GC-FID method for high-throughput analysis of residual solvents in pharmaceutical drugs and intermediates
Author:
Affiliation:
1. Process Research & Development
2. Merck Research Laboratories
3. Rahway
4. USA
Abstract
This approach simplifies tremendously the tedious task of residual solvent quantitation, resulting in significantly less labor, greater reliability, faster time to result and at least a 290 fold reduction in solvent consumption and hazardous waste disposal.
Publisher
Royal Society of Chemistry (RSC)
Subject
Pollution,Environmental Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/GC/C6GC01210H
Reference26 articles.
1. Analytical procedures for quality control of pharmaceuticals in terms of residual solvents content: Challenges and recent developments
2. UNDERSTANDING GOUT BEYOND DOUBT
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