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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:
2207864
EC Number:
202-730-7
MDL number:
MFCD00002512
UNSPSC Code:
12352100
PubChem Substance ID:
24893352
NACRES:
NA.22

Quality Level

100

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

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

392.0 °F - closed cup

Flash Point(C)

200 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Sunil Varughese et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(6), 1597-1609 (2005-10-27)
A molecular recognition study of 3,5-dihydroxybenzoic acid (1) and its bromo derivative 4-bromo-3,5-dihydroxybenzoic acid (2) with the N-donor compounds 1,2-bis(4-pyridyl)ethene (bpyee), 1,2-bis(4-pyridyl)ethane (bpyea), and 4,4'-bipyridine (bpy) is reported. Thus, the syntheses and structural analysis of molecular adducts 1 a-1 c
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