Effects of Reaction Time and Temperature on the Formation of Volatiles from l-Cysteine and Propanal Heated in a Triglyceride–Water System

J. Okumura
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引用次数: 2

Abstract

The effects of reaction time and temperature on the volatile compounds formed from l-cysteine and propanal were studied in model systems heated in triglyceride–water (75:25). The volatile compounds, flavor profiles and yields formed in these model systems varied according to the reaction conditions. At 90 and 110°C, 2-methyl-2-pentenal was the most predominant component formed. Its maximum proportion occurred after heating for 1.5 hr at 110°C, and markedly decreased with temperatures over 110°C. 2-Ethylthiazolidine was the major product in the system heated at 140°C for 1.5 hr. 2-Ethylthiazolidino [3,4-b] thiazolidine could be detected in the system heated at 90°C for 1.5 hr. At 170°C, the profile of the volatile products was very complex, higher temperatures favoring the formation of nitrogen- and sulfur-containing compounds, including pyrrole, pyridines, thiophenes, thiazolidines, 1,2,4,-trithiolanes and 1,2,4-trithianes.
反应时间和温度对甘油三酯-水体系中l-半胱氨酸和丙醛生成挥发物的影响
在甘油三酯-水(75:25)加热的模型体系中,研究了反应时间和温度对l-半胱氨酸和丙醛形成挥发性化合物的影响。这些模型体系的挥发性化合物、风味特征和产率随反应条件的不同而变化。在90°和110°C时,2-甲基-2-戊烯醛是形成的最主要组分。在110℃下加热1.5小时后,其比例达到最大,温度超过110℃时,比例显著下降。2-乙基噻唑烷为主要产物,在140℃下加热1.5 h。2-乙基噻唑烷[3,4-b]噻唑烷在90℃加热1.5 h时可以检测到。在170°C时,挥发产物的分布非常复杂,较高的温度有利于形成含氮和含硫化合物,包括吡咯、吡啶、噻吩、噻唑烷、1,2,4,-三硫烷和1,2,4-三硫烷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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