Heptafluorobutyl Chloroformate-Based Sample Preparation Protocol for Nonchiral and Chiral Amino Acid Analysis by Gas Chromatography-Mass Spectrometry
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- Keywords
- 2,3-Dimercapto-1-propanesulfonic acid, Amino acid, Amino acid analysis, Chiral analysis, Derivatization, Enantiomer, Gas chromatography, Heptafluorobutyl chloroformate, Mass spectrometry, Plasma, Serum,
- MeSH
- Amino Acids blood chemistry isolation & purification MeSH
- Deuterium analysis chemistry MeSH
- Liquid-Liquid Extraction instrumentation methods MeSH
- Fluorocarbons chemistry MeSH
- Formates chemistry MeSH
- Carbon Isotopes analysis chemistry MeSH
- Calibration MeSH
- Humans MeSH
- Gas Chromatography-Mass Spectrometry instrumentation methods MeSH
- Stereoisomerism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amino Acids MeSH
- Carbon-13 MeSH Browser
- Deuterium MeSH
- Fluorocarbons MeSH
- Formates MeSH
- heptafluorobutyl chloroformate MeSH Browser
- Carbon Isotopes MeSH
Gas chromatography (GC) is a commonly used technique in amino acid analysis (AAA). However, one of the requirements of the application of GC for AAA is a need for the polar analytes to be converted into their volatile, thermally stable derivatives. In the last two decades, alkyl chloroformates (RCFs) have become attractive derivatization reagents. The reagents react immediately with most amino acid functional groups in aqueous matrices, and the process can easily be coupled with liquid-liquid extraction of the resulting less polar derivatives into immiscible organic phase. Here we describe a simple protocol for in situ derivatization of amino acids with heptafluorobutyl chloroformate (HFBCF) followed by subsequent chiral as well as nonchiral GC/MS (mass spectrometric) analysis on a respective nonpolar fused silica and an enantioselective Chirasil-Val capillary column.
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