1(2H)-Anthracenone, 8-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-3,9-dihydroxy-6-methoxy-3-methyl-, (3S)- - Names and Identifiers
1(2H)-Anthracenone, 8-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-3,9-dihydroxy-6-methoxy-3-methyl-, (3S)- - Physico-chemical Properties
Molecular Formula | C28H36O15
|
Molar Mass | 612.58 |
Density | 1.66±0.1 g/cm3(Predicted) |
Boling Point | 950.7±65.0 °C(Predicted) |
Appearance | Powder |
pKa | 6.93±0.40(Predicted) |
Storage Condition | 2-8℃ |
1(2H)-Anthracenone, 8-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-3,9-dihydroxy-6-methoxy-3-methyl-, (3S)- - Introduction
Torosachrysone 8-O-beta-gentiobioside, also known as Hydroxyethyl carrylate, is a compound. The following is an introduction to its properties, uses, preparation methods and safety information:
Nature:
Torosachrysone 8-O-beta-gentiobioside is a natural product that belongs to the extract of the Rubiaceae plant Torosa chinensis. It is yellow crystalline powder. The chemical formula is C32H40O17 and the molecular weight is 664.66.
Use:
Torosachrysone 8-O-beta-gentiobioside has certain application value in pharmaceutical and cosmetic industries. Studies have shown that the compound has antioxidant, anti-inflammatory and anti-tumor activities. Therefore, it is widely used in anti-aging, skin care, anti-inflammatory and anti-cancer products.
Method:
The extraction method of Torosachrysone 8-O-beta-gentiobioside usually involves extraction and purification from Torosa chinensis plants. This process may include the steps of grinding, solvent extraction, and chromatographic separation of the plant material.
Safety Information:
There is a lack of adequate research and evaluation on the safety of Torosachrysone 8-O-beta-gentiobioside. Therefore, there is no definitive conclusion as to its safety and toxicity. When using the product, it is recommended to follow the manufacturer's instructions and the instructions on the product label to ensure safe use and avoid excessive or sensitive reactions.
Last Update:2024-04-09 21:54:55