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135070

Sigma-Aldrich

Benzenesulfonic acid

technical grade, 90%

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About This Item

Linear Formula:
C6H5SO3H
CAS Number:
98-11-3
Molecular Weight:
158.18
Beilstein:
742513
MDL number:
MFCD00011689
UNSPSC Code:
12352106
PubChem Substance ID:
24848198
NACRES:
NA.22

grade

technical grade

Quality Level

200

Assay

90%

form

solid

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, also known as besylic acid, is a strong organic acid commonly used as an acid catalyst in various organic reactions, such as esterification, alkylation, and condensation reactions. It is also used as a sulfonating agent to introduce sulfonic acid (SO3H) groups into organic compounds, which can be useful in the synthesis of several dye intermediates.

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H290,H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 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

Certificates of Analysis (COA)

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Chenghui Han et al.
Journal of hazardous materials, 168(1), 215-219 (2009-04-04)
A series of TiO(2)-Cu(2)O mixed oxides were prepared by the hydrolysis of titanium butoxide and reduction of copper acetate with hydrazine. These composite oxides were characterized by X-ray diffraction (XRD), inductively coupled plasma spectrometry (ICP), high-resolution transmission electron microscopy (HRTEM)
N V V S S Raman et al.
Journal of pharmaceutical and biomedical analysis, 48(1), 227-230 (2008-07-08)
The present paper describes a simple isocratic reverse phase HPLC method for the determination of four genotoxic alkyl benzenesulfonates (ABSs) viz. methyl, ethyl, n-propyl and isopropyl benzenesulfonates (MBS, EBS, NPBS and IPBS) in amlodipine besylate (ADB). Good resolution between benzene
Snehlata Yadav et al.
European journal of medicinal chemistry, 45(12), 5985-5997 (2010-10-26)
A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones.
Ramasubbu Ramani et al.
Biomacromolecules, 9(5), 1390-1397 (2008-04-19)
We present lamellar self-assembly of cationic poly(L-histidine) (PLH) stoichiometrically complexed with an anionic surfactant, dodecyl benzenesulfonic acid (DBSA), which allows a stabilized conformation reminiscent of polyproline type II (PPII) left-handed helices. Such a conformation has no intrapeptide hydrogen bonds, and
Wen Huang et al.
The Journal of organic chemistry, 73(17), 6845-6848 (2008-08-07)
A novel, convenient, and efficient method has been developed for selective synthesis of spirocycle, polycycle, and di- and tetrahydronaphthalene systems from aryl-substituted propargylic alcohols by FeCl3- or TsOH-catalyzed multiple activations of unsaturated C-C bonds and C-H bonds.
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