Method for preparing high-purity natural vitamin E monomers by separating mixed tocopherol
A natural vitamin and tocopherol technology, applied in the direction of organic chemistry, can solve the problems of inability to obtain various monomers of tocopherol, difficulties in solvent selection and recovery, and inability to obtain purity.
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Embodiment 1
[0022] Take 100 grams of low-purity mixed tocopherols (total VE: 50.69%, of which d-α-tocopherol: 13.60%, d-(β+γ)-tocopherol: 29.07%, d-δ-tocopherol: 8.02% , sterol: 9.28%, others: 40.03%, specific optical rotation is +19°) and 400ml volume concentration of 95% ethanol aqueous solution are fully mixed and dissolved at 40°C, and put into a silica gel alumina reverse phase chromatography column (φ20mm*800mm) Carry out adsorption, then continue to enter the column with acetone 300ml until the effluent flows out, discard the effluent less than 10% of the effluent volume, collect the effluent from 10% of the effluent volume to 29% of the effluent volume as effluent-13.8 grams, The purity of d-α-tocopherol was detected to be 91.33%;
[0023] Collect 30% of the effluent volume to 69% of the effluent volume as 28.9 grams of effluent liquid. After removing the solvent, detect that the purity of d-γ-tocopherol is 91.85%, and collect the remaining effluent liquid as 8.1 grams of effluent...
Embodiment 2
[0025] Take 100 grams of low-purity mixed tocopherols (total VE: 48.10%, of which d-α-tocopherol: 15.34%, d-(β+γ)-tocopherol: 27.17%, d-δ-tocopherol: 5.59% , sterol: 9.51%, others: 42.39%, specific optical rotation is +16°) and 500ml of methanol are fully mixed and dissolved at 45°C, and then enter the polystyrene reverse phase chromatography column (φ20mm*800mm) for adsorption, and then use n-hexane and ethyl acetate (volume ratio is 1: 1) 400ml continue to enter the column until the effluent flows out, collect the first 10-30% effluent-15.8 grams, detect wherein the d-alpha-tocopherol purity is 91.26%, collect 30-70 % 27.5 grams of effluent liquid 2, wherein the purity of d-γ-tocopherol was detected to be 90.79%, and the remaining effluent liquid 3 was collected to be 5.7 grams, and the purity of d-δ-tocopherol was detected to be 85.81%. After molecular distillation, the purity of d-α-tocopherol in effluent 1 was 96.31%, the purity of d-γ-tocopherol in effluent 2 was 97.12%,...
Embodiment 3
[0027] A method for separating and preparing high-purity natural vitamin E monomer from mixed tocopherols, comprising the steps of:
[0028] 1) Adsorption: 1 part by volume of mixed tocopherols with a mass concentration of 30% was dissolved in 5 parts by volume of isopropanol at 45°C, and fully dissolved to obtain a sample solution;
[0029] In the reverse phase chromatography column, install the fixed reverse phase filler octylsilane bonded silica gel, add the sample solution at 45°C to the chromatography column, and let the sample solution pass through the filler;
[0030] 2) Analysis: add methanol 1 times the volume of the sample solution into the chromatographic column;
[0031] Discard the effluent that is less than 10% of the volume of the effluent, collect the effluent that is greater than or equal to 10% of the volume of the effluent, and the effluent that is less than 30% of the volume of the effluent is the effluent one. After removing the solvent, d-alpha-tocopherol...
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