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12635

Sigma-Aldrich

Benzenesulfonic acid

98.0% (T)

Synonym(s):

Phenylsulfonic acid

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About This Item

Linear Formula:
C6H5SO3H
CAS Number:
Molecular Weight:
158.18
Beilstein:
742513
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98.0% (T)

form

solid

impurities

≤1.0% water

SMILES string

OS(=O)(=O)c1ccccc1

InChI

1S/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9)

InChI key

SRSXLGNVWSONIS-UHFFFAOYSA-N

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General description

Benzenesulfonic acid (BSA), also known as phenylsulfonic acid, is the simplest aromatic sulfonic acid. It is also used as a catalyst for Michael′s reactions and in the oxidative alkenylation process.

Application

Benzenesulfonic acid is an aryl sulfonic acid that can be used:
  • As an oxidizing agent in the synthesis of Fe(III) benzenesulfonate.
  • As a catalyst during the vapor-phase nitration of benzene.
  • As a reagent in the synthesis of organic salts.
  • To form an organic salt with 5,7-dimethyl-1,8-naphthyridine-2-amine, that can be a synthon for developing supramolecular structures.
  • As a dopant for the polymerization of pyrrole to form poly(pyrrole), a conducting polymer useful in the development of flexible capacitors.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

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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Supramolecular salts of 5, 7-dimethyl-1, 8-naphthyridine-2-amine and acids through classical H-Bonds and other intermolecular interactions.
Dong L
Journal of Molecular Structure, 1153, 311-323 (2018)
Durable Flexible Supercapacitors Utilizing the Multifunctional Role of Ionic Liquids.
Lorenzo M
Energy Technology, 6(1), 196-204 (2018)
David Scholz et al.
ChemSusChem, 11(13), 2189-2201 (2018-05-08)
The deactivation pathways of sulfonated carbon catalysts prepared from different carbons were studied during the aqueous-phase hydrolysis of cellobiose under continuous-flow conditions. The sulfonation of carbon materials with a low degree of graphitization introduced sulfonic acid groups that are partially
Bo Ram Lee et al.
Journal of colloid and interface science, 331(1), 55-59 (2008-12-09)
Sulfur hexafluoride (SF(6)) has been widely used in a variety of industrial processes, but it is one of the most potent greenhouse gases. For this reason, it is necessary to separate or collect it from waste gas streams. One separation
Yanlong Gu et al.
Organic letters, 9(2), 175-178 (2007-01-16)
A neutral catalytic system for Michael reactions of indoles has been developed by combining silica-supported benzenesulfonic acid sodium salt with hydrophobic ionic liquid in water. An efficient hydrophobic environment could be created on the surface of the silica-sodium material under

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