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V900790

Sigma-Aldrich

3,5-Dihydroxybenzoic acid

Vetec, reagent grade, 97%

Synonym(s):

α-Resorcylic acid

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About This Item

Linear Formula:
(HO)2C6H3CO2H
CAS Number:
Molecular Weight:
154.12
Beilstein/REAXYS Number:
2207864
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Pricing and availability is not currently available.

grade

reagent grade

product line

Vetec

assay

97%

mp

236-238 °C (dec.) (lit.)

SMILES string

OC(=O)c1cc(O)cc(O)c1

InChI

1S/C7H6O4/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,8-9H,(H,10,11)

InChI key

UYEMGAFJOZZIFP-UHFFFAOYSA-N

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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

392.0 °F - closed cup

flash_point_c

200 °C - closed cup


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Y Matsumoto et al.
Journal of pharmaceutical sciences, 81(5), 428-431 (1992-05-01)
To reveal the role of the band 3 anion transport protein of the erythrocyte membrane in drug transport through the membrane, the possible effects of inhibitors of anion transport on the permeability of some anionic drugs were examined. The amounts
Seetharaman Vaidyanathan et al.
Rapid communications in mass spectrometry : RCM, 20(8), 1192-1198 (2006-03-17)
Matrix-assisted laser desorption/ionisation (MALDI) mass spectrometry was investigated for the simultaneous detection of several metabolites, as applicable to global metabolite analysis (metabolomics). The commonly employed organic matrices alpha-cyano-4-hydroxycinnamic acid and 3,5-dihydroxybenzoic acid, in both the crystalline and ionic liquid forms
Silke C Wenzel et al.
Chembiochem : a European journal of chemical biology, 9(16), 2711-2721 (2008-10-31)
Kendomycin is a bioactive polyketide that is produced by various Streptomyces strains. It displays strong antibiotic activities against a wide range of bacteria and exhibits remarkable cytotoxic effects on the growth of several human cancer cell lines. In this study
Anja Koskela et al.
Journal of agricultural and food chemistry, 56(17), 7678-7681 (2008-08-12)
This study presents the optimization and validation of a rapid protocol for quantifying alkyresorcinol (AR) metabolites 3,5-dihydroxybenzoic acid (DHBA) and 3-(3,5-dihydroxyphenyl)-1-propanoic acid (DHPPA) in plasma, using high-performance liquid chromatography (HPLC) coupled with a coulometric electrode array detector. Syringic acid (SyrA)
Abigail E Wolfe et al.
Biochemistry, 46(19), 5741-5753 (2007-04-21)
Dihydroorotate dehydrogenases (DHODs) catalyze the oxidation of dihydroorotate to orotate in the only redox reaction in pyrimidine biosynthesis. The pyrimidine binding sites are very similar in all structurally characterized DHODs, suggesting that the prospects for identifying a class-specific inhibitor directed

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