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A86805

Sigma-Aldrich

Aniline-2-sulfonic acid

95%

Synonym(s):

Orthanilic acid, 2-Aminobenzenesulfonic acid, o-Sulfanilic acid

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About This Item

Linear Formula:
H2NC6H4SO3H
CAS Number:
88-21-1
Molecular Weight:
173.19
Beilstein/REAXYS Number:
1309204
EC Number:
201-810-9
MDL number:
MFCD00007705
UNSPSC Code:
12352100
PubChem Substance ID:
24891357
NACRES:
NA.22

Quality Level

200

assay

95%

form

solid

SMILES string

Nc1ccccc1S(O)(=O)=O

InChI

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

InChI key

ZMCHBSMFKQYNKA-UHFFFAOYSA-N

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Related Categories

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

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2-Aminobenzenesulfonamide 98%

Sigma-Aldrich

245887

2-Aminobenzenesulfonamide

Sangram S Kale et al.
Chemical communications (Cambridge, England), 49(22), 2222-2224 (2013-02-09)
Orthanilic acid (2-aminobenzenesulfonic acid, (S)Ant), an aromatic β-amino acid, has been shown to be highly useful in inducing a folded conformation in peptides. When incorporated into peptide sequences (Xaa-(S)Ant-Yaa), this rigid aromatic β-amino acid strongly imparts a reverse-turn conformation to
F Junker et al.
Microbiology (Reading, England), 140 ( Pt 7), 1713-1722 (1994-07-01)
Alcaligenes sp. strain O-1 utilizes three sulphonated aromatic compounds as sole sources of carbon and energy for growth in minimal salts medium-benzenesulphonate (BS), 4-toluenesulphonate (TS) and 2-aminobenzenesulphonate (2AS). The degradative pathway(s) in 2AS-grown cells are initiated with membrane transport, NADH-dependent
Jürgen Ruff et al.
Microbiological research, 165(4), 288-299 (2009-07-07)
Alcaligenes sp. strain O-1 inducibly deaminates 2-aminobenzenesulfonate (ABS) via dioxygenation to 3-sulfocatechol, which is desulfonated during meta ring-cleavage to yield 2-hydroxymuconate. This intermediate is transformed through the oxalocrotonate-branch of the sulfocatechol meta-pathway (Scm). The complete pathway is encoded on the
Determination of nitrite ion and sulfanilic and orthanilic acids by differential pulse polarography.
S T Sulaiman
Analytical chemistry, 56(13), 2405-2407 (1984-11-01)
Effect of taurine, L-cysteic and orthanilic acids on cardiac tension.
F Franconi et al.
Progress in clinical and biological research, 351, 175-184 (1990-01-01)
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