13(E)-Docosenoic Acid, a trans-acid, is a 22-carbon monounsaturated fatty acid [1]. 13(E)-Docosenoic Acid can react with primary amines, secondary amines, as well as aliphatic and aromatic amines to synthesize a series of novel amide compounds, which are widely used as the corrosion inhibitors[2]. 13(E)-Docosenoic Acid can be used as a model compound to develop gas chromatography methods for the separation of related compounds[3].
References:
[1] Astorg P O. Heart lipidosis induced by short-term feeding of cis-or trans-docosenoic acids in weanling or 7-week-old rats[J]. Annals of Nutrition and Metabolism, 1981, 25(4): 201-207.
[2] Elsharif A M, Abubshait S A, Abdulazeez I, et al. Synthesis of a new class of corrosion inhibitors derived from natural fatty acid: 13‐Docosenoic acid amide derivatives for oil and gas industry[J]. Arabian Journal of Chemistry, 2020, 13(5): 5363-5376.
[3] Shimizu K, Ando Y. Gas chromatographic separation of docosenoic acid positional isomers on an SLB-IL100 ionic liquid column[J]. Journal of Oleo Science, 2012, 61(8): 421-426.
13(E)-Docosenoic Acid是一种反式酸，为一种22碳单不饱和脂肪酸[1]。13(E)-Docosenoic Acid能与伯胺、仲胺以及脂肪族和芳香族胺反应，合成一系列新型酰胺化合物，这些化合物被广泛用作缓蚀剂[2]。13(E)-Docosenoic Acid可作为模型化合物，用于开发分离相关化合物的气相色谱方法[3]。