38916-91-5

Basic information

• Product Name: (+)-Erythro-guaiacylglycerol
• Synonyms: (+)-Erythro-guaiacylglycerol;(1R,2S)-rel-1-(4-Hydroxy-3-methoxyphenyl)-1,2,3-propanetriol
• CAS NO: 38916-91-5
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.21500
• Mol File: 38916-91-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (+)-Erythro-guaiacylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-Erythro-guaiacylglycerol(38916-91-5)
• EPA Substance Registry System: (+)-Erythro-guaiacylglycerol(38916-91-5)

Safety Data

• Hazardous Substances Data: 38916-91-5(Hazardous Substances Data)

Usage

Description

(+)-Erythro-guaiacylglycerol, also known as erythro-guaiacylglycerol, is a naturally occurring organic compound found in various plant sources, including Viticis Fructus (Vitex rotundifolia). It is characterized by its unique chemical structure and possesses analgesic properties, making it a potential candidate for pharmaceutical and therapeutic applications.

Uses

Used in Pharmaceutical Industry:
(+)-Erythro-guaiacylglycerol is used as an analgesic agent for its pain-relieving effects. It is particularly beneficial in managing various types of pain, such as chronic or acute pain, due to its natural origin and potential for minimal side effects.
Used in Traditional Medicine:
In traditional medicine, (+)-Erythro-guaiacylglycerol is utilized for its analgesic properties, often in the form of herbal remedies or supplements. It is commonly found in formulations targeting pain relief and inflammation reduction, making it a valuable component in the treatment of various ailments.
Used in Cosmetics Industry:
(+)-Erythro-guaiacylglycerol may also find application in the cosmetics industry, where it can be used as an ingredient in skincare and personal care products. Its analgesic and anti-inflammatory properties could be beneficial in products aimed at soothing and reducing skin irritation, redness, or inflammation.

Upstream product

• 14070-76-9 1-(4-hydroxy-3-methoxy)-phenyl-2-[4-(1,2,3- trihydroxypropyl)-2-methoxy]-phenoxy-1, 3-propandiol 
• 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 

Downstream Products

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

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.