Synthesis of Isopropyl palmitate

Synthesis of Isopropyl palmitate

Isopropyl palmitate is prepared by a two step lipase catalysed hydrolysis reaction with palm stearin as the raw material. The specific synthesis steps are as follows:

Step 1: hydrolysis of PS in water 

Step 2: esterification of the palmitic acid (PA) concentrate with isopropanol in a solvent-free system. 

Lewatit VP OC (LVO) 1600-immobilized Eversa Transform (ET) 2.0 was used as the biocatalyst in both reaction steps. The fixation level of proteins contained in ET 2.0 solution with a protein concentration of 34.7 mg/mL on LVO 1600 and the quantity of the proteins bound to LVO 1600 were 78.8 wt% and 214.5 mg per gram of the support material, respectively. The first-step reaction yielded a free fatty acid (FFA) fraction containing 99.4 area% FFAs using reaction conditions of 50 °C, 1:80 (PS-to-water molar ratio), 10 mg/g PS (enzyme loading), and 24 h (reaction time). Fractional crystallization of the FFA fraction in n-hexane for 2 h (crystallization time) at − 5 °C yielded a PA concentrate containing 91.0 wt% PA. Finally, a 90.1 area% conversion to IPP was achieved in the second-step reaction under reaction conditions of 55 °C, 1:1.5 (PA concentrate-to-isopropanol molar ratio), 20 mg/g total substrates (enzyme loading), and 24 h (reaction time).

References:

[1] SEOHYUN HONG; Byung H K; In Hwan Kim. Lipase-catalyzed hydroesterification process for isopropyl palmitate synthesis from palm stearin[J]. Process Biochemistry, 2023, 134: Pages 44-53. DOI:10.1016/j.procbio.2023.09.017.

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