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D110000

Sigma-Aldrich

3,5-Dihydroxybenzoic acid

97%

Synonym(s):

α-Resorcylic acid

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About This Item

Linear Formula:
(HO)2C6H3CO2H
CAS Number:
99-10-5
Molecular Weight:
154.12
Beilstein/REAXYS Number:
2207864
EC Number:
202-730-7
MDL number:
MFCD00002512
UNSPSC Code:
12352100
PubChem Substance ID:
24893352
NACRES:
NA.22

assay

97%

form

powder

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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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

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

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)
Matti Marklund et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 878(11-12), 888-894 (2010-03-13)
Alkylresorcinols (ARs) are phenolic lipids present at high concentrations in the outer parts of rye and wheat kernels and have been proposed as biomarkers for intake of whole grain and bran products of these cereals. AR are absorbed in the
Qian Cao et al.
Biosensors & bioelectronics, 25(12), 2680-2685 (2010-06-01)
A colorimetric, label-free, and nonaggregation-based gold nanoparticles probe has been developed for the detection of melamine. Gold nanoparticles were generated using 3,5-dihydroxybenzoic acid as a reducer without adding gold nanoparticle seeds at room temperature. Upon the addition of melamine, the
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
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
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