Method for purifying beta-sitosterol from cornel kernels
A technology of cornus kernel and sitosterol, which is applied in the field of separation and purification of biologically active substance phytosterol, can solve the problems of low purity of beta-sitosterol, difficult to achieve and high cost, and achieves good crystal shape, high separation speed and low cost. Effect
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Embodiment 1
[0018] A method for purifying β-sitosterol from cornus officinale, comprising the following steps:
[0019] 1) Crush the fruit core of dogwood into 15 mesh particles;
[0020] 2) Soak the crushed granules in 5 times the weight of 95% edible ethanol for 24 hours, filter, and squeeze out the oil;
[0021] 3) Combine the filtrate and squeezed liquid, concentrate under reduced pressure to remove the ethanol in the combined liquid, then mix the oil after removing ethanol with NaOH solution with a concentration of 25% (W / W) according to M / V=1:1, at 75 degrees Saponification under reflux for 3 hours;
[0022] 4) cooling the reaction solution prepared in step 3), and lowering the temperature to 0°C to precipitate the residue, filter to remove the saponification product, and concentrate the filtrate to 1 / 10 of the original volume under reduced pressure at 65°C;
[0023] 5) Add an equal volume of ethyl acetate to the filtrate to extract the filtrate 2 to 3 times, combine the extracts,...
Embodiment 2
[0030] A method for purifying β-sitosterol from cornus officinale, comprising the following steps:
[0031] 1) Crush the fruit core of dogwood into 20 mesh particles;
[0032] 2) Soak the crushed granules in 5 times the weight of 95% edible ethanol for 24 hours, filter, and squeeze out the oil;
[0033] 3) Combine the filtrate and squeezed liquid, concentrate under reduced pressure to remove the ethanol in the combined liquid, then mix the oil after removing ethanol with NaOH solution with a concentration of 25% (W / W) according to M / V=1:1, at 75 degrees Saponification under reflux for 3 hours;
[0034] 4) cooling the reaction solution prepared in step 3), and cooling it down to 0°C to precipitate the residue, filter to remove the saponification product, and concentrate the filtrate to 1 / 10 of the original volume under reduced pressure at 65°C;
[0035] 5) Add an equal volume of ethyl acetate to the filtrate to extract the filtrate 2 to 3 times, combine the extracts, adjust t...
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