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Merck

86090

Sulfanilic acid

≥99.0% (T), powder or crystals, purum p.a.

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
NACRES:
NA.21
PubChem Substance ID:
57653079
UNSPSC Code:
12352100
EC Number:
204-482-5
MDL number:
MFCD00007886
Beilstein/REAXYS Number:
908765

Product Name

Sulfanilic acid, puriss. p.a., ≥99.0% (T)

InChI key

HVBSAKJJOYLTQU-UHFFFAOYSA-N

InChI

1S/C6H7NO3S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H,8,9,10)

SMILES string

Nc1ccc(cc1)S(O)(=O)=O

grade

puriss. p.a.

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

Quality Level

200

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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

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN1902
BCCM5621
BCCM5445
BCCK8777
BCCK7810

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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)
Prashant Barsing et al.
Bioresource technology, 102(2), 765-771 (2010-09-25)
A novel bacterial consortium (TJ-2) for mineralization of aromatic amines resulting from decolorization of azo dyes was developed. Three bacterial strains were identified as Pseudomonas pseudoalcaligenes (TJ-21,EU072476), Pseudomonas citronellolis (TJ-22,EU072477) and Pseudomonas testosterone (TJ-23,EU072477) by 16S rRNA gene sequence analysis.
Nam Hoon Kim et al.
Nano letters, 10(10), 4181-4185 (2010-09-25)
A bifunctional adenosine-sensitive double-stranded DNA aptamer was used to create and control a surface-enhanced Raman spectroscopy (SERS) hot spot between a bulk Au surface and a gold nanoparticle (Au NP) attached to the aptamer via a biotin-avidin linkage. The Au
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