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邻氨基苯酚衍生气相色谱-质谱分析不饱和脂肪酸
引用本文:邹耀洪.邻氨基苯酚衍生气相色谱-质谱分析不饱和脂肪酸[J].食品科学,2007,28(3):277-281.
作者姓名:邹耀洪
作者单位:常熟理工学院化学系,江苏,常熟,215500
摘    要:以邻氨基苯酚为脂肪酸的衍生化试剂,柱前衍生气相色谱-EI质谱分析不饱和脂肪酸,邻氨基苯酚将不饱和脂肪酸羧基化学修饰成含氮杂环,从而避免了链烯基中碳碳双键在EI源中的移动,并使质谱呈现显示双键位置的规范信息。通过解析不饱和脂肪酸邻氨基苯酚衍生产物的EI质谱图,得到了不饱和脂肪酸中碳碳双键的定位规则,从而为分析不饱和脂肪酸精细结构提供了手段。用脂肪酸邻氨基苯酚衍生气相色谱-EI质谱法分析了葵子油脂肪酸,鉴定出2种不饱和脂肪酸,确定了脂肪酸中碳碳双键的位置,结果与文献一致。

关 键 词:不饱和脂肪酸  双键位置  邻氨基苯酚  衍生化  EI质谱
文章编号:1002-6630(2007)03-0277-05
修稿时间:2006-02-14

Analysis of Unsaturated Fatty Acids by Gas Chromatography-Mass Spectrometry with Ortho-Aminophenol Pre-Column Derivatization
ZOU Yao-hong.Analysis of Unsaturated Fatty Acids by Gas Chromatography-Mass Spectrometry with Ortho-Aminophenol Pre-Column Derivatization[J].Food Science,2007,28(3):277-281.
Authors:ZOU Yao-hong
Affiliation:Department of Chemistry, Changshu Institute of Technology, Changshu 215500, China
Abstract:A gas chromatography-electron impact mass spectrometric(GC-EIMS) method was developed for analyzing the unsaturated fatty acids, while ortho-aminophenol was used for the pre-column derivatization reagent of unsaturated fatty acids so as to modify carboxy1 group into nitrogen-containing heterocycle which effectively suppressed the migration of double bonds of the alkeny1 under the electron impact source and led to regular informative mass spectra regarding the position of the olefinic bonds in the chain .The empirical rule in which the position of double bonds of olefinic acids was located was refered to by analyzing electron impact spectra of the derivatives of the fatty acids modified by ortho-aminophenol reagent. This methodprovides a new technical tool for analyzing the fine structure of unsaturated fatty acids. Ortho-aminophenol is used as derivatization reagent to the fatty acids and 2 unsaturated fatty acids in sunflower oil are identified according to the analysis of GC-EIMS .The position of double bonds of the unsaturated fatty acids from sunflower oil is located and the results are in good agreement with bibliography.
Keywords:unsaturated fatty acids  position of double bond  ortho-aminophenol  derivatization  electron impact mass spectrometry
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