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86090

Sigma-Aldrich

Sulfanilic acid

puriss. p.a., ≥99.0% (T)

Synonym(s):

4-Aminobenzenesulfonic acid, Aniline-4-sulfonic acid

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About This Item

Linear Formula:
4-(H2N)C6H4SO3H
CAS Number:
121-57-3
Molecular Weight:
173.19
Beilstein:
908765
EC Number:
204-482-5
MDL number:
MFCD00007886
UNSPSC Code:
12352100
PubChem Substance ID:
57653079
NACRES:
NA.21

grade

puriss. p.a.

Quality Level

200

Assay

≥99.0% (T)

form

powder or crystals

impurities

≤1% ortho/meta-aminobenzene sulfonic acid (HPLC)

ign. residue

≤0.01% (as SO4)

mp

>300 °C (lit.)

anion traces

chloride (Cl-): ≤20 mg/kg
nitrite (NO2-): ≤0.5 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

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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Application

Sulfanilic acid may be used for the functionalization of single-walled carbon nanotubes (SWNTs) with aryl sulfonate groups.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H319

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9491
BCCH0242
BCCD7689
BCCC3918
BCCC4385

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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)
Adsorption of essential micronutrients by carbon nanotubes and the implications for nanotoxicity testing.
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Addressing potential sex differences in pre-clinical studies is crucial for developing therapeutic interventions. Although sex differences have been reported in epidemiological studies and from clinical experience, most pre-clinical studies of neuroinflammation use male rodents; however, sexual dimorphisms in microglia might
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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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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
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