1208-42-0

Basic information

• Product Name: 1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol
• CAS NO: 1208-42-0
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.2152
• Mol File: 1208-42-0.mol

Chemical Properties

• Boiling Point: 483.7°C at 760 mmHg
• Flash Point: 246.3°C
• Density: 1.383g/cm³
• Vapor Pressure: 3.62E-10mmHg at 25°C
• Refractive Index: 1.608
• CAS DataBase Reference: 1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol(1208-42-0)
• EPA Substance Registry System: 1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol(1208-42-0)

Safety Data

• Hazardous Substances Data: 1208-42-0(Hazardous Substances Data)

Usage

Uses

Used in Traditional Chinese Medicine:
Paeoniflorin is utilized as a medicinal ingredient for its analgesic and anti-inflammatory effects, traditionally employed to treat various ailments including pain and inflammation.
Used in Pharmaceutical Applications:
1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol is used as a therapeutic agent for its potential in managing conditions such as arthritis, diabetes, and neurodegenerative diseases, due to its antioxidant and anti-inflammatory properties.
Used in Health Supplements:
Paeoniflorin is used as an ingredient in health supplements for its liver-protective and cardiovascular health-promoting benefits, contributing to overall well-being and health maintenance.
Used in Scientific Research:
1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol is used as a subject of research in the scientific community to explore its potential applications in medicine and to understand its mechanisms of action in treating various diseases.

Upstream product

• 7213-02-7 D-threo-guaiacylglycerol 7-O-β-D-glucopyranoside 
• 2309-07-1 Methyl ferulate 
• 93722-55-5 (2RS,3SR)-2,3-diacetoxy-3-(4-acetoxy-3-methoxy-phenyl)-propionic acid methyl ester 
• 93728-44-0 (1RS,2RS)-1-(4-benzyloxy-3-methoxy-phenyl)-propane-1,2,3-triol 
• 60525-32-8 ethyl 3-[4-(benzyloxy)-3-methoxyphenyl]-3-oxopropanoate 
• 7572-99-8 α-(Acetoxy-benzylvanilloylessigsaeure-aethylester 
• 14065-26-0 (1RS,2SR)-1,2,3-triacetoxy-1-(4-acetoxy-3-methoxy-phenyl)-propane 
• 93722-55-5 (2RS,3RS)-2,3-diacetoxy-3-(4-acetoxy-3-methoxy-phenyl)-propionic acid methyl ester 
• 1370004-83-3 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)guaiacylglycerol 
• 14070-76-9 1-(4-hydroxy-3-methoxy)-phenyl-2-[4-(1,2,3- trihydroxypropyl)-2-methoxy]-phenoxy-1, 3-propandiol 

Downstream Products

• 4899-74-5 2-propanone,1-hydroxy-3-(4-hydroxy-3-methoxyphenyl)- 
• 4756-11-0 (1RS,2SR)-1-(3,4-dimethoxy-phenyl)-propane-1,2,3-triol 

Relevant articles and documents

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.

Studies on the constituents of Osmanthus species. X. Structures of phenolic glucosides from the leaves of Osmanthus asiaticus NAKAI

Three new phenolic glucosides were isolated from the leaves of Osmanthus asiaticus NAKAI (Oleaceae). The structures of 1, 2 and 3 were determined to be 2-hydroxy-5-(2-hydroxyethyl)phenyl β-D-glucopyranoside, 4-(2,3-dihydroxypropyl)-2,6-dimethoxyphenyl β-D-glucopyranoside and D-threo-guaiacylglycerol 7-O-β-D-glucopyranoside, respectively, on the basis of chemical and spectral data.