Method for preparing taxifolin from fruit of princesplume ladysthumb
A technology of taxifolin and safflower seeds, which is applied in the field of preparing taxifolin, and achieves the effects of high product purity, easy decolorization and good separation effect.
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Embodiment 1
[0022] Take 10g of safflower medicinal material, soak it with 60mL50% ethanol, place it in a crusher, crush and extract it for 15 minutes, put the extract in a centrifuge, and centrifuge it at 3000r / min for 10 minutes, repeat the operation 3 times, combine the centrifugate, and On the HPD300 macroporous resin on the centrifuge, the impurities were first eluted with 5 times the column volume of water at a flow rate of 1.5BV / h, and then eluted with 60% ethanol until no taxifolin fraction was detected by TLC, and the taxifolin fraction was collected , heated to 60°C, then added active carbon and stirred at constant temperature for decolorization for 1h, filtered, concentrated the filtrate into an extract, mixed the extract with dextran gel and dried it, then put it on a Sephadex LH-20 column in a dry method, chloroform-ethanol (6: 1) Elution, flow rate 4BV / h, thin-layer detection, collect taxifolin fraction, concentrate under reduced pressure to recover the solvent, and obtain the...
Embodiment 2
[0024] Take 10g of safflower medicinal material, soak it with 100mL45% ethanol, place it in a crusher and extract it for 20 minutes, put the extract in a centrifuge, and centrifuge it at 3500r / min for 15 minutes, repeat the operation twice, combine the centrifugate, and On the NKA-9 macroporous resin on the centrifuge, the impurities were first eluted with 4 times the column volume of water at a flow rate of 2 BV / h, and then eluted with 50% ethanol until no taxifolin fraction was detected by TLC, and the taxifolin flow was collected Separate, heat to 60°C, add active carbon and stir at constant temperature for decolorization for 1h, filter, concentrate the filtrate into an extract, mix the extract with dextran gel and dry it, then put it on a Sephadex LH-20 column in a dry method, chloroform-ethanol (9 : 1) elution, flow rate 4BV / h thin-layer detection, collect taxifolin fraction, concentrate under reduced pressure to recover the solvent, to obtain crude product, benzene-ethano...
Embodiment 3
[0026] Take 20g of Safflower medicinal material, soak it with 240mL A0% ethanol, place it in a crusher and extract it for 10 minutes, put the extract in a centrifuge, and centrifuge it at 4000r / min for 12 minutes, repeat the operation 3 times, combine the centrifugate, and On the HPD600 macroporous resin on the centrifuge, the impurities were first eluted with 5 times the column volume of water at a flow rate of 3 BV / h, and then eluted with 75% ethanol until no taxifolin fraction was detected by TLC, and the taxifolin fraction was collected. Heat to 60°C, add activated carbon and stir at constant temperature for decolorization for 1 hour, filter, concentrate the filtrate into an extract, mix the extract with dextran gel and dry it, then put it on a Sephadex LH-20 column by dry method, chloroform-ethanol (5:1 ) elution, flow rate 1.5BV / h, thin-layer detection, collect taxifolin fraction, concentrate under reduced pressure and recover the solvent to obtain a crude product, benzen...
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