High yield environmental protection type industrial separating method for ginseng saponin Rb1
A technology of ginsenoside and separation method, applied in the direction of organic chemistry, steroids, etc., can solve the problems of increased production cost, high production cost, and increased production equipment, and achieve the goal of reduced production cost, shortened production cycle, and long production cycle Effect
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Embodiment 1
[0022] 1. Column packing: take 12 kg of 200-300 mesh silica gel, add 24 liters of water-saturated n-butanol, stir while adding, remove air bubbles, soak for 10 hours, put it into a 100 cm high chromatography column, and add 36 liters of water-saturated n-butanol Alcohol elution is stable and ready for use;
[0023] 2. Separation: Take 240 grams of total ginsenosides as a sample, dissolve in a small amount of water-saturated n-butanol, add to the top of a stable chromatography column, elute with water-saturated n-butanol, and start when the color band reaches the bottom of the chromatography column Continuous sampling with a triangular flask, 50 milliliters each time, is detected by thin-layer chromatography while sampling, until no obvious spots are detected, the sampling is terminated;
[0024] 3. Recovered product: combined ginsenoside Rb 1 Part of the eluent, decompression recovery n-butanol, to obtain ginsenoside Rb 1 aqueous solution, vacuum freeze-drying, to obtain gin...
Embodiment 2
[0026] 1. Column packing: Take 12 kg of 200-300 mesh silica gel, add 24 liters of water-saturated n-butanol, stir while adding, remove air bubbles, soak for 12 hours, put it into a 100 cm high chromatography column, and add 36 liters of water-saturated n-butanol Alcohol elution is stable and ready for use;
[0027] 2. Separation: Take 300 grams of total ginsenosides as a sample, dissolve in a small amount of water-saturated n-butanol, add to the top of a stable chromatography column, and elute with water-saturated n-butanol until the color band reaches the bottom of the chromatography column. Continuous sampling with a triangular flask, 50 milliliters each time, is detected by thin-layer chromatography while sampling, until no obvious spots are detected, the sampling is terminated;
[0028] 3. Recovered product: combined ginsenoside Rb 1 Part of the eluent, decompression recovery n-butanol, to obtain ginsenoside Rb 1 aqueous solution, vacuum freeze-drying, to obtain ginsenos...
Embodiment 3
[0030] 1. Column packing: Take 12 kg of 200-300 mesh silica gel, add 24 liters of water-saturated n-butanol, stir while adding, remove air bubbles, soak for 15 hours, put it into a 100 cm high chromatography column, and add 36 liters of water-saturated n-butanol Alcohol elution is stable and ready for use;
[0031] 2. Separation: Take 400 grams of total ginsenosides as a sample, dissolve in a small amount of water-saturated n-butanol, add to the top of a stable chromatographic column, and elute with water-saturated n-butanol until the color band reaches the bottom of the chromatographic column. Continuous sampling with a triangular flask, 50 milliliters each time, is detected by thin-layer chromatography while sampling, until no obvious spots are detected, the sampling is terminated;
[0032] 3. Recovered product: combined ginsenoside Rb 1 Part of the eluent, decompression recovery n-butanol, to obtain ginsenoside Rb 1 aqueous solution, vacuum freeze-drying, to obtain ginsen...
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