Synthesis of lipophilic antioxidant tyrosol laurate using imidazolium ionic liquid [Bmim]HSO4 as a catalyst

被引:2
|
作者
Wang, Yimei [1 ]
Zhang, Yaoyao [1 ]
Qiao, Xing [1 ]
Sun, Shangde [1 ]
机构
[1] Henan Univ Technol, Natl Engn Res Ctr Wheat & Corn Further Proc, Sch Food Sci & Engn, Lianhua Rd 100, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Tyrosol laurate; Lauric acid; Ionic liquids; Esterification; Antioxidant activity; ENZYMATIC-SYNTHESIS; ACID; ESTERIFICATION; OIL; ESTERS;
D O I
10.1016/j.foodchem.2024.138418
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Tyrosol is a natural phenolic compound with potent antioxidant properties in the field of food manufacturing. However, the low lipophilicity of tyrosol limited its application. Therefore, the construction of tyrosol laurate (Tyr-L) could effectively overcome the limitations of tyrosol. In this work, four ionic liquids (ILs) were applied for TYr-L preparation. Among them, the 1-butyl-3-methylimidazolium hydrogen sulfate ([Bmim]HSO4) showed the best catalytic performance. The maximum TYr-L yield was achieved (94.24 +/- 1.23 %) under the optimal conditions (reaction temperature 119 degrees C, substrate ratio 1:6.7, IL dosage 9.2 %, and reaction time 12 h). The kinetic and thermodynamic parameters were also evaluated and it was found that Ea, Delta H, Delta S, and Delta G were 80.81 kJ<middle dot>mol(-1), 77.63 kJ<middle dot>mol(-1), -82.08 J<middle dot>(mol<middle dot>K)(-1), and 109.89 kJ<middle dot>mol(-1), respectively. The acidic [Bmim]HSO4 demonstrated excellent reusability and stability, even after 6 cycles. Furthermore, TYr-L showed superior ABTS radical scavenging ability, which could be further applied in various industrial processes.
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页数:11
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