Method for extracting dihydromyricetin, ampelopsis grossedentata amylase and ampelopsis grossedentata polyphenol from ampelopsis grossedentata
A technology of dihydromyricetin and rattan tea, applied in the direction of organic chemistry and the like, can solve the problems affecting the economic benefits of rattan tea resources, low resource utilization rate, etc., and achieve comprehensive development and utilization and economic benefits, low cost, and extraction yield. high effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0010] Dry and pulverize fresh rattan tea stems and leaves to obtain 500g of raw material powder, add 6L of distilled water, heat to 95°C and extract for 30min, filter with 100-mesh double-layer filter cloth while hot, then centrifuge while hot (4000rpm, 15min), collect For the supernatant I, add 4L of distilled water to the filter residue, heat to 95°C and repeat the extraction once, combine the supernatant I; concentrate the supernatant I under reduced pressure to 1 / 3 volume, fully cool, and stand at 4°C After 12 hours of crystallization, centrifuge (4000rpm, 15min) to collect the precipitate A and the supernatant II respectively; the precipitate A is recrystallized by adding water twice, and then the crystals are vacuum-dried at 40°C to obtain dihydromyricetin, the product Yield can reach 11% (dihydromyricetin is used as standard sample, aluminum nitrate-sodium nitrite colorimetric method is measured, and product dihydromyricetin content is more than or equal to 85%); Supern...
Embodiment 2
[0012] Dry and pulverize fresh rattan tea stems and leaves to obtain 1000g of raw material powder, add 12L of distilled water, heat to 95°C for extraction for 30min, filter with 100-mesh double-layer filter cloth while hot, then centrifuge while hot (4000rpm, 15min), collect For the supernatant I, add 8L of distilled water to the filter residue, heat to 95°C and repeat the extraction once, combine the supernatant I; concentrate the supernatant I under reduced pressure to 1 / 3 volume, fully cool, and stand at 4°C After 12 hours of crystallization, centrifuge (4000rpm, 15min) to collect the precipitate A and the supernatant II respectively; the precipitate A is recrystallized by adding water twice, and then the crystals are vacuum-dried at 40°C to obtain the dihydromyricetin product. The product yield can reach 11% (dihydromyricetin is used as a standard sample, and the aluminum nitrate-sodium nitrite colorimetric method determines that the product dihydromyricetin content is ≥ 85...
Embodiment 3
[0014] Dried and crushed fresh vine tea stems and leaves as raw materials for extraction; add 1500g of raw material powder, add 18L of distilled water, heat to 95°C and extract for 30min, filter with 100-mesh double-layer filter cloth while hot, and then centrifuge while hot (4000rpm, 15min) , collect the supernatant I, add 12L of distilled water to the filter residue, heat to 95°C and repeat the extraction once, combine the supernatant I; concentrate the supernatant I under reduced pressure to 1 / 3 volume, fully cool, at 4°C Stand still for 12 hours, after crystallization, centrifuge (4000rpm, 15min), collect precipitate A and supernatant II respectively; add water to precipitate A twice and recrystallize, then dry the crystals in vacuum at 40°C to obtain dihydromyricetin , the product yield can reach 11% (dihydromyricetin is used as a standard sample, measured by aluminum nitrate-sodium nitrite colorimetric method, product dihydromyricetin content ≥ 85%); the supernatant II is...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com