D110000
3,5-Dihydroxybenzoic acid
97%
Synonym(s):
α-Resorcylic acid
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About This Item
Linear Formula:
(HO)2C6H3CO2H
CAS Number:
Molecular Weight:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-730-7
Beilstein/REAXYS Number:
2207864
MDL number:
Product Name
3,5-Dihydroxybenzoic acid, 97%
InChI key
UYEMGAFJOZZIFP-UHFFFAOYSA-N
InChI
1S/C7H6O4/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3,8-9H,(H,10,11)
SMILES string
OC(=O)c1cc(O)cc(O)c1
assay
97%
form
powder
mp
236-238 °C (dec.) (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
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)
Determination of alkylresorcinol metabolites in human urine by gas chromatography-mass spectrometry.
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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