Download Analytical Profiles of Drug Substances, Excipients, and by Harry G. Brittain PDF

By Harry G. Brittain

ISBN-10: 0122608267

ISBN-13: 9780122608261

Even if the legitimate compendia outline a drug substance as to identification, purity, power, and caliber, they mostly don't supply different actual or chemical information, nor do they checklist tools of synthesis or pathways of actual or organic degradation and metabolism. Such info is scattered in the course of the clinical literature and the documents of pharmaceutical laboratories. Edited by means of the affiliate Director of Analytical study and improvement for the yank organization of Pharmaceutical Scientists, Analytical Profiles of Drug components and Excipients brings this knowledge jointly into one resource. The scope of the sequence has lately been improved to incorporate profiles of excipient fabrics.

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Clin. Pharm. , 12, 107 (1 987). 52. A. M. H. , 8, 157 (1955). BRINZOLAMIDE Rex Hall', Grey Wavner', John Baker', Glenn Stafford2, Wayne Schneider2, Way-Yu Lin2, Jesse May3, Michael Curtis4,Craig Struble4, Bette McCue4, Dan Jasheway4, and David McGee' (1) Analytical Chemistry (2) Research SuppodPharmaceutics (3) Research/Discovery Synthesis (4)PharmacokineticslDrug Metabolism ( 5 ) Toxicology Research and Development Alcon Laboratories, Inc. 00 47 Copyright 0 1999 by Academic Prrsc All nphlr ufrepruduutlon In any form recrrved 48 REX HALLETAL.

164-167. 29. Application Manual HPLCITLUHPTLC, E. Merck, Darmstad, Germany, 1986. 30. Hewlett Packard Analytical Columns and Supplies 199411995, Hewlett Packard Company, 1994. 31. Supelco International, Chromatography Products, Supelco Inc, Bellefonte, PA, 1995. 32. hmtl. 33. W. R. L. McKenzie, J. Pharm. , 68, 280 (1979). 34. zorbax. com. 35. dc08060 1. jp/shodex/english/ html. 36. S. Lee, J. , 78, 80 (1995). BENZOIC ACID 37. HPLC Application, BDH Ltd. (member of Merck Group), Product No. 44, 60-64, 70.

When the acid is heated to 370"C, it is irreversibly decomposed to benzene and carbon dioxide, and a small portion (2-8Y0)decomposes into phenol and carbon monoxide. Copper and cadmium powder increase the reaction rate by factors of approximately 9-fold and 200-fold, respectively. 2 Solution-PhaseStability Aqueous solutions of benzoic acid react with metals, and can generate hydrogen gas [46]. When a solution consisting of 1 mole of benzoic acid in 8 moles of water is heated in autoclave, a slight decomposition with gas BENZOIC ACID 41 formation is noted at 200°C.

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Analytical Profiles of Drug Substances, Excipients, and Related Methodology by Harry G. Brittain


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