27391-16-8

Basic information

• Product Name: threo-Guaiacylglycerol
• Synonyms: threo-Guaiacylglycerol
• CAS NO: 27391-16-8
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.22
• Mol File: 27391-16-8.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: threo-Guaiacylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: threo-Guaiacylglycerol(27391-16-8)
• EPA Substance Registry System: threo-Guaiacylglycerol(27391-16-8)

Safety Data

• Hazardous Substances Data: 27391-16-8(Hazardous Substances Data)

Usage

Description

threo-Guaiacylglycerol is a naturally occurring organic compound that can be found in various plants, including Viticis Fructus (Vitex rotundifolia). It is known for its analgesic properties, which make it a potential candidate for pharmaceutical applications.

Uses

Used in Pharmaceutical Industry:
threo-Guaiacylglycerol is used as an analgesic agent for its pain-relieving effects. It is particularly beneficial in managing various types of pain due to its natural origin and potential for minimal side effects.
Used in Traditional Medicine:
In traditional medicine, threo-Guaiacylglycerol is utilized for its analgesic properties, often as a component of herbal remedies and treatments aimed at alleviating pain and discomfort.
Used in Nutraceutical Industry:
threo-Guaiacylglycerol can also be used as an ingredient in the development of nutraceutical products, targeting consumers seeking natural alternatives for pain management and overall wellness.

Upstream product

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• 2309-07-1 Methyl ferulate 
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• 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.