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
• Article Data: 2

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

General Description

1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol, also known as paeoniflorin, is a natural chemical compound found in the roots of Paeonia lactiflora, a flowering plant commonly known as peony. It is classified as a phenolic compound and is known for its antioxidant and anti-inflammatory properties. Paeoniflorin has been used in traditional Chinese medicine for centuries and is believed to have various health benefits, including reducing pain and inflammation, protecting the liver, and promoting cardiovascular health. It has also been the subject of scientific research for its potential therapeutic applications in treating conditions such as arthritis, diabetes, and neurodegenerative diseases. Overall, paeoniflorin is a biologically active compound that shows promise for its potential medicinal properties.

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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.