Principles of Chemical Nomenclature A Guide to IUPAC Recommendations
This book "Principles of Chemical Nomenclature A Guide to IUPAC Recommendations" also available from IUPAC as free download
Contents
Introduction;
Definitions;
Formulae;
Naming of substances;
Aspects of the nomenclature of organometallic compounds;Macromolecular (polymer) nomenclature;
Biochemical nomenclature;Nomenclature in the making;Appendices;
Indexfull text pdf 1.70MB, with bookmark by chapters and sections
Get Green Book, 2nd Edition for free!!
The second edition of Quantities, Units and Symbols in Physical Chemistry (ISBN 0-632-03583-8), also known as the Green Book, establishing standards for nomenclature in chemistry.
The green books are direct successors to the "Manual of Symbols and Terminology for Physicochemical Quantities and Units" prepared for publication on behalf of the Physical Chemistry Division of IUPAC by M. L. McGlashen in 1969. A full history of the 'Green Books" is provided in the historical Introduction to the 3rd Edition. The 2nd edition has been available online as a PDF file, and the third edition will be available as a pdf one year after publication.
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Goldify is a service provided by IUPAC. This online service allows you to submit your text and have links to the IUPAC Gold Book automatically inserted into it using the goldify software. Underlined linear structures display the actual structure of the molecule when you put a mouse cursor over them.
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This website is able to convert any website with chemical names into a nicely drawn chemical structure one.
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Drug Master File
Drug Master File or DMF is a document prepared by a pharmaceutical manufacturer and submitted solely at its discretion to the appropriate regulatory authority in the intended drug market. There is no regulatory requirement to file a DMF. However, the document provides the regulatory authority with confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of one or more human drugs.
Drug Master File (DMF) is a document containing complete information on an Active Pharmaceutical Ingredient (API) or finished drug dosage form. It is known as European Drug Master File (EDMF) or Active Substance Master File (ASMF) and US-Drug Master file (US-DMF) in Europe and United States respectively.
The DMF contains factual and complete information on a drug product's chemistry, manufacture, stability, purity, impurity profile, packaging, and the cGMP status of any human drug product.
Source: Wikipedia