Cat# Bc-0625 Cas# 331-39-5 

Synonym: 3,4-Dihydroxybenzeneacrylic acid, 3,4-Dihydroxycinnamic acid, 3-(3,4-Dihydroxyphenyl)2-propenoic acid

Properties

assay ≥98.0% (HPLC)
form powder
mp 211-213 °C (dec.) (lit.)
solubility ethanol: 50 mg/mL
SMILES string OC(=O)\C=C\c1ccc(O)c(O)c1
InChI 1S/C9H8O4/c10-7-3-1-6(5-8(7)11)2-4-9(12)13/h1-5,10-11H,(H,12,13)/b4-2+
InChI key QAIPRVGONGVQAS-DUXPYHPUSA-N
Gene Information human … ELA2(1991)
rat … Alox5(25290)

Safety Information

Symbol
GHS08  GHS08
Signal word
Warning
Hazard statements
RIDADR
NONH for all modes of transport
WGK Germany
WGK 3
RTECS
GD8950000
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable

Description

Description

General description

Caffeic acid exists in its free and ester form. It is considered as the predominant polyphenol, contributing to the hydroxycinnamic acid content in various fruits. Coffee is one of the major source of caffeic acid.[1]

Application

Caffeic acid has been used as a standard of phenolic acid in the study to determine the total phenolic acid content in vegetables after subjecting to alkaline and acid hydrolysis. It has also been used to determine its antioxidant activity by various assay methods.

Packaging

2, 5, 25 g in poly bottle

Biochem/physiol Actions

A natural dietary phenolic compound found in plants that is an anti-oxidant. Inhibits the synthesis of leukotrienes that are involved in immunoregulation, inflammation and allergy. Inhibits Cu2+-induced LDL oxidation.

Caffeic acid and other polyphenols are metabolized by going through enzyme catalysed methyl transfer, sulfation and glucuronic acid addition. It non-competitively prevents the action of 5-lipoxygenase. Caffeic acid ready undergoes hydrolysis in alkaline conditions.

Features and Benefits

This compound is a featured product for Gene Regulation research.

This compound is also offered as part of Sigma′s Library of Pharmacologically Active Compounds, a biologically annotated collection of high-quality, ready-to-screen compounds.

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