Pharmaceutical Chemical Analysis: Methods for Identification and Limit Tests (Record no. 16002)

MARC details
000 -LEADER
fixed length control field 02623nam a2200169Ia 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 140223b2006 xxu||||| |||| 00| 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9780849319785
Terms of availability 0.00
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 615.1901
Item number PED
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Pederson, Ole
245 ## - TITLE STATEMENT
Title Pharmaceutical Chemical Analysis: Methods for Identification and Limit Tests
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc. Boca Raton
Name of publisher, distributor, etc. Taylor & Francis
Date of publication, distribution, etc. 2006
300 ## - PHYSICAL DESCRIPTION
Extent 157p
500 ## - GENERAL NOTE
General note Complete, referenced information in an easy-to-use format Many of the monographs in the European Pharmacopiea, the industry standard test for certain groups of ingredients and excipients, do not describe the tests in full, but reference general methods based on test-tube chemistry. When a test fails, you need to know what went wrong, how it can be fixed, and how to convince QA\QC that the tested material is okay. This gives you little time to dig out the relevant scientific literature, literature that is often so old it doesn’t show up in an electronic search. Making this knowledge easily accessible and directly applicable to work in the lab, Pharmaceutical Chemical Analysis: Methods for Limit Tests and Identifications explains the purpose of these older tests, the chemistry involved, and hazards to avoid. The book covers the identification of ions and functional groups tests and limit tests respectively. It covers subjects relevant to all the pharmacopoeial identification/limit test and then goes on to describe the individual tests in chapters organized and named as they appear in the European Pharmacopoeia. Each chapter begins with a short discussion on the purpose and rationale of the tests, followed by a review of the physical and chemical characters of the target ion or compound. The author describes the chemical background and logic of the individual procedural steps of the test with formulas and reaction and provides tips on the strengths and weaknesses of these techniques in terms of specificity, ruggedness, and potential procedural pitfalls. Strict regulatory requirements and economic pressures make the pharmaceutical industry understandably reluctant to replace a test that is simple, cheap, and performs well with expensive, unvalidated instrumental techniques. This resource bridges the gap by providing an in-depth understanding of the principles behind the European Pharmacopoeia tests and how to use them, saving you valuable production time.
600 ## - SUBJECT ADDED ENTRY--PERSONAL NAME
Personal name Pharmaceutical Analysis
890 ## -
-- UK
995 ## - RECOMMENDATION 995 [LOCAL, UNIMARC FRANCE]
-- PED
-- 004443
-- PHA-NIP
-- 8108.00
-- 0
-- 049
-- 409
-- 0
-- 0.00
-- 20060302
-- 1
-- C
-- 20060413
-- Viraj Marketing-p
-- Reference

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