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163171

Sigma-Aldrich

4-Aminoresorcinol hydrochloride

96%

Synonym(s):

2,4-Dihydroxyaniline hydrochloride

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About This Item

Linear Formula:
H2NC6H3-1,3-(OH)2 · HCl
CAS Number:
34781-86-7
Molecular Weight:
161.59
MDL number:
MFCD00012963
UNSPSC Code:
12352100
PubChem Substance ID:
24850026
NACRES:
NA.22

Assay

96%

form

powder

mp

220 °C (dec.) (lit.)

SMILES string

Cl.Nc1ccc(O)cc1O

InChI

1S/C6H7NO2.ClH/c7-5-2-1-4(8)3-6(5)9;/h1-3,8-9H,7H2;1H

InChI key

LLJMPRKYLLJAEB-UHFFFAOYSA-N

Related Categories

General description

Electrochemical oxidation of 4-aminoresorcinol hydrochloride (2,4-dihydroxyaniline hydrochloride) has been studied using a boron-doped diamond electrode as anode. It is an inhibitor of meta-cleavage dioxygenase enzyme isolated from cell extracts of Bordetella sp. strain 10d.

Application

4-Aminoresorcinol hydrochloride was used in an enzyme assay during isolation of soil bacterium Bordetella sp. strain 10d.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

163171-1G:
163171-VAR:
163171-5G:
163171-BULK:

Certificates of Analysis (COA)

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Shinji Takenaka et al.
European journal of biochemistry, 269(23), 5871-5877 (2002-11-26)
A bacterial strain that grew on 4-amino-3-hydroxybenzoic acid was isolated from farm soil. The isolate, strain 10d, was identified as a species of Bordetella. Cell extracts of Bordetella sp. strain 10d grown on 4-amino-3-hydroxybenzoic acid contained an enzyme that cleaved
M J Pacheco et al.
Journal of hazardous materials, 186(2-3), 1033-1041 (2010-12-21)
The electrochemical oxidation of four aromatic amines, with different substituent groups, 3-amino-4-hydroxy-5-nitrobenzenesulfonic acid (A1), 5-amino-2-methoxybenzenesulfonic acid (A2), 2,4-dihydroxyaniline hydrochloride (A3) and benzene-1,4-diamine (A4), was performed using as anode a boron-doped diamond electrode, commercially available at Adamant Technologies. Tests were run

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