Commission Directive 2008/58/EC of 21 August 2008 amending, for the purpose of its adaptation to technical progress, for the 30th time, Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (Text with EEA relevance)
Date: 2008-08-21
Institutions: European Commission
Subjects: approximation of laws, chemical product, dangerous substance, labelling, packaging

15.9.2008

EN

Official Journal of the European Union

L 246/1

I

(Acts adopted under the EC Treaty/Euratom Treaty whose publication is obligatory)

DIRECTIVES

COMMISSION DIRECTIVE 2008/58/EC

of 21 August 2008

amending, for the purpose of its adaptation to technical progress, for the 30th time, Council Directive
67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to
the classification, packaging and labelling of dangerous substances

(Text with EEA relevance)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,

Having regard to the Treaty establishing the European Commu-
nity,

Having regard to Council Directive 67/548/EEC of 27 June 1967
on the approximation of the laws, regulations and administrative
provisions relating to the classification, packaging and labelling
of dangerous substances (1), and in particular Article 28 thereof,

Whereas:

(1) Annex I

together with particulars of

to Directive 67/548/EEC contains a list of
dangerous substances,
the
classification and labelling of each substance. That list needs
to be updated to include further notified new substances
and further existing substances, as well as to adapt certain
entries to technical progress. In addition, it is necessary, in
that Annex, to delete entries for certain substances. The
classification and labelling of
containing
benzene should be changed in order to reflect that benzene
is classified as a mutagen and some entries should be split
because the newly added or
revised physico-chemical
classification no longer applies to all the substances under
those entries.

substances

discussion of the classification of Nickel substances or any
new relevant scientific findings or interpretations given to
the data used to establish the current proposals for the
Nickel compounds concerned by this Directive.

(3) Certain notes in the foreword of Annex I should be
amended or added to clarify the obligations on manufac-
turers, distributors and importers of certain substances, to
reflect that benzene has, in addition to other effects, been
classified as mutagenic, and to reflect that the classification
and labelling in Annex I relating to physico-chemical
properties need not be applied when testing shows that the
specific form of a substance marketed has different physico-
chemical properties. Note 6 in the foreword of Annex I
should be deleted as the provisions of this note no longer
apply from the date on which Commission Directive 2001/
60/EC (2) enters into force. Consequently, the reference to
Note 6 should be deleted from certain entries in the Annex.
A new Note 7 should be added to the foreword of Annex I
to reflect that alloys containing nickel are to be classified for
sensitisation on the basis of their release rate rather than on
the concentration of nickel.

(2)

The classification and labelling of the substances listed in
this Directive should be reviewed if new scientific knowl-
edge becomes available. In this respect, considering recent
preliminary, partial and not peer-reviewed information
submitted by industry, special attention should be paid to
further results of epidemiological studies on the Borates
concerned by this Directive including the ongoing study
the IARC
conducted in China and the outcome of

(4)

in this Directive are in
The measures provided for
accordance with the opinion of the Committee on the
Adaptation to Technical Progress of the Directives for the
Elimination of Technical Barriers to Trade with Dangerous
Substances and Preparations,

(1) OJ L 196, 16.8.1967, p. 1.

(2) OJ L 226, 22.8.2001, p. 5.

L 246/2

EN

Official Journal of the European Union

15.9.2008

HAS ADOPTED THIS DIRECTIVE:

Article 1

Annex I of Directive 67/548/EEC is amended as follows:

1.

the foreword is amended as follows:

(a) Note H is replaced by the text set out in Annex 1A;

(b) Note J is replaced by the text set out in Annex 1B;

(c) Note P is replaced by the text set out in Annex 1C;

(d) The text set out in Annex 1D is added as Note T;

(e) Note 6 is deleted;

(f)

The text set out in Annex 1E is added as Note 7;

the entries corresponding to the entries set out in Annex 1F
are replaced by the entries set out in that Annex;

The entries set out in Annex 1G to this Directive are
inserted in accordance with the order of the entries set out
in Annex I to Directive 67/548/EEC;

2.

3.

4.

Directive by 1 June 2009 at the latest. They shall forthwith
communicate to the Commission the text of those provisions
and a correlation table between those provisions and this
Directive.

When Member States adopt those provisions, they shall contain a
reference to this Directive or be accompanied by such a reference
on the occasion of their official publication. Member States shall
determine how such reference is to be made.

2. Member States shall communicate to the Commission the
text of the main provisions of national law which they adopt in
the field covered by this Directive.

Article 3

This Directive shall enter into force on the 20th day following
that of its publication in the Official Journal of the European Union.

Article 4

This Directive is addressed to the Member States.

The entries set out in Annex 1H to this Directive are
deleted.

Done at Brussels, 21 August 2008.

Article 2

1. Member States shall bring into force the laws, regulations
and administrative provisions necessary to comply with this

For the Commission

Stavros DIMAS

Member of the Commission

15.9.2008

EN

Official Journal of the European Union

L 246/3

ANNEX 1A

‘Note H:

The classification and label shown for this substance applies to the dangerous property(ies) indicated by the risk phrase(s) in
combination with the category(ies) of danger shown. The manufacturers, distributors and importers of this substance shall
be obliged to carry out an investigation to make themselves aware of the relevant and accessible data which exists for all
other properties to classify and label the substance. The final label shall follow the requirements of section 7 of Annex VI of
this Directive.’

ANNEX 1B

‘Note J:

The classification as a carcinogen or mutagen need not apply if it can be shown that the substance contains less than 0,1 %
w/w benzene (Einecs No 200-753-7). This note applies only to certain complex coal- and oil-derived substances in Annex I.’

ANNEX 1C

‘Note P:

The classification as a carcinogen or mutagen need not apply if it can be shown that the substance contains less than 0,1 %
w/w benzene (Einecs No 200-753-7).

When the substance is classified as a carcinogen or mutagen, Note E shall also apply.

When the substance is not classified as a carcinogen or mutagen at least the S-phrases (2-)23-24-62 shall apply.

This note applies only to certain complex oil-derived substances in Annex I.’

ANNEX 1D

‘Note T:

This substance may be marketed in a form which does not have the physico-chemical properties as indicated by the
classification in the Annex I entry. If the result(s) of the relevant Annex V test method(s) show(s) that the specific form of the
substance marketed does not exhibit this (these) property (properties), the substance shall be classified in accordance with
the results(s) of this (these) test(s). Relevant information, including reference to the relevant Annex V test(s) method(s),
should be included in the safety data sheet.’

ANNEX 1E

‘Note 7:

Alloys containing nickel are classified for skin sensitisation when the release rate of 0,5 μg Ni/cm2/week, as measured by the
European Standard reference test method EN 1811, is exceeded.’

ANNEX 1F

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

‘006-011-00-7

carbaryl (ISO);
1-naphthyl methylcarbamate

200-555-0

63-25-2

Carc. Cat. 3; R40
Xn; R20/22
N; R50

Xn; N
R: 20/22-40-50
S: (2-)36/37-46-61

C ≥ 25 %: Xn, N; R20/22-40-50
1 % ≤ C < 25 %: Xn, N; R40-50
0,25 % ≤ C < 1 %: N; R50

006-045-00-2

methomyl (ISO);
1-(methylthio)ethylideneamino
N-methylcarbamate

240-815-0

16752-77-5

T+; R28
N; R50-53

T+; N
R: 28-50/53
S: (1/2-)28-36/37-45-60-
61

006-087-00-1

furathiocarb (ISO);
2,3-dihydro-2,2-dimethyl-7-ben-
zofuryl 2,4-dimethyl-6-oxa-5-
oxo-3-thia-2,4-diazadecanoate

265-974-3

65907-30-4

T+; R26
T; R25
Xn; R48/22
Xi; R36/38
R43
N; R50-53

T+; N
R: 25-26-36/38-43-48/
22-50/53
S: (1/2-)28-36/37-38-45-
60-61

C ≥ 7 %: T+, N; R28-50/53
1 % ≤ C < 7 %: T, N; R25-50/53
0,25 % ≤ C < 1 %: Xn, N; R22-50/
53
0,1 % ≤ C < 0,25 %: Xn, N; R22-
51/53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

C ≥ 25 %: T+, N; R25-26-36/38-
43-48/22-50/53
20 % ≤ C < 25 %: T+, N; R22-26-
36/38-43-48/22-50/53
10 % ≤ C < 20 %: T+, N; R22-26-
43-48/22-50/53
7 % ≤ C < 10 %: T+, N; R22-26-43-
50/53
3 % ≤ C < 7 %: T, N; R22-23-43-
50/53
1 % ≤ C < 3 %: T, N; R23-43-50/53
0,25 % ≤ C < 1 %: Xn, N; R20-50/
53
0,1 % ≤ C < 0,25 %: Xn, N; R20-
51/53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

L

2
4
6
/
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

007-007-00-8

ethyl nitrate

210-903-3

625-58-1

E; R3

009-001-00-0

fluorine

231-954-8

7782-41-4

O; R8
T+; R26
C; R35

E
R: 3
S: (2-)23-24/25

O; T+; C
R: 8-26-35
S: (1/2-)9-26-28-36/37/
39-45

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

013-002-00-1

aluminium powder (stabilised)

T

231-072-3

7429-90-5

F; R11-15

F
R: 11-15
S: (2-)7/8-43

015-003-00-2

calcium phosphide;
tricalcium diphosphide

215-142-0

1305-99-3

015-004-00-8

aluminium phosphide

244-088-0

20859-73-8

015-005-00-3

magnesium phosphide;
trimagnesium diphosphide

235-023-7

12057-74-8

015-006-00-9

trizinc diphosphide;
zinc phosphide

T

215-244-5

1314-84-7

015-019-00-X

dichlorvos (ISO);
2,2-dichlorovinyl dimethyl phos-
phate

200-547-7

62-73-7

F; R15/29
T+; R28
N; R50

F; R15/29
T+; R28
R32
N; R50

F; R15/29
T+; R28
N; R50

F; R15/29
T+; R28
R32
N; R50-53

T+; R26
T; R24/25
R43
N; R50

F; T+; N
R: 15/29-28-50
S: (1/2-)22-28-36/37-43-
45-61

C ≥ 7 %: T+, N; R28-50
1 % ≤ C < 7 %: T, N; R25-50
0,25 % ≤ C < 1 %: Xn, N; R22-50
0,1 % ≤ C < 0,25 %: Xn; R22

F; T+; N
R: 15/29-28-32-50
S: (1/2-)3/9/14-28-30-36/
37-43-45-61

C ≥ 7 %: T+, N; R28-50
1 % ≤ C < 7 %: T, N; R25-50
0,25 % ≤ C < 1 %: Xn, N; R22-50
0,1 % ≤ C < 0,25 %: Xn; R22

F; T+; N
R: 15/29-28-50
S: (1/2-)22-28-43-45-61

C ≥ 7 %: T+, N; R28-50
1 % ≤ C < 7 %: T, N; R25-50
0,25 % ≤ C < 1 %: Xn, N; R22-50
0,1 % ≤ C < 0,25 %: Xn; R22

F; T+; N
R: 15/29-28-32-50/53
S: (1/2-)28-30-36/37-43-
45-60-61

T+; N
R: 24/25-26-43-50
S: (1/2-)28-36/37-45-61

C ≥ 7 %: T+, N; R28-50/53
1 % ≤ C < 7 %: T, N; R25-50/53
0,25 % ≤ C < 1 %: Xn, N; R22-50/
53
0,1 % ≤ C < 0,25 %: Xn, N; R22-
R51/53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

C ≥ 25 %: T+, N; R24/25-26-43-50
7 % ≤ C < 25 %: T+, N; R21/22-26-
43-50
3 % ≤ C < 7 %: T, N; R21/22-23-
43-50
1 % ≤ C < 3 %: T, N; R23-43-50
0,1 % ≤ C < 1 %: Xn, N; R20-50
0,025 % ≤ C < 0,1 %: N; R50

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

015-048-00-8

fenthion (ISO);
O,O-dimethyl-O-(4-methylthion-
m-tolyl) phosphorothioate

200-231-9

55-38-9

Muta. Cat. 3; R68
T; R23-48/25
Xn; R21/22
N; R50-53

T; N
R: 21/22-23-48/25-68-
50/53
S: (1/2-)36/37-45-60-61

015-056-00-1

azinphos-ethyl (ISO);
O,O-diethyl 4-oxobenzotriazin-
3-ylmethyl phosphorodithioate

220-147-6

2642-71-9

T+; R28
T; R24
N; R50-53

T+; N
R: 24-28-50/53
S: (1/2-)28-36/37-45-60-
61

015-067-00-1

phosalone (ISO);
S-(6-chloro-2-oxobenzoxazolin-
3-ylmethyl) O,O-diethyl phos-
phorodithioate

218-996-2

2310-17-0

T; R25
Xn; R20/21
R43
N; R50-53

T; N
R: 20/21-25-43-50/53
S: (1/2-)36/37-45-60-61

015-114-00-6

chlormephos (ISO);
S-chloromethyl O,O-diethyl
phosphorodithioate

246-538-1

24934-91-6

T+; R27/28
N; R50-53

T+; N
R: 27/28-50/53
S: (1/2-)27-28-36/37-45-
60-61

C ≥ 25 %: T, N; R21/22-23-48/25-
68-50/53
10 % ≤ C < 25 %: T, N; R20-48/25-
68-50/53
3 % ≤ C < 10 %: Xn, N; R20-48/22-
68-50/53
1 % ≤ C < 3 %: Xn, N; R48/22-68-
50/53
0,25 % ≤ C < 1 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

C ≥ 25 %: T+, N; R24-28-50/53
7 % ≤ C < 25 %: T+, N; R21-28-50/
53
3 % ≤ C < 7 %: T, N; R21-25-50/53
1 % ≤ C < 3 %: T, N; R25-50/53
0,25 % ≤ C < 1 %: Xn, N; R22-50/
53
0,1 % ≤ C < 0,25 %: Xn, N; R22-
51/53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

C ≥ 25 %: T, N; R21-25-50/53
3 % ≤ C < 25 %: Xn, N; R22-50/53
0,025 % ≤ C < 3 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 7 %: T+, N; R27/28-50/53
2,5 % ≤ C < 7 %: T, N; R24/25-50/
53
1 % ≤ C < 2,5 %: T, N; R24/25-51/
53
0,25 % ≤ C < 1 %: Xn, N; R21/22-
51/53
0,1 % ≤ C < 0,25 %: Xn; R21/22-
52/53
0,025 % ≤ C < 0,1 %: R52/53

L

2
4
6
/
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

015-115-00-1

chlorthiophos (ISO);
[isomeric reaction mixture in
which O-2,5-dichlorophenyl-4-
methylthiophenyl O,O-diethyl
phosphorothioate predominates]

244-663-6

21923-23-9

T+; R28
T; R24
N; R50-53

T+; N
R: 24-28-50/53
S: (1/2-)28-36/37-45-60-
61

015-140-00-8

triazophos (ISO);
O,O-diethyl-O-1-phenyl-1H-
1,2,4-triazol-3-yl phosphor-
othioate

245-986-5

24017-47-8

T; R23/25
Xn; R21
N; R50-53

T; N
R: 21-23/25-50/53
S: (1/2-)36/37-45-60-61

C ≥ 25 %: T+, N; R24-28-50/53
7 % ≤ C < 25 %: T+, N; R21-28-50/
53
3 % ≤ C < 7 %: T, N; R21-25-50/53
1 % ≤ C < 3 %: T, N; R25-50/53
0,1 % ≤ C < 1 %: Xn, N; R22-50/53
0,025 % ≤ C < 0,1 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 25 %: T, N; R21-23/25-50/53
3 % ≤ C < 25 %: Xn, N; R20/22-50/
53
0,25 % ≤ C < 3 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

016-084-00-7

prosulfuron (ISO);
1-(4-methoxy-6-methyl-1,3,5-
triazin-2-yl)-3-[2-(3,3,3-trifluor-
opropyl)phenylsulfonyl]urea

—

94125-34-5

Xn; R22
N; R50-53

Xn; N
R: 22-50/53
S: (2-)60-61

C ≥ 25 %: Xn, N; R22-50/53
0,25 % ≤ C < 25 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

017-001-00-7

chlorine

231-959-5

7782-50-5

017-012-00-7

calcium hypochlorite

231-908-7

7778-54-3

T; R23
Xi; R36/37/38
N; R50

T; N
R: 23-36/37/38-50
S: (1/2-)9-45-61

C ≥ 25 %: T, N; R23-36/37/38-50
20 % ≤ C < 25 %: Xn, N; R20-36/
37/38-50
3 % ≤ C < 20 %: Xn, N; R20-50
0,25 % ≤ C < 3 %: N; R50

O; R8
C; R34
Xn; R22
R31
N; R50

O; C; N
R: 8-22-31-34-50
S: (1/2-)26-36/37/39-45-
61

C ≥ 25 %: C, N; R22-34-50
10 % ≤ C < 25 %: C, N; R34-50
3 % ≤ C < 10 %: Xi, N; R37/38-41-
50
2,5 % ≤ C < 3 %: Xi, N; R36-50
0,5 % ≤ C < 2,5 %: Xi; R36

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

5

017-026-00-3

chlorine dioxide

233-162-8

10049-04-4

017-026-01-0

chlorine dioxide ... %

B

233-162-8

10049-04-4

027-004-00-5

cobalt dichloride

E

231-589-4

7646-79-9

027-005-00-0

cobalt sulfate

E

233-334-2

10124-43-3

O; R8
R6
T+; R26
C; R34
N; R50

T; R25
C; R34
N; R50

O; T+; N
R: 6-8-26-34-50
S: (1/2-)23-26-28-36/37/
39-38-45-61

C ≥ 5 %: T+, N; R26-34-50
2,5 % ≤ C < 5 %: T+, N; R26-36/
37/38-50
1 % ≤ C < 2,5 %: T+; R26-36/37/38
0,5 % ≤ C < 1 %: T; R23-36/37/38
0,2 % ≤ C < 0,5 %: T; R23
0,02 % ≤ C < 0,2 %: Xn; R20

T; N
R: 25-34-50
S: (1/2-)23-26-28-36/37/
39-45-61

C ≥ 25 %: T, N; R25-34-50
10 % ≤ C < 25 %: C, N; R22-34-50
3 % ≤ C < 10 %: Xn, N; R22-36/37/
38-50
2,5 % ≤ C < 3 %: Xi, N; R36-50
0,3 % ≤ C < 2,5 %: Xi; R36

Carc. Cat. 2; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R60
Xn; R22
R42/43
N; R50-53

T; N
R: 49-60-22-42/43-68-
50/53
S: 53-45-60-61

Carc. Cat. 2; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R60
Xn; R22
R42/43
N; R50-53

T; N
R: 49-60-22-42/43-68-
50/53
S: 53-45-60-61

1

1

C ≥ 25 %: T, N; R49-60-22-42/43-
68-50/53
2,5 % ≤ C < 25 %: T, N; R49-60-
42/43-68-50/53
1 % ≤ C < 2,5 %: T, N; R49-60-42/
43-68-51/53
0,5 % ≤ C < 1 %: T, N; R49-60-51/
53
0,25 % ≤ C < 0,5 %: T, N; R49-51/
53
0,025 % ≤ C < 0,25 %: T; R49-52/
53
0,01 % ≤ C < 0,025 %: T; R49

C ≥ 25 %: T, N; R49-60-22-42/43-
68-50/53
2,5 ≤ C < 25 %: T, N; R49-60-42/
43-68-50/53
1 % ≤ C < 2,5 %: T, N; R49-60-42/
43-68-51/53
0,5 % ≤ C < 1 %: T, N; R49-60-51/
53
0,25 % ≤ C < 0,5 %: T, N; R49-51/
53
0,025 % ≤ C < 0,25 %: T; R49-52/
53
0,01 % ≤ C < 0,025 %: T; R49

L

2
4
6
/
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

231-111-4

7440-02-0

Carc. Cat. 3; R40
T; R48/23
R43

T
R: 40-43-48/23
S: (2-)36/37/39-45

S

E

E

028-002-00-7

nickel

028-009-00-5

nickel sulfate

028-010-00-0

nickel carbonate;
basic nickel carbonate;
carbonic acid, nickel (2+) salt; [1]
carbonic acid, nickel salt; [2]
[μ-[carbonato(2-)-O:O’]] dihy-
droxy trinickel; [3]
[carbonato(2-)] tetrahydroxytri-
nickel [4]

232-104-9

7786-81-4

222-068-2 [1]
240-408-8 [2]
265-748-4 [3]
235-715-9 [4]

3333-67-3 [1]
16337-84-1 [2]
65405-96-1 [3]
12607-70-4 [4]

Carc. Cat. 1; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R61
T; R48/23
Xn; R20/22
Xi; R38
R42/43
N; R50-53

Carc. Cat. 1; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R61
T; R48/23
Xn; R20/22
Xi; R38
R42/43
N; R50-53

Carc. Cat. 3; R40
Xi; R36/37

042-001-00-9

molybdenum trioxide

215-204-7

1313-27-5

042-002-00-4

tetrakis(dimethylditetradecylam-
monium) hexa-μ-oxotetra-μ3-
oxodi-μ5-oxotetradecaoxoocta-
molybdate(4-)

404-760-8

117342-25-3

T; R23
Xi; R41

080-006-00-8

dimercury dicyanide oxide;
mercuric oxycyanide

215-629-8

1335-31-5

E; R2
T; R23/24/25
R33
N; R50-53

.

.

1
5
9
2
0
0
8

Notes
related to
prepa-
rations

7

C ≥ 25 %: T, N; R49-61-20/22-38-
42/43-48/23-68-50/53
20 % ≤ C < 25 %: T, N; R49-61-38-
42/43-48/23-68-51/53
2,5 % ≤ C < 20 %: T, N; R49-61-
42/43-48/23-68-51/53
1 % ≤ C < 2,5 %: T; R49-61-42/43-
48/23-68-52/53
0,5 % ≤ C < 1 %: T; R49-61-43-48/
20-52/53
0,25 % ≤ C < 0,5 %: T; R49-43-48/
20-52/53
0,1 % ≤ C < 0,25 %: T; R49-43-48/
20
0,01 % ≤ C < 0,1 %: Xi; R43

T; N
R: 49-61-20/22-38-42/
43-48/23-68-50/53
S: 53-45-60-61

T; N
R: 49-61-20/22-38-42/
43-48/23-68-50/53
S: 53-45-60-61

Xn
R: 36/37-40
S: (2-)22-36/37

T
R: 23-41
S: (1/2-)26-36/37/39-45

E; T; N
R: 2-23/24/25-33-50/53
S: (1/2-)28-36/37-45-60-
61

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

082-004-00-2

lead chromate

231-846-0

7758-97-6

082-009-00-X

lead sulfochromate yellow;
C.I. Pigment Yellow 34;
[This substance is identified in
the Colour Index by Colour Index
Constitution Number, C.I.
77603.]

082-010-00-5

lead chromate molybdate sulfate
red;
C.I. Pigment Red 104;
[This substance is identified in
the Colour Index by Colour Index
Constitution Number, C.I.
77605.]

601-006-00-1

pentane; [1]
isopentane;
2-methylbutane [2]

601-007-00-7

hexane (containing < 5 % n-
hexane (203-777-6));
2-methylpentane; [1]
3-methylpentane; [2]
2,2-dimethylbutane; [3]
2,3-dimethylbutane [4]

215-693-7

1344-37-2

235-759-9

12656-85-8

C

C

203-692-4 [1]
201-142-8 [2]

109-66-0 [1]
78-78-4 [2]

203-523-4 [1]
202-481-4 [2]
200-906-8 [3]
201-193-6 [4]

107-83-5 [1]
96-14-0 [2]
75-83-2 [3]
79-29-8 [4]

Carc. Cat. 2; R45
Repr. Cat. 1; R61
Repr. Cat. 3; R62
R33
N; R50-53

Carc. Cat. 2; R45
Repr. Cat. 1; R61
Repr. Cat. 3; R62
R33
N; R50-53

Carc. Cat. 2; R45
Repr. Cat. 1; R61
Repr. Cat. 3; R62
R33
N; R50-53

F+; R12
Xn; R65
R66
R67
N; R51-53

F; R11
Xn; R65
Xi; R38
R67
N; R51-53

T; N
R: 45-61-33-62-50/53
S: 53-45-60-61

T; N
R: 45-61-33-62-50/53
S: 53-45-60-61

T; N
R: 45-61-33-62-50/53
S: 53-45-60-61

F+; Xn; N
R: 12-65-66-67-51/53
S: (2-)9-16-29-33-61-62

F; Xn; N
R: 11-38-65-67-51/53
S: (2-)9-16-29-33-61-62

1

1

1

4

4

L

2
4
6
/
1
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

F; Xn; N
R: 11-38-65-67-50/53
S: (2-)9-16-29-33-60-61-
62

F; Xn; N
R: 11-38-65-67-50/53
S: (2-)9-16-29-33-60-61-
62

601-008-00-2

601-009-00-8

C

C

heptane;
n-heptane; [1]
2,4-dimethylpentane; [2]
2,2,3-trimethylbutane; [3]
3,3-dimethylpentane; [4]
2,3-dimethylpentane; [5]
3-methylhexane; [6]
2,2-dimethylpentane; [7]
2-methylhexane; [8]
3-ethylpentane; [9]
isoheptane; [10]

octane;
n-octane; [1]
2,2,4-trimethylpentane; [2]
2,3,3-trimethylpentane; [3]
3,3-dimethylhexane; [4]
2,2,3-trimethylpentane; [5]
2,3,4-trimethylpentane; [6]
3,4-dimethylhexane; [7]
2,3-dimethylhexane; [8]
2,4-dimethylhexane; [9]
4-methylheptane; [10]
3-methylheptane; [11]
2,2-dimethylhexane; [12]
2,5-dimethylhexane; [13]
2-methylheptane; [14]
2,2,3,3-tetramethylbutane; [15]
3-ethyl-2-methylpentane; [16]
3-ethylhexane; [17]
3-ethyl-3-methylpentane; [18]
isooctane; [19]

F; R11
Xn; R65
Xi; R38
R67
N; R50-53

F; R11
Xn; R65
Xi; R38
R67
N; R50-53

205-563-8 [1]
203-548-0 [2]
207-346-3 [3]
209-230-8 [4]
209-280-0 [5]
209-643-3 [6]
209-680-5 [7]
209-730-6 [8]
210-529-0 [9]
250-610-8 [10]

142-82-5 [1]
108-08-7 [2]
464-06-2 [3]
562-49-2 [4]
565-59-3 [5]
589-34-4 [6]
590-35-2 [7]
591-76-4 [8]
617-78-7 [9]
31394-54-4
[10]

203-892-1 [1]
208-759-1 [2]
209-207-2 [3]
209-243-9 [4]
209-266-4 [5]
209-292-6 [6]
209-504-7 [7]
209-547-1 [8]
209-649-6 [9]
209-650-1 [10]
209-660-6 [11]
209-689-4 [12]
209-745-8 [13]
209-747-9 [14]
209-855-6 [15]
210-187-2 [16]
210-621-0 [17]
213-923-0 [18]
247-861-0 [19]

111-65-9 [1]
540-84-1 [2]
560-21-4 [3]
563-16-6 [4]
564-02-3 [5]
565-75-3 [6]
583-48-2 [7]
584-94-1 [8]
589-43-5 [9]
589-53-7 [10]
589-81-1 [11]
590-73-8 [12]
592-13-2 [13]
592-27-8 [14]
594-82-1 [15]
609-26-7 [16]
619-99-8 [17]
1067-08-9 [18]
26635-64-3
[19]

601-017-00-1

cyclohexane

203-806-2

110-82-7

F; R11
Xn; R65
Xi; R38
R67
N; R50-53

F; Xn; N
R: 11-38-65-67-50/53
S: (2-)9-16-25-33-51-60-
61-62

4

4

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

601-018-00-7

methylcyclohexane

203-624-3

108-87-2

601-019-00-2

1,4-dimethylcyclohexane

209-663-2

589-90-2

601-021-00-3

toluene

203-625-9

108-88-3

601-033-00-9

benz[a]anthracene

200-280-6

56-55-3

601-037-00-0

n-hexane

203-777-6

110-54-3

601-041-00-2

dibenz[a,h]anthracene

200-181-8

53-70-3

4

4

4

4

F; R11
Xn; R65
Xi; R38
R67
N; R51-53

F; R11
Xn; R65
Xi; R38
R67
N; R51-53

F; R11
Repr.Cat.3; R63
Xn; R48/20-65
Xi; R38
R67

Carc. Cat. 2; R45
N; R50-53

F; Xn; N
R: 11-38-65-67-51/53
S: (2-)9-16-33-61-62

F; Xn; N
R: 11-38-65-67-51/53
S: (2-)9-16-33-61-62

F; Xn
R: 11-38-48/20-63-65-67
S: (2-)36/37-62

T; N
R: 45-50/53
S: 53-45-60-61

C ≥ 0,25 %: T, N; R45-50/53
0,1 % ≤ C < 0,25 %: T, N; R45-51/
53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

F; R11
Repr. Cat. 3; R62
Xn; R48/20-65
Xi; R38
R67
N; R51-53

F; Xn; N
R: 11-38-48/20-62-65-
67-51/53
S: (2-)9-16-29-33-36/37-
61-62

C ≥ 25 %: Xn, N; R38-48/20-62-
51/53
20 % ≤ C < 25 %: Xn; R38-48/20-
62-52/53
5 % ≤ C < 20 %: Xn; R48/20-62-
52/53
2,5 % ≤ C < 5 %: R52/53

Carc. Cat. 2; R45
N; R50-53

T; N
R: 45-50/53
S: 53-45-60-61

C ≥ 0,25 %: T, N; R45-50/53
0,025 % ≤ C < 0,25 %: T, N; R45-
51/53
0,01 % ≤ C < 0,025 %: T; R45-52/
53
0,0025 % ≤ C < 0,01 %: R52/53

L

2
4
6
/
1
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

602-050-00-4

isodrin;
(1α,4α,4aβ,5β,8β,8aβ)-
1,2,3,4,10,10-hexachloro-
1,4,4a,5,8,8a-hexahydro-1,4:5,8-
dimethanonaphthalene

207-366-2

465-73-6

T+; R26/27/28
N; R50-53

T+; N
R: 26/27/28-50/53
S: (1/2-)13-28-36/37-45-
60-61

C ≥ 7 %: T+, N; R26/27/28-50/53
1 % ≤ C < 7 %: T, N; R23/24/25-
50/53
0,25 % ≤ C < 1 %: Xn, N; R20/21/
22-50/53
0,1 % ≤ C < 0,25 %: Xn, N; R20/21/
22-51/53
0,025 % ≤ C < 0,1 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

602-052-00-5

endosulfan (ISO);
1,2,3,4,7,7-hexachloro-8,9,10-
trinorborn-2-en-5,6-ylenedi-
methyl sulfite;
1,4,5,6,7,7-hexachloro-8,9,10-
trinorborn-5-en-2,3-ylenedi-
methylene) sulfite

204-079-4

115-29-7

T+; R26/28
Xn; R21
N; R50-53

T+; N
R: 21-26/28-50/53
S: (1/2-)28-36/37-45-60-
61-63

602-076-00-6

2,3,4-trichlorobut-1-ene

219-397-9

2431-50-7

Carc. Cat. 3; R40
T; R23
Xn; R22
Xi; R36/37/38
N; R50-53

T; N
R: 22-23-36/37/38-40-
50/53
S: (1/2-)36/37-45-60-61

C ≥ 25 %: T, N; R22-23-36/37/38-
40-50/53
20 % ≤ C < 25 %: Xn, N; R20-36/
37/38-40-51/53
3 % ≤ C < 20 %: Xn, N; R20-40-51/
53
2,5 % ≤ C < 3 %: Xn, N; R40-51/53
0,25 % ≤ C < 2,5 %: Xn; R40-52/53
0,1 % ≤ C < 0,25 %: Xn; R40

602-080-00-8

alkanes, C10-13, chloro;
chlorinated paraffins, C10-13

287-476-5

85535-84-8

Carc. Cat. 3; R40
R66
N; R50-53

Xn; N
R: 40-66-50/53
S: (2-)24-36/37-46-60-61

603-003-00-0

propan-1-ol;
n-propanol

200-746-9

71-23-8

603-004-00-6

butan-1-ol;
n-butanol

200-751-6

71-36-3

F; R11
Xi; R41
R67

R10
Xn; R22
Xi; R37/38-41
R67

F; Xi
R: 11-41-67
S: (2-)7-16-24-26-39

Xn
R: 10-22-37/38-41-67
S: (2-)7/9-13-26-37/39-46

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

603-022-00-4

diethyl ether;
ether

200-467-2

60-29-7

603-032-00-9

ethylene dinitrate;
ethylene glycol dinitrate

211-063-0

628-96-6

F+; R12
R19
Xn; R22
R66
R67

E; R3
T+; R26/27/28
R33

603-037-00-6

cellulose nitrate;
nitrocellulose, containing more
than 12,6 % nitrogen

—

—

E; R3

603-045-00-X

diisopropyl ether; [1]
dipropyl ether [2]

C

203-560-6 [1]
203-869-6 [2]

108-20-3 [1]
111-43-3 [2]

F; R11
R19
R66
R67

F+; Xn
R: 12-19-22-66-67
S: (2-)9-16-29-33

E; T+
R: 3-26/27/28-33
S: (1/2-)27/28-33-35-36/
37-45

E
R: 3
S: (2-)35

F
R: 11-19-66-67
S: (2-)9-16-29-33

603-085-00-8

bronopol (INN);
2-bromo-2-nitropropane-1,3-
diol

200-143-0

52-51-7

Xn; R21/22
Xi; R37/38-41
N; R50

Xn; N
R: 21/22-37/38-41-50
S: (2-)26-36/37/39-61

603-108-00-1

2-methylpropan-1-ol;
iso-butanol

201-148-0

78-83-1

R10
Xi; R37/38-41
R67

Xi
R: 10-37/38-41-67
S: (2-)7/9-13-26-37/39-46

603-117-00-0

603-127-00-5

propan-2-ol;
isopropyl alcohol;
isopropanol

butan-2-ol; [1]
(S)-butan-2-ol; [2]
(R)-butan-2-ol; [3]
(±)-butan-2-ol [4]

200-661-7

67-63-0

F; R11
Xi; R36
R67

F; Xi
R: 11-36-67
S: (2-)7-16-24/25-26

C

201-158-5 [1]
224-168-1 [2]
238-967-8 [3]
240-029-8 [4]

78-92-2 [1]
4221-99-2 [2]
14898-79-4 [3]
15892-23-6 [4]

R10
Xi; R36/37
R67

Xi
R: 10-36/37-67
S: (2-)7/9-13-24/25-26-46

C ≥ 25 %: Xn, N; R21/22-37/38-
41-50
20 % ≤ C < 25 %: Xi, N; R37/38-
41-50
10 % ≤ C < 20 %: Xi, N; R41-50
5 % ≤ C < 10 %: Xi, N; R36-50
2,5 % ≤ C < 5 %: N; R50

L

2
4
6
/
1
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

604-005-00-4

1,4-dihydroxybenzene;
hydroquinone;
quinol

204-617-8

123-31-9

604-030-00-0

bisphenol A;
4,4'-isopropylidenediphenol

201-245-8

80-05-7

604-055-00-7

2,2'-((3,3',5,5'-tetramethyl-(1,1'-
biphenyl)-4,4'-diyl)-bis(oxy-
methylene))-bis-oxirane

413-900-7

85954-11-6

605-010-00-4

2-furaldehyde

202-627-7

98-01-1

606-001-00-8

acetone;
propan-2-one;
propanone

200-662-2

67-64-1

606-002-00-3

butanone;
ethyl methyl ketone

201-159-0

78-93-3

606-006-00-5

pentan-3-one;
diethyl ketone

202-490-3

96-22-0

Carc. Cat. 3; R40
Muta. Cat. 3; R68
Xn; R22
Xi; R41
R43
N; R50

Repr. Cat. 3; R62
Xi; R37-41
R43
R52

Carc. Cat. 3; R40
R43

Carc. Cat. 3; R40
T; R23/25
Xn; R21
Xi; R36/37/38

F; R11
Xi; R36
R66
R67

F; R11
Xi; R36
R66
R67

F; R11
Xi; R37
R66
R67

Xn; N
R: 22-40-41-43-68-50
S: (2-)26-36/37/39-61

C ≥ 25 %: Xn, N; R22-40-41-43-
68-50
10 % ≤ C < 25 %: Xn, N; R40-41-
43-68-50
5 % ≤ C < 10 %: Xn, N; R36-40-43-
68-50
2,5 % ≤ C < 5 %: Xn, N; R40-43-
68-50
1 % ≤ C < 2,5 %: Xn; R40-43-68

Xn
R: 37-41-43-62-52
S: (2-)26-36/37-39-46-61

Xn
R: 40-43
S: (2-)22-36/37

T
R: 21-23/25-36/37/38-40
S: (1/2-)26-36/37-45

F; Xi
R: 11-36-66-67
S: (2-)9-16-26-46

F; Xi
R: 11-36-66-67
S: (2-)9-16

F; Xi
R: 11-37-66-67
S: (2-)9-16-25-33

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

606-013-00-3

p-benzoquinone;
quinone

203-405-2

106-51-4

T; R23/25
Xi; R36/37/38
N; R50

T; N
R: 23/25-36/37/38-50
S: (1/2-)26-28-45-61

C ≥ 25 %: T, N; R23/25-36/37/38-
50
20 % ≤ C < 25 %: Xn, N; R20/22-
36/37/38-50
3 % ≤ C < 20 %: Xn, N; R20/22-50
2,5 % ≤ C < 3 %: N; R50

606-030-00-6

hexan-2-one;
methyl butyl ketone;
butyl methyl ketone;
methyl-n-butyl ketone

209-731-1

591-78-6

R10
Repr. Cat. 3; R62
T; R48/23
R67

T
R: 10-48/23-62-67
S: (1/2-)36/37-45

C ≥ 10 %: T; R48/23-62
5 % ≤ C < 10 %: Xn; R48/20-62
1 % ≤ C < 5 %: Xn; R48/20

606-034-00-8

metribuzin (ISO);
4-amino-6-tert-butyl-3-
methylthio-1,2,4-triazin-5(4H)-
one;
4-amino-4,5-dihydro-6-(1,1-
dimethylethyl)-3-methylthio-
1,2,4-triazin-5-one

244-209-7

21087-64-9

Xn; R22
N; R50-53

Xn; N
R: 22-50/53
S: (2-)60-61

C ≥ 25 %: Xn, N; R22-50/53
2,5 % ≤ C < 25 %: N; R50/53
0,25 % ≤ C < 2,5 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

607-003-00-1

chloroacetic acid

201-178-4

79-11-8

607-016-00-2

propyl formate; [1]
isopropyl formate [2]

C

203-798-0 [1]
210-901-2 [2]

110-74-7 [1]
625-55-8 [2]

607-021-00-X

methyl acetate

201-185-2

79-20-9

607-022-00-5

ethyl acetate

205-500-4

141-78-6

T; R23/24/25
C; R34
N; R50

F; R11
Xi; R36/37
R67

F; R11
Xi; R36
R66
R67

F; R11
Xi; R36
R66
R67

T; N
R: 23/24/25-34-50
S: (1/2-)26-36/37/39-45-
61-63

C ≥ 25 %: T, N; R23/24/25-34-50
10 % ≤ C < 25 %: C; R20/21/22-34
5 % ≤ C < 10 %: Xn; R20/21/22-
36/37/38
3 % ≤ C < 5 %: Xn; R20/21/22

F; Xi
R: 11-36/37-67
S: (2-)9-16-24-33

F; Xi
R: 11-36-66-67
S: (2-)16-26-29-33

F; Xi
R: 11-36-66-67
S: (2-)16-26-33

L

2
4
6
/
1
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

607-024-00-6

propyl acetate; [1]
isopropyl acetate [2]

Notes
related to
substances

C

203-686-1 [1]
203-561-1 [2]

109-60-4 [1]
108-21-4 [2]

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-025-00-1

n-butyl acetate

204-658-1

123-86-4

607-065-00-X

bromoacetic acid

201-175-8

79-08-3

F; R11
Xi; R36
R66
R67

R10
R66
R67

F; Xi
R: 11-36-66-67
S: (2-)16-26-29-33

R: 10-66-67
S: (2-)25

T; R23/24/25
C; R35
R43
N; R50

T; C; N
R: 23/24/25-35-43-50
S: (1/2-)26-36/37/39-45-
61

607-162-00-7

dalapon;
2,2-dichloropropionic acid; [1]
dalapon-sodium;
sodium 2,2-dichloropropionate
[2]

