A method for enriching branched-chain fatty acids
A branched-chain fatty acid and fatty acid technology, applied in the production of fatty acids, chemical modification of fatty acids, etc., can solve the problems of unsuitability for large-scale industrial production, low purity of branched-chain fatty acids, small processing capacity, etc., and achieve mild reaction conditions and high purity. , the effect of low energy consumption
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Embodiment 1
[0024] Mix 20 grams of lanolin fatty acid, 40 grams of urea, and 200 milliliters of anhydrous methanol, reflux in a water bath at 60°C for 2 hours, cool and crystallize at 10°C for 12 hours, and filter quickly. After removing most of the solvent by rotary evaporation of the filtrate, add water to dissolve, then add petroleum ether to extract the fatty acid for 3 times, separate the liquid, wash the residual urea in the organic phase with water, add anhydrous sodium sulfate to absorb the residual water in the organic phase, 60 ℃ The solvent was removed by rotary evaporation to obtain high-purity branched-chain fatty acid with a purity of 94.17% and a recovery of branched-chain fatty acid of 38.24%.
Embodiment 2
[0026] Mix 20 grams of lanolin fatty acid, 50 grams of urea, and 50 milliliters of 80% methanol, reflux in a water bath at 60° C. for 2 hours, cool and crystallize at 20° C. for 6 hours, and quickly filter with suction. After removing most of the solvent by rotary evaporation of the filtrate, add water to dissolve, add petroleum ether to extract the fatty acid three times, separate the liquid, wash the residual urea in the organic phase with water, add anhydrous sodium sulfate to absorb the residual water in the organic phase, and rotate at 60°C Evaporate and remove the solvent to obtain high-purity branched chain fatty acid fatty acid, the purity is 91.28%, and the recovery rate of branched chain fatty acid is 21.24%.
Embodiment 3
[0028] Mix 20 grams of fish oil fatty acid, 20 grams of urea, and 100 milliliters of 90% ethanol, reflux in a water bath at 60°C for 4 hours, cool and crystallize at 10°C for 24 hours, and quickly filter with suction. After removing most of the solvent by rotary evaporation of the filtrate, add water to dissolve, extract the fatty acid three times with petroleum ether, separate the liquid, wash the residual urea in the organic phase with water, add anhydrous sodium sulfate to absorb the residual water in the organic phase, and rotate to evaporate at 60°C The high-purity branched-chain fatty acid is obtained by removing the solvent, the purity is 68.40%, and the recovery rate of the branched-chain fatty acid is 44.85%.
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