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Key Documents

28-5740

Sigma-Aldrich

Sulfanilic acid

JIS special grade, 99.0-100.5%

Synonym(s):

4-Aminobenzenesulfonic acid, Aniline-4-sulfonic acid

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About This Item

Linear Formula:
4-(H2N)C6H4SO3H
CAS Number:
Molecular Weight:
173.19
Beilstein/REAXYS Number:
908765
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
Pricing and availability is not currently available.

grade

JIS special grade

assay

99.0-100.5%

form

powder

availability

available only in Japan

mp

>300 °C (lit.)

solubility

water: soluble 12.51 g/L at 20 °C

density

1.4862 g/cm3 at 20 °C

SMILES string

Nc1ccc(cc1)S(O)(=O)=O

InChI

1S/C6H7NO3S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H,8,9,10)

InChI key

HVBSAKJJOYLTQU-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Han Ming Gan et al.
Chemosphere, 82(4), 507-513 (2010-11-26)
A co-culture consisting of Hydrogenophaga sp. PBC and Ralstonia sp. PBA, isolated from textile wastewater treatment plant could tolerate up to 100 mM 4-aminobenzenesulfonate (4-ABS) and utilize it as sole carbon, nitrogen and sulfur source under aerobic condition. The biodegradation
Han Ming Gan et al.
Microbiology (Reading, England), 158(Pt 8), 1933-1941 (2012-05-23)
The gene coding for the oxygenase component, sadA, of 4-aminobenzenesulfonate (4-ABS) 3,4-dioxygenase in Hydrogenophaga sp. PBC was previously identified via transposon mutagenesis. Expression of wild-type sadA in trans restored the ability of the sadA mutant to grow on 4-ABS. The
Luís Belo et al.
PloS one, 9(6), e98467-e98467 (2014-06-06)
Bilirubin has potential antioxidant and anti-inflammatory properties. The UGT1A1*28 polymorphism (TA repeats in the promoter region) is a major determinant of bilirubin levels and recent evidence suggests that raised adiposity may also be a contributing factor. We aimed to study
Yunfeng Liao et al.
Organic letters, 14(23), 6004-6007 (2012-11-16)
2-Aryl benzothiazole formation from aryl ketones and 2-aminobenzenethiols under metal- and I(2)-free conditions was described. Various 2-aryl benzothiazoles were selectively obtained in good yields using molecular oxygen as oxidant. DMSO played an important role in this transformation. Functional groups such
Kwan Kim et al.
The journal of physical chemistry. B, 109(40), 18929-18934 (2006-07-21)
Raman scattering measurements were conducted for 4-aminobenzenethiol (4-ABT) assembled on powdered copper substrates. Initially, very weak Raman peaks were detected, but upon attaching Ag nanoparticles probably via NH2 groups onto 4-ABT/Cu, distinct Raman spectra were observed. Considering the fact that

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