200-923-0 [1]
204-828-5 [2]

75-99-0 [1]
127-20-8 [2]

Xi; R38-41
R52-53

607-189-00-4

trimethylenediaminetetraacetic
acid

400-400-9

1939-36-2

607-213-00-3

ethyl 3,3-bis(tert-pentylperoxy)
butyrate

403-320-2

67567-23-1

415-130-7

91465-08-6

607-252-00-6

lambda-cyhalothrin (ISO);
A 1:1 mixture of: (S)-α-cyano-3-
phenoxybenzyl(Z)-(1R)-cis-3-(2-
chloro-3,3,3-trifluoropropenyl)-
2,2-dimethylcyclopropanecar-
boxylate;
(R)-α-cyano-3-phenoxybenzyl
(Z)-(1S)-cis-3-(2-chloro-3,3,3-tri-
fluoropropenyl)-2,2-dimethylcy-
clopropanecarboxylate

Xn; R22
Xi; R41

E; R3
O; R7
R10
N; R51-53

T+; R26
T; R25
Xn; R21
N; R50-53

Xi
R: 38-41-52/53
S: (2-)26-39-61

Xn
R: 22-41
S: (2-)22-26-39

E; N
R: 3-7-10-51/53
S: (2-)3/7-14-33-36/37/
39-61

T+; N
R: 21-25-26-50/53
S: (1/2-)28-36/37/39-38-
45-60-61

C ≥ 25 %: T+, N; R21-25-26-50/53
7 % ≤ C < 25 %: T+, N; R22-26-50/
53
3 % ≤ C < 7 %: T, N; R22-23-50/53
1 % ≤ C < 3 %: T, N; R23-50/53
0,1 % ≤ C < 1 %: Xn, N; R20-50/53
0,0025 % ≤ C < 0,1 %: N; R50/53
0,00025 % ≤ C < 0,0025 %: N;
R51/53
0,000025 % ≤ C < 0,00025 %:
R52/53

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-253-00-1

cyfluthrin (ISO);
α-cyano-4-fluoro-3-phenoxyben-
zyl-3-(2,2-dichlorovinyl)-2,2-
dimethylcyclopropanecarboxylate

269-855-7

68359-37-5

T+; R28
T; R23
N; R50-53

T+; N
R: 23-28-50/53
S: (1/2-)28-36/37/39-45-
60-61

C ≥ 25 %: T+, N; R23-28-50/53
7 % ≤ C < 25 %: T+, N; R20-28-50/
53
3 % ≤ C < 7 %: T, N; R20-25-50/53
1 % ≤ C < 3 %: T, N; R25-50/53
0,1 % ≤ C < 1 %: Xn, N; R22-50/53
0,025 % ≤ C < 0,1 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

607-319-00-X

deltamethrin (ISO);
(S)-α-cyano-3-phenoxybenzyl
(1R, 3R)-3-(2,2-dibromovinyl)-
2,2-dimethylcyclopropanecar-
boxylate

258-256-6

52918-63-5

T; R23/25
N; R50-53

T; N
R: 23/25-50/53
S: (1/2-)24-28-36/37/39-
38-45-60-61

C ≥ 25 %: T, N; R23/25-50/53
3 % ≤ C < 25 %: Xn, N; R20/22-50/
53
0,000025 % ≤ C < 3 %: N; R50/53
0,0000025 % ≤ C < 0,000025 %:
N; R51/53
0,00000025 % ≤ C <
0,0000025 %: R52/53

607-422-00-X

α-cypermethrin (ISO);
racemate comprising (R)-α-
cyano-3-phenoxybenzyl (1S,3S)-
3-(2,2-dichlorovinyl)-2,2-
dimethylcyclopropanecarboxy-
late;
(S)-α-cyano-3-phenoxybenzyl
(1R,3R)-3-(2,2-dichlorovinyl)-
2,2-dimethylcyclopropanecar-
boxylate

257-842-9

67375-30-8

T; R25
Xn; R48/22
Xi; R37
N; R50-53

T; N
R: 25-37-48/22-50/53
S: (1/2-)36/37/39-45-60-
61

C ≥ 25 %: T, N; R25-37-48/22-50/
53
20 % ≤ C < 25 %: Xn, N; R22-37-
48/22-50/53
10 % ≤ C < 20 %: Xn, N; R22-48/
22-50/53
3 % ≤ C < 10 %: Xn, N; R22-50/53
0,025 % ≤ C < 3 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

L

2
4
6
/
1
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

608-014-00-4

chlorothalonil (ISO);
tetrachloroisophthalonitrile

217-588-1

1897-45-6

Carc. Cat. 3; R40
T+; R26
Xi; R37-41
R43
N; R50-53

T+; N
R: 26-37-40-41-43-50/53
S: (1/2-)28-36/37/39-45-
60-61

C ≥ 20 %: T+, N; R26-37-40-41-
43-50/53
10 % ≤ C < 20 %: T+, N; R26-40-
41-43-50/53
7 % ≤ C < 10 %: T+, N; R26-40-36-
43-50/53
5 % ≤ C < 7 %: T, N; R23-40-36-
43-50/53
2,5 % ≤ C < 5 %: T, N; R23-40-43-
50/53
1 % ≤ C < 2,5 %: T, N; R23-40-43-
51/53
0,25 % ≤ C < 1 %: Xn, N; R20-51/
53
0,1 % ≤ C < 0,25 %: Xn; R20-52/53
0,025 % ≤ C < 0,1 %: R52/53

608-034-00-3

chlorfenapyr (ISO);
4-bromo-2-(4-chlorophenyl)-1-
ethoxymethyl-5-trifluoromethyl-
pyrrole-3-carbonitrile

—

122453-73-0

608-058-00-4

esfenvalerate (ISO);
(S)-α-cyano-3-phenoxybenzyl-(S)-
2-(4-chlorophenyl)-3-methylbu-
tyrate

—

66230-04-4

T; R23
Xn; R22
N; R50-53

T; R23/25
R43
N; R50-53

T; N
R: 22-23-50/53
S: (1/2-)13-36/37-45-60-
61

C ≥ 25 %: T, N; R23-22-50/53
3 % ≤ C < 25 %: Xn, N; R20-50/53
0,25 % ≤ C < 3 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

T; N
R: 23/25-43-50/53
S: (1/2-)24-36/37/39-45-
60-61

C ≥ 25 %: T, N; R23/25-43-50/53
3 % ≤ C < 25 %: Xn, N; R20/22-43-
50/53
1 % ≤ C < 3 %: Xi, N; R43-50/53
0,0025 % ≤ C < 1 %: N; R50/53
0,00025 % ≤ C < 0,0025 %: N;
R51/53
0,000025 % ≤ C < 0,00025 %:
R52/53

609-005-00-8

1,3,5-trinitrobenzene

202-752-7

99-35-4

609-009-00-X

2,4,6-trinitrophenol;
picric acid

201-865-9

88-89-1

E; R3
T+; R26/27/28
R33
N; R50-53

E; R3
R4
T; R23/24/25

E; T+; N
R: 3-26/27/28-33-50/53
S: (1/2-)28-36/37-45-60-
61

E; T
R: 3-4-23/24/25
S: (1/2-)28-35-36/37-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

609-018-00-9

2,4,6-trinitroresorcinol;
styphnic acid

201-436-6

82-71-3

E; R3
R4
Xn; R20/21/22

E; Xn
R: 3-4-20/21/22
S: (2-)35-36/37

609-023-00-6

dinocap (ISO);
(RS)-2,6-dinitro-4-octylphenyl
crotonates and (RS)-2,4-dinitro-
6-octylphenyl crotonates in
which “octyl” is a mixture of 1-
methylheptyl, 1-ethylhexyl and
1-propylpentyl groups

E

254-408-0

39300-45-3

Repr. Cat. 2; R61
Xn; R20/22-48/22
Xi; R38
R43
N; R50-53

T; N
R: 61-20/22-38-43-48/
22-50/53
S: 53-45-60-61

609-046-00-1

611-067-00-6

trifluralin (ISO) (containing
< 0.5 ppm NPDA);
α,α,α-trifluoro-2,6-dinitro-N,N-
dipropyl-p-toluidine (containing
< 0.5 ppm NPDA);
2,6-dinitro-N,N-dipropyl-4-tri-
fluoromethylaniline (containing
< 0.5 ppm NPDA);
N,N-dipropyl-2,6-dinitro-4-tri-
fluoromethylaniline (containing
< 0.5 ppm NPDA)

A mixture of: bis(tris(2-(2-
hydroxy(1-methyl)ethoxy)ethyl)
ammonium) 7-anilino-4-
hydroxy-3-(2-methoxy-5-methyl-
4-(4-sulfonatophenylazo)pheny-
lazo)naphthalene-2-sulfonate;
bis(tris(2-(2-hydroxy(2-methyl)
ethoxy)ethyl)ammonium) 7-ani-
lino-4-hydroxy-3-(2-methoxy-5-
methyl-4-(4-sulfonatophenylazo)
phenylazo)naphthalene-2-sulfo-
nate

216-428-8

1582-09-8

Carc. Cat. 3; R40
R43
N; R50-53

Xn; N
R: 40-43-50/53
S: (2-)36/37-46-60-61

406-910-8

—

Xn; R22
R52-53

Xn
R: 22-52/53
S: (2-)22-61

C ≥ 25 %: T, N; R61-20/22-38-43-
48/22-50/53
20 % ≤ C < 25 %: T, N; R61-38-43-
48/22-50/53
10 % ≤ C < 20 %: T, N; R61-43-48/
22-50/53
1 % ≤ C < 10 %: T, N; R61-43-50/
53
0,5 % ≤ C < 1 %: T, N; R61-50/53
0,25 % ≤ C < 0,5 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

C ≥ 2,5 %: Xn, N; R40-43-50/53
1 % ≤ C < 2,5 %: Xn, N; R40-43-
51/53
0,25 % ≤ C < 1 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

L

2
4
6
/
2
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

611-130-00-8

tetra-ammonium 2-[6-[7-(2-car-
boxylato-phenylazo)-8-hydroxy-
3,6-disulfonato-1-naphthyla-
mino]-4-hydroxy-1,3,5-triazin-2-
ylamino]benzoate

612-017-00-6

N-methyl-N-2,4,6-tetranitroani-
line;
tetryl

418-520-5

183130-96-3

Xi; R36
R52-53

207-531-9

479-45-8

612-018-00-1

bis(2,4,6-trinitrophenyl)amine;
hexyl

205-037-8

131-73-7

612-019-00-7

dipicrylamine, ammonium salt

220-639-0

2844-92-0

612-034-00-9

2-amino-4,6-dinitrophenol;
picramic acid

202-544-6

96-91-3

E; R3
T; R23/24/25
R33

E; R3
T+; R26/27/28
R33
N; R51-53

E; R3
T+; R26/27/28
R33
N; R51-53

E; R2
Xn; R20/21/22
R52-53

Xi
R: 36-52/53
S: (2-)26-39-61

E; T
R: 3-23/24/25-33
S: (1/2-)35-36/37-45-63

E; T+; N
R: 3-26/27/28-33-51/53
S: (1/2-)27/28-35-36/37-
45-61-63

E; T+; N
R: 3-26/27/28-33-51/53
S: (1/2-)27/28-36/37-45-
61-63

E; Xn
R: 2-20/21/22-52/53
S: (2-)35-36/37-46-61

612-057-00-4

piperazine;
[solid]

203-808-3

110-85-0

Repr. Cat. 3; R62-63
C; R34
R42/43

Xn; C
R: 34-42/43-62-63
S: (1/2-)22-26-36/37/39-
45

612-083-00-6

1-methyl-3-nitro-1-nitrosoguani-
dine

E

200-730-1

70-25-7

612-094-00-6

4-(2-chloro-4-trifluoromethyl)
phenoxy-2-fluoroaniline hydro-
chloride

402-190-4

113674-95-6

Carc. Cat. 2; R45
Xn; R20
Xi; R36/38
N; R51-53

T; R48/25
Xn; R22-48/20
Xi; R41
R43
N; R50-53

T; N
R: 45-20-36/38-51/53
S: 53-45-61

C ≥ 25 %: T, N; R45-20-36/38-51/
53
20 % ≤ C < 25 %: T; R45-36/38-
52/53
2,5 % ≤ C < 20 %: T; R45-52/53
0,01 % ≤ C < 2,5 %: T; R45

T; N
R: 22-41-43-48/20-48/
25-50/53
S: (1/2-)26-36/37/39-45-
60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
2
1

Index No

Chemical name

612-098-00-8

nitrosodipropylamine

612-122-00-7

hydroxylamine .... %
[> 55 % in aqueous solution]

Notes
related to
substances

E

B

232-259-2

7803-49-8

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

210-698-0

621-64-7

Carc. Cat. 2; R45
Xn; R22
N; R51-53

T; N
R: 45-22-51/53
S: 53-45-61

C ≥ 25 %: T, N; R45-22-51/53
2,5 % ≤ C < 25 %: T; R45-52/53
0,001 % ≤ C < 2,5 %: T; R45

612-123-00-2

hydroxylammonium chloride;
hydroxylamine hydrochloride; [1]
bis(hydroxylammonium) sulfate;
hydroxylamine sulfate (2:1) [2]

226-798-2 [1]
233-118-8 [2]

5470-11-1 [1]
10039-54-0 [2]

613-003-00-2

1,2,3,4-tetranitrocarbazole

—

6202-15-9

613-010-00-0

ametryn (ISO);
2-ethylamino-4-isopropylamino-
6-methylthio-1,3,5-triazine

212-634-7

834-12-8

Xn; R22
N; R50-53

E; R2
Carc. Cat. 3; R40
Xn; R21/22-48/22
Xi; R37/38-41
R43
N; R50

E; R2
Carc. Cat. 3; R40
Xn; R21/22-48/22
Xi; R36/38
R43
N; R50

E; R2
Xn; R20/21/22

E; Xn; N
R: 2-21/22-37/38-40-41-
43-48/22-50
S: (2-)26-36/37/39-61

E; Xn; N
R: 2-21/22-36/38-40-43-
48/22-50
S: (2-)36/37-61

E; Xn
R: 2-20/21/22
S: (2-)35-36/37

Xn; N
R: 22-50/53
S: (2-)36-60-61

C ≥ 25 %: Xn, N; R22-50/53
0,25 % ≤ C < 25 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

613-030-00-X

troclosene potassium; [1]
troclosene sodium [2]

T

218-828-8 [1]
220-767-7 [2]

2244-21-5 [1]
2893-78-9 [2]

E; R2
O; R8
Xn; R22
Xi; R36/37
R31
N; R50-53

E; Xn; N
R: 2-8-22-31-36/37-50/
53
S: (2-)8-26-41-45-60-61

C ≥ 25 %: Xn, N; R22-36/37-50/53
10 % ≤ C < 25 %: Xn, N; R22-31-
36/37-51/53
2,5 % ≤ C < 10 %: N; R51/53
0,25 % ≤ C < 2,5 %: R52/53

L

2
4
6
/
2
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

613-044-00-6

captan (ISO);
1,2,3,6-tetrahydro-N-(trichloro-
methylthio)phthalimide

205-087-0

133-06-2

Carc. Cat. 3; R40
T; R23
Xi; R41
R43
N; R50

T; N
R: 23-40-41-43-50
S: (1/2-)26-29-36/37/39-
45-61

613-045-00-1

folpet (ISO);
N-(trichloromethylthio)phthali-
mide

205-088-6

133-07-3

Carc. Cat. 3; R40
Xn; R20
Xi; R36
R43
N; R50

Xn; N
R: 20-36-40-43-50
S: (2-)36/37-46-61

613-060-00-3

resmethrin (ISO);
5-benzyl-3-furylmethyl (±)-cis-
trans-chrysanthemate

233-940-7

10453-86-8

Xn; R22
N; R50-53

Xn; N
R: 22-50/53
S: (2-)60-61

613-120-00-9

bioresmethrin (ISO);
(5-benzylfur-3-yl)methyl(1R)-
trans-2,2-dimethyl-3-(2-methyl-
propenyl)cyclopropanecarboxy-
late

613-139-00-2

metsulfuron-methyl (ISO);
2-(4-methoxy-6-methyl-1,3,5-
triazin-2-ylcarbamoylsulfamoyl)
benzoic acid

613-163-00-3

azimsulfuron (ISO);
1-(4,6-dimethoxypyrimidin-2-yl)-
3-[1-methyl-4-(2-methyl-2H-tet-
razol-5-yl)pyrazol-5-ylsulfonyl]
urea

249-014-0

28434-01-7

N; R50-53

—

74223-64-6

N; R50-53

—

120162-55-2

N; R50-53

N
R: 50/53
S: 60-61

N
R: 50/53
S: 60-61

N
R: 50/53
S: 60-61

C ≥ 25 %: T, N; R23-40-41-43-50
10 % ≤ C < 25 %: Xn, N; R20-40-
41-43-50
5 % ≤ C < 10 %: Xn, N; R20-36-40-
43-50
3 % ≤ C < 5 %: Xn, N; R20-40-43-
50
2,5 % ≤ C < 3 %: Xn, N; R40-43-50
1 % ≤ C < 2,5 %: Xn; R40-43

C ≥ 25 %: Xn, N; R20-36-40-43-50
20 % ≤ C < 25 %: Xn, N; R36-40-
43-50
2,5 % ≤ C < 20 %: Xn, N; R40-43-
50
1 % ≤ C < 2,5 %: Xn; R40-43

C ≥ 25 %: Xn, N; R22-50/53
0,025 % ≤ C < 25 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 0,025 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 0,025 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 0,025 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
2
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-164-00-9

flufenacet (ISO);
N-(4-fluorophenyl)-N-isopropyl-
2-(5-trifluoromethyl-[1,3,4]thia-
diazol-2-yloxy)acetamide

—

142459-58-3

Xn; R22-48/22
R43
N; R50-53

Xn; N
R: 22-43-48/22-50/53
S: (2-)13-24-37-60-61

C ≥ 25 %: Xn, N; R22-43-48/22-
50/53
10 % ≤ C < 25 %: Xn, N; R43-48/
22-50/53
1 % ≤ C < 10 %: Xi, N; R43-50/53
0,25 % ≤ C < 1 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

613-165-00-4

flupyrsulfuron-methyl-sodium
(ISO);
methyl 2-[[(4,6-dimethoxypyri-
midin-2-ylcarbamoyl)sulfamoyl]-
6-trifluoromethyl]nicotinate,
monosodium salt

613-166-00-X

flumioxazin (ISO);
N-(7-fluoro-3,4-dihydro-3-oxo-
4-prop-2-ynyl-2H-1,4-benzoxa-
zin-6-yl)cyclohex-1-ene-1,2-
dicarboxamide

—

144740-54-5

N; R50-53

N
R: 50/53
S: 60-61

C ≥ 0,25 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

—

103361-09-7

Repr. Cat. 2; R61
N; R50-53

T; N
R: 61-50/53
S: 53-45-60-61

613-169-00-6

9-vinylcarbazole

216-055-0

1484-13-5

Muta. Cat. 3; R68
Xn; R21/22
Xi; R38
R43
N; R50-53

Xn; N
R: 21/22-38-43-68-50/53
S: (2-)22-23-36/37-60-61

613-174-00-3

tetraconazole (ISO);
(+/-) 2-(2,4-dichlorophenyl)-3-
(1H-1,2,4-triazol-1-yl)propyl-
1,1,2,2-tetrafluoroethylether

407-760-6

112281-77-3

Xn; R20/22
N; R51-53

Xn; N
R: 20/22-51/53
S: (2-)36-61

C ≥ 0,5 %: T, N; R61-50/53
0,025 % ≤ C < 0,5 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

C ≥ 25 %: Xn, N; R21/22-38-43-
68-50/53
20 % ≤ C < 25 %: Xn, N; R38-43-
68-50/53
1 % ≤ C < 20 %: Xn, N; R43-68-50/
53
0,25 % ≤ C < 1 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

L

2
4
6
/
2
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-203-00-X

613-204-00-5

pyraflufen-ethyl (ISO);
2-chloro-5-(4-chloro-5-difluoro-
methoxy-1-methylpyrazol-3-yl)-
4-fluorophenoxyacetic acid ethyl
ester; [1]
pyraflufen (ISO);
2-chloro-5-(4-chloro-5-difluoro-
methoxy-1-methylpyrazol-3-yl)-
4-fluorophenoxyacetic acid [2]

oxadiargyl (ISO);
3-[2,4-dichloro-5-(2-propyny-
loxy)phenyl]-5-(1,1-dimethy-
lethyl)-1,3,4-oxadiazol-2(3H)-
one;
5-tert-butyl-3-[2,4-dichloro-5-
(prop-2-ynyloxy)phenyl]-1,3,4-
oxadiazol-2(3H)-one

614-005-00-6

colchicine

615-005-00-9

4,4'-methylenediphenyl diisocya-
nate;
diphenylmethane-4,4'-diisocya-
nate; [1]
2,2'-methylenediphenyl diisocya-
nate;
diphenylmethane-2,2'-diisocya-
nate; [2]
o-(p-isocyanatobenzyl)phenyl iso-
cyanate;
diphenylmethane-2,4'-diisocya-
nate; [3]
methylenediphenyl diisocyanate
[4]

E

C

— [1]
— [2]

N; R50-53

129630-19-9
[1]
129630-17-7
[2]

N
R: 50/53
S: 60-61

C ≥ 0,025 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

254-637-6

39807-15-3

Repr. Cat. 3; R63
Xn; R48/22
N; R50-53

Xn; N
R: 48/22-63-50/53
S: (2-)36/37-46-60-61

200-598-5

64-86-8

Muta. Cat. 2; R46
T+; R28

T+
R: 46-28
S: 53-45

202-966-0 [1]
219-799-4 [2]
227-534-9 [3]
247-714-0 [4]

101-68-8 [1]
2536-05-2 [2]
5873-54-1 [3]
26447-40-5 [4]

Carc. Cat. 3; R40
Xn; R20-48/20
Xi; R36/37/38
R42/43

Xn
R: 20-36/37/38-40-42/
43-48/20
S: (1/2-)23-36/37-45

C ≥ 10 %: Xn, N; R48/22-63-50/53
5 % ≤ C < 10 %: Xn, N; R63-50/53
0,025 % ≤ C < 5 %: N; R50/53
0,0025 % ≤ C < 0,025 %: N; R51/
53
0,00025 % ≤ C < 0,0025 %: R52/
53

2

C ≥ 25 %: Xn; R20-36/37/38-40-
42/43-48/20
10 % ≤ C < 25 %: Xn; R36/37/38-
40-42/43-48/20
5 % ≤ C < 10 %: Xn; R36/37/38-
40-42/43
1 % ≤ C < 5 %: Xn; R40-42/43
0,1 % ≤ C < 1 %: Xn; R42

615-022-00-1

methyl 3-isocyanatosulfonyl-2-
thiophene-carboxylate

410-550-7

79277-18-2

R14
Xn; R48/22
R42/43

Xn
R: 14-42/43-48/22
S: (2-)22-30-35-36/37-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
2
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

616-006-00-7

dichlofluanid (ISO);
N-dichlorofluoromethylthio-N',
N'-dimethyl-N-phenylsulfamide

214-118-7

1085-98-9

616-009-00-3

propanil (ISO);
3',4'-dichloropropionanilide

211-914-6

709-98-8

617-008-00-0

dibenzoyl peroxide;
benzoyl peroxide

202-327-6

94-36-0

Xn; R20
Xi; R36
R43
N; R50

Xn; R22
N; R50

E; R3
O; R7
Xi; R36
R43

Xn; N
R: 20-36-43-50
S: (2-)24-37-61

C ≥ 25 %: Xn, N; R20-36-43-50
20 % ≤ C < 25 %: Xi, N; R36-43-50
2,5 % ≤ C < 20 %: Xi, N; R43-50
1 % ≤ C < 2,5 %: Xi; R43

Xn; N
R: 22-50
S: (2-)22-61

C ≥ 25 %: Xn, N; R22-50
2,5 % ≤ C < 25 %: N; R50

E; Xi
R: 3-7-36-43
S: (2-)3/7-14-36/37/39

617-010-00-1

C

1-hydroperoxycyclohexyl 1-
hydroxycyclohexyl peroxide; [1]
1,1'-dioxybiscyclohexan-1-ol; [2]
cyclohexylidene hydroperoxi-
de; [3]
cyclohexanone, peroxide [4]

201-091-1 [1]
219-306-2 [2]
220-279-4 [3]
235-527-7 [4]

78-18-2 [1]
2407-94-5 [2]
2699-11-8 [3]
12262-58-7 [4]

E; R3
O; R7
C; R34
Xn; R22

E; C
R: 3-7-22-34
S: (1/2-)3/7-14-36/37/39-
45

C ≥ 25 %: C; R22-34
10 % ≤ C < 25 %: C; R34
5 % ≤ C < 10 %: Xi; R36/37/38

L

2
4
6
/
2
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

648-002-00-6

648-003-00-1

Tar oils, brown-coal;
Light Oil;
[The distillate from lignite tar
boiling in the range of approxi-
mately 80 °C to 250 °C (176 °F to
482 °F). Composed primarily of
aliphatic and aromatic hydrocar-
bons and monobasic phenols.]

Benzol forerunnings (coal);
Light Oil Redistillate, low boiling;
[The distillate from coke oven
light oil having an approximate
distillation range below 100 °C
(212 °F). Composed primarily of
C4 to C6 aliphatic hydrocarbons.]

H J

302-674-4

94114-40-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

266-023-5

65996-88-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-004-00-7

Distillates (coal tar), benzole
fraction, BTX-rich;
Light Oil Redistillate, low boiling;
[A residue from the distillation of
crude benzole to remove benzole
fronts. Composed primarily of
benzene, toluene and xylenes
boiling in the range of approxi-
mately 75 °C to 200 °C (167 °F to
392 °F).]

H J

309-984-9

101896-26-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-005-00-2

Aromatic hydrocarbons, C6-10,
C8-rich;
Light Oil Redistillate, low boiling

H J

292-697-5

90989-41-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-006-00-8

Solvent naphtha (coal), light;
Light Oil Redistillate, low boiling

H J

287-498-5

85536-17-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-007-00-3

Solvent naphtha (coal), xylene-
styrene cut;
Light Oil Redistillate, intermedi-
ate boiling

648-008-00-9

Solvent naphtha (coal), coumar-
one-styrene contg.;
Light Oil Redistillate, intermedi-
ate boiling

648-009-00-4

Naphtha (coal), distn. residues;
Light Oil Redistillate, high boil-
ing;
[The residue remaining from the
distillation of recovered naphtha.
Composed primarily of naphtha-
lene and condensation products
of indene and styrene.]

H J

287-502-5

85536-20-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

H J

287-500-4

85536-19-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

H J

292-636-2

90641-12-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-010-00-X

Aromatic hydrocarbons, C8;
Light Oil Redistillate, high boiling

H J

292-694-9

90989-38-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
2
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

295-281-1

91995-20-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-012-00-0

Aromatic hydrocarbons, C8-9,
hydrocarbon resin polymn. by-
product;
Light Oil Redistillate, high boil-
ing;
[A complex combination of
hydrocarbons obtained from the
evaporation of solvent under
vacuum from polymerized
hydrocarbon resin. It consists
predominantly of aromatic
hydrocarbons having carbon
numbers predominantly in the
range of C8 through C9 and
boiling in the range of approxi-
mately 120 °C to 215 °C (248 °F
to 419 °F).]

648-013-00-6

Aromatic hydrocarbons, C9-12,
benzene distn.;
Light Oil Redistillate, high boiling

H J

295-551-9

92062-36-7

H J

295-323-9

91995-61-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

648-014-00-1

648-015-00-7

Extract residues (coal), benzole
fraction alk., acid ext.;
Light Oil Extract Residues, low
boiling;
[The redistillate from the distil-
late, freed of tar acids and tar
bases, from bituminous coal high
temperature tar boiling in the
approximate range of 90 °C to
160 °C (194 °F to 320 °F). It
consists predominantly of ben-
zene, toluene and xylenes.]

Extract residues (coal tar), ben-
zole fraction alk., acid ext.;
Light Oil Extract Residues, low
boiling;
[A complex combination of
hydrocarbons obtained by the
redistillation of the distillate of
high temperature coal tar (tar
acid and tar base free). It consists
predominantly of unsubstituted
and substituted mononuclear
aromatic hydrocarbons boiling in
the range of 85 °C to 195 °C
(185 °F to 383 °F).]

H J

309-868-8

101316-63-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
2
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

298-725-2

93821-38-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

292-625-2

90641-02-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-016-00-2

648-017-00-8

Extract residues (coal), benzole
fraction acid;
Light Oil Extract Residues, low
boiling;
[An acid sludge by-product of the
sulfuric acid refining of crude
high temperature coal. Composed
primarily of sulfuric acid and
organic compounds.]

Extract residues (coal), light oil
alk., distn. overheads;
Light Oil Extract Residues, low
boiling;
[The first fraction from the dis-
tillation of aromatic hydrocar-
bons, coumarone, naphthalene
and indene rich prefractionator
bottoms or washed carbolic oil
boiling substantially below
145 °C (293 °F).Composed pri-
marily of C7 and C8 aliphatic and
aromatic hydrocarbons.]

648-018-00-3

Extract residues (coal), light oil
alk., acid ext., indene fraction;
Light Oil Extract Residues, inter-
mediate boiling

H J

309-867-2

101316-62-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

H J

292-626-8

90641-03-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-019-00-9

Extract residues (coal), light oil
alk., indene naphtha fraction;
Light Oil Extract Residues, high
boiling;
[The distillate from aromatic
hydrocarbons, coumarone,
naphthalene and indene rich
prefractionator bottoms or
washed carbolic oils, having an
approximate boiling range of
155 °C to 180 °C (311 °F to
356 °F).Composed primarily of
indene, indan and trimethylben-
zenes.]

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
2
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

266-013-0

65996-79-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

309-971-8

101794-90-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

292-609-5

90640-87-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

283-483-2

84650-03-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-020-00-4

648-021-00-X

648-022-00-5

648-023-00-0

Solvent naphtha (coal);
[The distillate from either high
temperature coal tar, coke oven
light oil, or coal tar oil alkaline
extract residue having an
approximate distillation range of
130 °C to 210 °C (266 °F to
410 °F). Composed primarily of
indene and other polycyclic ring
systems containing a single aro-
matic ring. May contain phenolic
compounds and aromatic nitro-
gen bases.]; Light Oil Extract
Residues, high boiling

Distillates (coal tar), light oils,
neutral fraction; Light Oil Extract
Residues, high boiling;
[A distillate from the fractional
distillation of high temperature
coal tar. Composed primarily of
alkyl-substituted one ring aro-
matic hydrocarbons boiling in
the range of approximately
135 °C to 210 °C (275 °F to
410 °F). May also include unsa-
turated hydrocarbons such as
indene and coumarone.]

Distillates (coal tar), light oils,
acid exts.; Light Oil Extract Resi-
dues, high boiling;
[This oil is a complex mixture of
aromatic hydrocarbons, primarily
indene, naphthalene, coumarone,
phenol, and o-, m- and p-cresol
and boiling in the range of
140 °C to 215 °C (284 °F to
419 °F).]

Distillates (coal tar), light oils;
Carbolic Oil;
[A complex combination of
hydrocarbons obtained by distil-
lation of coal tar. It consists of
aromatic and other hydrocar-
bons, phenolic compounds and
aromatic nitrogen compounds
and distills at the approximate
range of 150 °C to 210 °C
(302 °F to 410 °F).]

L

2
4
6
/
3
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-024-00-6

648-026-00-7

648-027-00-2

648-028-00-8

Tar oils, coal;
Carbolic Oil;
[The distillate from high tem-
perature coal tar having an
approximate distillation range of
130 °C to 250 °C (266 °F to
410 °F). Composed primarily of
naphthalene, alkylnaphthalenes,
phenolic compounds, and aro-
matic nitrogen bases.]

Extract residues (coal), light oil
alk., acid ext.;
Carbolic Oil Extract Residue;
[The oil resulting from the acid
washing of alkali-washed carbolic
oil to remove the minor amounts
of basic compounds (tar bases).
Composed primarily of indene,
indan and alkylbenzenes.]

Extract residues (coal), tar oil alk.;
Carbolic Oil Extract Residue;
[The residue obtained from coal
tar oil by an alkaline wash such as
aqueous sodium hydroxide after
the removal of crude coal tar
acids. Composed primarily of
naphthalenes and aromatic
nitrogen bases.]

Extract oils (coal), light oil;
Acid Extract;
[The aqueous extract produced
by an acidic wash of alkali-
washed carbolic oil. Composed
primarily of acid salts of various
aromatic nitrogen bases includ-
ing pyridine, quinoline and their
alkyl derivatives.]

H J

266-016-7

65996-82-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

292-624-7

90641-01-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

266-021-4

65996-87-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

292-622-6

90640-99-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
3
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

269-929-9

68391-11-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

295-548-2

92062-33-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-029-00-3

648-030-00-9

Pyridine, alkyl derivs.;
Crude Tar Bases;
[The complex combination of
polyalkylated pyridines derived
from coal tar distillation or as
high-boiling distillates approxi-
mately above 150 °C (302 °F)
from the reaction of ammonia
with acetaldehyde, formaldehyde
or paraformaldehyde.]

Tar bases, coal, picoline fraction;
Distillate Bases;
[Pyridine bases boiling in the
range of approximately 125 °C to
160 °C (257 °F 320 °F) obtained
by distillation of neutralized acid
extract of the base-containing tar
fraction obtained by the distilla-
tion of bituminous coal tars.
Composed chiefly of lutidines
and picolines.]

648-031-00-4

Tar bases, coal, lutidine fraction;
Distillate Bases

H J

293-766-2

91082-52-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

H J

273-077-3

68937-63-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-032-00-X

Extract oils (coal), tar base, colli-
dine fraction;
Distillate Bases;
[The extract produced by the
acidic extraction of bases from
crude coal tar aromatic oils,
neutralization, and distillation of
the bases. Composed primarily of
collidines, aniline, toluidines,
lutidines, xylidines.]

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

L

2
4
6
/
3
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

295-543-5

92062-28-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

295-541-4

92062-27-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-033-00-5

648-034-00-0

Tar bases, coal, collidine fraction;
Distillate Bases;
[The distillation fraction boiling
in the range of approximately
181 °C to 186 °C (356 °F to
367 °F) from the crude bases
obtained from the neutralized,
acid-extracted base-containing tar
fractions obtained by the distilla-
tion of bituminous coal tar. It
contains chiefly aniline and col-
lidines.]

Tar bases, coal, aniline fraction;
Distillate Bases;
[The distillation fraction boiling
in the range of approximately
180 °C to 200 °C (356 °F to
392 °F) from the crude bases
obtained by dephenolating and
debasing the carbolated oil from
the distillation of coal tar. It
contains chiefly aniline, colli-
dines, lutidines and toluidines.]

648-035-00-6

Tar bases, coal, toluidine fraction;
Distillate Bases

H J

293-767-8

91082-53-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

H J

295-292-1

91995-31-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-036-00-1

Distillates (petroleum), alkene-
alkyne manuf. pyrolysis oil,
mixed with high-temp. coal tar,
indene fraction;
Redistillates;
[A complex combination of
hydrocarbons obtained as a
redistillate from the fractional
distillation of bituminous coal
high temperature tar and residual
oils that are obtained by the
pyrolytic production of alkenes
and alkynes from petroleum
products or natural gas. It con-
sists predominantly of indene
and boils in a range of approxi-
mately 160 °C to 190 °C (320 °F
to 374 °F).]

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
3
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

295-295-8

91995-35-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

295-329-1

91995-66-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

310-170-0

122070-79-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-037-00-7

648-038-00-2

648-039-00-8

Distillates (coal), coal tar-residual
pyrolysis oils, naphthalene oils;
Redistillates;
[The redistillate obtained from
the fractional distillation of
bituminous coal high tempera-
ture tar and pyrolysis residual oils
and boiling in the range of
approximately 190 °C to 270 °C
(374 °F to 518 °F). Composed
primarily of substituted dinuclear
aromatics.]

Extract oils (coal), coal tar-resi-
dual pyrolysis oils, naphthalene
oil, redistillate;
Redistillates;
[The redistillate from the frac-
tional distillation of dephenolated
and debased methylnaphthalene
oil obtained from bituminous
coal high temperature tar and
pyrolysis residual oils boiling in
the approximate range of 220 °C
to 230 °C (428 °F to 446 °F). It
consists predominantly of
unsubstituted and substituted
dinuclear aromatic hydrocar-
bons.]

Extract oils (coal), coal tar-resi-
dual pyrolysis oils, naphthalene
oils;
Redistillates;
[A neutral oil obtained by
debasing and dephenolating the
oil obtained from the distillation
of high temperature tar and
pyrolysis residual oils which has a
boiliing range of 225 °C to
255 °C (437 °F to 491 °F).
Composed primarily of substi-
tuted dinuclear aromatic hydro-
carbons.]

L

2
4
6
/
3
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

310-171-6

122070-80-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H M

292-606-9

90640-85-0

Carc. Cat. 2; R45

H M

295-506-3

92061-93-3

Carc. Cat. 2; R45

T
R: 45
S: 53-45

T
R: 45
S: 53-45

HJM

285-076-5

85029-51-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-040-00-3

648-043-00-X

648-080-00-1

648-084-00-3

Extract oils (coal), coal tar resi-
dual pyrolysis oils, naphthalene
oil, distn. residues;
Redistillates;
[Residue from the distillation of
dephenolated and debased
methylnaphthalene oil (from
bituminous coal tar and pyrolysis
residual oils) with a boiling range
of 240 °C to 260 °C (464 °F to
500 °F). Composed primarily of
substituted dinuclear aromatic
and heterocyclic hydrocarbons.]

Creosote oil, acenaphthene frac-
tion, acenaphthene-free;
Wash Oil Redistillate;
[The oil remaining after removal
by a crystallization process of
acenaphthene from ace-
naphthene oil from coal tar.
Composed primarily of naphtha-
lene and alkylnaphthalenes.]

Residues (coal tar), creosote oil
distn.;
Wash Oil Redistillate;
[The residue from the fractional
distillation of wash oil boiling in
the approximate range of 270 °C
to 330 °C (518 °F to 626 °F). It
consists predominantly of dinuc-
lear aromatic and heterocyclic
hydrocarbons.]

Distillates (coal), coke-oven light
oil, naphthalene cut;
Naphthalene Oil;
[The complex combination of
hydrocarbons obtained from
prefractionation (continuous dis-
tillation) of coke oven light oil. It
consists predominantly of
naphthalene, coumarone and
indene and boils above 148 °C
(298 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
3
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-085-00-9

648-086-00-4

648-087-00-X

648-088-00-5

Distillates (coal tar), naphthalene
oils;
Naphthalene Oil;
[A complex combination of
hydrocarbons obtained by the
distillation of coal tar. It consists
primarily of aromatic and other
hydrocarbons, phenolic com-
pounds and aromatic nitrogen
compounds and distills in the
approximate range of 200 °C to
250 °C (392 °F to 482 °F).]

Distillates (coal tar), naphthalene
oils, naphthalene-low;
Naphthalene Oil Redistillate;
[A complex combination of
hydrocarbons obtained by crys-
tallization of naphthalene oil.
Composed primarily of naphtha-
lene, alkyl naphthalenes and
phenolic compounds.]

Distillates (coal tar), naphthalene
oil crystn. mother liquor;
Naphthalene Oil Redistillate;
[A complex combination of
organic compounds obtained as a
filtrate from the crystallization of
the naphthalene fraction from
coal tar and boiling in the range
of approximately 200 °C to 230 °
C (392 °F to 446 °F). Contains
chiefly naphthalene, thio-
naphthene and alkylnaphtha-
lenes.]

Extract residues (coal), naphtha-
lene oil, alk.;
Naphthalene Oil Extract Residue;
[A complex combination of
hydrocarbons obtained from the
alkali washing of naphthalene oil
to remove phenolic compounds
(tar acids). It is composed of
naphthalene and alkyl naphtha-
lenes.]

