幸运8平台彩票

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Application Note

幸运8平台彩票Residual Solvents in Pharmaceuticals by USP Chapter 467 Methodology

Introduction

The synthesis of active pharmaceutical ingredients (API) may require multiple reaction steps that produce undesirable reaction byproducts or utilize various solvents that have to be removed from the finished product. These solvents and byproducts may be measured with headspace gas chromatography for those volatile residual organic solvents according to the USP chapter 467 method. Method USP 467 classifies residual solvents into three classes according to toxicity; class 1 solvents are to be avoided unless there is strong justification, class 2 solvents are those that should be limited due to toxicity concerns.