A86805
Aniline-2-sulfonic acid
95%
Synonym(s):
Orthanilic acid, 2-Aminobenzenesulfonic acid, o-Sulfanilic acid
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All Photos(2)
About This Item
Linear Formula:
H2NC6H4SO3H
CAS Number:
Molecular Weight:
173.19
Beilstein:
1309204
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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In this work, we electrochemically deposited self-doped polyanilines (SPANI) on the surface of carbon-nanoparticle (CNP) film, enhancing the superficial faradic reactions in supercapacitors and thus improving their performance. SPANI was electrodeposited on the CNP-film employing electropolymerization of aniline (AN) and
T Thurnheer et al.
Biodegradation, 1(1), 55-64 (1990-01-01)
Alcaligenes sp. strain O-1 grew with benzene sulfonate (BS) as sole carbon source for growth with either NH4+ or NH4+ plus orthanilate (2-aminobenzene sulfonate, OS) as the source(s) of nitrogen. The intracellular desulfonative enzyme did not degrade 3- or 4-aminobenzene
J Mampel et al.
Microbiology (Reading, England), 145 ( Pt 11), 3255-3264 (1999-12-10)
Growth of Alcaligenes sp. strain O-1 with 2-aminobenzenesulfonate (ABS; orthanilate) as sole source of carbon and energy requires expression of the soluble, multicomponent 2-aminobenzenesulfonate 2,3-dioxygenase system (deaminating) (ABSDOS) which is plasmid-encoded. ABSDOS was separated by anion-exchange chromatography to yield a
Inotropic activity of orthanilic and L-cysteic acid on isolated guinea-pig ventricular strips.
F Franconi et al.
Advances in experimental medicine and biology, 217, 159-165 (1987-01-01)
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
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