HJM

283-484-8

84650-04-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

284-898-1

84989-09-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

295-310-8

91995-49-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

310-166-9

121620-47-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
3
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

310-167-4

121620-48-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-612-1

90640-90-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-627-3

90641-04-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

309-985-4

101896-27-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-089-00-0

648-090-00-6

648-091-00-1

648-092-00-7

Extract residues (coal), naphtha-
lene oil, alk., naphthalene-low;
Naphthalene Oil Extract Residue;
[A complex combination of
hydrocarbons remaining after the
removal of naphthalene from
alkali-washed naphthalene oil by
a crystallization process. It is
composed primarily of naphtha-
lene and alkyl naphthalenes.]

Distillates (coal tar), naphthalene
oils, naphthalene-free, alk. exts.;
Naphthalene Oil Extract Residue;
[The oil remaining after the
removal of phenolic compounds
(tar acids) from drained
naphthalene oil by an alkali wash.
Composed primarily of naphtha-
lene and alkyl naphthalenes.]

Extract residues (coal), naphtha-
lene oil alk., distn. overheads;
Naphthalene Oil Extract Residue;
[The distillate from alkali-washed
naphthalene oil having an
approximate distillation range of
180 °C to 220 °C (356 °F to
428 °F). Composed primarily of
naphthalene, alkylbenzenes,
indene and indan.]

Distillates (coal tar), naphthalene
oils, methylnaphthalene fraction;
Methylnaphthalene Oil;
[A distillate from the fractional
distillation of high temperature
coal tar. Composed primarily of
substituted two ring aromatic
hydrocarbons and aromatic
nitrogen bases boiling in the
range of approximately 225 °C to
255 °C (437 °F to 491 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
3
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

309-972-3

101794-91-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

295-309-2

91995-48-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-628-9

90641-05-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-093-00-2

648-094-00-8

648-095-00-3

Distillates (coal tar), naphthalene
oils, indole-methylnaphthalene
fraction;
Methylnaphthalene Oil;
[A distillate from the fractional
distillation of high temperature
coal tar. Composed primarily of
indole and methylnaphthalene
boiling in the range of approxi-
mately 235 °C to 255 °C (455 °F
to 491 °F).]

Distillates (coal tar), naphthalene
oils, acid exts.;
Methylnaphthalene Oil Extract
Residue;
[A complex combination of
hydrocarbons obtained by
debasing the methylnaphthalene
fraction obtained by the distilla-
tion of coal tar and boiling in the
range of approximately 230 °C to
255 °C (446 °F to 491 °F).
Contains chiefly 1(2)-methyl-
naphthalene, naphthalene,
dimethylnaphthalene and biphe-
nyl.]

Extract residues (coal), naphtha-
lene oil alk., distn. residues;
Methylnaphthalene Oil Extract
Residue;
[The residue from the distillation
of alkali-washed naphthalene oil
having an approximate distilla-
tion range of 220 °C to 300 °C
(428 °F to 572 °F). Composed
primarily of naphthalene, alkyl-
naphthalenes and aromatic
nitrogen bases.]

L

2
4
6
/
3
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

284-901-6

84989-12-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

310-165-3

121620-46-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H M

292-605-3

90640-84-9

Carc. Cat. 2; R45

T
R: 45
S: 53-45

648-096-00-9

648-097-00-4

648-098-00-X

Extract oils (coal), acidic, tar-base
free;
Methylnaphthalene Oil Extract
Residue;
[The extract oil boiling in the
range of approximately 220 °C to
265 °C (428 °F to 509 °F) from
coal tar alkaline extract residue
produced by an acidic wash such
as aqueous sulfuric acid after
distillation to remove tar bases.
Composed primarily of alkyl-
naphthalenes.]

Distillates (coal tar), benzole
fraction, distn. residues;
Wash Oil;
[A complex combination of
hydrocarbons obtained from the
distillation of crude benzole (high
temperature coal tar). It may be a
liquid with the approximate dis-
tillation range of 150 °C to 300 °
C (302 °F to 572 °F) or a semi-
solid or solid with a melting
point up to 70 °C (158 °F). It is
composed primarily of naphtha-
lene and alkyl naphthalenes.]

Creosote oil, acenaphthene frac-
tion;
Wash Oil;
[A complex combination of
hydrocarbons produced by the
distillation of coal tar and boiling
in the range of approximately
240 °C to 280 °C (464 °F to
536 °F). Composed primarily of
acenaphthene, naphthalene and
alkyl naphthalene.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
3
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-099-00-5

648-100-00-9

648-102-00-X

648-103-00-5

Creosote oil;
[A complex combination of
hydrocarbons obtained by the
distillation of coal tar. It consists
primarily of aromatic hydrocar-
bons and may contain appreci-
able quantities of tar acids and tar
bases. It distills at the approxi-
mate range of 200 °C to 325 °C
(392 °F to 617 °F).]

Creosote oil, high-boiling distil-
late;
Wash Oil;
[The high-boiling distillation
fraction obtained from the high
temperature carbonization of
bituminous coal which is further
refined to remove excess crystal-
line salts. It consists primarily of
creosote oil with some of the
normal polynuclear aromatic
salts, which are components of
coal tar distillates, removed. It is
crystal free at approximately 5 °C
(41 °F).]

Extract residues (coal), creosote
oil acid;
Wash Oil Extract Residue;
[A complex combination of
hydrocarbons from the base-
freed fraction from the distilla-
tion of coal tar, boiling in the
range of approximately 250 °C to
280 °C (482 °F to 536 °F). It
consists predominantly of biphe-
nyl and isomeric diphenyl-
naphthalenes.]

Anthracene oil, anthracene paste;
Anthracene Oil Fraction;
[The anthracene-rich solid
obtained by the crystallization
and centrifuging of anthracene
oil. It is composed primarily of
anthracene, carbazole and phe-
nanthrene.]

H M

263-047-8

61789-28-4

Carc. Cat. 2; R45

H M

274-565-9

70321-79-8

Carc. Cat. 2; R45

H M

310-189-4

122384-77-4

Carc. Cat. 2; R45

T
R: 45
S: 53-45

T
R: 45
S: 53-45

T
R: 45
S: 53-45

HJM

292-603-2

90640-81-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
4
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

292-604-8

90640-82-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

295-505-8

92061-92-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

295-275-9

91995-15-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

295-276-4

91995-16-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-104-00-0

648-105-00-6

648-106-00-1

648-107-00-7

Anthracene oil, anthracene-low;
Anthracene Oil Fraction;
[The oil remaining after the
removal, by a crystallization
process, of an anthracene-rich
solid (anthracene paste) from
anthracene oil. It is composed
primarily of two, three and four
membered aromatic com-
pounds.]

Residues (coal tar), anthracene oil
distn.;
Anthracene Oil Fraction;
[The residue from the fraction
distillation of crude anthracene
boiling in the approximate range
of 340 °C to 400 °C (644 °F to
752 °F). It consists predomi-
nantly of tri- and polynuclear
aromatic and heterocyclic hydro-
carbons.]

Anthracene oil, anthracene paste,
anthracene fraction;
Anthracene Oil Fraction;
[A complex combination of
hydrocarbons from the distilla-
tion of anthracene obtained by
the crystallization of anthracene
oil from bituminous high tem-
perature tar and boiling in the
range of 330 °C to 350 °C (626 °
F to 662 °F). It contains chiefly
anthracene, carbazole and phe-
nanthrene.]

Anthracene oil, anthracene paste,
carbazole fraction;
Anthracene Oil Fraction;
[A complex combination of
hydrocarbons from the distilla-
tion of anthracene obtained by
crystallization of anthracene oil
from bituminous coal high tem-
perature tar and boiling in the
approximate range of 350 °C to
360 °C (662 °F to 680 °F). It
contains chiefly anthracene, car-
bazole and phenanthrene.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
4
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

295-278-5

91995-17-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

309-889-2

101316-87-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

310-191-5

122384-78-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

284-881-9

84988-93-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-108-00-2

648-109-00-8

648-110-00-3

648-111-00-9

Anthracene oil, anthracene paste,
distn. lights;
Anthracene Oil Fraction;
[A complex combination of
hydrocarbons from the distilla-
tion of anthracene obtained by
crystallization of anthracene oil
from bituminous high tempera-
ture tar and boiling in the range
of approximately 290 °C to 340 °
C (554 °F to 644 °F). It contains
chiefly trinuclear aromatics and
their dihydro derivatives.]

Tar oils, coal, low-temp.;
Tar Oil, high boiling;
[A distillate from low-tempera-
ture coal tar. Composed primarily
of hydrocarbons, phenolic com-
pounds and aromatic nitrogen
bases boiling in the range of
approximately 160 °C to 340 °C
(320 °F to 644 °F).]

Extract residues (coal), low temp.
coal atar alk.;
[The residue from low tempera-
ture coal tar oils after an alkaline
wash, such as aqueous sodium
hydroxide, to remove crude coal
tar acids. Composed primarily of
hydrocarbons and aromatic
nitrogen bases.]

Phenols, ammonia liquor ext.;
Alkaline Extract;
[The combination of phenols
extracted, using isobutyl acetate,
from the ammonia liquor con-
densed from the gas evolved in
low-temperature (less than 700 °
C (1 292 °F)) destructive distilla-
tion of coal. It consists predomi-
nantly of a mixture of
monohydric and dihydric phe-
nols.]

L

2
4
6
/
4
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-112-00-4

Distillates (coal tar), light oils, alk.
exts.;
Alkaline Extract;
[The aqueous extract from car-
bolic oil produced by an alkaline
wash such as aqueous sodium
hydroxide. Composed primarily
of the alkali salts of various
phenolic compounds.]

648-113-00-X

Extracts, coal tar oil alk.;
Alkaline Extract;
[The extract from coal tar oil
produced by an alkaline wash
such as aqueous sodium hydro-
xide. Composed primarily of the
alkali salts of various phenolic
compounds.]

648-114-00-5

648-115-00-0

Distillates (coal tar), naphthalene
oils, alk. exts.;
Alkaline Extract;
[The aqueous extract from
naphthalene oil produced by an
alkaline wash such as aqueous
sodium hydroxide. Composed
primarily of the alkali salts of
various phenolic compounds.]

Extract residues (coal), tar oil alk.,
carbonated, limed;
Crude Phenols;
[The product obtained by treat-
ment of coal tar oil alkaline
extract with CO2 and CaO.
Composed primarily of CaCO3,
Ca(OH)2, Na2CO3 and other
organic and inorganic impuri-
ties.]

HJM

292-610-0

90640-88-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

266-017-2

65996-83-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-611-6

90640-89-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-629-4

90641-06-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
4
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-116-00-6

648-117-00-1

648-118-00-7

648-119-00-2

648-120-00-8

Tar acids, coal, crude;
Crude Phenols;
[The reaction product obtained
by neutralizing coal tar oil alka-
line extract with an acidic solu-
tion, such as aqueous sulfuric
acid, or gaseous carbon dioxide,
to obtain the free acids. Com-
posed primarily of tar acids such
as phenol, cresols, and xylenols.]

Tar acids, brown-coal, crude;
Crude Phenols;
[An acidified alkaline extract of
brown coal tar distillate. Com-
posed primarily of phenol and
phenol homologs.]

Tar acids, brown-coal gasifica-
tion;
Crude Phenols;
[A complex combination of
organic compounds obtained
from brown coal gasification.
Composed primarily of C6-10
hydroxy aromatic phenols and
their homologs.]

Tar acids, distn. residues;
Distillate Phenols;
[A residue from the distillation of
crude phenol from coal. It con-
sists predominantly of phenols
having carbon numbers in the
range of C8 through C10 with a
softening point of 60 °C to 80 °C
(140 °F to 176 °F).]

Tar acids, methylphenol fraction;
Distillate Phenols;
[The fraction of tar acid rich in 3-
and 4-methylphenol, recovered
by distillation of low-temperature
coal tar crude tar acids.]

HJM

266-019-3

65996-85-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

309-888-7

101316-86-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46

HJM

295-536-7

92062-22-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

HJM

306-251-5

96690-55-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

284-892-9

84989-04-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
4
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-121-00-3

648-122-00-9

Tar acids, polyalkylphenol frac-
tion;
Distillate Phenols;
[The fraction of tar acids, recov-
ered by distillation of low-tem-
perature coal tar crude tar acids,
having an approximate boiling
range of 225 °C to 320 °C (437 °
F to 608 °F).Composed primarily
of polyalkylphenols.]

Tar acids, xylenol fraction;
Distillate Phenols;
[The fraction of tar acids, rich in
2,4- and 2,5-dimethylphenol,
recovered by distillation of low-
temperature coal tar crude tar
acids.]

648-123-00-4

Tar acids, ethylphenol fraction;
Distillate Phenols;
[The fraction of tar acids, rich in
3- and 4-ethylphenol, recovered
by distillation of low-temperature
coal tar crude tar acids.]

648-124-00-X

Tar acids, 3,5-xylenol fraction;
Distillate Phenols;
[The fraction of tar acids, rich in
3,5-dimethylphenol, recovered by
distillation of low-temperature
coal tar acids.]

648-125-00-5

Tar acids, residues, distillates,
first-cut;
Distillate Phenols;
[The residue from the distillation
in the range of 235 °C to 355 °C
(481 °F to 697 °F) of light
carbolic oil.]

HJM

284-893-4

84989-05-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

284-895-5

84989-06-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

284-891-3

84989-03-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46

HJM

284-896-0

84989-07-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

HJM

270-713-1

68477-23-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
4
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-126-00-0

Tar acids, cresylic, residues;
Distillate Phenols;
[The residue from crude coal tar
acids after removal of phenol,
cresols, xylenols and any higher
boiling phenols. A black solid
with a melting point approxi-
mately 80 °C (176 °F). Composed
primarily of polyalkylphenols,
resin gums, and inorganic salts.]

HJM

271-418-0

68555-24-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

648-127-00-6

Phenols, C9-11;
Distillate Phenols

HJM

293-435-2

91079-47-9

HJM

295-540-9

92062-26-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

648-128-00-1

648-129-00-7

648-130-00-2

Tar acids, cresylic;
Distillate Phenols;
[A complex combination of
organic compounds obtained
from brown coal and boiling in
the range of approximately 200 °
C to 230 °C (392 °F to 446 °F). It
contains chiefly phenols and
pyridine bases.]

Tar acids, brown-coal, C2-alkyl-
phenol fraction;
Distillate Phenols;
[The distillate from the acidifica-
tion of alkaline washed lignite tar
distillate boiling in the range of
approximately 200 °C to 230 °C
(392 °F to 446 °F). Composed
primarily of m- and p-ethylphe-
nol as well as cresols and xyle-
nols.]

Extract oils (coal), naphthalene
oils;
Acid Extract;
[The aqueous extract produced
by an acidic wash of alkali-
washed naphthalene oil. Com-
posed primarily of acid salts of
various aromatic nitrogen bases
including pyridine, quinoline and
their alkyl derivatives.]

HJM

302-662-9

94114-29-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

292-623-1

90641-00-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
4
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-131-00-8

Tar bases, quinoline derivs.;
Distillate Bases

HJM

271-020-7

68513-87-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

648-132-00-3

Tar bases, coal, quinoline derivs.
fraction;
Distillate Bases

HJM

274-560-1

70321-67-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

HJM

295-544-0

92062-29-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

648-133-00-9

648-134-00-4

648-135-00-X

Tar bases, coal, distn. residues;
Distillate Bases;
[The distillation residue remain-
ing after the distillation of the
neutralized, acid-extracted base-
containing tar fractions obtained
by the distillation of coal tars. It
contains chiefly aniline, colli-
dines, quinoline and quinoline
derivatives and toluidines.]

Hydrocarbon oils, arom., mixed
with polyethylene and polypro-
pylene, pyrolyzed, light oil frac-
tion;
Heat Treatment Products;
[The oil obtained from the heat
treatment of a polyethylene/
polypropylene mixture with coal
tar pitch or aromatic oils. It
consists predominantly of ben-
zene and its homologs boiling in
a range of approximately 70 °C to
120 °C (158 °F to 248 °F).]

Hydrocarbon oils, arom., mixed
with polyethylene, pyrolyzed,
light oil fraction;
Heat Treatment Products;
[The oil obtained from the heat
treatment of polyethylene with
coal tar pitch or aromatic oils. It
consists predominantly of ben-
zene and its homologs boiling in
a range of 70 °C to 120 °C (158 °
F to 248 °F).]

HJM

309-745-9

100801-63-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

309-748-5

100801-65-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
4
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HJM

309-749-0

100801-66-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

HJM

277-567-8

73665-18-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H M

274-566-4

70321-80-1

Carc. Cat. 2; R45

T
R: 45
S: 53-45

648-136-00-5

648-137-00-0

648-138-00-6

Hydrocarbon oils, arom., mixed
with polystyrene, pyrolyzed, light
oil fraction;
Heat Treatment Products;
[The oil obtained from the heat
treatment of polystyrene with
coal tar pitch or aromatic oils. It
consists predominantly of ben-
zene and its homologs boiling in
a range of approximately 70 °C to
210 °C (158 °F to 410 °F).]

Extract residues (coal), tar oil alk.,
naphthalene distn. residues;
Naphthalene Oil Extract Residue;
[The residue obtained from che-
mical oil extracted after the
removal of naphthalene by dis-
tillation composed primarily of
two to four membered con-
densed ring aromatic hydrocar-
bons and aromatic nitrogen
bases.]

Creosote oil, low-boiling distil-
late;
Wash Oil;
[The low-boiling distillation frac-
tion obtained from the high
temperature carbonization of
bituminous coal, which is further
refined to remove excess crystal-
line salts. It consists primarily of
creosote oil with some of the
normal polynuclear aromatic
salts, which are components of
coal tar distillate, removed. It is
crystal free at approximately 38 °
C (100 °F).]

648-139-00-1

Tar acids, cresylic, sodium salts,
caustic solns.;
Alkaline Extract

HJM

272-361-4

68815-21-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

L

2
4
6
/
4
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-140-00-7

Extract oils (coal), tar base;

HJM

266-020-9

65996-86-3

Acid Extract;

[The extract from coal tar oil
alkaline extract residue produced
by an acidic wash such as
aqueous sulfuric acid after dis-
tillation to remove naphthalene.
Composed primarily of the acid
salts of various aromatic nitrogen
bases including pyridine, quino-
line, and their alkyl derivatives.]

648-141-00-2

Tar bases, coal, crude;

HJM

266-018-8

65996-84-1

Crude Tar Bases;

[The reaction product obtained
by neutralizing coal tar base
extract oil with an alkaline solu-
tion, such as aqueous sodium
hydroxide, to obtain the free
bases. Composed primarily of
such organic bases as acridine,
phenanthridine, pyridine, quino-
line and their alkyl derivatives.]

648-147-00-5

Light oil (coal), coke-oven;

H J

266-012-5

65996-78-3

Crude benzole;

[The volatile organic liquid
extracted from the gas evolved in
the high temperature (greater
than 700 °C (1 292 °F)) destruc-
tive distillation of coal. Com-
posed primarily of benzene,
toluene, and xylenes. May contain
other minor hydrocarbon con-
stituents.]

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
4
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-148-00-0

Distillates (coal), liq. solvent extn.,
primary;

H J

302-688-0

94114-52-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46

[The liquid product of condensa-
tion of vapors emitted during the
digestion of coal in a liquid
solvent and boiling in the range
of approximately 30 °C to 300 °C
(86 °F to 572 °F). Composed
primarily of partly hydrogenated
condensed-ring aromatic hydro-
carbons, aromatic compounds
containing nitrogen, oxygen and
sulfur, and their alkyl derivatives
having carbon numbers predo-
minantly in the range of C4
through C14.]

648-149-00-6

Distillates (coal), solvent extn.,
hydrocracked;

H J

302-689-6

94114-53-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46

[Distillate obtained by hydro-
cracking of coal extract or solu-
tion produced by the liquid
solvent extraction or supercritical
gas extraction processes and
boiling in the range of approxi-
mately 30 °C to 300 °C (86 °F to
572 °F). Composed primarily of
aromatic, hydrogenated aromatic
and naphthenic compounds,
their alkyl derivatives and alkanes
with carbon numbers predomi-
nantly in the range of C4 through
C14. Nitrogen, sulfur and oxygen-
containing aromatic and hydro-
genated aromatic compounds are
also present.]

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

L

2
4
6
/
5
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

648-150-00-1

Naphtha (coal), solvent extn.,
hydrocracked;

H J

302-690-1

94114-54-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46

[Fraction of the distillate obtained
by hydrocracking of coal extract
or solution produced by the
liquid solvent extraction or
supercritical gas extraction pro-
cesses and boiling in the range of
approximately 30 °C to 180 °C
(86 °F to 356 °F). Composed
primarily of aromatic, hydroge-
nated aromatic and naphthenic
compounds, their alkyl deriva-
tives and alkanes with carbon
numbers predominantly in the
range of C4 to C9. Nitrogen, sulfur
and oxygen-containing aromatic
and hydrogenated aromatic
compounds are also present.]

648-152-00-2

Distillates (coal), solvent extn.,
hydrocracked middle;

H J

302-692-2

94114-56-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46

[Distillate obtained from the
hydrocracking of coal extract or
solution produced by the liquid
solvent extraction or supercritical
gas extraction processes and
boiling in the range of approxi-
mately 180 °C to 300 °C (356 °F
to 572 °F. Composed primarily of
two-ring aromatic, hydrogenated
aromatic and naphthenic com-
pounds, their alkyl derivatives
and alkanes having carbon num-
bers predominantly in the range
of C9 through C14. Nitrogen,
sulfur and oxygen-containing
compounds are also present.]

T
R: 45-46
S: 53-45

T
R: 45-46
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H J

302-693-8

94114-57-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H J

292-635-7

90641-11-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46

T
R: 45-46
S: 53-45

H K

270-755-0

68477-73-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

648-153-00-8

Distillates (coal), solvent extn.,
hydrocracked hydrogenated mid-
dle;
[Distillate from the hydrogena-
tion of hydrocracked middle dis-
tillate from coal extract or
solution produced by the liquid
solvent extraction or supercritical
gas extraction processes and
boiling in the range of approxi-
mately 180 °C to 280 °C (356 °F
to 536 °F). Composed primarily
of hydrogenated two- ring carbon
compounds and their alkyl deri-
vatives having carbon numbers
predominantly in the range of C9
through C14.]

648-156-00-4

Light oil (coal), semi-coking pro-
cess;
Fresh oil;
[The volatile organic liquid con-
densed from the gas evolved in
the low-temperature (less than
700 °C (1 292 °F)) destructive
distillation of coal. Composed
primarily of C6-10 hydrocarbons.]

649-062-00-6

Gases (petroleum), catalytic
cracked naphtha depropanizer
overhead, C3-rich acid-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation of catalytic cracked
hydrocarbons and treated to
remove acidic impurities. It con-
sists of hydrocarbons having
carbon numbers in the range of
C2 through C4, predominantly
C3.]

L

2
4
6
/
5
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-756-6

68477-74-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-757-1

68477-75-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-758-7

68477-76-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-760-8

68477-79-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-063-00-1

649-064-00-7

649-065-00-2

649-066-00-8

Gases (petroleum), catalytic
cracker;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of the products from a
catalytic cracking process. It
consists predominantly of ali-
phatic hydrocarbons having car-
bon numbers predominantly in
the range of C1 through C6.]

Gases (petroleum), catalytic
cracker, C1-5-rich;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
catalytic cracking process. It
consists of aliphatic hydrocar-
bons having carbon numbers in
the range of C1 through C6,
predominantly C1 through C5.]

Gases (petroleum), catalytic
polymd. naphtha stabilizer over-
head, C2-4-rich;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
fractionation stabilization of cat-
alytic polymerized naphtha. It
consists of aliphatic hydrocar-
bons having carbon numbers in
the range of C2 through C6,
predominantly C2 through C4.]

Gases (petroleum), catalytic
reformer, C1-4-rich;
Petroleum gas;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from a
catalytic reforming process. It
consists of hydrocarbons having
carbon numbers in the range of
C1 through C6, predominantly C1
through C4.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-765-5

68477-83-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-767-6

68477-85-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-768-1

68477-86-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-769-7

68477-87-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-067-00-3

649-068-00-9

649-069-00-4

649-070-00-X

Gases (petroleum), C3-5 olefinic-
paraffinic alkylation feed;
Petroleum gas;
[A complex combination of ole-
finic and paraffinic hydrocarbons
having carbon numbers in the
range of C3 through C5 which are
used as alkylation feed. Ambient
temperatures normally exceed the
critical temperature of these
combinations.]

Gases (petroleum), C4-rich;
Petroleum gas;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from a
catalytic fractionation process. It
consists of aliphatic hydrocar-
bons having carbon numbers in
the range of C3 through C5,
predominantly C4.]

Gases (petroleum), deethanizer
overheads;
Petroleum gas;
[A complex combination of
hydrocarbons produced from
distillation of the gas and gaso-
line fractions from the catalytic
cracking process. It contains pre-
dominantly ethane and ethylene.]

Gases (petroleum), deisobutani-
zer tower overheads;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
atmospheric distillation of a
butane-butylene stream. It con-
sists of aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C3
through C4.]

L

2
4
6
/
5
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-772-3

68477-90-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-773-9

68477-91-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-777-0

68477-94-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-778-6

68477-95-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-071-00-5

649-072-00-0

649-073-00-6

649-074-00-1

Gases (petroleum), depropanizer
dry, propene-rich;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from the
gas and gasoline fractions of a
catalytic cracking process. It
consists predominantly of pro-
pylene with some ethane and
propane.]

Gases (petroleum), depropanizer
overheads;
Petroleum gas;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from the gas
and gasoline fractions of a cata-
lytic cracking process. It consists
of aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C2 through C4.]

Gases (petroleum), gas recovery
plant depropanizer overheads;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by frac-
tionation of miscellaneous
hydrocarbon streams. It consists
predominantly of hydrocarbons
having carbon numbers in the
range of C1 through C4, predo-
minantly propane.]

Gases (petroleum), Girbotol unit
feed;
Petroleum gas;
[A complex combination of
hydrocarbons that is used as the
feed into the Girbatol unit to
remove hydrogen sulfide. It con-
sists of aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C2
through C4.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-075-00-7

Gases (petroleum), isomerized
naphtha fractionator, C4-rich,
hydrogen sulfide-free;
Petroleum gas

H K

270-782-8

68477-99-6

H K

270-802-5

68478-21-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

649-076-00-2

649-077-00-8

649-078-00-3

Tail gas (petroleum), catalytic
cracked clarified oil and thermal
cracked vacuum residue frac-
tionation reflux drum;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation of catalytic cracked
clarified oil and thermal cracked
vacuum residue. It consists pre-
dominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C6.]

Tail gas (petroleum), catalytic
cracked naphtha stabilization
absorber;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
stabilization of catalytic cracked
naphtha. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C6.]

Tail gas (petroleum), catalytic
cracker, catalytic reformer and
hydrodesulfurizer combined
fractionater;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
fractionation of products from
catalytic cracking, catalytic
reforming and hydrodesulfuriz-
ing processes treated to remove
acidic impurities. It consists pre-
dominantly of hydrocarbons
having cabon numbers predomi-
nantly in the range of C1 through
C5.]

H K

270-803-0

68478-22-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-804-6

68478-24-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
5
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-079-00-9

Tail gas (petroleum), catalytic
reformed naphtha fractionation
stabilizer;

H K

270-806-7

68478-26-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

Petroleum gas;

[A complex combination of
hydrocarbons obtained from the
fractionation stabilization of cat-
alytic reformed naphtha. It con-
sists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C4.]

649-080-00-4

Tail gas (petroleum), saturate gas
plant mixed stream, C4-rich;

H K

270-813-5

68478-32-0

Petroleum gas;

[A complex combination of
hydrocarbons obtained from the
fractionation stabilization of
straight-run naphtha, distillation
tail gas and catalytic reformed
naphtha stabilizer tail gas. It
consists of hydrocarbons having
carbon numbers in the range of
C3 through C6, predominantly
butane and isobutane.]

649-081-00-X

Tail gas (petroleum), saturate gas
recovery plant, C1-2-rich;

H K

270-814-0

68478-33-1

Petroleum gas;

[A complex combination of
hydrocarbons obtained from
fractionation of distillate tail gas,
straight-run naphtha, catalytic
reformed naphtha stabilizer tail
gas. It consists predominantly of
hydrocarbons having carbon
numbers in the range of
C1through C5, predominantly
methane and ethane.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-815-6

68478-34-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-990-9

68512-91-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-000-8

68513-15-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-001-3

68513-16-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-082-00-5

649-083-00-0

649-084-00-6

649-085-00-1

Tail gas (petroleum), vacuum
residues thermal cracker;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
thermal cracking of vacuum
residues. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C5.]

Hydrocarbons, C3-4-rich, petro-
leum distillate;
Petroleum gas;
[A complex combination of
hydrocarbons produced by dis-
tillation and condensation of
crude oil. It consists of hydro-
carbons having carbon numbers
in the range of C3 through C5,
predominantly C3 through C4.]

Gases (petroleum), full-range
straight-run naphtha dehexanizer
off;
petroleum gas;
[A complex combination of
hydrocarbons obtained by the
fractionation of the full-range
straight-run naphtha. It consists
of hydrocarbons having carbon
numbers predominantly in the
range of C2 through C6.]

Gases (petroleum), hydrocracking
depropanizer off, hydrocarbon-
rich;
Petroleum gas;
[A complex combination of
hydrocarbon produced by the
distillation of products from a
hydrocracking process. It consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C4. It may also contain
small amounts of hydrogen and
hydrogen sulfide.]

L

2
4
6
/
5
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-086-00-7

Gases (petroleum), light straight-
run naphtha stabilizer off;

H K

271-002-9

68513-17-7

Petroleum gas;

[A complex combination of
hydrocarbons obtained by the
stabilization of light straight-run
naphtha. It consists of saturated
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C2 through C6.]

649-087-00-2

Residues (petroleum), alkylation
splitter, C4-rich;

H K

271-010-2

68513-66-6

Petroleum gas;

[A complex residuum from the
distillation of streams various
refinery operations. It consists of
hydrocarbons having carbon
numbers in the range of C4
through C5, predominantly
butane and boiling in the range
of approximately -11.7 °C to
27.8 °C (11 °F to 82 °F).]

649-088-00-8

Hydrocarbons, C1-4;

H K

271-032-2

68514-31-8

Petroleum gas;

[A complex combination of
hydrocarbons provided by ther-
mal cracking and absorber
operations and by distillation of
crude oil. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C1
through C4 and boiling in the
range of approximately minus
164 °C to minus 0.5 °C (-263 °F
to 31 °F).]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
5
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-089-00-3

649-090-00-9

Hydrocarbons, C1-4, sweetened;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by sub-
jecting hydrocarbon gases to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C1
through C4 and boiling in the
range of approximately -164 °C
to -0.5 °C (-263 °F to 31 °F).]

Hydrocarbons, C1-3;
Petroleum gas;
[A complex combination of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C3 and
boiling in the range of approxi-
mately minus 164 °C to minus
42 °C (-263 °F to -44 °F).]

H K

271-038-5

68514-36-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-259-7

68527-16-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-091-00-4

Hydrocarbons, C1-4, debutanizer
fraction;
Petroleum gas

H K

271-261-8

68527-19-5

H K

271-624-0

68602-83-5

649-092-00-X

Gases (petroleum), C1-5, wet;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of crude oil and/or the
cracking of tower gas oil. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

649-093-00-5

Hydrocarbons, C2-4;
Petroleum gas

H K

271-734-9

68606-25-7

649-094-00-0

Hydrocarbons, C3;
Petroleum gas

H K

271-735-4

68606-26-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
6
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-095-00-6

Gases (petroleum), alkylation
feed;

H K

271-737-5

68606-27-9

Petroleum gas;

[A complex combination of
hydrocarbons produced by the
catalytic cracking of gas oil. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C3 through C4.]

649-096-00-1

Gases (petroleum), depropanizer
bottoms fractionation off;

H K

271-742-2

68606-34-8

Petroleum gas;

[A complex combination of
hydrocarbons obtained from the
fractionation of depropanizer
bottoms. It consists predomi-
nantly of butane, isobutane and
butadiene.]

649-097-00-7

Gases (petroleum), refinery blend;

H K

272-183-7

68783-07-3

Petroleum gas;

[A complex combination
obtained from various processes.
It consists of hydrogen, hydrogen
sulfide and hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

649-098-00-2

Gases (petroleum), catalytic
cracking;

H K

272-203-4

68783-64-2

Petroleum gas;

[A complex combination of
hydrocarbons produced by the
distillation of the products from a
catalytic cracking process. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C3 through C5.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
6
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-099-00-8

Gases (petroleum), C2-4, swee-
tened;

H K

272-205-5

68783-65-3

Petroleum gas;

[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum distillate to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists predomi-
nantly of saturated and unsatu-
rated hydrocarbons having
carbon numbers predominantly
in the range of C2 through C4 and
boiling in the range of approxi-
mately -51 °C to -34 °C (-60 °F to
-30 °F).]

649-100-00-1

Gases (petroleum), crude oil
fractionation off;

H K

272-871-7

68918-99-0

Petroleum gas;

[A complex combination of
hydrocarbons produced by the
fractionation of crude oil. It
consists of saturated aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

649-101-00-7

Gases (petroleum), dehexanizer
off;

H K

272-872-2

68919-00-6

Petroleum gas;

[A complex combination of
hydrocarbons obtained by the
fractionation of combined
naphtha streams. It consists of
saturated aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C5.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
6
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-102-00-2

649-103-00-8

649-104-00-3

649-105-00-9

Gases (petroleum), light straight
run gasoline fractionation stabi-
lizer off;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by the
fractionation of light straight-run
gasoline. It consists of saturated
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

Gases (petroleum), naphtha uni-
finer desulfurization stripper off;
Petroleum gas;
[A complex combination of
hydrocarbons produced by a
naphtha unifiner desulfurization
process and stripped from the
naphtha product. It consists of
saturated aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C4.]

Gases (petroleum), straight-run
naphtha catalytic reforming off;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by the
catalytic reforming of straight-
run naphtha and fractionation of
the total effluent. It consists of
methane, ethane, and propane.]

Gases (petroleum), fluidized cat-
alytic cracker splitter overheads;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
fractionation of the charge to the
C3 -C4 splitter. It consists pre-
dominantly of C3 hydrocarbons.]

H K

272-878-5

68919-05-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-879-0

68919-06-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-882-7

68919-09-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-893-7

68919-20-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
6
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

272-883-2

68919-10-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-169-3

68952-76-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-170-9

68952-77-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-175-6

68952-81-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-106-00-4

649-107-00-X

649-108-00-5

649-109-00-0

Gases (petroleum), straight-run
stabilizer off;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
fractionation of the liquid from
the first tower used in the
distillation of crude oil. It consists
of saturated aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C4.]

Gases (petroleum), catalytic
cracked naphtha debutanizer;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation of catalytic cracked
naphtha. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C4.]

Tail gas (petroleum), catalytic
cracked distillate and naphtha
stabilizer;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by the
fractionation of catalytic cracked
naphtha and distillate. It consists
pre-
dominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C4.]

Tail gas (petroleum), thermal-
cracked distillate, gas oil and
naphtha absorber;
petroleum gas;
[A complex combination of
hydrocarbons obtained from the
separation of thermal-cracked
distillates, naphtha and gas oil. It
consists pedrominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

L

2
4
6
/
6
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

273-176-1

68952-82-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-265-5

68955-28-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-270-2

68955-34-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-110-00-6

649-111-00-1

649-112-00-7

Tail gas (petroleum), thermal
cracked hydrocarbon fractiona-
tion stabilizer, petroleum coking;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
fractionation stabilization of
thermal cracked hydrocarbons
from petroleum coking process.
It consists of hydrocarbons hav-
ing carbon numbers predomi-
nantly in the range of C1 through
C6.]

Gases (petroleum, light steam-
cracked, butadiene conc.;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
thermal cracking process. It con-
sists of hydrocarbons having a
carbon number predominantly of
C4.]

Gases (petroleum), straight-run
naphtha catalytic reformer stabi-
lizer overhead;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by the
catalytic reforming of straight-
run naphtha and the fractiona-
tion of the total effluent. It
consists of saturated aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C2 through C4.]

649-113-00-2

Hydrocarbons, C4;
Petroleum gas

H K

289-339-5

87741-01-3

649-114-00-8

Alkanes, C1-4, C3-rich;
Petroleum gas

H K

292-456-4

90622-55-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
6
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

295-404-9

92045-22-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

295-405-4

92045-23-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

HKS

295-463-0

92045-80-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-115-00-3

649-116-00-9

649-117-00-4

Gases (petroleum), steam-cracker
C3-rich;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
steam cracking process. It con-
sists predominantly of propylene
with some propane and boils in
the range of approximately -70 °
C to 0 °C (-94 °F to 32 °F).]

Hydrocarbons, C4, steam-cracker
distillate;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of the products of a
steam cracking process. It con-
sists predominantly of hydrocar-
bons having a carbon number of
C4, predominantly 1-butene and
2-butene, containing also butane
and isobutene and boiling in the
range of approximately minus
12 °C to 5 °C (10.4 °F to 41 °F).]

Petroleum gases, liquefied,
sweetened, C4 fraction;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by sub-
jecting a liquified petroleum gas
mix to a sweetening process to
oxidize mercaptans or to remove
acidic impurities. It consists pre-
dominantly of C4 saturated and
unsaturated hydrocarbons.]

649-118-00-X

Hydrocarbons, C4, 1,3-butadiene-
and isobutene-free;
Petroleum gas

H K

306-004-1

95465-89-7

649-119-00-5

Raffinates (petroleum), steam-
cracked C4 fraction cuprous
ammonium acetate extn., C3-5
and C3-5 unsatd., butadiene-free;
Petroleum gas

H K

307-769-4

97722-19-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
6
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-120-00-0

Gases (petroleum), amine system
feed;

H K

270-746-1

68477-65-6

Refinery gas;

[The feed gas to the amine system
for removal of hydrogen sulfide.
It consists of hydrogen. Carbon
monoxide, carbon dioxide,
hydrogen sulfide and aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5 may also
be present.]

649-121-00-6

Gases (petroleum), benzene unit
hydrodesulfurizer off;

H K

270-747-7

68477-66-7

Refinery gas;

[Off gases produced by the
benzene unit. It consists primar-
ily of hydrogen. Carbon monox-
ide and hydrocarbons having
carbon numbers predominantly
in the range of C1 through C6,
including benzene, may also be
present.]

649-122-00-1

Gases (petroleum), benzene unit
recycle, hydrogen-rich;

H K

270-748-2

68477-67-8

Refinery gas;

[A complex combination of
hydrocarbons obtained by recy-
cling the gases of the benzene
unit. It consists primarily of
hydrogen with various small
amounts of carbon monoxide
and hydrocarbons having carbon
numbers in the range of C1
through C6.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
6
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-123-00-7

Gases (petroleum), blend oil,
hydrogen-nitrogen-rich;

H K

270-749-8

68477-68-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

Refinery gas;

[A complex combination of
hydrocarbons obtained by distil-
lation of a blend oil. It consists
primarily of hydrogen and nitro-
gen with various small amounts
of carbon monoxide, carbon
dioxide, and aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C5.]

Gases (petroleum), catalytic
reformed naphtha stripper over-
heads;

Refinery gas;

[A complex combination of
hydrocarbons obtained from sta-
bilization of catalytic reformed
naphtha. Its consists of hydrogen
and saturated hydrocarbons hav-
ing carbon numbers predomi-
nantly in the range of C1 through
C4.]

649-124-00-2

H K

270-759-2

68477-77-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-125-00-8

Gases (petroleum), C6-8 catalytic
reformer recycle;

H K

270-761-3

68477-80-5

Refinery gas;

[A complex combination of
hydrocarbons produced by dis-
tillation of products from cataly-
tic reforming of C6-C8 feed and
recycled to conserve hydrogen. It
consists primarily of hydrogen. It
may also contain various small
amounts of carbon monoxide,
carbon dioxide, nitrogen, and
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
6
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-126-00-3

Gases (petroleum), C6-8 catalytic
reformer;
Refinery gas;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from cataly-
tic reforming of C6-C8feed. It
consists of hydrocarbons having
carbon numbers in the range of
C1 through C5 and hydrogen.]

