emodin-6-O-β-D-glucopyranoside
emodin-6-O-β-D-glucopyranoside
CAS: 34298-85-6
Molecular Formula: C21H20O10
emodin-6-O-β-D-glucopyranoside - Names and Identifiers
emodin-6-O-β-D-glucopyranoside - Physico-chemical Properties
| Molecular Formula | C21H20O10 |
| Molar Mass | 432 |
| Density | 1.667g/cm3 |
| Melting Point | 189 °C (甲醇) |
| Boling Point | 801.9°C at 760 mmHg |
| Flash Point | 285.3°C |
| Vapor Presure | 3.83E-27mmHg at 25°C |
| pKa | 5.99±0.20(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.725 |
emodin-6-O-β-D-glucopyranoside - Upstream Downstream Industry
| Raw Materials | Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester 2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide 2-CHLORO-4-NITROPHENYL-BETA-D-GLUCO- PYRANOSIDE* Emodin |
emodin-6-O-β-D-glucopyranoside - Introduction
It is a naturally occurring organic compound with the chemical formula C21H20O10. It is a glycoside compound formed by the combination of emodin and glucose molecules.
It is a yellow crystalline powder, soluble in hot water and ethanol, and almost insoluble in ether and chloroform. It has a certain bitterness and cherry floral smell.
This compound has important uses in pharmaceutical and biomedical research. It has a variety of pharmacological activities, including anti-inflammatory, antioxidant, anti-tumor and antibacterial effects. It is often used in the field of traditional Chinese medicine to treat inflammatory diseases, tumors and infections.
The method of preparing the salt is usually to convert the substrate of emodin and glucose through an enzyme-catalyzed reaction. First, emodin reacts with glucose through the enzyme to form an enzyme-catalyzed glycosidic bond, combining the two into glycosidic compounds.
There is no clear toxicity data report regarding the safety information of the phenol. However, as a natural compound, it should be used appropriately and follow appropriate dosage and usage recommendations. If necessary, consult a professional doctor or pharmacist before use. In addition, for pregnant, lactating women and children, consult a doctor or professional before use.
It is a yellow crystalline powder, soluble in hot water and ethanol, and almost insoluble in ether and chloroform. It has a certain bitterness and cherry floral smell.
This compound has important uses in pharmaceutical and biomedical research. It has a variety of pharmacological activities, including anti-inflammatory, antioxidant, anti-tumor and antibacterial effects. It is often used in the field of traditional Chinese medicine to treat inflammatory diseases, tumors and infections.
The method of preparing the salt is usually to convert the substrate of emodin and glucose through an enzyme-catalyzed reaction. First, emodin reacts with glucose through the enzyme to form an enzyme-catalyzed glycosidic bond, combining the two into glycosidic compounds.
There is no clear toxicity data report regarding the safety information of the phenol. However, as a natural compound, it should be used appropriately and follow appropriate dosage and usage recommendations. If necessary, consult a professional doctor or pharmacist before use. In addition, for pregnant, lactating women and children, consult a doctor or professional before use.
Last Update：2024-04-10 22:29:15
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CAS: 34298-85-6
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Product Name: Emodin-6-O-glucopyranoside Visit Supplier Webpage Request for quotation
CAS: 34298-85-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 34298-85-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
View History
Raw Materials for emodin-6-O-β-D-glucopyranoside
Uridine 5'-(trihydrogen diphosphate), mono-alpha-d-glucopyranosyl ester
2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide
2-CHLORO-4-NITROPHENYL-BETA-D-GLUCO- PYRANOSIDE*
Emodin
2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide
2-CHLORO-4-NITROPHENYL-BETA-D-GLUCO- PYRANOSIDE*
Emodin