A86805
Aniline-2-sulfonic acid
95%
Synonym(s):
Orthanilic acid, 2-Aminobenzenesulfonic acid, o-Sulfanilic acid
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100 G
562,00 kr
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100 G
562,00 kr
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
form:
solid
Assay:
95%
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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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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
Po-Hsin Wang et al.
Nanomaterials (Basel, Switzerland), 8(4) (2018-04-05)
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
F Junker et al.
The Biochemical journal, 300 ( Pt 2), 429-436 (1994-06-01)
2-Aminobenzenesulphonic acid (2AS) is degraded by Alcaligenes sp. strain O-1 via a previously detected but unidentified intermediate. A mutant of strain O-1 was found to excrete this intermediate, which was isolated and identified by m.s., 1H- and 13C-n.m.r. as 3-sulphocatechol
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)
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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