H K

270-762-9

68477-81-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-127-00-9

Gases (petroleum), C6-8 catalytic
reformer recycle, hydrogen-rich;
Refinery gas

H K

270-763-4

68477-82-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-128-00-4

649-129-00-X

Gases (petroleum), C2-return
stream;
Refinery gas;
[A complex combination of
hydrocarbons obtained by the
extraction of hydrogen from a
gas stream which consists pri-
marily of hydrogen with small
amounts of nitrogen, carbon
monoxide, methane, ethane, and
ethylene. It contains predomi-
nantly hydrocarbons such as
methane, ethane, and ethylene
with small amounts of hydrogen,
nitrogen and carbon monoxide.]

Gases (petroleum), dry sour, gas-
concn.-unit-off;
Refinery gas;
[The complex combination of dry
gases from a gas concentration
unit. It consists of hydrogen,
hydrogen sulfide and hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C3.]

H K

270-766-0

68477-84-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-774-4

68477-92-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
6
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-130-00-5

Gases (petroleum), gas concn.
reabsorber distn.;

H K

270-776-5

68477-93-0

Refinery gas;

[A complex combination of
hydrocarbons produced by dis-
tillation of products from com-
bined gas streams in a gas
concentration reabsorber. It con-
sists predominantly of hydrogen,
carbon monoxide, carbon diox-
ide, nitrogen, hydrogen sulfide
and hydrocarbons having carbon
numbers in the range of C1
through C3.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-131-00-0

Gases (petroleum), hydrogen
absorber off;

H K

270-779-1

68477-96-3

Refinery gas;

[A complex combination
obtained by absorbing hydrogen
from a hydrogen rich stream. It
consists of hydrogen, carbon
monoxide, nitrogen, and
methane with small amounts of
C2 hydrocarbons.]

649-132-00-6

Gases (petroleum), hydrogen-
rich;

H K

270-780-7

68477-97-4

Refinery gas;

[A complex combination sepa-
rated as a gas from hydrocarbon
gases by chilling. It consists
primarily of hydrogen with var-
ious small amounts of carbon
monoxide, nitrogen, methane,
and C2 hydrocarbons.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
7
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-133-00-1

Gases (petroleum), hydrotreater
blend oil recycle, hydrogen-
nitrogen-rich;

H K

270-781-2

68477-98-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

Refinery gas;

[A complex combination
obtained from recycled hydro-
treated blend oil. It consists
primarily of hydrogen and nitro-
gen with various small amounts
of carbon monoxide, carbon
dioxide and hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

649-134-00-7

Gases (petroleum), recycle,
hydrogen-rich;

H K

270-783-3

68478-00-2

Refinery gas;

[A complex combination
obtained from recycled reactor
gases. It consists primarily of
hydrogen with various small
amounts of carbon monoxide,
carbon dioxide, nitrogen, hydro-
gen sulfide, and saturated alipha-
tic hydrocarbons having carbon
numbers in the range of C1
through C5.]

649-135-00-2

Gases (petroleum), reformer
make-up, hydrogen-rich;

H K

270-784-9

68478-01-3

Refinery gas;

[A complex combination
obtained from the reformers. It
consists primarily of hydrogen
with various small amounts of
carbon monoxide and aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-136-00-8

Gases (petroleum), reforming
hydrotreater;

H K

270-785-4

68478-02-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-137-00-3

649-138-00-9

Refinery gas;

[A complex combination
obtained from the reforming
hydrotreating process. It consists
primarily of hydrogen, methane,
and ethane with various small
amounts of hydrogen sulfide and
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C3 through C5.]

Gases (petroleum), reforming
hydrotreater, hydrogen-methane-
rich;

Refinery gas;

[A complex combination
obtained from the reforming
hydrotreating process. It consists
primarily of hydrogen and
methane with various small
amounts of carbon monoxide,
carbon dioxide, nitrogen and
saturated aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C2
through C5.]

Gases (petroleum), reforming
hydrotreater make-up, hydrogen-
rich;

Refinery gas;

[A complex combination
obtained from the reforming
hydrotreating process. It consists
primarily of hydrogen with var-
ious small amounts of carbon
monoxide and aliphatic hydro-
carbons having carbon numbers
predominantly in the range of C1
through C5.]

H K

270-787-5

68478-03-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-788-0

68478-04-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
7
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-139-00-4

649-140-00-X

649-141-00-5

649-142-00-0

Gases (petroleum), thermal
cracking distn.;
Refinery gas;
[A complex combination pro-
duced by distillation of products
from a thermal cracking process.
It consists of hydrogen, hydrogen
sulfide, carbon monoxide, carbon
dioxide and hydrocarbons having
carbon numbers predominantly
in the range of C1 through C6.]

Tail gas (petroleum), catalytic
cracker refractionation absorber;
Refinery gas;
[A complex combination of
hydrocarbons obtained from
refractionation of products from
a catalytic cracking process. It
consists of hydrogen and hydro-
carbons having carbon numbers
predominantly in the range of C1
through C3.]

Tail gas (petroleum), catalytic
reformed naphtha separator;
Refinery gas;
[A complex combination of
hydrocarbons obtained from the
catalytic reforming of straight
run naphtha. It consists of
hydrogen and hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C6.]

Tail gas (petroleum), catalytic
reformed naphtha stabilizer;
Refinery gas;
[A complex combination of
hydrocarbons obtained from the
stabilization of catalytic reformed
naphtha. It consists of hydrogen
and hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

H K

270-789-6

68478-05-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-805-1

68478-25-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-807-2

68478-27-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-808-8

68478-28-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-809-3

68478-29-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-810-9

68478-30-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-999-8

68513-14-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-003-4

68513-18-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-143-00-6

649-144-00-1

649-145-00-7

649-146-00-2

Tail gas (petroleum), cracked dis-
tillate hydrotreater separator;
Refinery gas;
[A complex combination of
hydrocarbons obtained by treat-
ing cracked distillates with
hydrogen in the presence of a
catalyst. It consists of hydrogen
and saturated aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C5.]

Tail gas (petroleum), hydrodesul-
furized straight-run naphtha
separator;
Refinery gas;
[A complex combination of
hydrocarbons obtained from
hydrodesulfurization of straight-
run naphtha. It consists of
hydrogen and saturated aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

Gases (petroleum), catalytic
reformed straight-run naphtha
stabilizer overheads;
Refinery gas;
[A complex combination of
hydrocarbons obtained from the
catalytic reforming of straight-
run naphtha followed by fractio-
nation of the total effluent. It
consists of hydrogen, methane,
ethane and propane.]

Gases (petroleum), reformer
effluent high-pressure flash drum
off;
Refinery gas;
[A complex combination pro-
duced by the high-pressure
flashing of the effluent from the
reforming reactor. It consists
primarily of hydrogen with var-
ious small amounts of methane,
ethane, and propane.]

L

2
4
6
/
7
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

271-005-5

68513-19-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-258-1

68527-15-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-623-5

68602-82-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-147-00-8

649-148-00-3

649-149-00-9

Gases (petroleum), reformer
effluent low-pressure flash drum
off;
Refinery gas;
[A complex combination pro-
duced by low-pressure flashing of
the effluent from the reforming
reactor. It consists primarily of
hydrogen with various small
amounts of methane, ethane, and
propane.]

Gases (petroleum), oil refinery
gas distn. off;
Refinery gas;
[A complex combination sepa-
rated by distillation of a gas
stream containing hydrogen, car-
bon monoxide, carbon dioxide
and hydrocarbons having carbon
numbers in the range of C1
through C6 or obtained by
cracking ethane and propane. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C2,
hydrogen, nitrogen, and carbon
monoxide.]

Gases (petroleum), benzene unit
hydrotreater depentanizer over-
heads;
Refinery gas;
[A complex combination pro-
duced by treating the feed from
the benzene unit with hydrogen
in the presence of a catalyst
followed by depentanizing. It
consists primarily of hydrogen,
ethane and propane with various
small amounts of nitrogen, car-
bon monoxide, carbon dioxide
and hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6. It may
contain trace amounts of ben-
zene.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-150-00-4

649-151-00-X

649-152-00-5

649-153-00-0

Gases (petroleum), secondary
absorber off, fluidized catalytic
cracker overheads fractionator;
Refinery gas;
[A complex combination pro-
duced by the fractionation of the
overhead products from the cat-
alytic cracking process in the
fluidized catalytic cracker. It
consists of hydrogen, nitrogen,
and hydrocarbons having carbon
numbers predominantly in the
range of C1 through C3.]

Petroleum products, refinery
gases;
Refinery gas;
[A complex combination which
consists primarily of hydrogen
with various small amounts of
methane, ethane, and propane.]

Gases (petroleum), hydrocracking
low-pressure separator;
Refinery gas;
[A complex combination
obtained by the liquid-vapor
separation of the hydrocracking
process reactor effluent. It con-
sists predominantly of hydrogen
and saturated hydrocarbons hav-
ing carbon numbers predomi-
nantly in the range of C1 through
C3.]

Gases (petroleum), refinery;
Refinery gas;
[A complex combination
obtained from various petroleum
refining operations. It consists of
hydrogen and hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C3.]

H K

271-625-6

68602-84-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

271-750-6

68607-11-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-182-1

68783-06-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-338-9

68814-67-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
7
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

272-343-6

68814-90-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-775-5

68911-58-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-776-0

68911-59-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-154-00-6

649-155-00-1

649-156-00-7

Gases (petroleum), platformer
products separator off;
Refinery gas;
[A complex combination
obtained from the chemical
reforming of naphthenes to aro-
matics. It consists of hydrogen
and saturated aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C2
through C4.]

Gases (petroleum), hydrotreated
sour kerosine depentanizer stabi-
lizer off;
Refinery gas;
[The complex combination
obtained from the depentanizer
stabilization of hydrotreated ker-
osine. It consists primarily of
hydrogen, methane, ethane, and
propane with various small
amounts of nitrogen, hydrogen
sulfide, carbon monoxide and
hydrocarbons having carbon
numbers predominantly in the
range of C4 through C5.]

Gases (petroleum), hydrotreated
sour kerosine flash drum;
Refinery gas;
[A complex combination
obtained from the flash drum of
the unit treating sour kerosine
with hydrogen in the presence of
a catalyst. It consists primarily of
hydrogen and methane with var-
ious small amounts of nitrogen,
carbon monoxide, and hydrocar-
bons having carbon numbers
predominantly in the range of C2
through C5.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

272-873-8

68919-01-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-874-3

68919-02-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-875-9

68919-03-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-876-4

68919-04-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-157-00-2

649-158-00-8

649-159-00-3

649-160-00-9

Gases (petroleum), distillate uni-
finer desulfurization stripper off;
Refinery gas;
[A complex combination
stripped from the liquid product
of the unifiner desulfurization
process. It consists of hydrogen
sulfide, methane, ethane, and
propane.]

Gases (petroleum), fluidized cat-
alytic cracker fractionation off;
Refinery gas;
[A complex combination pro-
duced by the fractionation of the
overhead product of the fluidized
catalytic cracking process. It
consists of hydrogen, hydrogen
sulfide, nitrogen, and hydrocar-
bons having carbon numbers
predominantly in the range of C1
through C5.]

Gases (petroleum), fluidized cat-
alytic cracker scrubbing second-
ary absorber off;
Refinery gas;
[A complex combination pro-
duced by scrubbing the overhead
gas from the fluidized catalytic
cracker. It consists of hydrogen,
nitrogen, methane, ethane and
propane.]

Gases (petroleum), heavy distil-
late hydrotreater desulfurization
stripper off;
Refinery gas;
[A complex combination
stripped from the liquid product
of the heavy distillate hydrotrea-
ter desulfurization process. It
consists of hydrogen, hydrogen
sulfide, and saturated aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

L

2
4
6
/
7
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-161-00-4

649-162-00-X

649-163-00-5

Gases (petroleum), platformer
stabilizer off, light ends frac-
tionation;
Refinery gas;
[A complex combination
obtained by the fractionation of
the light ends of the platinum
reactors of the platformer unit. It
consists of hydrogen, methane,
ethane and propane.]

Gases (petroleum), preflash tower
off, crude distn.;
Refinery gas;
[A complex combination pro-
duced from the first tower used
in the distillation of crude oil. It
consists of nitrogen and saturated
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

Gases (petroleum), tar stripper
off;
Refinery gas;
[A complex combination
obtained by the fractionation of
reduced crude oil. It consists of
hydrogen and hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C4.]

649-164-00-0

Gases (petroleum), unifiner strip-
per off;
Refinery gas;
[A combination of hydrogen and
methane obtained by fractiona-
tion of the products from the
unifiner unit.]

H K

272-880-6

68919-07-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-881-1

68919-08-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-884-8

68919-11-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

272-885-3

68919-12-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
7
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

273-173-5

68952-79-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-174-0

68952-80-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-269-7

68955-33-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

273-563-5

68989-88-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-165-00-6

649-166-00-1

649-167-00-7

649-168-00-2

Tail gas (petroleum), catalytic
hydrodesulfurized naphtha
separator;
Refinery gas;
[A complex combination of
hydrocarbons obtained from the
hydrodesulfurization of naphtha.
It consists of hydrogen, methane,
ethane, and propane.]

Tail gas (petroleum), straight-run
naphtha hydrodesulfurizer;
Refinery gas;
[A complex combination
obtained from the hydrodesul-
furization of straight-run
naphtha. It consists of hydrogen
and hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

Gases (petroleum), sponge
absorber off, fluidized catalytic
cracker and gas oil desulfurizer
overhead fractionation;
Refinery gas;
[A complex combination
obtained by the fractionation of
products from the fluidized cat-
alytic cracker and gas oil desul-
furizer. It consists of hydrogen
and hydrocarbons having carbon
numbers predominantly in the
range of C1 through C4.]

Gases (petroleum), crude distn.
and catalytic cracking;
Refinery gas;
[A complex combination pro-
duced by crude distillation and
catalytic cracking processes. It
consists of hydrogen, hydrogen
sulfide, nitrogen, carbon monox-
ide and paraffinic and olefinic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

L

2
4
6
/
8
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

295-397-2

92045-15-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

295-398-8

92045-16-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

295-399-3

92045-17-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

295-400-7

92045-18-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-169-00-8

649-170-00-3

649-171-00-9

649-172-00-4

Gases (petroleum), gas oil
diethanolamine scrubber off;
Refinery gas;
[A complex combination pro-
duced by desulfurization of gas
oils with diethanolamine. It con-
sists predominantly of hydrogen
sulfide, hydrogen and aliphatic
hydrocarbons having carbon
numbers in the range of C1
through C5.]

Gases (petroleum), gas oil hydro-
desulfurization effluent;
Refinery gas;
[A complex combination
obtained by separation of the
liquid phase from the effluent
from the hydrogenation reaction.
It consists predominantly of
hydrogen, hydrogen sulfide and
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C1 through C3.]

Gases (petroleum), gas oil hydro-
desulfurization purge;
Refinery gas;
[A complex combination of gases
obtained from the reformer and
from the purges from the hydro-
genation reactor. It consists pre-
dominantly of hydrogen and
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C1 through C4.]

Gases (petroleum), hydrogenator
effluent flash drum off;
Refinery gas;
[A complex combination of gases
obtained from flash of the efflu-
ents after the hydrogenation
reaction. It consists predomi-
nantly of hydrogen and aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
8
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

295-401-2

92045-19-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

295-402-8

92045-20-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

268-629-5

68131-75-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-173-00-X

649-174-00-5

649-177-00-1

Gases (petroleum), naphtha
steam cracking high-pressure
residual;
Refinery gas;
[A complex combination
obtained as a mixture of the non-
condensable portions from the
product of a naphtha steam
cracking process as well as resi-
dual gases obtained during the
preparation of subsequent prod-
ucts. It consists predominantly of
hydrogen and paraffinic and ole-
finic hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5 with
which natural gas may also be
mixed.]

Gases (petroleum), residue vis-
baking off;
Refinery gas;
[A complex combination
obtained from viscosity reduction
of residues in a furnace. It
consists predominantly of
hydrogen sulfide and paraffinic
and olefinic hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

Gases (petroleum), C3-4;
Petroleum gas;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from the
cracking of crude oil. It consists
of hydrocarbons having carbon
numbers in the range of C3
through C4, predominantly of
propane and propylene, and
boiling in the range of approxi-
mately -51 °C to -1 °C (-60 °F to
30 °F.)]

L

2
4
6
/
8
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

269-617-2

68307-98-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-618-8

68307-99-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-619-3

68308-00-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-178-00-7

649-179-00-2

649-180-00-8

Tail gas (petroleum), catalytic
cracked distillate and catalytic
cracked naphtha fractionation
absorber;
Petroleum gas;
[The complex combination of
hydrocarbons from the distilla-
tion of the products from cata-
lytic cracked distillates and
catalytic cracked naphtha. It
consists predominantly of
hydrocarbons having carbon
numbers in the range of C1
through C4.]

Tail gas (petroleum), catalytic
polymn. naphtha fractionation
stabilizer;
Petroleum gas;
[A complex combination of
hydrocarbons from the fractio-
nation stabilization products
from polymerization of naphtha.
It consists predominantly of
hydrocarbons having carbon
numbers in the range of C1
through C4.]

Tail gas (petroleum), catalytic
reformed naphtha fractionation
stabilizer, hydrogen sulfide-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation stabilization of cat-
alytic reformed naphtha and
from which hydrogen sulfide has
been removed by amine treat-
ment. It consists predominantly
of hydrocarbons having carbon
numbers predominantly in the
range of C1 through C4.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
8
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

269-620-9

68308-01-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-630-3

68308-10-1

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-623-5

68308-03-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-181-00-3

649-182-00-9

649-183-00-4

Tail gas (petroleum), cracked dis-
tillate hydrotreater stripper;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by treat-
ing thermal cracked distillates
with hydrogen in the presence of
a catalyst. It consists predomi-
nantly of saturated hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C6.]

Tail gas (petroleum), straight-run
distillate hydrodesulfurizer,
hydrogen sulfide-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from cat-
alytic hydrodesulfurization of
straight run distillates and from
which hydrogen sulfide has been
removed by amine treatment. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C4.]

Tail gas (petroleum), gas oil
catalytic cracking absorber;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
distillation of products from the
catalytic cracking of gas oil. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

L

2
4
6
/
8
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

269-624-0

68308-04-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-625-6

68308-05-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-626-1

68308-06-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-184-00-X

Tail gas (petroleum), gas recovery
plant;
Petroleum gas;
[A complex combination of
hydrocarbons from the distilla-
tion of products from miscella-
neous hydrocarbon streams. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

649-185-00-5

Tail gas (petroleum), gas recovery
plant deethanizer;
Petroleum gas;
[A complex combination of
hydrocarbons from the distilla-
tion of products from miscella-
neous hydrocarbon streams. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C4.]

649-186-00-0

Tail gas (petroleum), hydrodesul-
furized distillate and hydrodesul-
furized naphtha fractionator,
acid-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation of hydrodesulfur-
ized naphtha and distillate
hydrocarbon streams and treated
to remove acidic impurities. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
8
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

269-627-7

68308-07-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-629-8

68308-09-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

269-631-9

68308-11-2

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-187-00-6

649-188-00-1

649-189-00-7

Tail gas (petroleum), hydrodesul-
furized vacuum gas oil stripper,
hydrogen sulfide-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
stripping stabilization of catalytic
hydrodesulfurized vacuum gas oil
and from which hydrogen sulfide
has been removed by amine
treatment. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C6.]

Tail gas (petroleum), light
straight-run naphtha stabilizer,
hydrogen sulfide-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation stabilization of light
straight run naphtha and from
which hydrogen sulfide has been
removed by amine treatment. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C5.]

Tail gas (petroleum), propane-
propylene alkylation feed prep
deethanizer;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
distillation of the reaction prod-
ucts of propane with propylene.
It consists of hydrocarbons hav-
ing carbon numbers predomi-
nantly in the range of C1 through
C4.]

L

2
4
6
/
8
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

269-632-4

68308-12-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-071-2

68409-99-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-190-00-2

649-191-00-8

Tail gas (petroleum), vacuum gas
oil hydrodesulfurizer, hydrogen
sulfide-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from cat-
alytic hydrodesulfurization of
vacuum gas oil and from which
hydrogen sulfide has been
removed by amine treatment. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C6.]

Gases (petroleum), catalytic
cracked overheads;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from the
catalytic cracking process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C3 through C5 and
boiling in the range of approxi-
mately -48 °C to 32 °C (-54 °F to
90 °F).]

649-193-00-9

Alkanes, C1-2;
Petroleum gas

H K

270-651-5

68475-57-0

649-194-00-4

Alkanes, C2-3;
Petroleum gas

H K

270-652-0

68475-58-1

649-195-00-X

Alkanes, C3-4;
petroleum gas

H K

270-653-6

68475-59-2

649-196-00-5

Alkanes, C4-5;
Petroleum gas

H K

270-654-1

68475-60-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
8
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-667-2

68476-26-6

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-670-9

68476-29-9

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-197-00-0

649-198-00-6

Fuel gases;
Petroleum gas;
[A combination of light gases. It
consists predominantly of
hydrogen and/or low molecular
weight hydrocarbons.]

Fuel gases, crude oil of distillates;
Petroleum gas;
[A complex combination of light
gases produced by distillation of
crude oil and by catalytic
reforming of naphtha. It consists
of hydrogen and hydrocarbons
having carbon numbers predo-
minantly in the range of C1
through C4 and boiling in the
range of approximately -217 °C
to -12 °C (-423 °F to 10 °F).]

649-199-00-1

Hydrocarbons, C3-4;
Petroleum gas

H K

270-681-9

68476-40-4

649-200-00-5

Hydrocarbons, C4-5;
Petroleum gas

H K

270-682-4

68476-42-6

649-201-00-0

Hydrocarbons, C2-4, C3-rich;
Petroleum gas

H K

270-689-2

68476-49-3

HKS

270-704-2

68476-85-7

649-202-00-6

Petroleum gases, liquefied;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of crude oil. It consists
of hydrocarbons having carbon
numbers predominantly in the
range of C3 through C7 and
boiling in the range of approxi-
mately -40 °C to 80 °C (-40 °F to
176 °F).]

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

F+; T
R: 45-46-12
S: 53-45

L

2
4
6
/
8
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

HKS

270-705-8

68476-86-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-724-1

68477-33-8

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-726-2

68477-35-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-203-00-1

649-204-00-7

649-205-00-2

Petroleum gases, liquefied,
sweetened;
Petroleum gas;
[A complex combination of
hydrocarbons obtained by sub-
jecting liquefied petroleum gas
mix to a sweetening process to
convert mercaptans or to remove
acidic impurities. It consists of
hydrocarbons having carbon
numbers predominantly in the
range of C3 through C7 and
boiling in the range of approxi-
mately -40 °C to 80 °C (-40 °F to
176 °F).]

gases (petroleum), C3-4, isobu-
tane-rich;
Petroleum gas;
[A complex combination of
hydrocarbons from the distilla-
tion of saturated and unsaturated
hydrocarbons usually ranging in
carbon numbers from C3 through
C6, predominantly butane and
isobutane. It consists of saturated
and unsaturated hydrocarbons
having carbon numbers in the
range of C3 through C4,
predominantly isobutane.]

Distillates (petroleum), C3-6,
piperylene-rich;
Petroleum gas;
[A complex combination of
hydrocarbons from the distilla-
tion of saturated and unsaturated
aliphatic hydrocarbons usually
ranging in the carbon numbers
C3 through C6. It consists of
saturated and unsaturated hydro-
carbons having carbon numbers
in the range of C3 through C6,
predominantly piperylenes.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
8
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H K

270-750-3

68477-69-0

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-751-9

68477-70-3

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-752-4

68477-71-4

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H K

270-754-5

68477-72-5

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

649-206-00-8

649-207-00-3

649-208-00-9

649-209-00-4

Gases (petroleum), butane splitter
overheads;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
distillation of the butane stream.
It consists of aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C3
through C4.]

Gases (petroleum), C2-3;
Petroleum gas;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
catalytic fractionation process. It
contains predominantly ethane,
ethylene, propane, and propy-
lene.]

Gases (petroleum), catalytic-
cracked gas oil depropanizer
bottoms, C4-rich acid-free;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from
fractionation of catalytic cracked
gas oil hydrocarbon stream and
treated to remove hydrogen sul-
fide and other acidic compo-
nents. It consists of hydrocarbons
having carbon numbers in the
range of C3 through C5,
predominantly C4.]

Gases (petroleum), catalytic-
cracked naphtha debutanizer
bottoms, C3-5-rich;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
stabilization of catalytic cracked
naphtha. It consists of aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C3 through C5.]

L

2
4
6
/
9
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

649-210-00-X

649-261-00-8

649-262-00-3

649-263-00-9

Tail gas (petroleum), isomerized
naphtha fractionation stabilizer;
Petroleum gas;
[A complex combination of
hydrocarbons obtained from the
fractionation stabilization prod-
ucts from isomerized naphtha. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C1 through C4.]

Gasoline, natural;
Low boiling point naphtha;
[A complex combination of
hydrocarbons separated from
natural gas by processes such as
refrigeration or absorption. It
consists predominantly of satu-
rated aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C8 and boiling in the
range of approximately minus
20 °C to 120 °C (-4 °F to 248 °F).]

Naphtha;
Low boiling point naphtha;
[Refined, partly refined, or unre-
fined petroleum products pro-
duced by the distillation of
natural gas. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C5
through C6 and boiling in the
range of approximately 100 °C to
200 °C (212 °F to 392 °F).]

Ligroine;
Low boiling point naphtha;
[A complex combination of
hydrocarbons obtained by the
fractional distillation of petro-
leum. This fraction boils in a
range of approximately 20 °C to
135 °C (58 °F to 275 °F).]

H K

269-628-2

68308-08-7

F+; R12
Carc. Cat. 1; R45
Muta. Cat. 2; R46

F+; T
R: 45-46-12
S: 53-45

H P

232-349-1

8006-61-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

232-443-2

8030-30-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

232-453-7

8032-32-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-264-00-4

Naphtha (petroleum), heavy
straight-run;

H P

265-041-0

64741-41-9

Low boiling point naphtha;

[A complex combination of
hydrocarbons produced by dis-
tillation of crude oil. It consists of
hydrocarbons having carbon
numbers predominantly in the
range of C6 through C12 and
boiling in the range of approxi-
mately 65 °C to 230 °C (149 °F to
446 °F).]

649-265-00-X

Naphtha (petroleum), full-range
straight-run;

H P

265-042-6

64741-42-0

Low boiling point naphtha;

[A complex combination of
hydrocarbons produced by dis-
tillation of crude oil. It consists of
hydrocarbons having carbon
numbers predominantly in the
range of C4 through C11 and
boiling in the range of approxi-
mately -20 °C to 220 °C (-4 °F to
428 °F).]

649-266-00-5

Naphtha (petroleum), light
straight-run;

H P

265-046-8

64741-46-4

Low boiling point naphtha;

[A complex combination of
hydrocarbons produced by dis-
tillation of crude oil. It consists
predominantly of aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C4 through C10 and
boiling in the range of approxi-
mately -20 °C to 180 °C (-4 °F to
356 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C <10 %: T; R45-46

4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

L

2
4
6
/
9
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

649-267-00-0

649-268-00-6

649-269-00-1

649-270-00-7

Solvent naphtha (petroleum),
light aliph.;
Low boiling point naphtha;
[A complex combination of
hydrocarbons obtained from the
distillation of crude oil or natural
gasoline. It consists predomi-
nantly of saturated hydrocarbons
having carbon numbers predo-
minantly in the range of C5
through C10 and boiling in the
range of approximately 35 °C to
160 °C (95 °F to 320 °F).]

Distillates (petroleum), straight-
run light;
Low boiling point naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of crude oil It consists
of hydrocarbons having carbon
numbers predominantly in the
range of C2 through C7 and
boiling in the range of approxi-
mately -88 °C to 99 °C (-127 °F
to 210 °F).]

Gasoline, vapor-recovery;
Low boiling point naphtha;
[A complex combination of
hydrocarbons separated from the
gases from vapor recovery sys-
tems by cooling. It consists of
hydrocarbons having carbon
numbers predominantly in the
range of C4 through C11 and
boiling in the range of approxi-
mately -20 °C to 196 °C(-4 °F to
384 °F).]

Gasoline, straight-run, topping-
plant;
Low boiling point naphtha;
[A complex combination of
hydrocarbons produced from the
topping plant by the distillation
of crude oil. It boils in the range
of approximately 36.1 °C to
193.3 °C (97 °F to 380 °F).]

H P

265-192-2

64742-89-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-077-5

68410-05-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

271-025-4

68514-15-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

271-727-0

68606-11-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 ≤ C < 10 %: T; R45-46

4

4

4

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-271-00-2

Naphtha (petroleum),
unsweetened;

H P

272-186-3

68783-12-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Low boiling point naphtha;

[A complex combination of
hydrocarbons produced from the
distillation of naphtha streams
from various refinery processes It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C12
and boiling in the range of
approximately 0 °C to 230 °C
(25 °F to 446 °F).]

Distillates (petroleum), light
straight-run gasoline fractiona-
tion stabilizer overheads;

Low boiling point naphtha;

[A complex combination of
hydrocarbons obtained by the
fractionation of light straight-run
gasoline. It consists of saturated
aliphatic hydrocarbons having
carbon numbers predominantly
in the range of C3 through C6.]

649-272-00-8

H P

272-931-2

68921-08-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-273-00-3

Naphtha (petroleum), heavy
straight run, arom.-contg.;

H P

309-945-6

101631-20-3

Low boiling point naphtha;

[A complex combination of
hydrocarbons obtained from a
distillation process of crude
petroleum. It consists predomi-
nantly of hydrocarbons having
carbon numbers in the range of
C8 through C12 and boiling in the
range of approximately 130 °C to
210 °C (266 °F to 410 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

L

2
4
6
/
9
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

649-274-00-9

Naphtha (petroleum), full-range
alkylate;

H P

265-066-7

64741-64-6

Low boiling point modified
naphtha;

[A complex combination of
hydrocarbons produced by dis-
tillation of the reaction products
of isobutane with monoolefinic
hydrocarbons usually ranging in
carbon numbers from C3 through
C5. It consists of predominantly
branched chain saturated hydro-
carbons having carbon numbers
predominantly in the range of C7
through C12 and boiling in the
range of approximately 90 °C to
220 °C (194 °F to 428 °F).]

649-275-00-4

Naphtha (petroleum), heavy
alkylate;

H P

265-067-2

64741-65-7

Low boiling point modified
naphtha;

[A complex combination of
hydrocarbons produced by dis-
tillation of the reaction products
of isobutane with monoolefinic
hydrocarbons usually ranging in
carbon numbers from C3 to C5. It
consists of predominantly
branched chain saturated hydro-
carbons having carbon numbers
predominantly in the range of C9
through C12 and boiling in the
range of approximately 150 °C to
220 °C (302 °F to 428 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

E
N

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-068-8

64741-66-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-073-5

64741-70-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-086-6

64741-84-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-276-00-X

649-277-00-5

649-278-00-0

Naphtha (petroleum), light alky-
late;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons produced by dis-
tillation of the reaction products
of isobutane with monoolefinic
hydrocarbons usually ranging in
carbon numbers from C3 through
C5. It consists of predominantly
branched chain saturated hydro-
carbons having carbon numbers
predominantly in the range of C7
through C10 and boiling in the
range of approximately 90 °C to
160 °C (194 °F to 320 °F).]

Naphtha (petroleum), isomeriza-
tion;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained from cat-
alytic isomerization of straight
chain paraffinic C4 through C6
hydrocarbons. It consists predo-
minantly of saturated hydrocar-
bons such as isobutane,
isopentane, 2,2-dimethylbutane,
2-methylpentane, and 3-methyl-
pentane.]

Naphtha (petroleum), solvent-
refined light;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained as the
raffinate from a solvent extrac-
tion process. It consists predo-
minantly of aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C5 through C11 and
boiling in the range of approxi-
mately 35 °C to 190 °C (95 °F to
374 °F).]

L

2
4
6
/
9
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-095-5

64741-92-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-088-5

68410-71-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-349-3

68425-35-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-279-00-6

649-280-00-1

649-281-00-7

Naphtha (petroleum), solvent-
refined heavy;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained as the
raffinate from a solvent extrac-
tion process. It consists predo-
minantly of aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C12 and
boiling in the range of approxi-
mately 90 °C to 230 °C (194 °F to
446 °F).]

Raffinates (petroleum), catalytic
reformer ethylene glycol-water
countercurrent exts.;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained as the
raffinate from the UDEX extrac-
tion process on the catalytic
reformer stream. It consists of
saturated hydrocarbons having
carbon numbers predominantly
in the range of C6 through C9.]

Raffinates (petroleum), reformer,
Lurgi unit-sepd.;
Low boiling point modified
naphtha;
[The complex combination of
hydrocarbons obtained as a raf-
finate from a Lurgi separation
unit. It consists predominantly of
non-aromatic hydrocarbons with
various small amounts of aro-
matic hydrocarbons having car-
bon numbers predominantly in
the range of C6 through C8.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

271-267-0

68527-27-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-315-5

91995-53-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

295-430-0

92045-49-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

649-282-00-2

649-283-00-8

649-284-00-3

Naphtha (petroleum), full-range
alkylate, butane-contg.;
Low boiling point modified
naphta;
[A complex combination of
hydrocarbons produced by the
distillation of the reaction prod-
ucts of isobutane with monoole-
finic hydrocarbons usually
ranging in carbon numbers from
C3 through C5. It consists of
predominantly branched chain
saturated hydrocarbons having
carbon numbers predominantly
in the range of C7 through C12
with some butanes and boiling in
the range of approximately 35 °C
to 200 °C (95 °F to 428 °F).]

Distillates (petroleum), naphtha
steam cracking-derived, solvent-
refined light hydrotreated;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained as the
raffinates from a solvent extrac-
tion process of hydrotreated light
distillate from steam-cracked
naphtha.]

Naphtha (petroleum), C4-12
butane-alkylate, isooctane-rich;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained by alky-
lation of butanes. It consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C12, rich in isooctane,
and boiling in the range of
approximately 35 °C to 210 °C
(95 °F to 410 °F).]

L

2
4
6
/
9
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-436-3

92045-55-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-440-5

92045-58-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

295-446-8

92045-64-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

649-285-00-9

649-286-00-4

649-287-00-X

Hydrocarbons, hydrotreated light
naphtha distillates, solvent-
refined;
Low boiling point modified
naphtha;
[A combination of hydrocarbons
obtained from the distillation of
hydrotreated naphtha followed
by a solvent extraction and dis-
tillation process. It consists pre-
dominantly of saturated
hydrocarbons boiling in the
range of approximately 94 °C to
99 °C (201 °F to 210 °F).]

Naphtha (petroleum), isomeriza-
tion, C6-fraction;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained by distil-
lation of a gasoline which has
been catalytically isomerized. It
consists predominantly of hexane
isomers boiling in the range of
approximately 60 °C to 66 °C
(140 °F to 151 °F).]

Hydrocarbons, C6-7, naphtha-
cracking, solvent-refined;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained by the
sorption of benzene from a
catalytically fully hydrogenated
benzene-rich hydrocarbon cut
that was distillatively obtained
from prehydrogenated cracked
naphtha. It consists predomi-
nantly of paraffinic and
naphthenic hydrocarbons having
carbon numbers predominantly
in the range of C6 through C7 and
boiling in the range of approxi-
mately 70 °C to 100 °C (158 °F to
212 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
9
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

309-871-4

101316-67-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-055-7

64741-54-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-056-2

64741-55-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-288-00-5

649-289-00-0

649-290-00-6

Hydrocarbons, C6-rich, hydro-
treated light naphtha distillates,
solvent-refined;
Low boiling point modified
naphtha;
[A complex combination of
hydrocarbons obtained by distil-
lation of hydrotreated naphtha
followed by solvent extraction. It
consists predominantly of satu-
rated hydrocarbons and boiling
in the range of approximately
65 °C to 70 °C (149 °F to 158 °
F).]

Naphtha (petroleum), heavy cat-
alytic cracked;
Low boiling point cat-cracked
naphtha;
[A complex combination of
hydrocarbons produced by a
distillation of products from a
catalytic cracking process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C6 through C12
and boiling in the range of
approximately 65 °C to 230 °C
(148 °F to 446 °F). It contains a
relatively large proportion of
unsaturated hydrocarbons.]

Naphtha (petroleum), light cata-
lytic cracked;
Low boiling point cat-cracked
naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
catalytic cracking process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C4 through C11
and boiling in the range of
approximately -20 °C to 190 °C
(-4 °F to 374 °F). It contains a
relatively large proportion of
unsaturated hydrocarbons.]

L

2
4
6
/
1
0
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-291-00-1

Hydrocarbons, C3-11, catalytic
cracker distillates;

H P

270-686-6

68476-46-0

Low boiling point cat-cracked
naphtha;

[A complex combination of
hydrocarbons produced by the
distillations of products from a
catalytic cracking process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C3 through C11
and boiling in a range approxi-
mately up to 204 °C (400 °F).]

649-292-00-7

Naphtha (petroleum), catalytic
cracked light distd.;

H P

272-185-8

68783-09-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-311-3

91995-50-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Low boiling point cat-cracked
naphtha;

[A complex combination of
hydrocarbons produced by the
distillation of products from a
catalytic cracking process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C1 through C5.]

Distillates (petroleum), naphtha
steam cracking-derived, hydro-
treated light arom.;

Low boiling point cat-cracked
naphtha.;

[A complex combination of
hydrocarbons obtained by treat-
ing a light distillate from steam-
cracked naphtha. It consists pre-
dominantly of aromatic hydro-
carbons.]

649-293-00-2

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
0
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-431-6

92045-50-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-441-0

92045-59-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-794-0

92128-94-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-294-00-8

649-295-00-3

649-296-00-9

Naphtha (petroleum), heavy cat-
alytic cracked, sweetened;
Low boiling point cat-cracked
naphtha;
[A complex combination of
hydrocarbons obtained by sub-
jecting a catalytic cracked petro-
leum distillate to a sweetening
process to convert mercaptans or
to remove acidic impurities. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C6 through C12 and
boiling in the range of approxi-
mately 60 °C to 200 °C (140 °F to
392 °F).]

Naphtha (petroleum), light cata-
lytic cracked sweetened;
Low boiling point cat-cracked
naphtha;
[A complex combination of
hydrocarbons obtained by sub-
jecting naphtha from a catalytic
cracking process to a sweetening
process to convert mercaptans or
to remove acidic impurities. It
consists predominantly of
hydrocarbons boiling in a range
of approximately 35 °C to 210 °C
(95 °F to 410 °F).]

Hydrocarbons, C8-12, catalytic-
cracking, chem. neutralized;
Low boiling point cat-cracked
naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of a cut from the
catalytic cracking process, having
undergone an alkaline washing. It
consists predominantly of
hydrocarbons having carbon
numbers in the range of C8
through C12 and boiling in the
range of approximately 130 °C to
210 °C (266 °F to 410 °F).]

L

2
4
6
/
1
0
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-297-00-4

Hydrocarbons, C8-12, catalytic
cracker distillates;

H P

309-974-4

101794-97-2

Low boiling point cat-cracked
naphtha;

[A complex combination of
hydrocarbons obtained by distil-
lation of products from a cataly-
tic cracking process. It consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C8
through C12 and boiling in the
range of approximately 140 °C to
210 °C (284 °F to 410 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-298-00-X

Hydrocarbons, C8-12, catalytic
cracking, chem. neutralized,
sweetened;

Low boiling point cat-cracked
naphtha

H P

309-987-5

101896-28-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-299-00-5

Naphtha (petroleum), light cata-
lytic reformed;

H P

265-065-1

64741-63-5

Low boiling point cat-reformed
naphtha;

[A complex combination of
hydrocarbons produced from the
distillation of products from a
catalytic reforming process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C11
and boiling in the range of
approximately 35 °C to 190 °C
(95 °F to 374 °F). It contains a
relatively large proportion of
aromatic and branched chain
hydrocarbons. This stream may
contain 10 vol. % or more ben-
zene.]

4

4

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
0
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-070-9

64741-68-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-660-4

68475-79-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-300-00-9

649-301-00-4

Naphtha (petroleum), heavy cat-
alytic reformed;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons produced from the
distillation of products from a
catalytic reforming process. It
consists of predominantly aro-
matic hydrocarbons having car-
bon numbers predominantly in
the range of C7 through C12 and
boiling in the range of approxi-
mately 90 °C to 230 °C (194 °F to
446 °F).]

