A method for separating and preparing petunienin-3-o-(6-o-p-coumaroyl) glucoside
A technology for petunidin and glucoside, which is applied in the field of separation and preparation of petunidin-3-O-glucoside, can solve the problem that there is no acylated anthocyanin, the separation and purification of acylated anthocyanin is difficult, and it is difficult to obtain target anthocyanin and other problems, to achieve the effect of good repeatability and large processing capacity
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Embodiment 1
[0048] Wash and peel the grapes to obtain 1 kg of grape skins, add 70% ethanol solution containing 0.5% (v / v) hydrochloric acid according to the ratio of solid to liquid 1g: 6mL, mix well, and extract by ultrasonic for 60min, (control the temperature below 50°C , protected from light), filtered through gauze, the filtrate was centrifuged at 4000rpm for 10min, and the supernatant was taken. The filter residue was extracted once more in the same way. The filtrates were combined and filtered one more time using a Buchner funnel. The filtrate was evaporated under reduced pressure at 45°C to remove ethanol and concentrated to obtain a crude grape skin anthocyanin extract. The high performance liquid chromatogram of grape skin anthocyanin crude extract is as follows figure 2 shown.
[0049] Put the AB-8 macroporous resin into the chromatographic column, and use ethanol, 0.5mol / L hydrochloric acid solution, 0.5mol / L sodium hydroxide solution, and water to wash in sequence, and th...
Embodiment 2
[0054] Wash and peel the grapes to obtain 4kg of grape skins, add 70% ethanol solution containing 0.5% (v / v) hydrochloric acid according to the ratio of solid to liquid 1g: 6mL, mix well, and ultrasonically extract for 90min, (control the temperature below 50°C , protected from light), filtered through gauze, the filtrate was centrifuged at 4000rpm for 10min, and the supernatant was taken. The filter residue was extracted once more in the same way. The filtrates were combined and filtered one more time using a Buchner funnel. The filtrate was evaporated under reduced pressure at 45°C to remove ethanol and concentrated to obtain a crude grape skin anthocyanin extract.
[0055] Put the AB-8 macroporous resin into the chromatographic column, and use ethanol, 0.5mol / L hydrochloric acid solution, 0.5mol / L sodium hydroxide solution, and water to wash in sequence, and then wash the crude anthocyanin extract at 0.2BV / The flow rate of h is injected into the chromatography column. A...
Embodiment 3
[0059] Wash and peel the grapes to obtain 10kg of grape skins, add 70% ethanol solution containing 0.5% (v / v) hydrochloric acid according to the ratio of solid to liquid 1g: 6mL, fully mix, ultrasonically extract for 60min, (control the temperature below 50°C , protected from light), filtered through gauze, the filtrate was centrifuged at 4000rpm for 10min, and the supernatant was taken. The filter residue was extracted once more in the same way. The filtrates were combined and filtered one more time using a Buchner funnel. The filtrate was evaporated under reduced pressure at 45°C to remove ethanol and concentrated to obtain a crude grape skin anthocyanin extract.
[0060] Put the AB-8 macroporous resin into the chromatographic column, and use ethanol, 0.5mol / L hydrochloric acid solution, 0.5mol / L sodium hydroxide solution, and water to wash in sequence, and then wash the crude anthocyanin extract at 0.2BV / The flow rate of h is injected into the chromatography column. Aft...
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