【IUPAC命名法】
IUPAC命名法（International Union of Pure and Applied Chemistry chemical nomenclature）包括国际纯化学和应用化学联合会（IUPAC）规定的一系列的命名法，它规定从有机到无机、从分子到高分子及各方面化学术语。IUPAC已将命名法出版为一系列的颜色书。
== IUPAC颜色书 ==
*总则（General）
**化学命名原理（Principles of Chemical Nomenclature: a Guide to IUPAC Recommendations）
*蓝皮书（Blue Book）
**有机化学命名法，A、B、C、D、E、F和H部（Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H）
**有机物IUPAC命名法指南，1993年推荐（A Guide to IUPAC Nomenclature of Organic Compounds, Recommendations 1993）
*金皮书（Gold Book）：
**化学术语概略（Compendium of Chemical Terminology）
*绿皮书（Green Book）：
**物理化学中的量、单位和符号（Quantities, Units and Symbols in Physical Chemistry）
*橙皮书（Orange Book）：
**分析命名概略（Compendium of Analytical Nomenclature）
*紫皮书（Purple Book）：
**高分子命名概略（Compendium of Macromolecular Nomenclature）
*红皮书（Red Book）：
**无机化学命名法，IUPAC2005年推荐（Nomenclature of Inorganic Chemistry - IUPAC Recommendations 2005）
**无机化学命名法，1990年推荐（Nomenclature of Inorganic Chemistry, Recommendations 1990）
**无机化学命名法第二部，2000年推荐（Nomenclature of Inorganic Chemistry II. Recommendations 2000）
**怎样命名无机物质，1977年（How to Name an Inorganic Substance, 1977）
*银皮书（Silver Book）
**临床实验科学术语及命名法概略（Compendium of Terminology and Nomenclature of Properties in Clinical Laboratory Sciences）
*白皮书（White Book）
**生物化学命名法及相关文档（Biochemical Nomenclature and Related Documents）
== IUPAC命名法 ==
IUPAC已发布的命名法有：
* 有机化学命名法，E部：立体化学1
* 有机化学命名法，F部：天然产物和有关化合物2
* 有机化学命名法，H部：同位素标记化合物3
* 修订的杂环命名法Hantzsch-Widman系统的延伸4
* 对于有机化学的可变价的命名法（Lambda约定）5
* 规则A-1.1和A-2.5的扩充，关于有机化学中的数字6
* 具有累积双键的环状有机物命名法（Delta约定）7
* 修订的基、离子、基离子及相关物种的命名法8
* 有机化学类名和基与结构的反映中间产物的术语表9
* 立体化学基本术语10
* 稠环及桥稠环系统的命名法11
* 芬命名法，第一部分：芬的母体名称12
* 扩展及修订的命名多环化合物的von Baeyer系统（包括双环化合物）13
* 扩展及修订的螺化合物的的命名法14
* 修订的F部：天然产物和有关化合物15
* C60-Ih及C70-D5h(6)球碳的命名法16
* 芬命名法，第二部分：加氢度的修正和芬母体取代产物17
* 球碳的编号18
== 参阅 ==
* 国际化合物标识
* IUPAC数值前缀
*IUPAC有机物命名法
== 参考文献 ==
# 1 Nomenclature of organic chemistry, section E: stereochemistry. Recommendations 1974, Pure Appl. Chem., 1976, 45, 11-30
# 2 Nomenclature of organic chemistry, section F: natural products and related compounds. Recommendations 1976, Eur. J. Biochem., 1978, 86, 1-8
# 3 Nomenclature of organic chemistry, section H: isotopically modified compounds. Recommendations 1977, Eur. J. Biochem., 1978, 86, 9-25; 1979, 102, 315-316; Pure Appl. Chem., 1979, 51, 353-380
# 4 Revision of the extended Hantzsch-Widman system of nomenclature for heteromonocycles. Recommendations 1982, Pure Appl. Chem., 1983, 55, 409-416.
# 5 Treatment of variable valence in organic nomenclature (lambda convention). Recommendations 1983, Pure Appl. Chem., 1984, 56, 769-778
# 6 Extension of rules A-1.1 and A-2.5 concerning numerical term used in organic chemical nomenclature. Recommendations 1986, Pure Appl. Chem., 1986, 58, 1693-1696 numerical terms to 9999。
# 7 Nomenclature for cyclic organic compounds with formal contiguous double bonds (the δ-convention). Recommendations 1988, Pure Appl. Chem., 1988, 60, 1395-1401.
# 8 Revised nomenclature for radicals, ions, radical ions and related species. Pure Appl. Chem., 65, 1993, 1357-1455
# 9 Glossary of class names of organic compounds and reactive intermediates based on structure. Recommendations 1995, Pure Appl. Chem., 67, 1995, 1307-1375.
# 10 Basic Terminology of Stereochemistry. IUPAC recommendations 1996, Pure Appl. Chem., 68, 1996, 2193-2222.
# 11 Nomenclature of Fused and Bridged Fused Ring Systems. IUPAC Recommendations 1998, Pure Appl. Chem., 1998, 70, 143-216.
# 12 Phane Nomenclature. Part I: Phane Parent Names. IUPAC Recommendations 1998, Pure Appl. Chem., 1998, 70, 1513-1545.
# 13 Extension and Revision of the von Baeyer System for Naming Polycyclic Compounds (Including Bicyclic Compounds).  IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 513-529.
# 14 Extension and Revision of the Nomenclature for Spiro Compounds. IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 531-558.
# 15 Revised Section F: Natural products and related compounds. IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 587-643.
# 16 Nomenclature for the C60-Ih and C70-D5h(6) Fullerenes. IUPAC Recommendations 2002, Pure Appl. Chem., 2002, 74, 629-695.
# 17 Phane nomenclature. Part II. Modification of the degree of hydrogenation and substitution derivatives of phane parent hydrides. IUPAC Recommendations 2002, Pure Appl. Chem., 2002, 74, 809-834.
# 18 Numbering of Fullerenes. IUPAC Recommendations 2004. Pure Appl. Chem., 2005, 77, 843-923.
==外部连结==
* Interactive  IUPAC Compendium of Chemical Terminologydate=20161124233000 （interactive "Gold Book"）
*  IUPAC Nomenclature Books Seriesdate=20100208200456 （list of all IUPAC nomenclature books, and means of accessing them）
*  IUPAC Compendium of Chemical Terminology（"Gold Book"）
*  Quantities, Units and Symbols in Physical Chemistrydate=20100311071751 （"Green Book"）
*  IUPAC Nomenclature of Organic Chemistrydate=20110608140820 （"Blue Book"）
*  Nomenclature of Inorganic Chemistry IUPAC Recommendations 2005date=20100216154328 （"Red Book"）
*  IUPAC Recommendations on Organic & Biochemical Nomenclature, Symbols, Terminology, etc.date=20060105051351 （includes IUBMB Recommendations for biochemistry）
*  chemicalize.orgdate=20160913080333  A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.
*  ChemAxon Name  Structure – IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at  chemicalize.orgdate=20160913080333
*  ACD/Namedate=20131102101820  – Generates IUPAC, INDEX (CAS), InChi, Smiles, etc. for drawn structures in 10 languages and translates names to structures. Also available as batch tool and for Pipeline Pilot. Part of   I-Lab 2.0