Distillates (petroleum), catalytic
reformed depentanizer;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons from the distilla-
tion of products from a catalytic
reforming process. It consists
predominantly of aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C3 through C6 and
boiling in the range of approxi-
mately -49 °C to 63 °C (-57 °F to
145 °F).]

649-302-00-X

Hydrocarbons, C2-6, C6-8 catalytic
reformer;
Low boiling point cat-reformed
naphtha

H P

270-687-1

68476-47-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-303-00-5

Residues (petroleum), C6-8 cata-
lytic reformer;
Low boiling point cat-reformed
naphtha;
[A complex residuum from the
catalytic reforming of C6-8 feed. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C2 through C6.]

H P

270-794-3

68478-15-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

L

2
4
6
/
1
0
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-304-00-0

649-305-00-6

649-306-00-1

Naphtha (petroleum), light cata-
lytic reformed, arom.-free;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons obtained from dis-
tillation of products from a
catalytic reforming process. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C5 through C8 and
boiling in the range of approxi-
mately 35 °C to 120 °C (95 °F to
248 °F). It contains a relatively
large proportion of branched
chain hydrocarbons with the
aromatic components removed.]

Distillates (petroleum), catalytic
reformed straight-run naphtha
overheads;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons obtained by the
catalytic reforming of straight-
run naphtha followed by the
fractionation of the total effluent.
It consists of saturated aliphatic
hydrocarbons having carbon
numbers predominantly in the
range of C2 through C6.]

Petroleum products, hydrofiner-
powerformer reformates;
Low boiling point cat-reformed
naphtha;
[The complex combination of
hydrocarbons obtained in a
hydrofiner-powerformer process
and boiling in a range of
approximately 27 °C to 210 °C
(80 °F to 410 °F).]

H P

270-993-5

68513-03-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

271-008-1

68513-63-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

271-058-4

68514-79-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
0
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

H P

272-895-8

68919-37-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C <10 %: T; R45-46

Notes
related to
prepa-
rations

4

H P

273-271-8

68955-35-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

285-509-8

85116-58-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-307-00-7

649-308-00-2

649-309-00-8

Naphtha (petroleum), full-range
reformed;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of the products from a
catalytic reforming process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C12
and boiling in the range of
approximately 35 °C to 230 °C
(95 °F to 446 °F).]

Naphtha (petroleum), catalytic
reformed;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
catalytic reforming process. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C4 through C12
and boiling in the range of
approximately 30 °C to 220 °C
(90 °F to 430 °F). It contains a
relatively large proportion of
aromatic and branched chain
hydrocarbons. This stream may
contain 10 vol. % or more ben-
zene.]

Distillates (petroleum), catalytic
reformed hydrotreated light, C8-12
arom. fraction;
Low boiling point cat-reformed
naphtha;
[A complex combination of
alkylbenzenes obtained by the
catalytic reforming of petroleum
naphtha. It consists predomi-
nantly of alkylbenzenes having
carbon numbers predominantly
in the range of C8 through C10
and boiling in the range of
approximately 160 °C to 180 °C
(320 °F to 356 °F).]

L

2
4
6
/
1
0
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

649-310-00-3

Aromatic hydrocarbons, C8, cat-
alytic reforming-derived;

H P

295-279-0

91995-18-5

Low boiling point cat-reformed
naphtha

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-311-00-9

Aromatic hydrocarbons, C7-12,
C8-rich;

H P

297-401-8

93571-75-6

Low boiling point cat-reformed
naphtha;

[A complex combination of
hydrocarbons obtained by separ-
ation from the platformate-con-
taining fraction. It consists
predominantly of aromatic
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C12 (pri-
marily C8) and can contain non-
aromatic hydrocarbons, both
boiling in the range of approxi-
mately 130 °C to 200 °C (266 °F
to 392 °F).]

649-312-00-4

Gasoline, C5-11, high-octane sta-
bilized reformed;

H P

297-458-9

93572-29-3

Low boiling point cat-reformed
naphtha;

[A complex high octane combi-
nation of hydrocarbons obtained
by the catalytic dehydrogenation
of a predominantly naphthenic
naphtha. It consists predomi-
nantly of aromatics and non-
aromatics having carbon num-
bers predominantly in the range
of C5 through C11 and boiling in
the range of approximately 45 °C
to 185 °C (113 °F to 365 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Notes
related to
prepa-
rations

4

4

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
0
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

297-465-7

93572-35-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

297-466-2

93572-36-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-075-6

64741-74-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-313-00-X

649-314-00-5

649-316-00-6

Hydrocarbons, C7-12, C >9-arom.-
rich, reforming heavy fraction;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons obtained by separ-
ation from the platformate-con-
taining fraction. It consists
predominantly of nonaromatic
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C12 and
boiling in the range of approxi-
mately 120 °C to 210 °C (248 °F
to 380 °F) and C9 and higher
aromatic hydrocarbons.]

Hydrocarbons, C5-11, nonaroms.-
rich, reforming light fraction;
Low boiling point cat-reformed
naphtha;
[A complex combination of
hydrocarbons obtained by separ-
ation from the platformate-con-
taining fraction. It consists
predominantly of nonaromatic
hydrocarbons having carbon
numbers predominantly in the
range of C5 through C11 and
boiling in the range of approxi-
mately 35 °C to 125 °C (94 °F to
257 °F), benzene and toluene.]

Naphtha (petroleum), light ther-
mal cracked;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons from distillation of
products from a thermal cracking
process. It consists predomi-
nantly of unsaturated hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C8 and boiling in the
range of approximately -10 °C to
130 °C (14 °F to 266 °F).]

L

2
4
6
/
1
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-085-0

64741-83-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

267-563-4

67891-79-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

267-565-5

67891-80-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-317-00-1

649-318-00-7

649-319-00-2

Naphtha (petroleum), heavy
thermal cracked;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons from distillation of
the products from a thermal
cracking process. It consists pre-
dominantly of unsaturated
hydrocarbons having carbon
numbers predominantly in the
range of C6 through C12 and
boiling in the range of approxi-
mately 65 °C to 220 °C (148 °F to
428 °F).]

Distillates (petroleum), heavy
arom.;
Low boiling point thermally
cracked naphtha;
[The complex combination of
hydrocarbons from the distilla-
tion of the products from the
thermal cracking of ethane and
propane. This higher boiling
fraction consists predominantly
of C5-7 aromatic hydrocarbons
with some unsaturated aliphatic
hydrocarbons having carbon
number predominantly of C5.
This stream may contain ben-
zene.]

Distillates (petroleum), light
arom.;
Low boiling point thermally
cracked naphtha;
[The complex combination of
hydrocarbons from the distilla-
tion of the products from the
thermal cracking of ethane and
propane. This lower boiling frac-
tion consists predominantly of
C5-7 aromatic hydrocarbons with
some unsaturated aliphatic
hydrocarbons having a carbon
number predominantly of C5.
This stream may contain ben-
zene.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
0
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

270-344-6

68425-29-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-658-3

68475-70-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

271-631-9

68603-00-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-320-00-8

649-321-00-3

649-322-00-9

Distillates (petroleum), naphtha-
raffinate pyrolyzate-derived,
gasoline-blending;
Low boiling point thermally
cracked naphtha;
[The complex combination of
hydrocarbons obtained by the
pyrolysis fractionation at 816 °C
(1 500 °F) of naphtha and raffi-
nate. It consists predominantly of
hydrocarbons having a carbon
number of C9 and boiling at
approximately 204 °C (400 °F).]

Aromatic hydrocarbons, C6-8,
naphtha-raffinate pyrolyzate-
derived;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons obtained by the
fractionation pyrolysis at 816 °C
(1 500 °F) of naphtha and raffi-
nate. It consists predominantly of
aromatic hydrocarbons having
carbon numbers predominantly
in the range of C6 through C8,
including benzene.]

Distillates (petroleum), thermal
cracked naphtha and gas oil;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons produced by dis-
tillation of thermally cracked
naphtha and/or gas oil. It consists
predominantly of olefinic hydro-
carbons having a carbon number
of C5 and boiling in the range of
approximately 33 °C to 60 °C
(91 °F to 140 °F).]

L

2
4
6
/
1
1
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

271-632-4

68603-01-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

271-634-5

68603-03-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

273-266-0

68955-29-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 %≤ C <10 %: T; R45-46

4

649-323-00-4

649-324-00-X

649-325-00-5

Distillates (petroleum), thermal
cracked naphtha and gas oil, C5-
dimer-contg.;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons produced by the
extractive distillation of thermal
cracked naphtha and/or gas oil. It
consists predominantly of
hydrocarbons having a carbon
number of C5 with some dimer-
ized C5 olefins and boiling in the
range of approximately 33 °C to
184 °C (91 °F to 363 °F).]

Distillates (petroleum), thermal
cracked naphtha and gas oil,
extractive;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons produced by the
extractive distillation of thermal
cracked naphtha and/or gas oil.. It
consists of paraffinic and olefinic
hydrocarbons, predominantly
isoamylenes such as 2-methyl-1-
butene and 2-methyl-2-butene
and boiling in the range of
approximately 31 °C to 40 °C
(88 °F to 104 °F).]

Distillates (petroleum), light ther-
mal cracked, debutanized arom.;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
thermal cracking process. It con-
sists predominantly of aromatic
hydrocarbons, primarily ben-
zene.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-447-3

92045-65-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-150-3

64742-48-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-151-9

64742-49-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-326-00-0

649-327-00-6

649-328-00-1

Naphtha (petroleum), light ther-
mal cracked, sweetened;
Low boiling point thermally
cracked naphtha;
[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum distillate from
the high temperature thermal
cracking of heavy oil fractions to
a sweetening process to convert
mercaptans. It consists predomi-
nantly of aromatics, olefins and
saturated hydrocarbons boiling in
the range of approximately 20 °C
to 100 °C (68 °F to 212 °F).]

Naphtha (petroleum), hydro-
treated heavy;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by treat-
ing a petroleum fraction with
hydrogen in the presence of a
catalyst. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C6
through C13 and boiling in the
range of approximately 65 °C to
230 °C (149 °F to 446 °F).]

Naphtha (petroleum), hydro-
treated light;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by treat-
ing a petroleum fraction with
hydrogen in the presence of a
catalyst. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C11 and boiling in the
range of approximately minus
20 °C to 190 °C (-4 °F to 374 °F).]

L

2
4
6
/
1
1
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-178-6

64742-73-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-185-4

64742-82-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-092-7

68410-96-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-329-00-7

649-330-00-2

649-331-00-8

Naphtha (petroleum), hydrode-
sulfurized light;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained from a
catalytic hydrodesulfurization
process. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C11 and boiling in the
range of approximately -20 °C to
190 °C (-4 °F to 374 °F).]

Naphtha (petroleum), hydrode-
sulfurized heavy;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained from a
catalytic hydrodesulfurization
process. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C7
through C12 and boiling in the
range of approximately 90 °C to
230 °C (194 °F to 446 °F).]

Distillates (petroleum), hydro-
treated middle, intermediate
boiling;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by the
distillation of products from a
middle distillate hydrotreating
process. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C5
through C10 and boiling in the
range of approximately 127 °C to
188 °C (262 °F to 370 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

270-093-2

68410-97-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

270-094-8

68410-98-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 %≤ C <10 %: T; R45-46

4

H P

270-988-8

68512-78-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-332-00-3

649-333-00-9

649-334-00-4

Distillates (petroleum), light dis-
tillate hydrotreating process, low-
boiling;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by the
distillation of products from the
light distillate hydrotreating pro-
cess. It consists of hydrocarbons
having carbon numbers predo-
minantly in the range of C6
through C9 and boiling in the
range of approximately 3 °C to
194 °C (37 °F to 382 °F).]

Distillates (petroleum), hydro-
treated heavy naphtha, deisohex-
anizer overheads;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by distil-
lation of the products from a
heavy naphtha hydrotreating
process. It consists of hydrocar-
bons having carbon numbers
predominantly in the range of C3
through C6 and boiling in the
range of approximately -49 °C to
68 °C (-57 °F to 155 °F).]

Solvent naphtha (petroleum),
light arom., hydrotreated;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by treat-
ing a petroleum fraction with
hydrogen in the presence of a
catalyst. It consists predomi-
nantly of aromatic hydrocarbons
having carbon numbers predo-
minantly in the range of C8
through C10 and boiling in the
range of approximately 135 °C to
210 °C (275 °F to 410 °F).]

L

2
4
6
/
1
1
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

H P

285-511-9

85116-60-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-335-00-X

649-336-00-5

Naphtha (petroleum), hydrode-
sulfurized thermal cracked light;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by frac-
tionation of hydrodesulfurized
thermal cracker distillate. It con-
sists predominantly of hydrocar-
bons having carbon numbers
predominantly in the range of C5
to C11 and boiling in the range of
approximately 23 °C to 195 °C
(73 °F to 383 °F).]

Naphtha (petroleum), hydro-
treated light, cycloalkane-contg.;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained from the
distillation of a petroleum frac-
tion. It consists predominantly of
alkanes and cycloalkanes boiling
in the range of approximately
-20 °C to 190 °C (-4 °F to 374 °
F).]

H P

285-512-4

85116-61-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-337-00-0

Naphtha (petroleum), heavy
steam-cracked, hydrogenated;
Low boiling point hydrogen
treated naphtha

H P

295-432-1

92045-51-7

H P

295-433-7

92045-52-8

649-338-00-6

Naphtha (petroleum), hydrode-
sulfurized full-range;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained from a
catalytic hydrodesulfurization
process. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C4 through C11
and boiling in the range of
approximately 30 °C to 250 °C
(86 °F to 482 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-438-4

92045-57-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-443-1

92045-61-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-529-9

92062-15-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-339-00-1

649-340-00-7

649-341-00-2

Naphtha (petroleum), hydro-
treated light steam-cracked;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by treat-
ing a petroleum fraction, derived
from a pyrolysis process, with
hydrogen in the presence of a
catalyst. It consists predomi-
nantly of unsaturated hydrocar-
bons having carbon numbers
predominantly in the range of C5
through C11 and boiling in the
range of approximately 35 °C to
190 °C (95 °F to 374 °F).]

Hydrocarbons, C4-12, naphtha-
cracking, hydrotreated;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by distil-
lation from the product of a
naphtha steam cracking process
and subsequent catalytic selective
hydrogenation of gum formers. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C4 through C12
and boiling in the range of
approximately 30 °C to 230 °C
(86 °F to 446 °F).]

Solvent naphtha (petroleum),
hydrotreated light naphthenic;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained by treat-
ing a petroleum fraction with
hydrogen in the presence of a
catalyst. It consists predomi-
nantly of cycloparaffinic hydro-
carbons having carbon numbers
predominantly in the range of C6
through C7 and boiling in the
range of approximately 73 °C to
85 °C (163 °F to 185 °F).]

L

2
4
6
/
1
1
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-342-00-8

649-343-00-3

649-344-00-9

Naphtha (petroleum), light
steam-cracked, hydrogenated;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons produced from the
separation and subsequent
hydrogenation of the products of
a steam-cracking process to pro-
duce ethylene. It consists predo-
minantly of saturated and
unsaturated paraffins, cyclic par-
affins and cyclic aromatic hydro-
carbons having carbon numbers
predominantly in the range of C4
through C10 and boiling in the
range of approximately 50 °C to
200 °C (122 °F to 392 °F).The
proportion of benzene hydrocar-
bons may vary up to 30 wt. %
and the stream may also contain
small amounts of sulfur and
oxygenated compounds.]

Hydrocarbons, C6-11, hydro-
treated, dearomatized;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained as sol-
vents which have been subjected
to hydrotreatment in order to
convert aromatics to naphthenes
by catalytic hydrogenation.]

Hydrocarbons, C9-12, hydro-
treated, dearomatized;
Low boiling point hydrogen
treated naphtha;
[A complex combination of
hydrocarbons obtained as sol-
vents which have been subjected
to hydrotreatment in order to
convert aromatics to naphthenes
by catalytic hydrogenation.]

H P

296-942-7

93165-55-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

297-852-0

93763-33-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

297-853-6

93763-34-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

649-345-00-4

Stoddard solvent;

H P

232-489-3

8052-41-3

Low boiling point naphtha —
unspecified;

[A colorless, refined petroleum
distillate that is free from rancid
or objectionable odors and that
boils in a range of approximately
148.8 °C to 204.4 °C. (300 °F to
400 °F).]

649-346-00-X

Natural gas condensates (petro-
leum);

H P

265-047-3

64741-47-5

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons separated as a
liquid from natural gas in a
surface separator by retrograde
condensation. It consists mainly
of hydrocarbons having carbon
numbers predominantly in the
range of C2 to C20. It is a liquid at
atmospheric temperature and
pressure.]

649-347-00-5

Natural gas (petroleum), raw liq.
mix;

H P

265-048-9

64741-48-6

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons separated as a
liquid from natural gas in a gas
recycling plant by processes such
as refrigeration or absorption. It
consists mainly of saturated ali-
phatic hydrocarbons having car-
bon numbers in the range of C2
through C8.]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 %≤ C <10 %: T; R45-46

Notes
related to
prepa-
rations

4

4

L

2
4
6
/
1
1
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-071-4

64741-69-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-079-8

64741-78-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-089-2

64741-87-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-348-00-0

649-349-00-6

649-350-00-1

Naphtha (petroleum), light
hydrocracked;
Low boiling naphtha — unspe-
cified;
[A complex combination of
hydrocarbons from distillation of
the products from a hydrocrack-
ing process. It consists predomi-
nantly of saturated hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C10, and boiling in the
range of approximately -20 °C to
180 °C (-4 °F to 356 °F).]

Naphtha (petroleum), heavy
hydrocracked;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons from distillation of
the products from a hydrocrack-
ing process. It consists predomi-
nantly of saturated hydrocarbons
having carbon numbers predo-
minantly in the range of C6
through C12, and boiling in the
range of approximately 65 °C to
230 °C (148 °F to 446 °F).]

Naphtha (petroleum), sweetened;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum naphtha to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C4
through C12 and boiling in the
range of approximately -10 °C to
230 °C (14 °F to 446 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
1
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-115-2

64742-15-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-351-00-7

Naphtha (petroleum), acid-trea-
ted;

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons obtained as a raf-
finate from a sulfuric acid treat-
ing process. It consists of
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C12 and
boiling in the range of approxi-
mately 90 °C to 230 °C (194 °F to
446 °F).]

649-352-00-2

Naphtha (petroleum), chemically
neutralized heavy;

H P

265-122-0

64742-22-9

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons produced by a
treating process to remove acidic
materials. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C6
through C12 and boiling in the
range of approximately 65 °C to
230 °C (149 °F to 446 °F).]

649-353-00-8

Naphtha (petroleum), chemically
neutralized light;

H P

265-123-6

64742-23-0

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons produced by a
treating process to remove acidic
materials. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C4
through C11 and boiling in the
range of approximately -20 °C to
190 °C (-4 °F to 374 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

L

2
4
6
/
1
2
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

265-170-2

64742-66-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-187-5

64742-83-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

265-199-0

64742-95-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-354-00-3

649-355-00-9

649-356-00-4

Naphtha (petroleum), catalytic
dewaxed;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from the
catalytic dewaxing of a petroleum
fraction. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C12
and boiling in the range of
approximately 35 °C to 230 °C
(95 °F to 446 °F).]

Naphtha (petroleum), light
steam-cracked;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
distillation of the products from a
steam cracking process. It con-
sists predominantly of unsatu-
rated hydrocarbons having
carbon numbers predominantly
in the range of C4 through C11
and boiling in the range of
approximately minus 20 °C to
190 °C
(-4 °F to 374 °F).This stream is
likely to contain 10 vol. % or
more benzene.]

Solvent naphtha (petroleum),
light arom.;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from dis-
tillation of aromatic streams. It
consists predominantly of aro-
matic hydrocarbons having car-
bon numbers predominantly in
the range of C8 through C10 and
boiling in the range of approxi-
mately 135 °C to 210 °C (275 °F
to 410 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
2
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

649-357-00-X

Aromatic hydrocarbons, C6-10,
acid-treated, neutralized;
Low boiling point naphtha —
unspecified

H P

268-618-5

68131-49-7

H P

270-725-7

68477-34-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-358-00-5

649-359-00-0

649-360-00-6

Distillates (petroleum), C3-5,
2-methyl-2-butene-rich;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons from the distilla-
tion of hydrocarbons usually
ranging in carbon numbers from
C3 through C5, predominantly
isopentane and 3-methyl-1-bu-
tene. It consists of saturated and
unsaturated hydrocarbons having
carbon numbers in the range of
C3 through C5, predominantly 2-
methyl-2-butene.]

Distillates (petroleum), polymd.
steam-cracked petroleum distil-
lates, C5-12 fraction;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from the
distillation of polymerized steam-
cracked petroleum distillate. It
consists predominantly of
hydrocarbons having carbon
numbers predominantly in the
range of C5 through C12.]

Distillates (petroleum), steam-
cracked, C5-12 fraction;
Low boiling point naphtha —
unspecified;
[A complex combination of
organic compounds obtained by
the distillation of products from a
steam cracking process. It con-
sists of unsaturated hydrocarbons
having carbon numbers predo-
minantly in the range of C5
through C12.]

H P

270-735-1

68477-50-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-736-7

68477-53-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

4

4

L

2
4
6
/
1
2
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

649-361-00-1

649-362-00-7

649-363-00-2

649-364-00-8

Distillates (petroleum), steam-
cracked, C5-10 fraction, mixed
with light steam-cracked petro-
leum naphtha C5 fraction;
Low boiling point naphtha —
unspecified

Extracts (petroleum), cold-acid,
C4-6;
Low boiling point naphtha —
unspecified;
[A complex combination of
organic compounds produced by
cold acid unit extraction of
saturated and unsaturated ali-
phatic hydrocarbons usually ran-
ging in carbon numbers from C3
through C6, predominantly pen-
tanes and amylenes. It consists
predominantly of saturated and
unsaturated hydrocarbons having
carbon numbers in the range of
C4 through C6, predominantly
C5.]

Distillates (petroleum), depenta-
nizer overheads;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from a
catalytic cracked gas stream. It
consists of aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C6.]

Residues (petroleum), butane
splitter bottoms;
Low boiling point naphtha —
unspecified;
[A complex residuum from the
distillation of butane stream. It
consists of aliphatic hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C6.]

H P

270-738-8

68477-55-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-741-4

68477-61-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-771-8

68477-89-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-791-7

68478-12-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C <10 %: T; R45-46

4

4

4

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
2
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

H P

270-795-9

68478-16-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

270-991-4

68513-02-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Notes
related to
prepa-
rations

4

4

L

2
4
6
/
1
2
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

H P

271-138-9

68516-20-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

.

.

1
5
9
2
0
0
8

649-365-00-3

649-366-00-9

649-367-00-4

Residual oils (petroleum), deiso-
butanizer tower;
Low boiling point naphtha —
unspecified;
[A complex residuum from the
atmospheric distillation of the
butane-butylene stream. It con-
sists of aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C6.]

Naphtha (petroleum), full-range
coker;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
fluid coker. It consists predomi-
nantly of unsaturated hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C15 and boiling in the
range of approximately 43 °C to
250 °C (110 °F-500 °F).]

Naphtha (petroleum), steam-
cracked middle arom.;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons produced by the
distillation of products from a
steam-cracking process. It con-
sists predominantly of aromatic
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C12 and
boiling in the range of approxi-
mately 130 °C to 220 °C (266 °F
to 428 °F).]

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-368-00-X

Naphtha (petroleum), clay-treated
full-range straight-run;

H P

271-262-3

68527-21-9

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons resulting from
treatment of full-range straight-
run naphtha with natural or
modified clay, usually in a per-
colation process to remove the
trace amounts of polar com-
pounds and impurities present. It
consists of hydrocarbons having
carbon numbers predominantly
in the range of C4 through C11
and boiling in the range of
approximately -20 °C to 220 °C
(-4 °F to 429 °F).]

649-369-00-5

Naphtha (petroleum), clay-treated
light straight-run;

H P

271-263-9

68527-22-0

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons resulting from
treatment of light straight-run
naphtha with a natural or modi-
fied clay, usually in a percolation
process to remove the trace
amounts of polar compounds
and impurities present. It consists
of hydrocarbons having carbon
numbers predominantly in the
range of C7 through C10 and
boiling in the range of approxi-
mately 93 °C to 180 °C (200 °F to
356 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
2
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

271-264-4

68527-23-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

271-266-5

68527-26-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-370-00-0

649-371-00-6

Naphtha (petroleum), light
steam-cracked arom.;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from a
steam-cracking process. It con-
sists predominantly of aromatic
hydrocarbons having carbon
numbers predominantly in the
range of C7 through C9 and
boiling in the range of approxi-
mately 110 °C to 165 °C (230 °F
to 329 °F).]

Naphtha (petroleum), light
steam-cracked, debenzenized;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons produced by dis-
tillation of products from a
steam-cracking process.t consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C12 and boiling in the
range of approximately 80 °C to
218 °C (176 °F to 424 °F).]

649-372-00-1

Naphtha (petroleum), arom.-
contg.;
Low boiling point naphtha —
unspecified

H P

271-635-0

68603-08-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-373-00-7

Gasoline, pyrolysis, debutanizer
bottoms;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from the
fractionation of depropanizer
bottoms. It consists of hydrocar-
bons having carbon numbers
predominantly greater than C5.]

H P

271-726-5

68606-10-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

L

2
4
6
/
1
2
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

272-206-0

68783-66-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H J

272-896-3

68919-39-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

272-932-8

68921-09-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-374-00-2

649-375-00-8

649-376-00-3

Naphtha (petroleum), light,
sweetened;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum distillate to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists predomi-
nantly of saturated and unsatu-
rated hydrocarbons having
carbon numbers predominantly
in the range of C3 through C6 and
boiling in the range of approxi-
mately -20 °C to 100 °C (-4 °F to
212 °F).]

Natural gas condensates;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons separated and/or
condensed from natural gas dur-
ing transportation and collected
at the wellhead and/or from the
production, gathering, transmis-
sion, and distribution pipelines in
deeps, scrubbers, etc. It consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C2
through C8.]

Distillates (petroleum), naphtha
unifiner stripper;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons produced by strip-
ping the products from the
naphtha unifiner. It consists of
saturated aliphatic hydrocarbons
having carbon numbers predo-
minantly in the range of C2
through C6.]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
2
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

285-510-3

85116-59-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-377-00-9

Naphtha (petroleum), catalytic
reformed light, arom.-free frac-
tion;

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons remaining after
removal of aromatic compounds
from catalytic reformed light
naphtha in a selective absorption
process. It consists predomi-
nantly of paraffinic and cyclic
compounds having carbon num-
bers predominantly in the range
of C5 to C8 and boiling in the
range of approximately 66 °C to
121 °C (151 °F to 250 °F).]

649-378-00-4

Gasoline;

H P

289-220-8

86290-81-5

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons consisting primar-
ily of paraffins, cycloparaffins,
aromatic and olefinic hydrocar-
bons having carbon numbers
predominantly greater than C3
and boiling in the range of 30 °C
to 260 °C (86 °F to 500 °F).]

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-379-00-X

Aromatic hydrocarbons, C7-8,
dealkylation products, distn. resi-
dues;

Low boiling point naphtha —
unspecified

H P

292-698-0

90989-42-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

L

2
4
6
/
1
2
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-298-4

91995-38-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-302-4

91995-41-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-331-2

91995-68-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-380-00-5

649-381-00-0

649-382-00-6

Hydrocarbons, C4-6, depentanizer
lights, arom. hydrotreater;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained as first
runnings from the depentanizer
column before hydrotreatment of
the aromatic charges. It consists
predominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C4
through C6, predominantly pen-
tanes and pentenes, and boiling
in the range of approximately
25 °C to 40 °C (77 °F to 104 °F).]

Distillates (petroleum), heat-
soaked steam-cracked naphtha,
C5-rich;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by distil-
lation of heat-soaked steam-
cracked naphtha. It consists pre-
dominantly of hydrocarbons
having carbon numbers in the
range of C4 through C6, predo-
minantly C5.]

Extracts (petroleum), catalytic
reformed light naphtha solvent;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained as the
extract from the solvent extrac-
tion of a catalytically reformed
petroleum cut. It consists pre-
dominantly of aromatic hydro-
carbons having carbon numbers
predominantly in the range of C7
through C8 and boiling in the
range of approximately 100 °C to
200 °C (212 °F to 392 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
2
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-434-2

92045-53-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-442-6

92045-60-8

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

295-444-7

92045-62-0

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-383-00-1

649-384-00-7

649-385-00-2

Naphtha (petroleum), hydrode-
sulfurized light, dearomatized;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by distil-
lation of hydrodesulfurized and
dearomatized light petroleum
fractions. It consists predomi-
nantly of C7 paraffins and cyclo-
paraffins boiling in a range of
approximately 90 °C to 100 °C
(194 °F to 212 °F).]

Naphtha (petroleum), light, C5-
rich, sweetened;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum naphtha to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists of hydro-
carbons having carbon numbers
predominantly in the range of C4
through C5, predominantly C5,
and boiling in the range of
approximately minus 10 °C to
35 °C (14 °F to 95 °F).]

Hydrocarbons, C8-11, naphtha-
cracking, toluene cut;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by distil-
lation from prehydrogenated
cracked naphtha. It consists pre-
dominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C8
through C11 and boiling in the
range of approximately 130 °C to
205 °C (266 °F to 401 °F).]

L

2
4
6
/
1
3
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

295-445-2

92045-63-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

296-028-8

92201-97-3

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

296-903-4

93165-19-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

649-386-00-8

649-387-00-3

649-388-00-9

Hydrocarbons, C4-11, naphtha-
cracking, arom.-free;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from
prehydrogenated cracked
naphtha after distillative separ-
ation of benzene- and toluene-
containing hydrocarbon cuts and
a higher boiling fraction. It con-
sists predominantly of hydrocar-
bons having carbon numbers
predominantly in the range of C4
through C11 and boiling in the
range of approximately 30 °C to
205 °C (86 °F to 401 °F).]

Naphtha (petroleum), light heat-
soaked, steam-cracked;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
fractionation of steam cracked
naphtha after recovery from a
heat soaking process. It consists
predominantly of hydrocarbons
having a carbon number pre-
dominantly in the range of C4
through C6 and boiling in the
range of approximately 0 °C to
80 °C (32 °F to 176 °F).]

Distillates (petroleum), C6-rich;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained from the
distillation of a petroleum feed-
stock. It consists predominantly
of hydrocarbons having carbon
numbers of C5 through C7, rich
in C6, and boiling in the range of
approximately 60 °C to 70 °C
(140 °F to 158 °F).]

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

H P

302-639-3

94114-03-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

305-750-5

95009-23-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Notes
related to
prepa-
rations

4

4

L

2
4
6
/
1
3
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

H P

308-261-5

97926-43-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

.

.

1
5
9
2
0
0
8

649-389-00-4

649-390-00-X

649-391-00-5

Gasoline, pyrolysis, hydroge-
nated;

Low boiling point naphtha-
unspecified;

[A distillation fraction from the
hydrogenation of pyrolysis gaso-
line boiling in the range of
approximately 20 °C to 200 °C
(68 °F to 392 °F).]

Distillates (petroleum), steam-
cracked, C8-12 fraction, polymd.,
distn. lights;

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons obtained by distil-
lation of the polymerized C8
through C12 fraction from steam-
cracked petroleum distillates. It
consists predominantly of aro-
matic hydrocarbons having car-
bon numbers predominantly in
the range of C8 through C12.]

Extracts (petroleum) heavy
naphtha solvent, clay-treated;

Low boiling point naphtha —
unspecified;

[A complex combination of
hydrocarbons obtained by the
treatment of heavy naphthic sol-
vent petroleum extract with
bleaching earth. It consists pre-
dominantly of hydrocarbons
having carbon numbers pre-
dominantly in the range of C6
through C10 and boiling in the
range of approximately 80 °C to
180 °C (175 °F to 356 °F).]

.

.

1
5
9
2
0
0
8

Notes
related to
prepa-
rations

4

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

649-392-00-0

649-393-00-6

649-394-00-1

Naphtha (petroleum), light
steam-cracked, debenzenized,
thermally treated;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
treatment and distillation of
debenzenized light steam-cracked
petroleum naphtha. It consists
predominantly of hydrocarbons
having carbon numbers pre-
dominantly in the range of C7
through C12 and boiling in the
range of approximately 95 °C to
200 °C (203 °F to 392 °F).]

Naphtha (petroleum), light
steam-cracked, thermally treated;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
treatment and distillation of light
steam-cracked petroleum
naphtha. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C6 and
boiling in the range of approxi-
mately 35 °C to 80 °C (95 °F to
176 °F).]

Distillates (petroleum), C7-9, C8-
rich, hydrodesulfurized dearoma-
tized;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
distillation of petroleum light
fraction, hydrodesulfurized and
dearomatized. It consists pre-
dominantly of hydrocarbons
having carbon numbers in the
range of C7 through C9, predo-
minantly C8 paraffins and cyclo-
paraffins, boiling in the range of
approximately 120 °C to 130 °C
(248 °F to 266 °F).]

H P

308-713-1

98219-46-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

308-714-7

98219-47-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

H P

309-862-5

101316-56-7

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

H P

309-870-9

101316-66-9

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

309-879-8

101316-76-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

309-976-5

101795-01-1

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

649-395-00-7

649-396-00-2

649-397-00-8

Hydrocarbons, C6-8, hydroge-
nated sorption-dearomatized,
toluene raffination;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained during
the sorptions of toluene from a
hydrocarbon fraction from
cracked gasoline treated with
hydrogen in the presence of a
catalyst. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C6 through C8 and
boiling in the range of approxi-
mately 80 °C to 135 °C (176 °F to
275 °F).]

Naphtha (petroleum), hydrode-
sulfurised full-range coker;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by frac-
tionation from hydrodesulfurised
coker distillate. It consists pre-
dominantly of hydrocarbons
having carbon numbers predo-
minantly in the range of C5 to C11
and boiling in the range of
approximately 23 °C to 196 °C
(73 °F to 385 °F).]

Naphtha (petroleum), sweetened
light;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by sub-
jecting a petroleum naphtha to a
sweetening process to convert
mercaptans or to remove acidic
impurities. It consists predomi-
nantly of hydrocarbons having
carbon numbers predominantly
in the range of C5 through C8 and
boiling in the range of approxi-
mately 20 °C to 130 °C (68 °F to
266 °F).]

L

2
4
6
/
1
3
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

Notes
related to
prepa-
rations

4

4

4

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

H P

310-012-0

102110-14-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

310-013-6

102110-15-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

H P

310-057-6

102110-55-4

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

4

4

649-398-00-3

649-399-00-9

649-400-00-2

Hydrocarbons, C3-6, C5-rich,
steam-cracked naphtha;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by distil-
lation of steam-cracked naphtha.
It consists predominantly of
hydrocarbons having carbon
numbers in the range of C3
through C6, predominantly C5.]

Hydrocarbons, C5-rich, dicyclo-
pentadiene-contg.;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by distil-
lation of the products from a
steam-cracking process. It con-
sists predominantly of hydrocar-
bons having carbon numbers of
C5 and dicyclopentadiene and
boiling in the range of approxi-
mately 30 °C to 170 °C (86 °F to
338 °F).]

Residues (petroleum), steam-
cracked light, arom.;
Low boiling point naphtha —
unspecified;
[A complex combination of
hydrocarbons obtained by the
distillation of the products of
steam cracking or similar pro-
cesses after taking off the very
light products resulting in a
residue starting with hydrocar-
bons having carbon numbers
greater than C5. It consists pre-
dominantly of aromatic hydro-
carbons having carbon numbers
greater than C5 and boiling above
approximately 40 °C (104 °F).]

