以邻苯二甲醛与N-乙酰-L-半胱氨酸作为柱前手性衍生化试剂拆分 DL-氨基酸的反相高效液相色谱法研究  

Separation of Enantiomeric Amino Acids by Reversed phase High-performance Liquid Chromatography

作　　者：李惠芝[1] 赵华[1] 胡湘南[1] 邱宗荫[1] 

机构地区：[1]重庆医科大学化学教研室,重庆630046

出　　处：《分析化学》1992年第12期1425-1428,共4页Chinese Journal of Analytical Chemistry

摘　　要：本文用邻苯二甲醛和N-乙酰-L-半胱氨酸作柱前手性衍生化试剂,经反相高效液相色谱法拆分DL-氨基酸。研究了衍生化反应条件以及固定相、流动相对出峰顺序和分离效果的影响。实现了11对DL-氨基酸的同时拆分。本方法用于(±)-2,4,6三甲基苯丙氨酸的分离取得满意结果。Enantiomeric amino acid reacted rapidly with o-phthaldehyde in the presence of N-acetyl-L-cysteine to give intensely fluorescent products, which were diastereoisomers. These diasteremeric derivatives were efficiently resolved on a reversed-phase column. Simultaneous analysis of 11 pairs of different enantiomeric amino acids was achieved by gradient elution. The effects of both stationary and mobile phase on the resolution and the eluting order were also discussed. The method was applied to the separation of (±)-2,4,6-trimethylphenylalanine.

关 键 词：邻苯二甲醛 AcCYs DL-氨基酸 

分 类 号：O629.7[理学—有机化学]