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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

functional group

sulfonic acid

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
BCCM5621
BCCM5445
BCCK8777
BCCK7810
BCCG9491

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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)
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
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)
Luís Belo et al.
PloS one, 9(6), e98467-e98467 (2014-06-06)
Bilirubin has potential antioxidant and anti-inflammatory properties. The UGT1A1*28 polymorphism (TA repeats in the promoter region) is a major determinant of bilirubin levels and recent evidence suggests that raised adiposity may also be a contributing factor. We aimed to study
Starlee Lively et al.
Frontiers in cellular neuroscience, 12, 433-433 (2018-12-14)
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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