Skip to Content
Merck
All Photos(2)

Key Documents

163171

Sigma-Aldrich

4-Aminoresorcinol hydrochloride

96%

Synonym(s):

2,4-Dihydroxyaniline hydrochloride

Sign Into View Organizational & Contract Pricing


About This Item

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

Quality Level

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service