649-401-00-8

Hydrocarbons, C≥5, C5-6-rich;
Low boiling point naphtha —
unspecified

H P

270-690-8

68476-50-6

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

4

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

649-402-00-3

649-403-00-9

Hydrocarbons, C5-rich;
Low boiling point naphtha —
unspecified

Aromatic hydrocarbons, C8-10;
Low boiling point naphtha —
unspecified

H P

270-695-5

68476-55-1

H P

292-695-4

90989-39-2

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R65

T
R: 45-46-65
S: 53-45

T
R: 45-46-65
S: 53-45

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

C ≥ 10 %: T; R45-46-65
0,1 % ≤ C < 10 %: T; R45-46

Notes
related to
prepa-
rations

4

4’

L

2
4
6
/
1
3
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

‘005-007-00-2

boric acid; [1]
boric acid, crude natural, con-
taining not more than 85 per
cent of H3BO3 calculated on the
dry weight [2]

ANNEX 1G

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

233-139-2 [1]
234-343-4 [2]

10043-35-3 [1]
11113-50-1 [2]

Repr. Cat. 2; R60-61

T
R: 60-61
S: 53-45

T
R: 60-61
S: 53-45

T
R: 60-61
S: 53-45

T
R: 60-61
S: 53-45

T
R: 60-61
S: 53-45

C ≥ 5,5 %: T; R60-61

C ≥ 3,1 %: T; R60-61

C ≥ 4,5 %: T; R60-61

C ≥ 8,5 %: T; R60-61

C ≥ 6,5 %: T; R60-61

005-008-00-8

diboron trioxide;
boric oxide

215-125-8

1303-86-2

Repr. Cat. 2; R60-61

005-011-00-4

disodium tetraborate, anhydrous;
boric acid, disodium salt; [1]
tetraboron disodium heptaoxide,
hydrate; [2]
orthoboric acid, sodium salt [3]

005-011-01-1

disodium tetraborate decahy-
drate;
borax decahydrate

005-011-02-9

disodium tetraborate pentahy-
drate;
borax pentahydrate

215-540-4 [1]
235-541-3 [2]
237-560-2 [3]

1330-43-4 [1]
12267-73-1 [2]
13840-56-7 [3]

Repr. Cat. 2; R60-61

215-540-4

1303-96-4

Repr. Cat. 2; R60-61

215-540-4

12179-04-3

Repr. Cat. 2; R60-61

005-015-00-6

1-chloromethyl-4-fluoro-1,4-dia-
zoniabicyclo[2.2.2]octane bis(tet-
rafluoroborate)

414-380-4

140681-55-6

Xn; R22
Xi; R41
R43
R52-53

Xn
R: 22-41-43-52/53
S: (2-)21-26-36/37/39-61

005-016-00-1

tetrabutylammonium butyl tris-
(4-trans-butylphenyl)borate

431-370-5

—

R53

R: 53
S: 61

006-091-00-3

propineb (ISO);
polymeric zinc propylenebis
(dithiocarbamate)

—

9016-72-2

Xn; R20-48/20/22
R43
N; R50

Xn; N
R: 20-43-48/20/22-50
S: (1/2-)24-37-46-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

006-092-00-9

trans-butyl (1S)-N-[1-((2S)-2-oxi-
ranyl)-2-phenylethyl]carbamate

425-420-5

98737-29-2

N; R50-53

006-093-00-4

2,2'-dithio di(ethylammonium)-
bis(dibenzyldithiocarbamate)

427-180-7

—

006-094-00-X

O-isobutyl-N-ethoxy carbo-
nylthiocarbamate

E

434-350-4

103122-66-3

Xn; R22
R43
N; R50-53

R10
Carc. Cat. 2; R45
Muta. Cat. 2; R46
Xn; R22-48/22
R43
N; R51-53

006-095-00-5

fosetyl-aluminium (ISO);
aluminium triethyl triphospho-
nate

254-320-2

39148-24-8

Xi; R41

006-096-00-0

chlorpropham (ISO);
isopropyl 3-chlorocarbanilate

202-925-7

101-21-3

007-028-00-2

hydroxylammonium nitrate

236-691-2

13465-08-2

Carc. Cat. 3; R40
Xn; R48/22
N; R51-53

E; R2
Carc. Cat. 3; R40
T; R24
Xn; R22-48/22
Xi; R36/38
R43
N; R50

N
R: 50/53
S: 60-61

Xn; N
R: 22-43-50/53
S: (2-)15-22-29-36/37-60-
61

T; N
R: 45-46-10-22-43-48/
22-51/53
S: 53-45-61

Xi
R: 41
S: (2-)26-39-46

Xn; N
R: 40-48/22-51/53
S: (2-)36/37-61

E; T; N
R: 2-22-24-36/38-40-43-
48/22-50
S: (1/2-)26-36/37-45-61

013-010-00-5

hydroxy aluminium bis(2,4,8,10-
tetra-trans-butyl-6-hydroxy-12H-
dibenzo[d, g][1.3.2]dioxapho-
sphocin-6-oxide)

430-650-4

151841-65-5

N; R51-53

014-033-00-3

2-methyl-3-(trimethoxysilyl)pro-
pyl-2-propenoate hydrolysis
product with silica

419-030-4

125804-20-8

F; R11
Xi; R36
R67

N
R: 51/53
S: 61

F; Xi
R: 11-36-67
S: (2-)16-26

L

2
4
6
/
1
3
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

014-034-00-9

3-hexylheptamethyltrisiloxane

428-700-5

1873-90-1

014-035-00-4

2-(3,4-epoxycyclohexyl)ethyl-
triethoxy silane

425-050-4

10217-34-2

015-113-00-0

tolclofos-methyl (ISO);
O-(2,6-dichloro-p-tolyl)-O,O-
dimethyl thiophosphate

260-515-3

57018-04-9

015-182-00-7

tetraisopropyldichloromethylene-
bisphosphonate

430-630-5

10596-22-2

015-183-00-2

(1-hydroxydodecylidene)dipho-
sphonic acid

425-230-2

16610-63-2

Xn; R20
R53

R43
R52-53

R43
N; R50-53

Xn; R22
Xi; R36
R43

C; R34
N; R50-53

015-188-00-X

(1-methylethylidene)di-4,1-phe-
nylenetetraphenyl diphosphate

425-220-8

5945-33-5

R53

016-092-00-0

A mixture of: 4,7-bis(mercapto-
methyl)-3,6,9-trithia-1,11-unde-
canedithiol-;
4,8-bis(mercaptomethyl)-3,6,9-
trithia-1,11-undecanedithiol;
5,7-bis(mercaptomethyl)-3,6,9-
trithia-1,11-undecanedithiol

017-023-00-7

[phosphinyldynetris(oxy)] tris[3-
aminopropyl-2-hydroxy-N,N-
dimethyl-N-(C6-18)-alkyl] trichlor-
ides

024-021-00-X

potassium tetrasodium bis[(N,N'-
n)-1'-(phenylcarbamoyl)-3,5-dis-
ulfonatobenzeneazo-1'-prop-1'-
ene-2,2'-diolato]chromate(III)

427-050-1

—

Repr. Cat. 3; R62
Xi; R38
R43
N; R50-53

425-520-9

197179-61-6

Xi; R41
N; R50-53

425-830-4

—

Xi; R41

Xn
R: 20-53
S: (2-)61

Xi
R: 43-52/53
S: (2-)24-37-61

Xi; N
R: 43-50/53
S: (2-)24-37-60-61

Xn
R: 22-36-43
S: (2-)24-26-37

C; N
R: 34-50/53
S: (1/2-)26-36/37/39-45-
60-61

R: 53
S: 61

Xn; N
R: 38-43-62-50/53
S: (2-)36/37-60-61

Xi; N
R: 41-50/53
S: (2-)26-39-60-61

Xi
R: 41
S: (2-)22-26-39

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
3
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

026-003-00-7

iron (II) sulfate

231-753-5

7720-78-7

Xn; R22
Xi; R36/38

026-003-01-4

iron (II) sulfate (1:1) heptahy-
drate;
sulfuric acid, iron(II) salt (1:1),
heptahydrate;
ferrous sulfate heptahydrate

231-753-5

7782-63-0

Xn; R22
Xi; R36/38

Xn
R: 22-36/38
S: (2-)46

Xn
R: 22-36/38
S: (2-)46

C ≥ 25 %: Xn; R22-36/38
20 % ≤ C < 25 %: Xi; R36

026-004-00-2

potassium ferrite

430-010-4

12160-44-0

027-006-00-6

cobalt acetate

200-755-8

71-48-7

C; R34
R43

Carc. Cat. 2; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R60
R42/43
N; R50-53

C
R: 34-43
S: (1/2-)22-26-36/37/39-
40-45

T; N
R: 49-60-42/43-68-50/53
S: 53-45-60-61

1

C ≥ 2,5 %: T, N; R49-60-42/43-68-
50/53
1 % ≤ C < 2,5 %: T, N; R49-60-42/
43-68-51/53
0,5 % ≤ C < 1 %: T, N; R49-60-51/
53
0,25 % ≤ C < 0,5 %: T, N; R49-51/
53
0,025 % ≤ C < 0,25 %: T; R49-52/
53
0,01 % ≤ C < 0,025 %: T; R49

L

2
4
6
/
1
4
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

027-007-00-1

zinc hexacyanocobaltate(III), ter-
tiary butyl alcohol/polypropylene
glycol complex

425-240-7

—

Xi; R41
N; R51-53

027-008-00-7

complex of cobalt(III)-bis(N-phe-
nyl-4-(5-ethylsulfonyl-2-hydroxy-
phenylazo)-3-hydroxynaphthyla-
mide), hydrated (n H2O, 2<n<3)

427-390-9

—

R43

Xi; N
R: 41-51/53
S: (2-)22-26-39-61

Xi
R: 43
S: (2-)24-37

.

.

1
5
9
2
0
0
8

Notes
related to
prepa-
rations

1

1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

027-009-00-2

cobalt nitrate

233-402-1

10141-05-6

Carc. Cat. 2; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R60
R42/43
N; R50-53

T; N
R: 49-60-42/43-68-50/53
S: 53-45-60-61

027-010-00-8

cobalt carbonate

208-169-4

513-79-1

Carc. Cat. 2; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R60
R42/43
N; R50-53

T; N
R: 49-60-42/43-68-50/53
S: 53-45-60-61

028-011-00-6

nickel dichloride

E

231-743-0

7718-54-9

Carc. Cat. 1; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R61
T; R23/25-48/23
Xi; R38
R42/43
N; R50-53

T; N
R: 49-61-23/25-38-42/
43-48/23-68-50/53
S: 53-45-60-61

C ≥ 2,5 %: T, N; R49-60-42/43-68-
50/53
1 % ≤ C < 2,5 %: T, N; R49-60-42/
43-68-51/53
0,5 % ≤ C < 1 %: T, N; R49-60-51/
53
0,25 % ≤ C < 0,5 %: T, N; R49-51/
53
0,025 % ≤ C < 0,25 %: T; R49-52/
53
0,01 % ≤ C < 0,025 %: T; R49

C ≥ 2,5 %: T, N; R49-60-42/43-68-
50/53
1 % ≤ C < 2,5 %: T, N; R49-60-42/
43-68-51/53
0,5 % ≤ C < 1 %: T, N; R49-60-51/
53
0,25 % ≤ C < 0,5 %: T, N; R49-51/
53
0,025 % ≤ C < 0,25 %: T; R49-52/
53
0,01 % ≤ C < 0,025 %: T; R49

C ≥ 25 %: T, N; R49-61-23/25-38-
42/43-48/23-68-50/53
20 % ≤ C < 25 %: T, N; R49-61-20/
22-38-42/43-48/23-68-51/53
3 % ≤ C < 20 %: T, N; R49-61-20/
22-42/43-48/23-68-51/53
2,5 % ≤ C < 3 %: T, N; R49-61-42/
43-48/23-68-51/53
1 % ≤ C < 2,5 %: T; R49-61-42/43-
48/23-68-52/53
0,5 % ≤ C < 1 %: T; R49-61-43-48/
20-52/53
0,25 % ≤ C < 0,5 %: T; R49-43-48/
20-52/53
0,1 % ≤ C < 0,25 %: T; R49-43-48/
20
0,01 % ≤ C < 0,1 %: Xi; R43

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
4
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

028-012-00-1

nickel dinitrate; [1]
nitric acid, nickel salt [2]

E

236-068-5 [1]
238-076-4 [2]

13138-45-9 [1]
14216-75-2 [2]

O; T; N
R: 49-61-8-20/22-38-41-
42/43-48/23-68-50/53
S: 53-45-60-61

O; R8
Carc. Cat. 1; R49
Muta. Cat. 3; R68
Repr. Cat. 2; R61
T; R48/23
Xn; R20/22
Xi; R38-41
R42/43
N; R50-53

C ≥ 25 %: T, N; R49-61-20/22-38-
41-42/43-48/23-68-50/53
20 % ≤ C < 25 %: T, N; R49-61-38-
41-42/43-48/23-68-51/53
10 % ≤ C < 20 %: T, N; R49-61-41-
42/43-48/23-68-51/53
5 % ≤ C < 10 %: T, N; R49-61-36-
42/43-48/23-68-51/53
2,5 % ≤ C < 5 %: T, N; R49-61-42/
43-48/23-68-51/53
1 % ≤ C < 2,5 %: T; R49-61-42/43-
48/23-68-52/53
0,5 % ≤ C < 1 %: T; R49-61-43-48/
20-52/53
0,25 % ≤ C < 0,5 %: T; R49-43-48/
20-52/53
0,1 % ≤ C < 0,25 %: T; R49-43-48/
20
0,01 % ≤ C < 0,1 %: Xi; R43

030-009-00-5

zinc-bis(4-(n-octyloxycarbonyla-
mino)salicylate) dihydrate

417-130-2

—

Xi; R41
N; R51-53

030-010-00-0

2-dodec-1-enylbutanedioic acid,
4-methyl ester zinc salt

430-740-3

—

N; R51-53

040-003-00-4

Reaction product of 3,5-di-trans-
butylsalicylic acid and zirconium
oxychloride, dehydrated, basic Zr:
DTBS = 1.0: 1.0 to 1.0: 1.5

430-610-6

226996-19-6

N; R50-53

Xi; N
R: 41-51/53
S: (2-)26-39-61

N
R: 51/53
S: 61

N
R: 50/53
S: 60-61

046-001-00-X

tetraammine palladium (II)
hydrogen carbonate

425-270-0

134620-00-1

Xn; R22-48/22
Xi; R41
R43
N; R50-53

Xn; N
R: 22-41-43-48/22-50/53
S: (2-)22-26-36/37/39-60-
61

047-002-00-8

polyphosphoric acid, copper,
sodium, magnesium, calcium,
silver and zinc salt

416-850-4

—

N; R50-53

N
R: 50/53
S: 60-61

L

2
4
6
/
1
4
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

050-021-00-4

dichlorodioctyl stannane

222-583-2

3542-36-7

050-022-00-X

dibutyltin dichloride;
(DBTC)

E

211-670-0

683-18-1

T; R23-48/25
R53

T
R: 23-48/25-53
S: (1/2-)38-45-61

Mut. Cat. 3; R68
Repr. Cat. 2; R60-61
T+; R26
T; R25-48/25
C; R34
Xn; R21
N; R50-53

T+; C; N
R: 60-61-21-25-26-34-
48/25-68-50/53
S: 53-45-60-61

078-010-00-X

tetraammine platinum (II)
hydrogen carbonate

426-730-3

123439-82-7

601-070-00-0

A mixture of: branched icosane;
branched docosane;
branched tetracosane

417-050-8

151006-58-5

Xn; R22
Xi; R41
R52-53

Xn; R20
R53

601-072-00-1

A mixture of: 1-(4-isopropylphe-
nyl)-1-phenylethane;
1-(3-isopropylphenyl)-1-pheny-
lethane;
1-(2-isopropylphenyl)-1-pheny-
lethane

430-690-2

52783-21-8

Xi; R38
N; R50-53

Xn
R: 22-41-52/53
S: (2-)22-26-39-61

Xn
R: 20-53
S: (2-)61

Xi; N
R: 38-50/53
S: (2-)37-60-61

C ≥ 25 %: T+, C, N; R60-61-21-25-
26-34-48/25-68-50/53
10 % ≤ C < 25 %: T+, C, N; R60-
61-22-26-34-48/25-68-50/53
7 % ≤ C < 10 %: T+, N; R60-61-22-
26-36/38-48/22-68-50/53
3 % ≤ C < 7 %: T, N; R60-61-22-
23-36/38-48/22-68-50/53
2,5 % ≤ C < 3 %: T, N; R60-61-23-
36/38-48/22-68-50/53
1 % ≤ C < 2,5 %: T, N; R60-61-23-
36/38-48/22-68-51/53
0,5 % ≤ C < 1 %: T, N; R60-61-20-
36/38-51/53
0,25 % ≤ C < 0,5 %: Xn, N; R20-
36/38-51/53
0,1 % ≤ C < 0,25 %: Xn; R20-36/
38-52/53
0,025 % ≤ C < 0,1 %: Xi; R36/38-
52/53
0,01 % ≤ C < 0,025 %: Xi; R36/38

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
4
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

601-075-00-8

4,4'-bis(N-carbamoyl-4-methyl-
benzenesulfonamide)diphenyl-
methane

418-770-5

151882-81-4

Carc. Cat. 3; R40

Xn
R: 40
S: (2-)22-36/37

601-076-00-3

ethynyl cyclopropane

425-430-1

6746-94-7

F; R11
R4
Xi; R38-41
R52-53

F; Xi
R: 4-11-38-41-52/53
S: (2-)9-16-26-33-37/39-
61

601-077-00-9

A mixture of: 1-heptyl-4-ethyl-
2,6,7-trioxabicyclo[2.2.2]octane;
1-nonyl-4-ethyl-2,6,7-trioxabicy-
clo[2.2.2]octane

601-078-00-4

A mixture of: 1,7-dimethyl-2-[(3-
methylbicyclo[2.2.1]hept-2-yl)
methyl]bicyclo[2.2.1]heptane;
2,3-dimethyl-2-[(3-methylbicyclo
[2.2.1]hept-2-yl)methyl]bicyclo
[2.2.1]heptane

426-510-7

196965-91-0

N; R50-53

427-040-5

—

C; R34
N; R50-53

601-079-00-X

A mixture of: trans–trans-cyclo-
hexadeca-1,9-diene;
cis–trans-cyclohexadeca-1,9-diene

429-620-3

—

602-095-00-X

alkanes, C14-17, chloro;
chlorinated paraffins, C14-17

287-477-0

85535-85-9

602-098-00-6

2-(3-bromophenoxy)tetrahydro-
2H-pyran

429-030-6

57999-49-2

602-099-00-1

3-(4-fluorophenyl)-2-methylpro-
pionylchloride

426-370-7

—

Xi; R38
R43
R53

R64
R66
N; R50-53

R43
N; R51-53

R14
R29
C; R35
Xn; R22
R52-53

N
R: 50/53
S: 60-61

C; N
R: 34-50/53
S: (1/2-)23-26-36/37/39-
45-57-60-61

Xi
R: 38-43-53
S: (2-)24-37-61

N
R: 64-66-50/53
S: (2-)24-60-61

Xi; N
R: 43-51/53
S: (2-)24-37-61

C
R: 14-22-29-35-52/53
S: (1/2-)26-36/37/39-45-
61

L

2
4
6
/
1
4
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

602-100-00-5

A mixture of: (R,R)-
1,1,1,2,2,3,4,5,5,5-decafluoro-
pentane;
(S,S)-1,1,1,2,2,3,4,5,5,5-deca-
fluoropentane

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

420-640-8

—

R52-53

R: 52/53
S: 61

602-101-00-0

2-chloro-4-fluoro-5-nitrophenyl
(isobutyl)carbonate

427-020-6

141772-37-4

Xn; R48/22
R43
N; R50-53

602-102-00-6

1,1,1,3,3-pentafluorobutane

430-250-1

406-58-6

F; R11

602-103-00-1

1-(chlorophenylmethyl)-2-
methylbenzene

431-450-1

41870-52-4

Xi; R38
N; R50-53

602-104-00-7

1,1,2,2,3,3,4-heptafluorocyclo-
pentane

430-710-1

15290-77-4

R52-53

603-109-00-7

A mixture of: 1-ethoxy-
1,1,2,3,3,3-hexafluoro-2-(tri-
fluoromethyl)propane;
1-ethoxy-1,1,2,2,3,3,4,4,4-nona-
fluorobutane

603-110-00-2

A mixture of: cis-2-isobutyl-5-
methyl 1,3-dioxane;
trans-2-isobutyl-5-methyl 1,3-
dioxane

603-111-00-8

A mixture of: 1-(1,1-dimethyl-
propyl)-4-ethoxy-cis-cyclohexane;
1-(1,1-dimethylpropyl)-4-ethoxy-
trans-cyclohexane

425-340-0

—

R53

426-130-1

166301-21-9

Xi; R38
R52-53

426-530-6

—

Xi; R38
N; R50-53

Xi; R38
N; R50-53

603-112-00-3

cyclopentyl 2-phenylethyl ether

428-340-9

—

Xn; N
R: 43-48/22-50/53
S: (2-)36/37-60-61

F
R: 11
S: (2-)3-9-16-41

Xi; N
R: 38-50/53
S: (2-)36/37-60-61

R: 52/53
S: 61

R: 53
S: 21-23-61

Xi
R: 38-52/53
S: (2-)23-37-61

Xi; N
R: 38-50/53
S: (2-)24-37-60-61

Xi; N
R: 38-50/53
S: (2-)37-60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
4
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

603-113-00-9

6-glycidyloxynapht-1-yl oxy-
methyloxirane

429-960-2

27610-48-6

Muta. Cat. 3; R68
Xn; R21
Xi; R38
R43
R52-53

Xn
R: 21-38-43-68-52/53
S: (2-)36/37/39-61

603-114-00-4

9-(2-propenyloxy)tricyclo[5.2.1.0
(2,6)]dec-3(or-4-)-ene

430-830-2

26912-64-1

603-115-00-X

A mixture of: O,O',O''-(methylsi-
lanetriyl)tris(4-methyl-2-penta-
none oxime) (3 stereoisomers)

423-580-0

—

603-116-00-5

(Z)-(2,4-difluorophenyl)piperi-
din-4-ylmethanone oxime
monohydrochloride

424-740-2

138271-16-6

Xi; R38
N; R51-53

Xn; R48/22
R53

Xn; R22
Xi; R41
R52-53

603-182-00-5

603-188-00-8

Reaction mixture of: saturated,
monounsaturated and multiple
unsaturated long-chained partly
estrified alcohols of vegetable
origin (Brassica napus L., Brassica
rapa L., Helianthus annuus L.,
Glycine hispida, Gossypium hirsutum
L., Cocos nucifera L., Elaeis gui-
neensis) with O,O-diisobutyl-
dithiophosphate and 2-ethyl-
hexylamine and hydrogen perox-
ide

A mixture of: 6,7-epoxy-
1,2,3,4,5,6,7,8-octahydro-
1,1,2,4,4,7-hexamethylnaphtha-
lene;
7,8-epoxy-1,2,3,4,6,7,8,8a-octa-
hydro-1,1,2,4,4,7-hexamethyl-
naphthalene

428-630-5

—

R43

426-970-9

—

N; R50-53

603-190-00-9

8,8-dimethyl-7-isopropyl-6,10-
dioxaspiro[4.5]decane

424-030-2

62406-73-9

Xi; R38
R52-53

Xi; N
R: 38-51/53
S: (2-)23-37-61

Xn
R: 48/22-53
S: 2-36-61

Xn
R: 22-41-52/53
S: (2-)22-26-39-61

Xi
R: 43
S: (2-)24-37

N
R: 50/53
S: 60-61

Xi
R: 38-52/53
S: (2-)24-37-61

L

2
4
6
/
1
4
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

603-192-00-X

(E,E)-3,7,11-trimethyldodeca-
1,4,6,10-tetraen-3-ol

423-240-1

125474-34-2

Xi; R38-41
R43
N; R50-53

Xi; N
R: 38-41-43-50/53
S: (2-)23-24-26-37/39-60-
61

603-193-00-5

disodium 9,10-anthracenedioxide

426-030-8

46492-07-3

C; R35

C
R: 35
S: (1/2-)26-36/37/39-45

603-194-00-0

2-(2-aminoethylamino)ethanol
(AEEA)

203-867-5

111-41-1

Repr. Cat. 2; R61
Repr. Cat. 3; R62
C; R34
R43

T
R: 61-34-43-62
S: 53-45

C ≥ 25 %: T; R61-34-43-62
10 % ≤ C < 25 %: T; R61-34-43-62
5 % ≤ C < 10 %: T; R61-36/37/38-
43-62
1 % ≤ C < 5 %: T; R61-43
0,5 % ≤ C < 1 %: T; R61

603-200-00-1

1-pentanol; [1]
3-pentanol [2]

200-752-1 [1]
209-526-7 [2]

71-41-0 [1]
584-02-1 [2]

R10
Xn; R20
Xi; R37/38

Xn
R: 10-20-37/38
S: (1/2-)36/37-46

603-201-00-7

(E)-(7R,11R)-3,7,11,15-tetra-
methylhexadec-2-ene-1-ol

416-120-5

—

603-202-00-2

4,4,5,5,5-pentafluoropentan-1-ol

421-360-9

148043-73-6

Xi; R38
R53

Xn; R22
R52-53

603-203-00-8

(1R,3S,7R,8R,10R,13R)-
5,5,7,9,9,13-hexamethyl-4,6-
dioxatetracyclo[6.5.1.01,10.03,7]
tetradecane

427-580-1

—

Xi; R38

Xi
R: 38-53
S: (2-)37-61

Xn
R: 22-52/53
S: (2-)23-61

Xi
R: 38
S: (2-)37

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
4
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

603-204-00-3

A mixture of: 2,2'-(heptane-1,7-
diyl)bis-1,3-dioxolane;
2,2'-(heptane-1,6-diyl)bis-1,3-
dioxolane

428-110-8

—

R52-53

R: 52/53
S: 61

603-205-00-9

(1S–cis)-4-(2-amino-6-chloro-
9H-purin-9-yl)-2-cyclopentene-
1-methanol hydrochloride

426-200-1

172015-79-1

603-206-00-4

2,2-dichloro-1,3-benzodioxol

426-850-6

2032-75-9

T; R48/25
Xn; R22
Xi; R41
R43
R52-53

R10
R14
C; R35
Xn; R22
R43

603-207-00-X

2-isobutyl-2-isopropyl-1,3-
dimethoxypropane

430-800-9

129228-21-3

Xi; R38
N; R51-53

603-208-00-5

1,2-diethoxyethane

211-076-1

629-14-1

F; R11
R19
Repr. Cat. 2; R61
Repr. Cat. 3; R62
Xi; R36

T
R: 22-41-43-48/25-52/53
S: (1/2-)22-26-36/37/39-
45-61

C
R: 10-14-22-35-43
S: (1/2-)7/8-23-26-36/37/
39-45

Xi; N
R: 38-51/53
S: (2-)23-37-61

F; T
R: 61-11-19-36-62
S: 53-45

603-209-00-0

spinosad (ISO) (a mixture of
spinosyn A and spinosyn D in
rations between 95:5 to 50:50);

— [1]
— [2]
— [3]

— [1]
131929-60-7
[2]
131929-63-0
[3]

N; R50-53

N
R: 50/53
S: 60-61

C ≥ 2,5 %: N; R50/53
0,25 % ≤ C < 2,5 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

L

2
4
6
/
1
4
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

mixture of 50-95 % of
(2R,3aS,5aR,5bS,9S,13S,14-
R,16aS,16bR)-2-(6-deoxy-2,3,4-
tri-O-methyl-α-L-mannopyrano-
syloxy)-13-(4-dimethylamino-
2,3,4,6-tetradeoxy-β-D-erythro-
pyranosyloxy)-9-ethyl-
2,3,3a,5a,5-
b,6,7,9,10,11,12,13,14,15,16-
a,16b-hexadecahydro-14-methyl-
1H-8-oxacyclododeca[b]as-inda-
cene-7,15-dione and 50-5 %
(2S,3aR,5a-
S,5bS,9S,13S,14R,16aS,16bS)-2-
(6-deoxy-2,3,4-tri-O-methyl-α-L-
mannopyranosyloxy)-13-(4-
dimethylamino-2,3,4,6-tetra-
deoxy-β-D-erythropyranosyloxy)-
9-ethyl-
2,3,3a,5a,5-
b,6,7,9,10,11,12,13,14,15,16-
a,16b-hexadecahydro-4,14-
dimethyl-1H-8-oxacyclododeca
[b]as-indacene-7,15-dione; [1]
spinosyn A; [2]
spinosyn D [3]

603-210-00-6

2,4-diethyl-1,5-pentanediol

429-310-8

57987-55-0

Xi; R41

604-071-00-4

4,4'-(1-{4-[1-(4-hydroxyphenyl)-
1-methylethyl]phenyl}ethylidene)
diphenol

425-600-3

110726-28-8

R53

604-072-00-X

1,2-bis(phenoxymethyl)benzene

428-620-0

10403-74-4

N; R50-53

Xi
R: 41
S: (2-)26-39

R: 53
S: 61

N
R: 50/53
S: 22-60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
4
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

604-073-00-5

(E)-3-[1-[4-[2-(dimethylamino)
ethoxy]phenyl]-2-phenylbut-1-
enyl]phenol

428-010-4

82413-20-5

Carc. Cat. 3; R40
Repr. Cat. 2; R60
R43
N; R50-53

605-023-00-5

5-chloro-2-(4-chlorophenoxy)
phe-
nol

429-290-0

3380-30-1

605-024-00-0

2-bromo-5-hydroxy-4-methoxy-
benzaldehyde

426-540-0

2973-59-3

605-032-00-4

3-[3-(4-fluorophenyl)-1-(1-
methylethyl)-1H-indol-2-yl]-(E)-
2-propenal

425-370-4

93957-50-7

605-033-00-X

A mixture of: 3,7,11-trimethyl-
cis-6,10-dodecadienal;
3,7,11-trimethyl-trans-6,10-
dodecadienal

425-910-9

32480-08-3

429-860-9

—

605-034-00-5

A mixture of:
(1RS,2RS,3SR,6RS,9SR)-9-meth-
oxytricyclo[5.2.1.0(2,6)]decane-
3-carbaldehyde;
(1RS,2RS,3RS,6RS,8SR)-8-meth-
oxytricyclo[5.2.1.0(2,6)]decane-
3-carbaldehyde;
(1RS,2RS,4SR,6RS,8SR)-8-meth-
oxytricyclo[5.2.1.0(2,6)]decane-
4-carbaldehyde

605-035-00-0

(E)-3-(4-(4-fluorophenyl)-5-
methoxymethyl-2,6-bis(1-meth-
oxymethyl)pyridin-3-yl)prop-2-
enal

426-330-9

177964-68-0

605-036-00-6

2-bromomalonaldehyde

430-470-6

2065-75-0

Xi; R41
N; R50-53

R43
N; R51-53

R43
N; R50-53

Xi; R38
N; R50-53

R43
N; R51-53

Xi; R36
R43
R53

Xn; R22
Xi; R41

T; N
R: 60-40-43-50/53
S: 53-45-60-61

Xi; N
R: 41-50/53
S: (2-)26-39-60-61

Xi; N
R: 43-51/53
S: (2-)24-37-61

Xi; N
R: 43-50/53
S: (2-)22-24-37-60-61

Xi; N
R: 38-50/53
S: (2-)37-60-61

Xi; N
R: 43-51/53
S: (2-)24-37-61

Xi
R: 36-43-53
S: (2-)24-26-37-61

Xn
R: 22-41
S: (2-)26-39

L

2
4
6
/
1
5
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

425-570-1

—

N; R50-53

Index No

Chemical name

Notes
related to
substances

606-074-00-6

A mixture of: (1R*,2S*)-2-acetyl-
1,2,3,4,5,6,7,8-octahydro-
1,2,8,8-tetramethylnaphthalene;
(2R*,3S*)-2-acetyl-
1,2,3,4,5,6,7,8-octahydro-
2,3,8,8-tetramethylnaphthalene

606-090-00-3

1-[3-[(dimethylamino)methyl]-4-
hydroxyphenyl]ethanone

430-920-1

73096-98-7

606-093-00-X

5-ethyl-2,4-dihydro-4-(2-phenox-
yethyl)-3H-1,2,4-triazol-3-one

414-470-3

95885-13-5

Xn; R22
Xi; R41
R52-53

Xn; R22
R52-53

606-094-00-5

N-[ethyl(3-methylbutyl)amino]-
3-methyl-1-phenyl-spiro[[1]
benzo-pyrano[2,3-c]pyrazole-4
(1H),1'(3'H)-isobenzofuran]-3'-
one

417-460-7

—

R53

606-095-00-0

(R,S)-2-azabicyclo[2.2.1]hept-5-
en-3-one

421-830-3

49805-30-3

606-096-00-6

3-(6-O-(6-desoxy-α-L-mannopy-
ranosyl-O-(α-D-glucopyranosyl)-
(β-D-glucopyranosyl)oxy)-2-(3,4-
dihydroxyphenyl)-5,7-dihydroxy-
4H-1-benzopyran-4-one

606-097-00-1

2,2''-dihydroxy-4,4''-(2-hydroxy-
propane-1,3-diyldioxy)dibenzo-
phenone

424-170-4

130603-71-3

Xn; R22
R43

R43
N; R51-53

424-210-0

23911-85-5

R53

606-098-00-7

1-benzyl-5-(hexadecyloxy)-2,4-
imidazolidinedione

431-220-9

158574-65-3

R53

606-099-00-2

5-methoxy-4'-(trifluoromethyl)
valerophenone

425-000-1

61718-80-7

N; R51-53

N
R: 50/53
S: 60-61

Xn
R: 22-41-52/53
S: (2-)22-26-39-61

Xn
R: 22-52/53
S: (2-)22-36-61

R: 53
S: 61

Xn
R: 22-43
S: (2-)22-24-37

Xi; N
R: 43-51/53
S: (2-)24-37-61

R: 53
S: 61

R: 53
S: 61

N
R: 51/53
S: 61

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

606-100-00-6

2-butyryl-3-hydroxy-5-thiocyclo-
hexan-3-yl-cyclohex-2-en-1-one

E

425-150-8

94723-86-1

Repr.Cat.2; R60
Xn; R22
R43
R52-53

T
R: 60-22-43-52/53
S: 53-45-61

426-050-7

165038-51-7

N; R50-53

N
R: 50/53
S: 60-61

606-101-00-1

A mixture of: 1,5-bis[(2-ethyl-
hexyl)amino]-9,10-anthracene-
dione;
1-[(2-ethylhexyl)amino]-5-[3-[(2-
ethylhexyl)oxy]propyl]amino-
9,10-anthracenedione;
1,5-bis[3-[(2-ethylhexyl)oxy]pro-
pyl]amino-9,10-anthracenedione;
1-[(2-ethylhexyl)amino]-5-[(3-
methoxypropyl)amino]-9,10-
anthracene dione;
1-[3-[(2-ethylhexyl)oxy]propyl]
amino-5-[(3-methoxypropyl)
amino]-9,10-anthracenedione;
1,5-bis[(3-methyloxypropyl)
amino]-9,10-anthracenedione

606-102-00-7

4-(3-triethoxysilylpropoxy)-2-
hydroxybenzophenone

431-490-8

79876-59-8

N; R51-53

606-103-00-2

1-(4-(trans-4-ethylcyclohexyl)phe-
nyl)ethanone

426-460-6

—

R43

606-104-00-8

1-(4-(trans-4-pentylcyclohexyl)
phenyl)ethanone

426-830-7

78531-59-6

606-105-00-3

3,4,3',4'-tetraphenyl-1,1'-ethan-
diylbispyrol-2,5-dione

431-500-0

226065-73-2

606-106-00-9

1-(4-(trans-4-butylcyclohexyl)
phenyl)ethanone

427-320-7

83626-30-6

R43
R53

R43
R53

R43
R53

N
R: 51/53
S: 61

Xi
R: 43
S: (2-)24-37

Xi
R: 43-53
S: (2-)24-37-61

Xi
R: 43-53
S: (2-)22-24-37-61

Xi
R: 43-53
S: (2-)24-37-61

L

2
4
6
/
1
5
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

606-107-00-4

8-azaspiro[4.5]decane-7,9-dione

427-770-4

1075-89-4

T; R25
N; R51-53

606-108-00-X

1,1,1,2,2,4,5,5,5-nonafluoro-4-
(trifluoromethyl)- 3-pentanone

436-710-6

756-13-8

R52-53

606-109-00-5

2-(4-methyl-3-pentenyl)anthra-
quinone

428-320-1

71308-16-2

Xn; R22
R43
R53

T; N
R: 25-51/53
S: (1/2-)22-36-45-61

R: 52/53
S: 61

Xn
R: 22-43-53
S: (2-)22-24-37-61

606-110-00-0

5-ethoxy-5H-furan-2-one

428-330-4

2833-30-9

C; R34
Xn; R21/22-48/22
R43

C
R: 21/22-34-43-48/22
S: (1/2-)23-26-36/37/39-
45

606-111-00-6

5-amino-6-methyl-1,3-dihydro-
benzoimidazol-2-one

428-410-9

67014-36-2

606-112-00-1

(4aR*,8aR*)-4a,5,9,10,11,12-
hexahydro-3-methoxy-11-
methyl-6H-benzofuro[3a,3,2-ef]
[2]benzazepin-6-one

428-690-2

1668-86-6

606-113-00-7

1-[4-(4-benzoylphenylsulfanyl)
phenyl]-2-methyl-2-(4-methyl-
phenylsulfonyl)propan-1-one

429-040-0

272460-97-6

Xn; R22
R43
N; R51-53

Xn; R22
Xi; R36
R52-53

Xi; R41
R53

429-150-9

67887-47-2

R53

Xn; N
R: 22-43-51/53
S: (2-)24-37-61

Xn
R: 22-36-52/53
S: (2-)22-26-61

Xi
R: 41-53
S: (2-)26-39-61

R: 53
S: 61

—

139001-49-3

Carc. Cat. 3; R40
Repr. Cat. 3; R63
R43

Xn
R: 40-43-63
S: (2-)36/37-46

606-114-00-2

4,4',5,5',6,6',7,7'-octachloro-
(2,2')biisoindolyl-1,1',3,3'-tetra-
one

606-115-00-8

profoxydim (ISO);
2-{(EZ)-1-[(2RS)-2-(4-chlorophe-
noxy)propoxyimino]butyl}-3-
hydroxy-5-(thian-3-yl)cyclohex-
2-en-1-one

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5
3

Index No

Chemical name

Notes
related to
substances

606-116-00-3

tepraloxydim (ISO);
(RS)-(EZ)-2-{1-[(2E)-3-chloroally-
loxyimino]propyl}-3-hydroxy-5-
perhydropyran-4-ylcyclohex-2-
en-1-one

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

—

149979-41-9

Carc. Cat. 3; R40
Repr. Cat. 3; R62-63

606-117-00-9

2,6-bis(1,1-dimethylethyl)-4-
(phenylenemethylene)cyclohexa-
2,5-dien-1-one

429-460-4

7078-98-0

606-118-00-4

N-(1,3-dimethylbutyl)-N'-(phe-
nyl)-1,4-benzoquinonediimine

429-640-2

52870-46-9

606-119-00-X

(E)-3-methyl-5-cyclopentadecen-
1-one

429-900-5

—

606-120-00-5

2,5-dihydroxy-5-methyl-3-(mor-
pholin-4-yl)-2-cyclopenten-1-one

430-170-5

114625-74-0

606-121-00-0

(+)-(1S,2S,3S,5R)-2,6,6-tri-
methylbicyclo[3.1.1]heptane-
3-spiro-1'-(cyclohex-2'-en-4'-one)

430-460-1

133636-82-5

606-122-00-6

3-(2-bromopropionoyl)-4,4-
dimethyl-1,3-oxazolan-2-one

430-820-8

114341-88-7

606-123-00-1

4-hexadecyl-1-phenylpyrazoli-
din-3-one

430-840-7

—

607-417-00-2

3-chloropropyl chloroformiate

425-770-9

628-11-5

R43
R53

Xi; R36
N; R50-53

R43
N; R50-53

Xn; R22
R52-53

C; R34
R43
N; R50-53

Xn; R22-48/22
Xi; R38-41
R43
N; R50-53

R43
R53

T; R23
Xn; R22-48/22
Xi; R38-41
R43

Xn
R: 40-62-63
S: (2-)36/37-46

Xi
R: 43-53
S: (2-)24-37-61

Xi; N
R: 36-50/53
S: (2-)26-60-61

Xi; N
R: 43-50/53
S: (2-)24-37-60-61

Xn
R: 22-52/53
S: (2-)46-61

C; N
R: 34-43-50/53
S: (1/2-)26-36/37/39-45-
57-60-61

Xn; N
R: 22-38-41-43-48/22-
50/53
S: (2-)26-36/37/39-60-61

Xi
R: 43-53
S: (2-)24-37-61

T
R: 22-23-38-41-43-48/22
S: (1/2-)26-36/37/39-45

L

2
4
6
/
1
5
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-428-00-2

tetrasodium ethylene diamine
tetraacetate

200-573-9

64-02-8

Xn; R22
Xi; R41

607-429-00-8

edetic acid
(EDTA)

200-449-4

60-00-4

Xi; R36

607-471-00-7

1,6-bis((dibenzylthiocarbamoyl)
disulfanyl)hexane

429-280-6

151900-44-6

R53

607-473-00-8

pentaerythritol, dipentaerythritol,
fatty acids, C6-10, mixed esters
with adipic acid, heptanoic acid
and isostearic acid

426-590-3

187412-41-5

R43

Xn
R: 22-41
S: (2-)26-39-46

Xi
R: 36
S: (2-)26

R: 53
S: 61

Xi
R: 43
S: (2-)24-37

607-477-00-X

(1α5α6α)-6-nitro-3-benzyl-3-aza-
bicyclo[3,1,0]hexane methane-
sulfonate salt

426-740-8

—

Xn; R22
Xi; R41
N; R51-53

Xn; N
R: 22-41-51/53
S: (2-)22-26-39-61

607-481-00-1

A mixture of: trihexyl citrate;
dihexyloctyl citrate;
dioctylhexyl citrate;
dihexyldecyl citrate

430-290-8

—

R53

R: 53
S: 61

607-482-00-7

N-[1-(S)-ethoxycarbonyl-3-phe-
nylpropyl]-L-alanyl-N-carboxyan-
hydride

430-360-8

84793-24-8

Xi; R41
R43

Xi
R: 41-43
S: (2-)22-24-26-37/39

607-483-00-2

1,2-benzenedicarboxylic acid;
di-C6-8-branched alkylesters,
C7-rich

607-484-00-8

ethyl 2-{[3-acetylamino-4-(6-
bromo-2-methyl-1,3-dioxo-2,3-
dihydro-1H-isoindol-5-ylazo)
phenyl]ethylamino}propionate

607-485-00-3

(3S—trans)-phenyl-3-[(1,3-ben-
zodioxol-5-yloxy)methyl]-4-(4-
fluorophenyl)-1-piperidinecar-
boxylate

276-158-1

71888-89-6

Repr. Cat. 2; R61

430-480-0

221452-67-1

R53

430-510-2

—

R53

T
R: 61
S: 53-45

R: 53
S: 61

R: 53
S: 22-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-486-00-9

potassium sodium 5'-(6-chloro-
4-(2-(2-vinylsulfonylethoxy)ethy-
lamino)-1,3,5-triazin-2-ylamino)-
4'-hydroxy-2,3'-azodinaphtha-
lene-1,2',5,7'-disulfonate

607-491-00-6

A mixture of: diester of 4,4'-
methylenebis[2-(2-hydroxy-5-
methylbenzyl)-3,6-dimethylphe-
nol] and 6-diazo-5,6-dihydro-5-
oxonaphthalene-1-sulfonic acid
(1:2);
triester of 4,4'-methylenebis[2-(2-
hydroxy-5-methylbenzyl)-3,6-
dimethylphenol] and 6-diazo-
5,6-dihydro-5-oxonaphthalene-
1-sulfonic acid (1:3)

402-110-8

110081-40-8

R52-53

427-140-9

—

Carc. Cat. 3; R40

R: 52/53
S: 22-61

Xn
R: 40
S: (2-)36/37

607-504-00-5

diammonium 1-hydroxy-2-(4-(4-
carboxyphenylazo)-2,5-
dimethoxyphenylazo)-7-amino-
3-naphthalenesulfonate

422-670-7

—

Repr. Cat. 3; R62
T; R25
Xn; R48/22
N; R50-53

T; N
R: 25-48/22-62-50/53
S: (1/2-)36/37-45-60-61

607-509-00-2

2-phenoxyethyl 4-aminobenzo-
ate

430-880-5

88938-23-2

N; R51-53

607-510-00-8

(2S,5R)-6,6-dibromo-3,3-
dimethyl-7-oxo-4-thia-1-azabicy-
clo[3.2.0]heptane-2-carboxylic
acid 4,4-dioxide

