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3,4-Dihydroxybenzoic acid

ALDRICH/37580 - ≥97.0% (T)

Synonym: Protocatechuic acid

CAS Number: 99-50-3
Empirical Formula (Hill Notation): C7H6O4
Molecular Weight: 154.12
EC Number: 202-760-0
MDL Number: MFCD00002509
Linear Formula: (HO)2C6H3CO2H
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-37580-25G-F 25 g
$121.00
1/EA
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45-37580-100G-F 100 g
$228.00
1/EA
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assay ≥97.0% (T)
InChI 1S/C7H6O4/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,8-9H,(H,10,11)
InChI key YQUVCSBJEUQKSH-UHFFFAOYSA-N
mp 197-200 °C (dec.) (lit.)
SMILES string OC(=O)c1ccc(O)c(O)c1
Application: 3,4-Dihydroxybenzoic acid is suitable for use in a study to investigate the effect of 4-coumaric and 3,4-dihydroxybenzoic acid on the basal oxidative DNA damage of rat colonic mucosa in vivo. It may be used in the derivatization of chitosan resin.
Biochem/physiol Actions: Chemopreventive in several animal models of carcinogenesis. Blocks cell proliferation in the post-initiation phase.
General description: 3,4-Dihydroxybenzoic acid is reported as dietery polyphenol. Antiviral activity of 3,4-dihydroxybenzoic acid (protocatechuic acid, PCA) against a virulent H9N2 strain in a mouse model is reported. Cytotoxic effects of PCA on 3 non-small cell lung cancer (NSCLC) cell lines, A549, H3255, and Calu-6 cell lines is reported. PCA is reported to prevent the carcinogenesis or antitumor growth in vivo. Signaling pathway involved in PCA-induced apoptosis in human gastric adenocarcinoma (AGS) cells is reported. The oxidation of 3,4-dihydroxybenzoic acid by H2O2 in aqueous/goethite slurry at varying operating conditions (catalyst load, temperature, pH, substrate and hydrogen peroxide starting concentration) is investigated.
Packaging: 25, 100 g in glass bottle
Purity ≥97.0% (T)
mp 197-200 °C (dec.) (lit.)
UNSPSC 12352100

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