112739
Sulfanilic acid
99%
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:
908765
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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Assay
99%
mp
>300 °C (lit.)
solubility
water: soluble 12.51 g/L 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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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Adsorption of essential micronutrients by carbon nanotubes and the implications for nanotoxicity testing.
Lin Guo et al.
Small (Weinheim an der Bergstrasse, Germany), 4(6), 721-727 (2008-05-28)
Kinetic, mechanistic and spectral studies for the oxidation of sulfanilic acid by alkaline hexacyanoferrate (III).
Farokhi SA and Nandibewoor ST.
Tetrahedron, 59(38), 7595-7602 (2003)
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
Jinsong Zhang et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 63(11), 2752-2758 (2011-11-05)
4-Aminobenzenesulfonate (4-ABS), an aromatic amine and recalcitrant toxic pollutant, is widely used in the dye and pharmaceutical industry. Pannonibactersp. W1 is a specialized microbial strain which can efficiently degrade 4-ABS. This study shows the feasibility of using the specialized strain
Yadong Sun et al.
Organic letters, 15(7), 1598-1601 (2013-03-19)
An efficient and convenient method was developed for the formation of 2-substituted benzothiazoles via a copper-catalyzed condensation of 2-aminobenzenethiols with nitriles. The developed method is applicable to a wide range of nitriles containing different functional groups furnishing excellent yields of
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