Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

93792

SAFC

Benzenesulfonic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5SO3H
CAS Number:
Molecular Weight:
158.18
Beilstein/REAXYS Number:
742513
MDL number:
UNSPSC Code:
12352005
NACRES:
NA.21

biological source

synthetic

Quality Level

assay

≥99.8% (area, HPLC)

form

solid

concentration

≥98.0 % (w/w) (T)

impurities

≤0.05% phenyl p-tolylsulfone (area)
≤0.1% any not specified impurity (area)
≤1% water (Karl Fischer)
≤2 mg/kg residual solvents (benzene) (GC)
≤5000 mg/kg residual solvents (heptane) (GC)
≤890 mg/kg residual solcents (toluene) (GC)

ign. residue

≤0.2%

solubility

H2O: 0.1 g/10 mL, clear, colorless

anion traces

chloride (Cl-): ≤500 mg/kg
sulfate (SO42-): ≤600 mg/kg

suitability

corresponds for identity (IR) (ATR)

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

Looking for similar products? Visit Product Comparison Guide

Analysis Note

white/colorless to slightly beige crystals; powder with lumps

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Wang-Ping Ting et al.
Journal of hazardous materials, 156(1-3), 421-427 (2008-02-05)
A new approach for promoting ferric reduction efficiency using a different electrochemical cell and the photoelectro-Fenton process has been developed. The use of UVA light and electric current as electron donors can efficiently initiate the Fenton reaction. Benzene sulfonic acid
Garry D Sisk et al.
Electrophoresis, 30(19), 3366-3371 (2009-09-04)
In this research, ion transfer across the interface between two immiscible electrolyte solutions (ITIES) was used as a method of detection in a CE separation system. This method allows for the electrochemical detection of ionic analytes that cannot be easily
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.
Erzsébet Szabó-Bárdos et al.
Water research, 45(4), 1617-1628 (2010-12-28)
Titanium dioxide-mediated photocatalyzed degradation of benzenesulfonate (BS) was investigated by monitoring chemical oxygen demand (COD), total organic carbon (TOC) content, sulfate concentration, pH as well as the absorption and emission spectral changes in both argon-saturated and aerated systems. Liquid chromatography-mass
M Jinish Antony et al.
The journal of physical chemistry. B, 114(3), 1314-1324 (2010-01-07)
Here, we report a unique molecular template approach, for the first time, to study the evolution of the different types of nanomaterial morphologies such as nanofiber, nanorod, nanosphere, and nanotube in a single system without changing their chemical composition or

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service