Method for effectively synthesizing phytosterol ester
A technology of phytosterol ester and synthesis method, which is applied in the field of high-efficiency synthesis of phytosterol ester, can solve the problems of harsh operating conditions and low catalyst safety, and achieve the effects of not easy oxidative denaturation, less by-products, and high product safety
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Embodiment 1
[0018] Embodiment 1: the synthesis of phytosterol laurate
[0019] Take by weighing 0.8g of mixed phytosterols and 0.8g of lauric acid in a 50mL Erlenmeyer flask with a stopper, add 1% free lipase (derived from Rhizopus Aspergillus niger, activity 700000U / g) of the total mass of phytosterols and lauric acid raw materials as a catalyst, Add 16 mL of n-hexane, control the water activity at 0.41, and react at a constant temperature of 45°C for 24 hours. The obtained reaction product is separated and purified to obtain phytosterol laurate with a purity of 95%.
Embodiment 2
[0020] Embodiment 2: the synthesis of phytosterol docosahexaenoate
[0021] Weigh mixed phytosterol 0.8g, docosahexaenoic acid (DHA) 4.0g in 50mL Erlenmeyer flask with stopper, add phytosterol and docosahexaenoic acid raw material gross mass 10% immobilized lipase (source In Candida, activity 10000U / g) as a catalyst in the above-mentioned Erlenmeyer flask with a stopper, add 20 mL of mixed solvent of n-hexane: cyclohexane: isooctane=6: 2: 1 (v / v) in the Erlenmeyer flask . Control the water activity at 0.87, and react at a constant temperature of 40°C for 96h. The obtained reaction product is separated and purified to obtain phytosterol docosahexaenoate with a purity of 92%.
Embodiment 3
[0022] Embodiment 3: the synthesis of phytosterol fatty acid ester
[0023] Weigh 0.8 g of mixed phytosterols and 8 g of mixed fatty acids in a 50 mL Erlenmeyer flask with a stopper. First add phytosterols and 5% free lipase (derived from Rhizopus, activity 30000U / g) of the total mass of mixed fatty acid raw materials as a catalyst in the above-mentioned Erlenmeyer flask with a stopper, and add 5 mL of solvent n-heptane in the Erlenmeyer flask. Control the water activity to 0.62, and after 24 hours of constant temperature reaction at 55°C, change the water activity of the system to 0.12, then add 3% immobilized lipase (derived from Aspergillus niger, 50000U / g) of the total mass of raw materials, and continue the reaction for 24 hours. The obtained reaction product is separated and purified to obtain a phytosterol fatty acid ester with a purity of 96%.
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