427-200-4

76646-91-8

607-511-00-3

A mixture of: 4-[(3-decyloxypro-
pyl)(3-isobutoxy-1-isobutoxycar-
bonyl-3-oxopropyl)amino]-4-
oxobutyric acid;
4-[(3-isobutoxy-1-isobutoxycar-
bonyl-3-oxopropyl)(3-octyloxy-
propyl)amino]-4-oxobutyric acid

423-750-4

—

Xn; R22
Xi; R38-41
R43

Xi; R36
N; R51-53

N
R: 51/53
S: 61

Xn
R: 22-38-41-43
S: (2-)24-26-37/39

Xi; N
R: 36-51/53
S: (2-)26-61

L

2
4
6
/
1
5
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-514-00-X

potassium N-(1-methoxy-1-oxo-
but-2-en-3-yl)valinate

427-240-2

134841-35-3

R43

607-518-00-1

3-oxoandrost-4-ene-17-β-car-
boxylic acid

414-990-0

302-97-6

Repr. Cat. 3; R62
R53

Xi
R: 43
S: (2-)24-37

Xn
R: 62-53
S: (2-)36/37-61

607-519-00-7

poly-[((4-((4-ethyl-ethylene)
amino)phenyl)-((4-(ethyl-(2-oxy-
ethylene)ami-
no)phenyl)methinyl)cyclohexa-
2,5-dienylidene)-N-ethyl-N-(2-
hydroxyethyl)ammonium acetate]

607-520-00-2

A mixture of: sodium 4,5-dihy-
dro-2-[(propionato)(C6-18)alkyl]-
3H-imidazolium-N-ethylpho-
sphate;
disodium 4,5-dihydro-2-[(dipro-
pionato)(C6-18)alkyl]-3H-imidazo-
lium-N-ethylphosphate

427-280-0

176429-27-9

Xi; R37/38-41
N; R50-53

Xi; N
R: 37/38-41-50/53
S: (2-)26-37/39-60-61

427-740-0

—

Xi; R41
R43

Xi
R: 41-43
S: (2-)24-26-37/39

607-521-00-8

tetraethyl N,N'-(methylenedicy-
clohexane-4,1-diyl)bis-DL-aspar-
tate

429-270-1

136210-30-5

R43
R52-53

607-522-00-3

sodium salt of the polymer of:
sodium 2-methyl-buta-1,3-diene-
1-sulfonate with acrylic acid and
2-hydroxyethyl-2-methylacrylate

429-720-7

184246-86-4

R52-53

Xi
R: 43-52/53
S: (2-)36/37-61

R: 52/53
S: 61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

430-200-7

—

Xi; R41
R52-53

Xi
R: 41-52/53
S: (2-)26-39-61

607-523-00-9

Mixture of mono to tetra(lithium
and/or sodium)3-amino-10-[4-
(4-amino-3-sulfonatoanilino)-6-
[methyl-(2-sulfonatoethyl)
amino]-1,3,5-triazin-2-ylamino]-
6-13-dichlorobenzo[1,2-B:4,5-B']
di[1,4]benzoxazine-4,11-disulfo-
nate; mono to tetra(lithium and/
or sodium)3-amino-10-[4,6-bis
(4-amino-3-sulfonatoanilino)-
1,3,5-triazin-2-ylamino]-6-13-
dichlorobenzo[1,2-B:4,5-B']di
[1,4]benzoxazine-4,11-disulfo-
nate; mono to penta(lithium and/
or sodium)10,10'-diamino-
6,6',13,13'-tetrachloro-3,3'-[6-
[methyl-(2-sulfonatoethyl)
amino]-1,3,5-triazin-2,4-diyldii-
mino]bis[benzo[1,2-B:4,5-B']di
[1,4]benzoxazine-4,11-disulfo-
nate; mono to hepta(lithium and/
or sodium)10-amino-6,6',13,13'-
tetrachloro-10'[4-(4-amino-3-sul-
fonatoanilino)-[6-methyl-(2-sul-
fonatoethl)amino]-1,3,5-triazin-
2,4-diimino]bis[benzo[1,2-B:4,5-
B']di[1,4]benzoxazine-4,11-disul-
fonate; mono to hepta(lithium
and/or sodium)10,10'-diamino-
6,6',3,3'[(2-sulfonato)-1,4-pheny-
lenediiminobis[6-methyl-(2-sul-
fonatoethyl)amino]-1,3,5-triazin-
2,4-diyldiimino]bis[benzo[1,2-
B:4,5-B']di[1,4]benzoxazine-
4,11-disulfonate

607-524-00-4

tall oil 2-[(tetrahydro-2H-pyran-
2-yl) thio]ethyl esters

430-310-5

—

R53

R: 53
S: 61

607-525-00-X

(Z)-2-methoxymino-2-[2-(trityla-
mino)thiazol-4-yl]acetic acid

431-520-1

64485-90-1

E; R2
Carc. Cat. 3; R40
R52-53

E; Xn
R: 2-40-52/53
S: (2-)23-25-35-36/37-61

607-528-00-6

(S)-3-methyl-2-(2-oxotetrahydro-
pyrimidine-1-yl)butyric acid

430-900-2

192725-50-1

Xi; R41

Xi
R: 41
S: (2-)26-39

L

2
4
6
/
1
5
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-529-00-1

benzyl cis-4-ammonium-4'-tolue-
nesulfonato-1-cyclohexanecar-
boxylate

607-530-00-7

A mixture of isomers of: C7-9-
alkyl 3-(3,5-di-trans-butyl-4-
hydroxyphenyl)propionate

426-070-6

67299-45-0

R52-53

406-040-9

125643-61-0

R53

607-531-00-2

methyl 3-amino-4,6-dibromo-2-
methyl-benzoate

425-190-6

119916-05-1

Xn; R48/22
N; R51-53

425-510-4

167944-94-7

R52-53

R: 52/53
S: 61

R: 53
S: 61

Xn; N
R: 48/22-51/53
S: (2-)22-36-61

R: 52/53
S: 61

414-910-4

—

Xi; R41
R43

Xi
R: 41-43
S: (2-)22-24-26-37/39

607-532-00-8

(S)-1-[2-trans-butoxycarbonyl-3-
(2-methoxyethoxy)propyl]-1-
cyclopentanecarboxylic acid,
cyclohexylamine salt

607-533-00-3

pentasodium monohydrogen 6-
chloro-3,10-bis[2-[4-chloro-6-
(2,4-disulfophenylamino)-1,3,5-
triazin-2-yl-amino]ethylamino]-
13-ethylbenzo[5.6][1.4]oxazino
[2,3-b]phenoxazine-4,11-disulfo-
nate

607-534-00-9

ethyl 2-(3-benzoylphenyl)pro-
panoate

414-920-9

60658-04-0

T; R25-48/25
R43
N; R51-53

T; N
R: 25-43-48/25-51/53
S: (1/2-)36/37-45-61

607-535-00-4

potassium 4-iodo-2-sulfonato-
benzoic acid

426-620-5

—

607-536-00-X

(2,6-xylyloxy) acetic acid

430-910-7

13335-71-2

607-537-00-5

isopropylammonium 2-(3-ben-
zoylphenyl)propionate

417-970-1

—

Xi; R41
R52-53

Xn; R22
Xi; R41
R52-53

T; R25-48/25
Xn; R21
Xi; R41
N; R50-53

Xi
R: 41-52/53
S: (2-)26-39-61

Xn
R: 22-41-52/53
S: (2-)26-39-61

T; N
R: 21-25-41-48/25-50/53
S: (1/2-)22-26-36/37/39-
45-60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
5
9

Index No

Chemical name

Notes
related to
substances

607-539-00-6

propyl((4-(5-oxo-3-propylisoxa-
zolidin-4-ylidenmethin)phenyl)
propoxycarbonylmethylenea-
mino)acetate

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

431-000-2

198705-81-6

R53

R: 53
S: 61

607-540-00-1

1-(mercaptomethyl)cyclopropyla-
cetic acid

420-240-3

162515-68-6

607-541-00-7

[(1-methyl-1,2-ethanediyl)bis
[nitrilobis(methylene)]]tetrakis
(phosphonic acid)

421-940-1

28698-31-9

C; R34
Xn; R21/22
R43
N; R51-53

Xi; R41
N; R50-53

607-542-00-2

methyl 2-(4-butanesulfonamido-
phenoxy)tetradecanoate

422-110-1

—

N; R50-53

607-543-00-8

poly-[((4-((4-(ethyl-ethylene)
amino)phenyl)-(4-(ethyl-(2-oxy-
ethylene)amino)phenyl)methi-
nyl)-3-methylcyclohexa-2,5-die-
nylidene)-N-ethyl-N-(2-hydro-
xyethyl)ammonium acetate]

607-544-00-3

ethyl 6,8-difluoro-1-(formyl-
methylamino)-1,4-dihydro-7-(4-
methyl)piperazin-1-yl)-4-oxo-qui-
noline-3-carboxylate

427-480-8

176429-22-4

Xi; R37/38-41
N; R50-53

427-490-2

158585-86-5

R52-53

607-545-00-9

1,2-dimethyl-3-(1-methylethenyl)
cyclopentyl acetate

424-070-0

94346-09-5

Xi; R38
N; R51-53

607-546-00-4

A mixture of: methyl {[5-acety-
lamino-4-(2-chloro-4-nitrophe-
nylazo)phenyl]methoxycarbonyl-
methylamino}acetate;
methyl {[5-acetylamino-4-(2-
chloro-4-nitrophenylazo)phenyl]
ethoxycarbonylmethylamino}
acetate

424-290-7

188070-47-5

R43

C; N
R: 21/22-34-43-51/53
S: (1/2-)22-26-36/37/39-
45-61

Xi; N
R: 41-50/53
S: (2-)26-39-60-61

N
R: 50/53
S: 60-61

Xi; N
R: 37/38-41-50/53
S: (2-)26-37/39-60-61

R: 52/53
S: 61

Xi; N
R: 38-51/53
S: (2-)37-61

Xi
R: 43
S: (2-)22-24-37

L

2
4
6
/
1
6
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-547-00-X

18-methylnonadecyl 2,2 -
dimethylpropanoate

424-370-1

125496-22-2

607-548-00-5

1-(2,4-dichlorophenyl)-2-(1H-
imidazol-1-yl)ethanone methane-
sulfonate

431-010-7

154486-26-7

Xi; R38
R43
R53

Xn; R22
Xi; R41
N; R51-53

607-549-00-0

methyl (E)-2((3-(1,3-benzodioxol-
5-yl)-2-methyl-1-propenyl)
amino)benzoate

424-430-7

125778-19-0

N; R50-53

607-550-00-6

2-amino-4-bromo-5-chloroben-
zoic acid

424-700-4

—

Xi; R41
R52-53

Xi
R: 38-43-53
S: (2-)24-37-61

Xn; N
R: 22-41-51/53
S: (2-)22-26-39-61

N
R: 50/53
S: 60-61

Xi
R: 41-52/53
S: (2-)26-39-61

607-551-00-1

tetrabutylammonium 2-amino-6-
iodopurinate

424-710-9

156126-48-6

Xn; R21/22-48/22
Xi; R38-41
R43
N; R51-53

Xn; N
R: 21/22-38-41-43-48/
22-51/53
S: (2-)26-36/37/39-61

607-552-00-7

hexadecyl 3-amino-4-isopro-
poxybenzoate

424-830-1

—

R53

607-553-00-2

7-amino-4-hydroxy-2-naphthale-
nesulfonic acid, coupled with 5
(or 8) -amino-8 (or 5)-[[4-[[4-[[4-
amino-6(or 7)-sulfo-1-naphthyl]
azo]phenyl]amino]-3-sulfophe-
nyl]azo]-2-naphthalenesulfonic
acid and 4-hydroxy-7-(phenyla-
mino)-2-naphthalenesulfonic
acid, sodium salt

424-850-0

—

Xi; R41

R: 53
S: 35-61

Xi
R: 41
S: (2-)26-39

607-554-00-8

2,4-diamino-5-[4-[(2-sulfoxyl
ethyl)sulfonyl]phenylazo]benze-
nesulfonic acid

424-870-1

27624-67-5

E; R3
Xi; R41
R52-53

E; Xi
R: 3-41-52/53
S: (2-)22-26-35-39-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
6
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-555-00-3

1,1,3,3-tetramethylbutylperoxy-
pivalate

424-980-8

22288-41-1

607-556-00-9

2-acetoxymethylene-4-acetylphe-
nylacetate

425-160-2

24085-06-1

F; R11
O; R7
Xi; R38
R43
N; R51-53

Xn; R22-48/22
Xi; R41
R43
N; R50-53

F; O; Xi; N
R: 7-11-38-43-51/53
S: (2-)7-14-16-36/37/39-
47-61

Xn; N
R: 22-41-43-48/22-50/53
S: (2-)22-26-36/37/39-60-
61

607-557-00-4

salt of: (1S–cis)-1-amino-2,3-
dihydro-1H-inden-2-ol and [R-
[R*R*]]-2,3-dihydroxybutane-
dioic acid

607-558-00-X

2S-isopropyl-5R-methyl-1R-
cyclohexyl (2R,5S)-5-(4-amino-2-
oxo-2H-pyrimidin-1-yl)-[1.3]-
oxathiolane-2-carboxylate

607-559-00-5

coconut oil, reaction products
with glycerol esters of 3,5-bis
(1,1-dimethylethyl)-4-hydroxy-
benzenepropanoic acid

425-210-3

169939-84-8

R43

425-250-1

147027-10-9

N; R51-53

425-400-6

179986-09-5

R53

607-560-00-0

(R,S)-2-butyloctanedioic acid

431-210-4

50905-10-7

Xi; R41

607-561-00-6

sodium 4-hydroxy-3-(N'-(2-(2-
hydroxyethylenesulfonyl)ethy-
lene)ureido)-5-nitrobenzenesulfo-
nate

607-562-00-1

A mixture of: (2R,3R)-3-(2-
ethoxyphenoxy)-2-hydroxy-3-
phenylpropylammonium metha-
nesulfonate;
(2S,3S)-3-(2-ethoxyphenoxy)-2-
hydroxy-3-phenylpropylammo-
nium methanesulfonate

425-460-3

—

425-530-3

98769-75-6

R43
R52-53

Xn; R22
Xi; R41
N; R51-53

Xi
R: 43
S: (2-)24-37

N
R: 51/53
S: 61

R: 53
S: 61

Xi
R: 41
S: (2-)26-39

Xi
R: 43-52/53
S: (2-)24-37-61

Xn; N
R: 22-41-51/53
S: (2-)22-26-39-61

L

2
4
6
/
1
6
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-563-00-7

5,7-dichloro-4-hydroxyquino-
line-3-carboxylic acid

431-250-2

171850-30-9

N; R51-53

607-564-00-2

1,6-hexanediammonium, sodium
5-sulfato-1,3-benzenedicarboxy-
late

425-730-0

51178-75-7

R43

N
R: 51/53
S: 61

Xi
R: 43
S: (2-)24-37

607-565-00-8

3-ethyl 5-methyl 2-(2-ami-
noethoxymethyl)-4-(2-chlorophe-
nyl)-1,4-dihydro-6-methyl-3,5-
pyridinedicarboxylate

425-820-1

88150-42-9

T; R25
Xn; R48/22
Xi; R41
N; R50-53

T; N
R: 25-41-48/22-50/53
S: (1/2-)26-36/37/39-45-
60-61

607-566-00-3

A mixture of: dodecylphenyl
dodecylhydroxybenzenecarboxy-
late;
bis(dodecylphenyl)dodecyl
hydroxybenzenedicarboxylate

426-140-6

—

R53

607-567-00-9

potassium 3-iodo-6-methylben-
zenesulfonate

426-300-5

—

Xi; R41

R: 53
S: 61

Xi
R: 41
S: (2-)26-39

607-568-00-4

potassium 2-chloro-3-(benzy-
loxy)propionate

426-350-8

138666-92-9

Xn; R22-48/22
Xi; R41
R43

Xn
R: 22-41-43-48/22
S: (2-)26-36/37/39

607-569-00-X

A mixture of: sodium 2-amino-4-
(2,6-difluoropyrimidin-4-yla-
mino)benzenesulfonate;
sodium 2-amino-4-(4,6-difluoro-
pyrimidin-4-ylamino)benzenesul-
fonate

607-570-00-5

sodium (6R—trans)-7-amino-8-
oxo-3-[[[1-(sulfomethyl)-1H-tet-
razol-5-yl]thio]methyl]-5-thia-1-
azabicyclo[4.2.0]oct-2-ene-2-car-
boxylate monohydrate

426-470-0

—

R43

426-520-1

71420-85-4

R43

Xi
R: 43
S: (2-)22-24-37

Xi
R: 43
S: (2-)24-37

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
6
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-571-00-0

2-cyclopentene-1-acetic acid, 3-
hydroxy-2-pentyl-, methyl ester
acetate

431-400-7

57374-49-9

R43
N; R51-53

Xi; N
R: 43-51/53
S: (2-)24-37-61

607-572-00-6

diethyl thiophosphoryl (Z)-(2-
aminothiazol-4-yl)methoxyimino
acetate

426-790-0

162208-27-7

Xn; R21/22-48/22
R43
N; R50-53

Xn; N
R: 21/22-43-48/22-50/53
S: (2-)36/37-60-61

607-573-00-1

A mixture of: disodium 7-(2,4-
difluoropyrimidin-6-ylamino)-4-
hydroxy-3-(4-methoxy-2-sulfona-
tophenylazo)naphthalene-2-sul-
fonate;
disodium 7-(4,6-difluoropyrimi-
din-2-ylamino)-4-hydroxy-3-(4-
methoxy-2-sulfonatophenylazo)
naphthalene-2-sulfonate

607-574-00-7

[1R-(1-α,2β,5α)]-mono[5-methyl-
2-(1-methylethyl)cyclohexyl]
butanedioate

607-575-00-2

4-(5-(5-[1-(4-carboxyphenyl)
hexa-
hydro-2,4,6-trioxopyrimidin-5-
ylidene]penta-1,3-dienyl)-
1,2,3,4-tetrahydro-6-hydroxy-
2,4-dioxopyrimidin-1-yl)benzoic
acid-triethylamine salt

607-576-00-8

branched, octyl 3-[3,5-di(trans-
butyl)-4-hydroxyphenyl]pro-
panoate

426-840-1

—

Xi; R41

426-890-4

77341-67-4

Xi; R41

426-900-7

—

Xi; R37
R52-53

427-030-0

—

N; R50-53

Xi
R: 41
S: (2-)22-26-39

Xi
R: 41
S: (2-)26-39

Xi
R: 37-52/53
S: (2-)61

N
R: 50/53
S: 60-61

607-577-00-3

(2R*,3S*)-2-(2,4-difluorophenyl)-
3-(5-fluoro-4-pyrimidinyl)-1-
(1H-1,2,4-triazol-1-yl)butan-2-ol
(1R)-10-camphorsulfonate

427-100-0

—

Xn; R22
Xi; R41
R43
R52-53

Xn
R: 22-41-43-52/53
S: (2-)22-24-26-37/39-61

607-578-00-9

ethyl 4-((4-diethylamino-2-
methylphenyl)imino)-4,5-dihy-
dro-1-isopropyl-5-oxo-1H-pyra-
zole-3-carboxylate

427-110-5

—

Xn; R22-48/22
R53

Xn
R: 22-48/22-53
S: (2-)36-61

L

2
4
6
/
1
6
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

.

.

1
5
9
2
0
0
8

607-579-00-4

diethyl[(p-ethoxyanilino)methy-
lene]malonate

431-430-0

103976-28-9

Xn; R22
N; R51-53

607-581-00-5

ethyl 2-ethoxy-4-carboxymethyl-
benzoate

427-630-2

99469-99-5

Xi; R41

427-650-1

—

R52-53

607-582-00-0

A mixture of: tetrasodium 7-(4-
(4-fluoro-6-(4-(2-sulfonatoethyl-
sulfonyl)phenylamino)-1,3,5-tria-
zin-2-ylamino)-2-ureidopheny-
lazo)naphthalene-1,3,6-trisulfo-
nate;
tetrasodium 7-(4-(4-hydroxy-6-
(4-(2-sulfonatoethylsulfonyl)phe-
nylamino)-1,3,5-triazin-2-yla-
mino)-2-ureidophenylazo)
naphthalene-1,3,6-trisulfonate

607-583-00-6

4-amino-3-[[4-[[2-(sulfooxy)
ethyl]sulfonyl]phenyl]azo]-1-
naphthalene sulfonic acid

427-680-5

188907-52-0

Xi; R41
R43
R52-53

Xi; R41
R43
R52-53

427-710-7

215612-56-9

427-930-3

—

R43

607-584-00-1

trisodium 3-[2-acetylamino-4-[4-
chloro-6-[4-(2-sulfonatoxyethyl-
sulfonyl)phenylamino]-1,3,5-tria-
zine-2-ylamino]phenylazo]
naphthalene-1,5-disulfonate

607-585-00-7

strontium 2-[(2-hydroxy-6-sulfo-
nato-1-naphthyl)azo]naphtha-
lene-1-sulfonate

607-586-00-2

dodecyl 3-amino-4-chlorobenzo-
ate

428-020-9

6195-20-6

R43
R53

607-587-00-8

ethyl cis-4-[4-[[2-(2,4-dichloro-
phenyl)-2-(1H-imidazol-1-
ylmethyl)-1,3-dioxolan-4-yl]
methoxy]phenyl]piperazine-1-
carboxylate

428-030-3

67914-69-6

Xn; R22-48/22
N; R50-53

Xn; N
R: 22-51/53
S: (2-)61

Xi
R: 41
S: (2-)26-39

R: 52/53
S: 22-61

Xi
R: 41-43-52/53
S: (2-)22-24-26-37/39-61

Xi
R: 41-43-52/53
S: (2-)24-26-37/39-61

Xi
R: 43
S: (2-)22-24-37

Xi
R: 43-53
S: (2-)24-37-61

Xn; N
R: 22-48/22-50/53
S: (2-)36-60-61

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
6
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-588-00-3

A mixture of: 2-ethylhexyl
2,3,4,5-tetrabromobenzoate;
bis(2-ethylhexyl)3,4,5,6-tetra-
bromo phthalate

428-050-2

—

607-589-00-9

tetrakis(1,2,2,6,6-pentamethyl-4-
piperidyl)-1,2,3,4-butanetetracar-
boxylate

428-070-1

91788-83-9

R43
N; R50-53

T; R48/25
Xn; R22
N; R50-53

428-140-1

210706-50-6

R53

428-400-4

—

Xi; R41

607-590-00-4

hexadecyl 3-[2-(5,5-dimethyl-
2,4-dioxo-1,3-oxazolidin-3-yl)-
4,4-dimethyl-3-oxovaleramido]-
4-isopropoxybenzoate

607-591-00-X

A mixture of: trisodium 5-(4-
fluoro-6-morpholin-4-yl-1,3,5-
triazin-2-ylamino)-4-hydroxy-3-
(4-(2-sulfooxyethanesulfonyl)phe-
nylazo)naphthalene-2,7-disulfo-
nate;
disodium 3-(4-ethenesulfonyl-
phenylazo)-5-(4-fluoro-6-mor-
pholin-4-yl-1,3,5-triazin-2-yla-
mino)-4-hydroxynaphthalene-
2,7-disulfonate

607-592-00-5

di(C9-11-alkyl) cyclohexane-1,4-
dicarboxylate

428-870-0

—

R53

607-593-00-0

4-(2-methylacryloyloxy)phenyl 4-
allyloxybenzoate

429-000-2

159235-16-2

607-594-00-6

ethyl (1S,5R,6S)-5-(1-ethylpro-
poxy)-7-oxabicyclo[4.1.0]hept-3-
ene-3-carboxylate

429-020-1

204254-96-6

R43
R52-53

Xn; R48/22
R43

607-595-00-1

N-amidino-N-methylglycine-2-
oxopropionate

429-120-5

208535-04-0

Xi; R41

Xi; N
R: 43-50/53
S: (2-)36/37-60-61

T; N
R: 22-48/25-50/53
S: (1/2-)22-36-45-57-60-
61

R: 53
S: 61

Xi
R: 41
S: (2-)22-26-39

R: 53
S: 61

Xi
R: 43-52/53
S: (2-)24-37-61

Xn
R: 43-48/22
S: (2-)22-36/37

Xi
R: 41
S: (2-)26-39

L

2
4
6
/
1
6
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-596-00-7

ethyl 2-(4-phenoxyphenyl)lactate

429-220-9

132584-17-9

R43
N; R50-53

Xi; N
R: 43-50/53
S: (2-)36/37-57-60-61

607-597-00-2

tetrasodium 4,4'-bis{4-[4-(2-
hydroxyethylamino)-6-(4-sulfo-
natoanilino)-1,3,5-triazin-2-yla-
mino]phenylazo}stilbene-2,2'-
disulfonate

607-598-00-8

trisodium 3-amino-4-[4-[4-(2-(2-
ethenylsulfonylethoxy)ethyla-
mino)-6-fluoro-1,3,5-triazine-2-
ylamino]-2-sulfophenylazo]-5-
hydroxynaphthalene-2,7-disulfo-
nate

429-230-3

—

Xi; R41

429-240-8

212652-59-0

Xi; R41

Xi
R: 41
S: (2-)22-26-39

Xi
R: 41
S: (2-)26-39

607-599-00-3

1,1-dimethylpropyl 3,5,5-tri-
methylperoxyhexanoate

431-610-9

68860-54-8

O; R7
R43
N; R50-53

O; Xi; N
R: 7-43-50/53
S: (2-)3-14-36/37/39-60-
61

607-600-00-7

(1S,1'R)-[1-(3',3'-dimethyl-1'-
cyclohexyl)ethoxycarbonyl]
methyl propanoate

431-700-8

—

N; R51-53

607-601-00-2

1,4-dihydroxy-2,2,6,6-tetra-
methylpiperidinium 2-hydroxy-
1,2,3-propanetricarboxylate

429-370-5

220410-74-2

Xn; R22

607-602-00-8

ethyl (3-cyanomethyl-3,4-dihy-
dro-4-oxophthalazin-1-yl)acetate

429-680-0

122665-86-5

607-603-00-3

lithium sodium 4,4',4''-(nitrilotris
(ethane-2,1-diylimino(6-chloro-
1,3,5-triazine-4,2-diyl)imino))tris
(5-hydroxy-6-(1-sulfonaphtha-
lene-2-ylazo)-2,7-naphthalene)
disulfonate

429-730-1

193562-37-7

R43
R52-53

Xi; R41
R43

N
R: 51/53
S: 61

Xn
R: 22
S: (2-)

Xi
R: 43-52/53
S: (2-)24-37-61

Xi
R: 41-43
S: (2-)22-24-26-37/39

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
6
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-604-00-9

guanidinium benzoate

429-820-0

26739-54-8

Xn; R22

607-605-00-4

methyl 4-iodo-2-(3-(4-methoxy-
6-methyl-1,3,5-triazine-2-yl)urei-
dosulfonyl)benzoate

429-890-2

144550-06-1

N; R50-53

607-606-00-X

(Z)-2-(2-t-butoxycarbonylamino-
4-thiazolyl)pent-2-enoic acid

430-100-3

86978-24-7

Xn; R22

607-607-00-5

607-608-00-0

A mixture of: calcium bis(C10-14
branched alkyl salicylate);
calcium bis(C18-30-alkyl salicy-
late);
calcium C10-14 branched alkylsa-
licylato-C18-30-alkyl salicylate;
calcium bis (C10-14 branched alkyl
phenolate);
calcium bis (C18-30-alkyl pheno-
late);
calcium C10-14 branched alkyl-
phenolato-C18-30-alkyl phenolate;
C10-14 branched alkyl phenol;
C18-30-alkyl phenol

pentapotassium 2-(4-{5-[1-(2,5-
disulfophenyl)-4,5-dihydro-3-
methylcarbamoyl-5-oxopyrazol-
4-ylidene]-3-(2-pyrrolidinone-1-
yl)-1,3-pentadienyl}-3-methylcar-
bamoyl-5-oxopyrazol-1-yl)ben-
zene-1,4-disulfonate

430-180-1

—

Xi; R38
N; R51-53

430-210-1

—

N; R50-53

607-609-00-6

ethyl (3R)-4-cyano-3-hydroxybu-
tanoate

430-220-6

141942-85-0

Xi; R36

607-610-00-1

trisodium 4-hydroxy-6-(sulfona-
tomethylamino)-5-(2-(2-sulfa-
toethylsulfonyl)phenylazo)
naphthalene-2-sulfonate

430-280-3

—

R43

Xn
R: 22
S: (2-)22-25

N
R: 50/53
S: 60-61

Xn
R: 22
S: (2-)22

Xi; N
R: 38-51/53
S: (2-)24-37-61

N
R: 50/53
S: 60-61

Xi
R: 36
S: (2-)26

Xi
R: 43
S: (2-)22-24-37

L

2
4
6
/
1
6
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-611-00-7

methyl 3-amino-2,2,3-trimethyl-
butyrate

431-720-7

90886-53-6

C; R34
Xn; R22
R52-53

C
R: 22-34-52/53
S: (1/2-)23-26-36/37/39-
45-61

607-612-00-2

A mixture of:
3,3,4,4,5,5,6,6,7,7,8,8,8-trideca-
fluoro-1-octanesulfonic acid;
ammonium
3,3,4,4,5,5,6,6,7,7,8,8,8-trideca-
fluoro-1-octanesulfonate

432-190-1

182176-52-9

Xn; R22-48/22
Xi; R41

Xn
R: 22-41-48/22
S: (2-)26-36/37/39

432-790-1

—

Muta. Cat. 3; R68
C; R34
Xn; R20/21/22

C
R: 20/21/22-34-68
S: (1/2-)26-28-36/37/39-
45

607-613-00-8

Mixture of: succinic acid;
monopersuccinic acid;
dipersuccinic acid;
monomethyl ester of succinic
acid;
monomethyl ester of persuccinic
acid;
dimethyl succinate;
glutaric acid;
monoperglutaric acid;
diperglutaric acid;
monomethyl ester of glutaric
acid;
monomethyl ester of perglutaric
acid;
dimethyl glutarate;
adipic acid;
monoperadipic acid;
diperadipic acid;
monomethyl ester of adipic acid;
monomethyl ester of peradipic
acid;
dimethyl adipate;
hydrogen peroxide;
methanol;
water

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
6
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

607-614-00-3

2-(10-oxo-10H-9-oxa-10-phos-
phaphenanthren-10-ylmethyl)
succinic acid

426-480-5

63562-33-4

607-615-00-9

Reaction product of thioglycerol
and mercaptoacetic acid consist-
ing mainly of 3-mercapto-1,2-
bismercaptoacetoxypropane and
oligomers of this substance

431-120-5

—

R43
R52-53

T; R23
Xn; R22
Xi; R36
R43

Xi
R: 43-52/53
S: (2-)24-37-61

T
R: 22-23-36-43
S: (1/2-)24-26-37-45

607-616-00-4

2,4-dichloro-5-fluoroben-
zoylchloride

428-390-1

86393-34-2

Xi; R37/38-41
R43
R52-53

Xi
R: 37/38-41-43-52/53
S: (2-)24-26-37/39-61

607-617-00-X

bis(2-ethylhexyl)-4,5-epoxycyclo-
hexane-1,2-dicarboxylate

430-700-5

10138-36-0

R43

608-020-00-7

diphenoxymethylenecyanamide

427-300-8

79463-77-7

608-032-00-2

acetamiprid (ISO);
(E)-N1-[(6-chloro-3-pyridyl)
methyl]-N2-cyano-N1-methylace-
tamidine

—

135410-20-7

Xi; R41
R52-53

Xn; R22
R52-53

608-044-00-8

2-cyclohexylidene-2-phenylaceto-
nitrile

423-740-1

10461-98-0

Xn; R22
N; R50-53

608-046-00-9

5-(4-chloro-2-nitro-phenylazo)-
1,2-dihydro-6-hydroxy-1,4-
dimethyl-2-oxo-pyridine-3-car-
bonitrile

425-310-7

77889-90-8

R53

608-047-00-4

2-piperidin-1-yl-benzonitrile

427-330-1

72752-52-4

N; R51-53

Xi
R: 43
S: (2-)24-37

Xi
R: 41-52/53
S: (2-)26-39-61

Xn
R: 22-52/53
S: (2-)46-61

Xn; N
R: 22-50/53
S: (2-)60-61

R: 53
S: 61

N
R: 51/53
S: 61

L

2
4
6
/
1
7
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

608-048-00-X

1-(3-cyclopentyloxy-4-methoxy-
phenyl)-4-oxo-cyclohexanecarbo-
nitrile

427-450-4

152630-47-2

Xn; R22-48/22
R43
N; R51-53

Xn; N
R: 22-43-48/22-51/53
S: (2-)36/37-61

608-049-00-5

2-(4-(4-(butyl-(1-methylhexyl)
amino)phenyl)-3-cyano-5-oxo-
1,5-dihydropyrrol-2-ylidene)pro-
pandinitrile

429-180-2

157362-53-3

R43
N; R50-53

Xi; N
R: 43-50/53
S: (2-)24-37-60-61

608-050-00-0

A mixture of: 5-(2-cyano-4-
nitrophenylazo)-2-(2-(2-hydro-
xyethoxy)ethylamino)-4-methyl-
6-phenylaminonicotinonitrile;
5-(2-cyano-4-nitrophenylazo)-6-
(2-(2-hydroxyethoxy)ethyla-
mino)-4-methyl-2-phenylamino-
nicotinonitrile

429-760-5

—

R53

R: 53
S: 61

608-051-00-6

(R)-4-(4-dimethylamino-1-(4-
fluorophenyl)-1-hydroxybutyl)-3-
(hydroxymethyl)benzonitrile

430-760-2

219861-18-4

608-052-00-1

(S)-4-(4-dimethylamino-1-(4-
fluorophenyl)-1-hydroxybutyl)-3-
(hydroxymethyl)benzonitrile

430-770-7

128173-52-4

608-053-00-7

(R,S)-4-(4-dimethylamino-1-(4-
fluorophenyl)-1-hydroxybutyl)-3-
(hydroxymethyl)benzonitrile

430-780-1

103146-25-4

608-054-00-2

(R,S)-4-(4-dimethylamino-1-(4-
fluorophenyl)-1-hydroxybutyl)-3-
(hydroxymethyl)benzonitrile
hemisulfate

430-790-6

—

Xn; R22
R43
N; R51-53

Xn; R22
R43
N; R51-53

Xn; R22
R43
N; R51-53

Xn; R22
Xi; R41
R43
N; R51-53

Xn; N
R: 22-43-51/53
S: (2-)36/37-61

Xn; N
R: 22-43-51/53
S: (2-)36/37-61

Xn; N
R: 22-43-51/53
S: (2-)36/37-61

Xn; N
R: 22-41-43-51/53
S: (2-)22-26-36/37/39-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

608-055-00-8

fipronil (ISO);
5-amino-1-[2,6-dichloro-4-(tri-
fluoromethyl)phenyl]-4-[(tri-
fluoromethyl)sulfinyl]-1H-pyra-
zole-3-carbonitrile

—

120068-37-3

T; R23/24/25-48/25
N; R50-53

T; N
R: 23/24/25-48/25-50/53
S: (1/2-)28-36/37-45-60-
61

C ≥ 25 %: T, N; R23/24/25-48/25-
50/53
10 % ≤ C < 25 %: T, N; R20/21/22-
48/25-50/53
3 % ≤ C < 10 %: Xn, N; R20/21/22-
48/22-50/53
2,5 % ≤ C < 3 %: Xn, N; R48/22-
50/53
1 % ≤ C < 2,5 %: Xn, N; R48/22-
51/53
0,25 % ≤ C < 1 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

608-056-00-3

N-methyl-N-cyanomethylmor-
pholiniummethylsulfate

429-340-1

—

608-057-00-9

4-cyanomethyl-4-methylmor-
pholin-4-iumhydrogene sulfate

431-200-1

208538-34-5

609-072-00-3

4-mesyl-2-nitrotoluene

430-550-0

1671-49-4

Xn; R22
Xi; R41

Xn; R22
Xi; R41
R43

Repr. Cat. 3; R62
Xn; R22
R43
R52-53

427-850-9

—

R43

Xn
R: 22-41
S: (2-)22-26-39

Xn
R: 22-41-43
S: (2-)22-24-26-37/39

Xn
R: 22-43-62-52/53
S: (2-)22-36/37-61

Xi
R: 43
S: (2-)22-24-37

415-350-3

—

Xi; R41
R52-53

Xi
R: 41-52/53
S: (2-)22-26-39-61

609-073-00-9

611-050-00-3

lithium potassium sodium N,N''-
bis{6-[7-[4-(4-chloro-1,3,5-tria-
zin-2-yl)amino-4-(2-ureidophe-
nylazo)]naphthalene-1,3,6-trisul-
fonato]}-N'-(2-aminoethyl)pipera-
zine

A mixture of: pentasodium 7-
amino-3-[[4-[[4-[[4-[[4-[(6-
amino-1-hydroxy-3-sulfonato-2-
naphthyl)azo]-7-sulfonato-1-
naphthyl]azo]phenyl]amino]-3-
sulfonatophenyl]azo]-6-sulfo-
nato-1-naphthyl]azo]-4-hydroxy-
naphthalen-2-sulfonate;

L

2
4
6
/
1
7
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

pentasodium 7-amino-8-[4-[4-
[4-[4-(2-amino-5-hydroxy-7-sul-
fonato-naphthalen-1-ylazo)-7-
sulfonatonaphthalen-1-ylazo]-
phenylamino]-3-sulfonato-phe-
nylazo]-6-sulfonato-naphthalen-
1-ylazo]-4-hydroxy-naphthalene-
2-sulfonate;
pentasodium 7-amino-8-[4-[4-
[4-[4-(6-amino-1-hydroxy-3-sul-
fonato-naphthalen-1-ylazo)-7-
sulfonatonaphthalen-1-ylazo]-
phenylamino]-3-sulfonato-phe-
nylazo]-6-sulfonato-naphthalen-
1-ylazo]-4-hydroxy-naphthalene-
2-sulfonate;
tetrasodium 7-amino-4-hydroxy-
3-[4-[4-[4-(4-hydroxy-7-sulfo-
nato-naphthalen-1-ylazo)-2-sul-
fonato-phenylamino]phenylazo]-
6-sulfonato-naphthalen-1-ylazo]
naphthalene-2-sulfonate;
tetrasodium 7-amino-4-hydroxy-
3-[4-[4-[4-(4-amino-7-sulfonato-
naphthalen-1-ylazo)-2-sulfonato-
phenylamino]phenylazo]-6-sulfo-
nato-naphthalen-1-ylazo]
naphthalene-2-sulfonate

Reaction product of: C.I. Leuco-
Sulfur Black 1 and a mixture of:
disodium 4-{4-[8-amino-1-
hydroxy-7-(4-sulfamoylpheny-
lazo)-3,6-disulfonato-2-naphthy-
lazo]phenylsulfonylamino}benze-
nediazonium chloride;
disodium 4-{4-[2,6-dihydroxy-3-
(8-hydroxy-3,6-disulfonato-1-
naphthylazo)phenylazo]phenyl-
sulfonylamino}benzene diazo-
nium chloride

611-102-00-5

424-500-7

—

R52-53

R: 52/53
S: 61

611-139-00-7

Reaction product of: C.I. Leuco
Sulfur Black 1 with (3-chloro-2-
hydroxypropyl)trimethylammo-
nium chloride

424-510-1

—

Xi; R41
N; R51-53

Xi; N
R: 41-51/53
S: (2-)26-39-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7
3

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

611-141-00-8

5-(4-[4-[4-(3,5-dicarboxy-phe-
nyl-azo)phenylamino]-6-mor-
pholin-4-yl-1,3,5-triazin-2-yla-
mino]phenylazo)isophthalic acid,
mixed monosodium and
diammonium salt

611-142-00-3

611-143-00-9

611-144-00-4

Product-by-process definition
polyazodyestuff obtained by
coupling 4-[4-(1-amino-8-
hydroxy-3,6-disulfo-2-naphthy-
lazo)phenylsulfonylamino]benze-
nediazonium with a mixture of
4-carboxybenzenediazonium and
diphenylamine-3-sulfo-4,4'-bis-
diazonium, and further coupling
of the obtained compounds with
a mixture of naphth-2-ol and 3-
aminophenol, sodium salts;
sodium chloride

