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2,4-Dihydroxybenzoic acid

Name: 2,4-Dihydroxybenzoic acid
Brand: SIAL

purum, ≥98.0% (T)

Synonym(s):

β-Resorcylic acid

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About This Item

Linear Formula:

(HO)₂C₆H₃CO₂H

CAS Number:

89-86-1

Molecular Weight:

154.12

EC Number:

201-946-9

UNSPSC Code:

12352100

PubChem Substance ID:

24863379

Beilstein/REAXYS Number:

1946213

MDL number:

MFCD00002451

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Properties

grade

purum

assay

≥98.0% (T)

mp

208-211 °C (dec.) (lit.)

SMILES string

OC(=O)c1ccc(O)cc1O

InChI

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

InChI key

UIAFKZKHHVMJGS-UHFFFAOYSA-N

Description

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pictograms

GHS07

signalword

Warning

hcodes

H317

pcodes

P261 - P272 - P280 - P302 + P352 - P333 + P313 - P362 + P364

Hazard Classifications

Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Crystal structures of wild-type p-hydroxybenzoate hydroxylase complexed with 4-aminobenzoate,2,4-dihydroxybenzoate, and 2-hydroxy-4-aminobenzoate and of the Tyr222Ala mutant complexed with 2-hydroxy-4-aminobenzoate. Evidence for a proton channel and a new binding mode of the flavin ring.

H A Schreuder et al.

Biochemistry, 33(33), 10161-10170 (1994-08-23)

The crystal structures of wild-type p-hydroxybenzoate hydroxylase from Pseudomonas fluorescens, complexed with the substrate analogues 4-aminobenzoate, 2,4-dihydroxybenzoate, and 2-hydroxy-4-aminobenzoate have been determined at 2.3-, 2.5-, and 2.8-A resolution, respectively. In addition, the crystal structure of a Tyr222Ala mutant, complexed with

Degradation of 2,4-dihydroxibenzoic acid by vacuum UV process in aqueous solution: kinetic, identification of intermediates and reaction pathway.

Kamal Azrague et al.

Journal of hazardous materials, 237-238, 71-78 (2012-09-15)

2,4-Dihydroxybenzoic acid (2,4-DHBA) is found frequently as a pollutant in natural waters and represents a threat to water quality because it is a precursor to the formation of quinones which are highly toxic. The degradation of 2,4-DHBA using the vacuum

Direct screening of G-quadruplex ligands from Kalopanax septemlobus (Thunb.) Koidz extract by high performance liquid chromatography.

Ge Bai et al.

Journal of chromatography. A, 1218(37), 6433-6438 (2011-08-13)

G-quadruplex DNA structure is considered to be a very attractive target for antitumor drug design due to its unique role in maintaining telomerase activities. Therefore, discovering ligands with high stability of G-quadruplex structure is of great interest. In this paper

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Global Trade Item Number

SKU	GTIN
279390-1G	04061837655876