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作 者:Toshio Hasegawa Tasuku Matsunaga Hideo Yamada
机构地区:[1]Department of Chemistry, Graduate School of Science and Engineering, Saitama University, Saitama 338-8570, Japan [2]Yamada-Matsu Co., Ltd., Kyoto 602-8014, Japan
出 处:《Journal of Chemistry and Chemical Engineering》2014年第2期112-117,共6页化学与化工(英文版)
摘 要:The authors examined the thermal change in the aroma profile of myrrh. The fresh odor of raw myrrh and its hexane extract depended on the amount of (E)-13-ocimene. Myrrh was extracted with hexane to avoid inducing changes in the constituents and odor. The main constituent, (E)-L3-ocimene (group A; low boiling point), and the other constituents (group B; high boiling point) of the hexane extract were separated by bulb-to-bulb distillation. The constituents of groups A and B were analyzed over time by nuclear magnetic resonance analysis and the odors were evaluated. Myrrh's odor depended on both the amount of thermally unstable (E)-[3-ocimene, which contributed to the fresh odor, and the constituents of group B (thermally stable), which contributed to the myrrh-like odor. Six compounds (c^-santalene, (Z)-a-bisabolene, c^-bergamotene, (E)-ct-santalal, c^-photosantalol and campherenol) were isolated from group B. No individual group B component had a myrrh-like odor, although the combined odor of group B was myrrh like. The authors demonstrated that the aroma profile of myrrh depends on the thermal instability of (E)-^-ocimene and a combination of six thermally stable terpenes with similar molecular structures.
关 键 词:Thermal variation thermal instability myrrh myrrh-like odor (E)-L3-ocimene.
分 类 号:TQ461[化学工程—制药化工] P467[天文地球—大气科学及气象学]
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