A mixture of: trisodium 2-(2-[α-
(2-carboxylato-κ-O-4-sulfonato-
phenylazo)benzylidene]hydra-
zino-κ-N')-6-(2,6-difluoropyrimi-
din-4-ylamino)-4-sulfonatophe-
nolatocuprate (II);
trisodium 2-(2-[α-(2-carboxylato-
κ-O-4-sulfonatophenylazo)ben-
zylidene]hydrazino-κ-N')-6-(4,6-
difluoropyrimidin-2-ylamino)-4-
sulfonatophenolatocuprate (II)

A mixture of: 7-amino-3,8-bis-
[4-(2-sulfoxyethylsulfonyl)pheny-
lazo]-4-hydroxynaphthalene-2-
sulfonic acid, Na/K salt;

7-amino-3-[4-(2-sulfoxyethylsul-
fonyl)phenylazo]-4-hydroxy-8-
[4-(2-sulfoxyethylsulfonyl)-2-sul-
fophenylazo]naphthalene-2-sul-
fonic acid, Na/K salt;

414-410-6

—

425-740-5

—

Xi; R41
R43

Xi; R41
R52-53

Xi
R: 41-43
S: (2-)22-24-26-37/39

Xi
R: 41-52/53
S: (2-)26-39-61

428-260-4

—

Xi; R41

429-070-4

214362-06-8

Xi; R41

Xi
R: 41
S: (2-)22-26-39

Xi
R: 41
S: (2-)22-26-39

L

2
4
6
/
1
7
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

611-145-00-X

611-146-00-5

7-amino-8-[4-(2-sulfoxyethylsul-
fonyl)-phenylazo]-4-hydroxy-3-
[4-(2-sulfoxyethylsulfonyl)-2-sul-
fophenylazo]naphthalene-2-sul-
fonic acid, Na/K salt;

7-amino-3,8-bis-[4-(2-sulfox-
yethylsulfonyl)-2-sulfopheny-
lazo]-4-hydroxynaphthalene-2-
sulfonic acid, Na/K salt

A mixture of: tetrasodium 3-(1,5-
disulfonatonaphthalene-2-ylazo)-
4-hydroxy-7-{4-chloro-6-[4-(2-
sulfoxyethylsulfonyl)phenyla-
mino]-1,3,5-triazine-2-ylamino}
naphthalene-2-sulfonate;

3-(2,5-disulfophenylazo)-4-
hydroxy-7-{4-chloro-6-[4-(2-sul-
foxyethylsulfonyl)phenylamino]-
1,3,5-triazine-2-ylamino}
naphthalene-2-sulfonic acid,
sodium salt

A mixture of: pentasodium 3-(4-
(4-(7-(2,4-diamino-5-sulfonato-
3-(4-sulfonatophenylazo)pheny-
lazo)-1-hydroxy-3-sulfonato-
naphthalen-2-ylazo)-2-sulfonato-
phenylamino)phenylazo)-4-
hydroxy-6-(2-oxo-1-phenylcarba-
moylpropylazo)naphthalene-2-
sulfonate;
pentasodium 6-((2,4-diamino-5-
sulfonatophenyl)azo)-3-((4-((4-
((7-((2,4-diamino-5-sulfonato-
phenyl)azo)-1-hydroxy-3-sulfo-
natonaphthalen-2-yl)azo)phenyl)
amino)-2-sulfonatophenyl)azo)-
4-hydroxynaphthalene-2-sulfo-
nate;
pentasodium 6-((2,4-diamino-5-
sulfonato-3-((4-sulfonatophenyl)
azo)phenyl)azo)-3-((4-((4-((1,7-
dihydroxy-3-sulfonatonaphtha-
len-2-yl)azo)-2-sulfonatophenyl)
amino)phenyl)azo)-4-hydroxy-
naphthalene-2-sulfonate;

429-440-5

—

Xi; R41

Xi
R: 41
S: (2-)22-26-39

430-070-1

—

N; R51-53

N
R: 51/53
S: 61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

hexasodium 6-((2,4-diamino-5-
sulfonatophenyl)azo)-3-((4-((4-
((7-((2,4-diamino-5-sulfonato-3-
((4-sulfonatophenyl)azo)phenyl)
azo)-1-hydroxy-3-sulfonato-
naphthalen-2-yl)azo)-2-sulfona-
tophenyl)amino)phenyl)azo)-4-
hydroxynaphthalene-2-sulfonate

611-147-00-0

sodium, potassium, lithium 5-
amino-3,6-bis(5-(4-chloro-6-
(methyl-(2-methylaminoacetyl)
amino)-1,3,5-triazin-2-ylamino)-
2-sulfonatophenylazo)-4-hydro-
xynaphthalene-2,7-disulfonate

611-148-00-6

A mixture of: 2-(3-(2,6-dichloro-
4-nitrophenylazo)carbazol-9-yl)
ethanol;
2-(2-(3-(2,6-dichloro-4-nitro-
phenylazo)-carbazol-9-yl)-
ethoxy)ethanol;
3-(2,6-dichloro-4-nitropheny-
lazo)carbazol

611-149-00-1

2-(2-chloroacetoxy)ethyl 3-((4-
(2,5-dichloro-4-fluorosulfonyl-
phenylazo)-3-methylphenyl)ethy-
lamino)propionate

611-150-00-7

tetralithium 2-[6-[7-[2-(carboxy-
lato)phenylazo]-8-hydroxy-3,6-
disulfonato-1-naphthylamino]-4-
hydroxy-1,3,5-triazine-2-yla-
mino]benzoate

430-090-0

205764-96-1

Xi; R41
R43

Xi
R: 41-43
S: (2-)22-24-26-37/39

429-590-1

—

R43
N; R50-53

Xi; N
R: 43-50/53
S: (2-)24-37-60-61

427-570-7

193486-83-8

N; R51-53

440-460-3

—

Xi; R36
R52-53

N
R: 51/53
S: 61

Xi
R: 36-52/53
S: (2-)26-39-61

611-151-00-2

chrysoidine;
4-(phenylazo)benzene-1,3-dia-
mine

207-803-7

495-54-5

Muta. Cat. 3; R68
Xn; R22
Xi; R38
N; R50-53

Xn; N
R: 22-38-68-50/53
S: (2-)23-26-36/37-46-60-
61

L

2
4
6
/
1
7
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

611-152-00-8

611-153-00-3

chrysoidine monohydrochloride;
4-phenylazophenylene-1,3-dia-
mine monohydrochloride; [1]
chrysoidine monoacetate;
4-(phenylazo)benzene-1,3-dia-
mine monoacetate; [2]
chrysoidine acetate;
4-(phenylazo)benzene-1,3-dia-
mine acetate; [3]
chrysoidine-p-dodecylbenzene-
sulfonate;
dodecylbenzenesulfonic acid,
compound with 4-(phenylazo)
benzene-1,3-diamine (1:1); [4]
chrysoidine dihydrochloride;
4-(phenylazo)benzene-1,3-dia-
mine dihydrochloride; [5]
chrysoidine sulfate;
bis[4-(phenylazo)benzene-1,3-
diamine] sulfate [6]

chrysoidine C10-14-alkyl deriva-
tives and;
benzenesulfonic acid, mono-
C10-14-alkyl derivatives, com-
pounds with 4-(phenylazo)-1,3-
benzenediamine; [1]
chrysoidine compound with
dibutylnaphthalene sulfonic acid;
dibutylnaphthalenesulfonic acid,
compound with 4-(phenylazo)
benzene-1,3-diamine (1:1) [2]

208-545-8 [1]
278-290-5 [2]
279-116-0 [3]
264-409-8 [4]
281-549-5 [5]
282-432-1 [6]

532-82-1 [1]
75660-25-2 [2]
79234-33-6 [3]
63681-54-9 [4]
83968-67-6 [5]
84196-22-5 [6]

Muta. Cat. 3; R68
Xn; R22
Xi; R38-41
N; R50-53

Xn; N
R: 22-38-41-68-50/53
S: (2-)23-26-36/37/39-46-
60-61

286-946-7 [1]
304-236-8 [2]

85407-90-5 [1]
94247-67-3 [2]

Muta. Cat. 3; R68
Xn; R22
Xi; R38-41

Xn
R: 22-38-41-68
S: (2-)23-26-36/37/39-46

612-057-01-1

piperazine;
[liquid]

203-808-3

110-85-0

Repr. Cat. 3; R62-63
C; R34
R42/43

Xn; C
R: 34-42/43-62-63
S: (1/2-)23-26-36/37/39-
45

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

612-122-01-4

hydroxylamine ...%
[≤ 55 % in aqueous solution]

B

232-259-2

7803-49-8

R5
Carc. Cat. 3; R40
Xn; R21/22-48/22
Xi; R37/38-41
R43
N; R50

Xn; N
R: 5-21/22-37/38-40-41-
43-48/22-50
S: (2-)26-36/37/39-46-61

612-169-00-3

bis(N-methyl-N-phenylhydra-
zine)sulfate

423-170-1

618-26-8

612-203-00-7

C8-10 alkyl dimethyl hydroxyethyl
ammoniumchloride (chain < C8:
<3 %, chain = C8: 15 %-70 %,
chain = C10: 30 %-85 %, chain >
C10: <3 %)

417-360-3

—

612-208-00-4

N-methylbenzene-1,2-diammo-
nium hydrogen phosphate

424-460-0

—

612-216-00-8

1-amino-1-cyanamino-2,2-dicya-
noethylene, sodium salt

425-870-2

19450-38-5

F; R11
T; R48/25
Xn; R22
Xi; R41
R43
N; R50-53

Xn; R21/22
Xi; R38

Xn; R22
R43
N; R51-53

R43
R52-53

612-219-00-4

(2-hydroxy-3-(3,4-dimethyl-9-
oxo-10-thiaanthracen-2-yloxy)
propyl)trimethylammonium
chloride

402-200-7

—

R52-53

F; T; N
R: 11-22-41-43-48/25-
50/53
S: (1/2-)22-26-33-36/37/
39-45-60-61

Xn
R: 21/22-38
S: (2-)25-36/37

Xn; N
R: 22-43-51/53
S: (2-)22-25-36/37-61

Xi
R: 43-52/53
S: (2-)24-37-61

R: 52/53
S: 61

612-220-00-X

N-nitro-N-(3-methyl-3,6-dihy-
dro-2H-1,3,5-oxadiazin-4-yl)
amine

431-060-1

153719-38-1

Xn; R22
R43
R52-53

Xn
R: 22-43-52/53
S: (2-)22-24-37-61

L

2
4
6
/
1
7
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

612-221-00-5

2-amino-4-(trifluoromethyl)ben-
zenethiol hydrochloride

429-560-8

4274-38-8

C; R34
Xn; R20/21/22-48/22
R43
N; R50

C; N
R: 20/21/22-34-43-48/
22-50
S: (1/2-)26-36/37/39-45-
61

612-222-00-0

cis-1-(3-(4-fluorophenoxy)pro-
pyl)-3-methoxy-4-piperidinamine

425-080-8

104860-26-6

Xn; R21/22-48/22
Xi; R41
N; R50-53

Xn; N
R: 21/22-41-48/22-50/53
S: (2-)26-36/37/39-60-61

612-223-00-6

N-benzyl-N-ethyl-(4-(5-nitro-
benzo[c]isothiazol-3-ylazo)phe-
nyl)amine

425-300-2

186450-73-7

R43
R53

612-224-00-1

N2,N4,N6-tris{4-[(1,4-dimethyl-
pentyl)amino]phenyl}-1,3,5-tria-
zine-2,4,6-triamine

426-150-0

121246-28-4

R43
N; R50-53

612-225-00-7

1,4,7,10-tetraazacyclododecane

425-450-9

294-90-6

612-226-00-2

3-(2'-phenoxyethoxy)propyla-
mine

427-870-8

6903-18-0

612-227-00-8

benzyl-N-(2-(2-methoxyphe-
noxy)ethyl)amine hydrochloride

428-290-8

120606-08-8

C; R34
Xn; R21/22
N; R50-53

Xn; R22
Xi; R38-41
R52-53

Xn; R22
Xi; R41
N; R50-53

Xi
R: 43-53
S: (2-)22-24-37-61

Xi; N
R: 43-50/53
S: (2-)24-37-60-61

C; N
R: 21/22-34-50/53
S: (1/2-)22-26-36/37/39-
45-60-61

Xn
R: 22-38-41-52/53
S: (2-)23-26-37/39-61

Xn; N
R: 22-41-50/53
S: (2-)22-26-39-60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
7
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

612-228-00-3

A mixture of: N-(3-(trimethoxy-
silyl)propyl)ethylenediamine;
N-benzyl-N-(3-(trimethoxysilyl)
propyl)ethylenediamine;
N-benzyl-N'-[3-(trimethoxysilyl)
propyl]ethylenediamine;
N,N'-bis-benzyl-N'-[3-(trimethox-
ysilyl)propyl]ethylenediamine;
N,N,N'-tris-benzyl-N'-[3-(tri-
methoxysilyl)propyl]ethylenedia-
mine;
N,N-bis-benzyl-N'-[3-(trimethox-
ysilyl)propyl]ethylenediamine

414-340-6

—

R10
Xn; R20/21/22-68/20/21/
22
Xi; R41
R43
R52-53

Xn
R: 10-20/21/22-41-43-
68/20/21/22-52/53
S: (2-)26-36/37/39-61

612-229-00-9

mepanipyrim;
4-methyl-N-phenyl-6-(1-propy-
nyl)-2-pyrimidinamine

—

110235-47-7

Carc. Cat. 3; R40
N; R50-53

612-230-00-4

N,N-bis(cocoyl-2-oxypropyl)-N,
N-dibutylammonium bromide

431-530-4

—

C; R35
R43
N; R50-53

Xi; R41
N; R50-53

427-370-1

164288-56-6

430-410-9

186148-38-9

R52-53

Xn; N
R: 40-50/53
S: (2-)36/37-46-60-61

C; N
R: 35-43-50/53
S: (1/2-)26-28-36/37/39-
45-60-61

Xi; N
R: 41-50/53
S: (2-)26-39-60-61

R: 52/53
S: 61

612-231-00-X

3-((C12-18)-acylamino)-N-(2-((2-
hydroxyethyl)amino)-2-
oxoethyl)-N,N-dimethyl-1-propa-
naminium chloride

612-232-00-5

A mixture of: triisopropanola-
mine salt of 1-amino-4-(3-pro-
pionamidoanilino)anthraqui-
none-2-sulfonic acid;
triisopropanolamine salt of
1-amino-4-[3,4-dimethyl-5-(2-
hydroxyethylaminosulfonyl)ani-
lino]anthraquinone-2-sulfonic
acid

612-237-00-2

hydroxylammonium hydrogen-
sulfate;
hydroxylamine sulfate (1:1)

T

233-154-4

10046-00-1

E; R2
Carc. Cat. 3; R40
Xn; R21/22-48/22
Xi; R36/38
R43
N; R50

E; Xn; N
R: 2-21/22-36/38-40-43-
48/22-50
S: (2-)36/37-61

L

2
4
6
/
1
8
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-161-00-2

2,4-diamino-6-hydroxymethylp-
teridinehydrobromide

430-620-0

76145-91-0

Xn; R48/22
R43
R52-53

Xn
R: 43-48/22-52/53
S: (2-)22-36/37-61

613-162-00-8

(6R–trans)-1-((7-ammonio-2-car-
boxylato-8-oxo-5-thia-1-azabicy-
clo-[4.2.0]oct-2-en-3-yl)methyl)
pyridinium iodide

423-260-0

100988-63-4

Muta. Cat. 3; R68
R43
N; R51-53

Xn; N
R: 43-68-51/53
S: (2-)36/37-61

613-187-00-4

5-(2-amino-5-cyano-6-[2-(2-
hydroxyethoxy)ethylamino]-4-
methylpyridin-3-ylazo)-3-
methyl-2,4-dicarbonitrilethio-
phene

410-530-8

—

R43

613-192-00-1

3-benzyl-exo-6-nitro-2,4-dioxo-
3-aza-cis-bicyclo[3.1.0]hexane

426-750-2

151860-15-0

R43
R52-53

613-198-00-4

2-amino-4-dimethylamino-6-tri-
fluoroethoxy-1,3,5-triazine

415-500-8

145963-84-4

Xn; R22-48/22
R52-53

613-229-00-1

1-acetyl-4-(3-dodecyl-2,5-dioxo-
1-pyrrolidinyl)-2,2,6,6-tetra-
methylpiperidine

411-930-5

106917-31-1

613-231-00-2

2,6-diamino-3-((pyridine-3-yl)
azo)pyridine

421-430-9

28365-08-4

613-232-00-8

3-(benzo[b]thien-2-yl)-5,6-dihy-
dro-1,4,2-oxathiazine-4-oxide

431-030-6

163269-30-5

613-234-00-9

imidazo[1,2-b]pyridazin hydro-
chloride

431-510-5

18087-70-2

Xi; R38
R43
N; R50-53

Xn; R22-48/22
N; R51-53

T; R23
Xn; R48/22
Xi; R41
N; R50-53

Xn; R22
Xi; R36

Xi
R: 43
S: (2-)24-37

Xi
R: 43-52/53
S: (2-)24-37-61

Xn
R: 22-48/22-52/53
S: (2-)22-36-61

Xi; N
R: 38-43-50/53
S: (2-)24-37-60-61

Xn; N
R: 22-48/22-51/53
S: (2-)22-36-61

T; N
R: 23-41-48/22-50/53
S: (1/2-)26-36/39-45-57-
60-61

Xn
R: 22-36
S: (2-)26

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
8
1

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-235-00-4

2,3-dihydro-2,2-dimethyl-1H-
perimidine

424-060-6

6364-17-6

613-236-00-X

2-chloro-3-trifluoromethylpyri-
dine

424-520-6

65753-47-1

Xn; R22-48/22
R43
N; R50-53

T; R24/25-48/25
C; R34
R52-53

613-237-00-5

6-trans-butyl-3-(3-dodecylsulfo-
nyl)propyl-7H-1,2,4-triazolo
[3.4b][1,3,4]thiadiazine

613-238-00-0

sodium 2-[[4-[(4,6-dichloro-
1,3,5-triazin-2-yl)amino]phenyl]
sulfonyl]ethyl sulfate

424-950-4

133949-92-5

R53

430-890-1

81992-66-7

613-239-00-6

2-[3-(methylamino)propyl]-1H-
benzimidazole

425-760-4

64137-52-6

R43
N; R50-53

Xi; R41
R52-53

613-241-00-7

3-(2H-tetrazol-5-yl)pyridine

426-810-8

3250-74-6

Xi; R41

613-242-00-2

Reaction products of 3,10-bis((2-
aminopropyl)amino)-6,13-
dichloro-4,11-triphenodioxazine-
disulfonic acid with 2-amino-1,4-
benzenedisulfonic acid, 2-((4-
aminophenyl)sulfonyl)ethyl
hydrogen sulfate and 2,4,6-tri-
fluoro-1,3,5-triazine, sodium
salts

426-860-0

191877-09-5

Xi; R41

613-243-00-8

4,4'-(1,6-hexamethylenebis(for-
mylimino))bis(2,2,6,6-tetra-
methyl-1-oxylpiperidine)

427-350-0

182235-14-9

N; R51-53

613-244-00-3

5,7-dichloro-4-hydroxyquinoline

427-420-0

21873-52-9

N; R51-53

Xn; N
R: 22-43-48/22-50/53
S: (2-)28-36/37-60-61

T
R: 24/25-34-48/25-52/53
S: (1/2-)23-26-36/37/39-
45-61

R: 53
S: 61

Xi; N
R: 43-50/53
S: (2-)22-24-37-60-61

Xi
R: 41-52/53
S: (2-)26-39-61

Xi
R: 41
S: (2-)22-26-39

Xi
R: 41
S: (2-)22-26-39

N
R: 51/53
S: 61

N
R: 51/53
S: 61

L

2
4
6
/
1
8
2

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-245-00-9

2-fluoro-6-trifluoromethylpyri-
dine

428-100-3

94239-04-0

R10
Xn; R20/22
R52-53

Xn
R: 10-20/22-52/53
S: (2-)16-61

613-246-00-4

2-hydroxymethyl-3-methyl-4-
(2,2,2-trifluoroethoxy)pyridine

428-200-7

103577-66-8

R52-53

613-247-00-X

3-(2-methoxy-4-methoxycarbox-
ybenzyl)-5-nitroindole

428-910-7

107786-36-7

R53

613-248-00-5

3,4-dimethyl-1H-pyrazole

429-130-1

2820-37-3

613-249-00-0

1-(2-hydroxyethyl)-1H-pyrazol-
4,5-diyldiammoniumsulfate

429-300-3

155601-30-2

613-250-00-6

A mixture of: carbonato-bis-N-
ethyl-2-isopropyl-1,3-oxazoli-
dine;
methyl carbonato-N-ethyl-2-iso-
propyl-1,3-oxazolidine;
2-isopropyl-N-hydroxyethyl 1,3-
oxazolidine

429-990-6

—

613-251-00-1

(R)-3-[(1-methylpyrrolidin-2-yl)
methyl]-5-[2-(phenylsulfonyl)
ethenyl]-1H-indole

430-560-5

180637-89-2

613-253-00-2

2,2-dialkyl-4-hydroxymethyl-1,3-
dioxolane;
reaction products with ethylene
oxide (alkyl is C1-12 and the sum
to C13, average degree of ethox-
ylation is 3.5)

430-580-4

—

Xn; R22
Xi; R41
R52-53

Xi; R41
R43
N; R51-53

Xi; R41
R43
R52-53

Xn; R22-48/22
Xi; R41
R43

R19
Xi; R38
N; R51-53

613-254-00-8

forchlorfenuron (ISO);
1-(2-chloro-4-pyridyl)-3-pheny-
lurea

—

68157-60-8

Carc. Cat. 3; R40
N; R51-53

R: 52/53
S: 61

R: 53
S: 61

Xn
R: 22-41-52/53
S: (2-)26-39-61

Xi; N
R: 41-43-51/53
S: (2-)24-26-37/39-61

Xi
R: 41-43-52/53
S: (2-)24-26-37/39-61

Xn
R: 22-41-43-48/22
S: (2-)26-36/37/39

Xi; N
R: 19-38-51/53
S: (2-)37-61

Xn; N
R: 40-51/53
S: (2-)36/37-46-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
8
3

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

424-270-8

—

Xi; R41

Index No

Chemical name

Notes
related to
substances

613-255-00-3

A mixture of isomers of: sodium
[(2-hydroxyethylsulfamoyl){[2-(2-
piperazin-1-ylethylamino)ethyl-
sulfamoyl][2-(4-aminoethylpiper-
azine-1-yl)ethylsulfamoyl](sulfa-
moyl)}(sulfonatophthalocyani-
nato)]copper(II)

613-256-00-9

3'5'-anhydro thymidine

425-810-5

38313-48-3

R52-53

613-257-00-4

2-phthalimidoethyl N-[4-(2-
cyano-4-nitrophenylazo)phenyl]-
N-methyl-β-alaninate

426-400-9

170222-39-6

427-730-6

202420-04-0

R43
R53

C; R34
R52-53

613-258-00-X

613-259-00-5

A mixture of: 4-chloro-7-
methylbenzotriazole sodium salt;
4-chloro-5-methylbenzotriazole
sodium salt;
5-chloro-4-methylbenzotriazole
sodium salt

A mixture of: [2,4-dioxo-(2-pro-
pyn-1-yl)imidazolidin-3-yl]
methyl(1R)-cis-chrysanthemate;
[2,4-dioxo-(2-propyn-1-yl)imida-
zolidin-3-yl]methyl(1R)-trans-
chrysanthemate

613-260-00-0

(±)-4-(3-chlorophenyl)-6-[(4-
chlorophenyl)hydroxy(1-methyl-
1H-imidazol-5-yl)methyl]-1-
methyl-2(1H)-quinolin

613-261-00-6

pyrazole-1-carboxamidine
monohydrochloride

429-520-1

4023-02-3

Xn; R22-48/22
Xi; R41
R43
R52-53

613-262-00-1

disodium (E)-1,2-bis-(4-(4-
methylamino-6-(4-methylcarba-
moylphenylamino)-1,3,5-triazin-
2-ylamino)phenyl-2-sulfonato)
ethene

427-310-2

180850-95-7

Xi; R41

428-790-6

72963-72-5

Xn; R22
N; R50-53

Xn; N
R: 22-50/53
S: (2-)60-61

430-730-9

—

Xi; R41
N; R50-53

Xi
R: 41
S: (2-)26-39

R: 52/53
S: 61

Xi
R: 43-53
S: (2-)24-37-61

C
R: 34-52/53
S: (1/2-)26-28-36/37/39-
45-61

Xi; N
R: 41-50/53
S: (2-)22-26-39-60-61

Xn
R: 22-41-43-48/22-52/53
S: (2-)22-26-36/37/39-61

Xi
R: 41
S: (2-)26-39

L

2
4
6
/
1
8
4

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-263-00-7

monosodium 3-cyano-5-fluoro-
6-hydroxypyridine-2-olate

429-570-2

—

R43

Xi
R: 43
S: (2-)24-37

613-265-00-8

tribenuron methyl (ISO);
2-[4-methoxy-6-methyl-1,3,5-
triazin-2-yl(methyl)carbamoylsul-
famoyl]benzoic acid

—

101200-48-0

613-266-00-3

2-chloro-5-chloromethylthiazole

429-830-5

105827-91-6

613-267-00-9

thiamethoxam (ISO);
3-(2-chloro-thiazol-5-ylmethyl)-
5-methyl[1,3,5]oxadiazinan-4-
ylidene-N-nitroamine

428-650-4

153719-23-4

R43
N; R50-53

T; R24
C; R34
Xn; R22
R43
N; R51-53

Xn; R22
N; R50-53

Xi; N
R: 43-50/53
S: (2-)24-37-46-60-61

C ≥ 1 %: Xi, N; R43-50/53
0,25 % ≤ C <1 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

T; N
R: 22-24-34-43-51/53
S: (1/2-)26-36/37/39-45-
61

Xn; N
R: 22-50/53
S: (2-)60-61

C ≥ 25 %: Xn, N; R22-50/53
2,5 % ≤ C < 25 %: N; R50/53
0,25 % ≤ C < 2,5 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

613-268-00-4

(4aS–cis-)-6-benzyl-octahydropyr-
rolo[3.4-b]pyridine

425-930-8

151213-39-7

C; R34
Xn; R20/22-48/22
N; R51-53

C; N
R: 20/22-34-48/22-51/53
S: (1/2-)26-36/37/39-45-
61

613-269-00-X

2-thiazolidinylidenecyanamide

427-720-1

26364-65-8

Xn; R22-48/22
R52-53

428-150-6

113171-13-4

R52-53

Xn
R: 22-48/22-52/53
S: (2-)22-36-61

R: 52/53
S: 61

—

142469-14-5

R43
N; R50-53

Xi; N
R: 43-50/53
S: (2-)24-37-46-60-61

C ≥ 2,5 %: Xi, N; R43-50/53
1 % ≤ C < 2,5 %: Xi, N; R43-51/53
0,25 % ≤ C < 1 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

613-270-00-5

5-amino-N-(2,6-dichloro-3-
methylphenyl)-1H-1,2,4-triazole-
3-sulfonamide

613-271-00-0

tritosulfuron (ISO) (containing
≤ 0,02 % AMTT);
1-[4-methoxy-6-(trifluoro-
methyl)-1,3,5-triazin-2-yl]-3-[2-
(trifluoromethyl)benzenesulfo-
nyl]urea (containing ≤ 0,02 %
AMTT)

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
8
5

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

613-272-00-6

pyraclostrobin (ISO);
methyl N-{2-[1-(4-chlorophenyl)-
1H-pyrazol-3-yloxymethyl]phe-
nyl}(N-methoxy)carbamate

—

—

T; R23
Xi; R38
N; R50-53

T; N
R: 23-38-50/53
S: (1/2-)45-60-61-63

C ≥ 25 %: T, N; 23-38-50/53
20 % ≤ C < 25 %: Xn, N; R20-38-
50/53
3 % ≤ C < 20 %: Xn, N; R20-50/53
0,25 % ≤ C < 3 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

613-273-00-1

tetrahydro-3-methyl-5-((2-phe-
nylthio)thiazol-5-ylmethyl)-[4H]-
1,3,5-oxadiazinan-4-ylidene-N-
nitroamine

427-600-9

192439-46-6

N; R51-53

613-274-00-7

2,6-dichloro-1-fluoropyridinium-
tetrafluoroborate

427-400-1

140623-89-8

613-275-00-2

3-(2-chloroethyl)-6,7,8,9-tetra-
hydro-2-methyl-4H-pyrido[1,2-
a]pyrimidin-4-one monohy-
drochloride

424-530-0

93076-03-0

C; R34
Xn; R22
R43
N; R50-53

T; R25
Xn; R68/21-48/22
Xi; R41
R43
N; R51-53

613-276-00-8

1-(2-chlorophenyl)-1,2-dihydro-
5H-tetrazol-5-one

426-110-2

98377-35-6

R43
R52-53

613-277-00-3

(4-(6-diethylamino-2-methylpyri-
din-3-yl)imino-4,5-dihydro-3-
methyl-1-(4-methylphenyl)-1H-
pyrazol-5-one

427-070-9

—

R53

613-278-00-9

(3-aminophenyl)pyridin-3-
ylmethanone

428-230-0

79568-06-2

Xn; R48/22
N; R50-53

613-279-00-4

2-ethyl-2,3-dihydro-2-methyl-
1H-perimidine

424-380-6

43057-68-7

Xn; R22-48/22
N; R50-53

N
R: 51/53
S: 61

C; N
R: 22-34-43-50/53
S: (1/2-)26-36/37/39-45-
60-61

T; N
R: 25-41-43-48/22-68/
21-51/53
S: (1/2-)22-26-36/37/39-
45-61

Xi
R: 43-52/53
S: (2-)24/25-37-61

R: 53
S: 61

Xn; N
R: 48/22-50/53
S: (2-)22-36-60-61

Xn; N
R: 22-48/22-50/53
S: (2-)36/37-60-61

L

2
4
6
/
1
8
6

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

615-033-00-1

615-034-00-7

615-035-00-2

615-036-00-8

615-037-00-3

615-038-00-9

615-039-00-4

616-107-00-6

Reaction product of diphenyl-
methanediisocyanate, octylamine,
oleylamine and cyclohexylamine
(1:1.58:0.32:0.097)

Reaction product of diphenyl-
methanediisocyanate, octylamine,
4-ethoxyaniline and ethylenedia-
mine (1:0,37:1,53:0,05)

Reaction product of diphenyl-
methanediisocyanate, octylamine
and oleylamine (molar ratio
1:1.86:0.14)

Reaction product of diphenyl-
methanediisocyanate, toluenedii-
socyanate (mixture of isomers:
65 % 2,4- and 35 % 2,6-diiso-
cyanate), octylamine, oleylamine
and 4-ethoxyaniline (molar ratio
4:1:7:1:2)

Reaction product of diphenyl-
methanediisocyanate, toluenedii-
socyanate (mixture of isomers:
65 % 2,4- and 35 % 2,6-diiso-
cyanate), octylamine and oleyla-
mine (molar ratio 4:1:9:1)

Reaction product of toluenedii-
socyanate (mixture of isomers:
65 % 2,4- and 35 % 2,6-diiso-
cyanate) and aniline (molarratio
1:2)

Reaction product of diphenyl-
methanediisocyanate, toluenedii-
socyanate (mixture of isomers:
65 % 2,4- and 35 % 2,6-diiso-
cyanate), octylamine, oleylamine
and 4-ethoxyaniline (molar ratio
3.88:1:6.38:0.47:2.91)

cinidon ethyl (ISO);
ethyl (Z)-2-chloro-3-[2-chloro-5-
(cyclohex-1-ene-1,2-dicarboxi-
mido)phenyl]acrylate

430-980-9

—

R53

430-750-8

—

R53

430-930-6

122886-55-9

R53

430-940-0

—

R53

430-950-5

—

R53

430-960-1

—

R53

430-970-4

—

R53

R: 53
S: 61

R: 53
S: 61

R: 53
S: 61

R: 53
S: 61

R: 53
S: 61

R: 53
S: 61

R: 53
S: 61

—

142891-20-1

Carc. Cat. 3; R40
R43
N; R50-53

Xn; N
R: 40-43-50/53
S: (2-)24-37-46-60-61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
8
7

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

616-122-00-8

methyl neodecanamide

414-460-9

105726-67-8

Xn; R22

Xn
R: 22
S: (2-)

616-131-00-7

1-aminocyclopentanecarboxa-
mide

422-950-9

17193-28-1

T; R48/25
Xn; R22
Xi; R41

T
R: 22-41-48/25
S: (1/2-)22-26-36/39-45

616-136-00-4

Reaction product of cocoalkyl-
diethanolamides and cocoalkyl-
monoglycerides and
molybdenumtrioxide (1.75-2.2:
0.75-1.0:0.1-1.1)

430-380-7

—

N; R51-53

616-137-00-X

4-dichloroacetyl-1-oxa-4-azas-
piro[4.5]decane

401-130-4

71526-07-3

616-138-00-5

benzoic acid, N–trans-butyl-N'-(4-
chlorobenzoyl)hydrazide

431-600-4

112226-61-6

616-139-00-0

(3S,4aS,8aS)-N–trans-butyldeca-
hydro-3-isoquinolinecarboxa-
mide

420-380-5

136465-81-1

616-140-00-6

N,N''-(methylenedi-4,1-pheny-
lene)bis[N'-(4-methylphenyl)urea]

429-380-1

133336-92-2

R43
N; R51-53

R43
N; R51-53

Xn; R22
Xi; R41
R52-53

R43
R53

N
R: 51/53
S: 61

Xi; N
R: 43-51/53
S: (2-)24-37-61

Xi; N
R: 43-51/53
S: (2-)24-37-61

Xn
R: 22-41-52/53
S: (2-)22-26-39-61

Xi
R: 43-53
S: (2-)24-37-61

616-141-00-1

zoxamide (ISO);
(RS)-3,5-dichloro-N-(3-chloro-1-
ethyl-1-methyl-2-oxopropyl)-p-
toluamide

616-144-00-8

3,4-dichloro-N-[5-chloro-4-[2-
[4-dodecyloxyphenylsulfonyl]
butyramido]-2-hydroxyphenyl]
benzamide

—

156052-68-5

R43
N; R50-53

Xi; N
R: 43-50/53
S: (2-)24-37-46-60-61

C ≥ 2,5 %: Xi, N; R43-50/53
1 % ≤ C < 2,5 %: Xi, N; R43-51/53
0,25 % ≤ C < 1 %: N; R51/53
0,025 % ≤ C < 0,25 %: R52/53

431-130-1

—

R53

R: 53
S: 61

L

2
4
6
/
1
8
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

616-145-00-3

pethoxamide (ISO);
2-chloro-N-(2-ethoxyethyl)-N-(2-
methyl-1-phenylprop-1-enyl)
acetamide

—

106700-29-2

Xn; R22
R43
N; R50-53

Xn; N
R: 22-43-50/53
S: (2-)24-37-46-60-61

C ≥ 25 %: Xn, N; R22-43-50/53
1 % ≤ C < 25 %: Xi, N; R43-50/53
0,25 % ≤ C < 1 %: N; R50/53
0,025 % ≤ C < 0,25 %: N; R51/53
0,0025 % ≤ C < 0,025 %: R52/53

616-146-00-9

N-(2-methoxy-5-octadecanoyla-
minophenyl)-2-(3-benzyl-2,5-
dioxoimidazolidin-1-yl)-4,4-
dimethyl-3-oxopentanoic acida-
mide

431-330-7

142776-95-2

R53

616-147-00-4

1-methyl-4-(2-methyl-2H-tetra-
zol-5-yl)-1H-pyrazole-5-sulfona-
mide

424-160-1

139481-22-4

Xn; R22
R52-53

R: 53
S: 22-61

Xn
R: 22-52/53
S: (2-)61

616-148-00-X

N-[6,9-dihydro-9-[[2-hydroxy-1-
(hydroxymethyl)ethoxy]methyl]-
6-oxo-1H-purin-2-yl]acetamide

424-550-1

84245-12-5

Carc. Cat. 2; R45
Muta. Cat. 2; R46
Repr. Cat. 2; R60-61

T
R: 45-46-60-61
S: 53-45

616-150-00-0

(2R,3S)-N-(3-amino-2-hydroxy-
4-phenylbutyl)-N-isobutyl-4-
nitrobenzenesulfonamide hydro-
chloride

425-260-6

—

616-151-00-6

N-(2-amino-4,6-dichloropyrimi-
din-5-yl)formamide

425-650-6

171887-03-9

Xn; R48/22
Xi; R41
R43
N; R51-53

Xn; R22
Xi; R41
R43
R52-53

616-152-00-1

4-(4-fluorophenyl)-2-(2-methyl-
1-oxopropyl)-4-oxo-3,N-diphe-
nylbutanamide

425-850-3

125971-96-2

R53

616-153-00-7

4-methyl-3-oxo-N-phenyl-2-
(phenylmethylene)pentanamide

425-860-8

125971-57-5

R43
N; R51-53

616-154-00-2

3,4-dichloro-N-[5-chloro-4-[2-
[4-(hexadecyloxy)phenylsulfonyl]
butyramido]-2-hydroxyphenyl]
benzamide

431-110-0

—

R53

Xn; N
R: 41-43-48/22-51/53
S: (2-)22-26-36/37/39-61

Xn
R: 22-41-43-52/53
S: (2-)24-26-37/39-61

R: 53
S: 61

Xi; N
R: 43-51/53
S: (2-)22-24-37-61

R: 53
S: 61

.

.

1
5
9
2
0
0
8

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

L

2
4
6
/
1
8
9

Index No

Chemical name

Notes
related to
substances

EC No

CAS No

Classification

Labelling

Concentration Limits

Notes
related to
prepa-
rations

616-155-00-8

N,N,N',N'-tetracyclohexyl-1,3-
benzenedicarboxamide

431-040-0

104560-40-9

N; R50-53

616-156-00-3

616-157-00-9

6-(2-chloro-6-cyano-4-nitrophe-
nylazo)-4-methoxy-3-[N-(meth-
oxycarbonylmethyl)-N-(1-meth-
oxycarbonylethyl)amino]acetani-
lide

3-amino-4-hydroxy-N-(3-isopro-
poxypropyl)benzenesulfonamide
hydrochloride

616-158-00-4

N-[4-cyano-3-trifluoromethyl-
phenyl]methacrylamide

430-500-8

204277-61-2

R53

427-780-9

114565-70-7

427-880-2

90357-53-2

Xn; R22
Xi; R41
N; R50-53

Xn; R48/22
N; R51-53

R43
R52-53

616-160-00-5

2,2'-azobis[N-(2-hydroxyethyl)-
2-methylpropionamide]

429-090-3

61551-69-7

616-161-00-0

2,4-dichloro-5-hydroxyacetani-
lide

616-162-00-6

isostearic acid monoisopropano-
lamide

616-163-00-1

617-021-00-1

4,4'-methylenebis[N-(4-chloro-
phenyl)-3-hydroxynaphthalene-
2-carboxamide]

methylethylketone peroxide tri-
mer

429-110-0

67669-19-6

R52-53

431-540-9

—

Xi; R38
N; R51-53

430-350-3

192463-88-0

R53

429-320-2

—

E; R2
O; R7
Xn; R65
Xi; R38
R43

N
R: 50/53
S: 60-61

R: 53
S: 61

Xn; N
R: 22-41-50/53
S: (2-)26-39-60-61

Xn; N
R: 48/22-51/53
S: (2-)36-61

Xi
R: 43-52/53
S: (2-)12-15-24-37-61

R: 52/53
S: 61

Xi; N
R: 38-51/53
S: (2-)37-61

R: 53
S: 61

E; Xn
R: 2-7-38-43-65
S: (2-)3/7-14-23-36/37/
39-62

4’

L

2
4
6
/
1
9
0

E
N

O

f
f
i
c
i
a
l

J
o
u
r
n
a
l

o
f

t
h
e

E
u
r
o
p
e
a
n

U
n
o
n

i

.

.

1
5
9
2
0
0
8

15.9.2008

EN

Official Journal of the European Union

L 246/191

ANNEX 1H

The entries in Annex I with the following entry numbers are deleted:

607-443-00-4, 607-472-00-2, and 606-080-00-9.