12635
Benzenesulfonic acid
98.0% (T)
Synonym(s):
Phenylsulfonic acid
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About This Item
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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.
Signal Word
Danger
Hazard Statements
Precautionary 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.
Journal of Molecular Structure, 1153, 311-323 (2018)
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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
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
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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