108111
Benzenesulfonyl chloride
96%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C6H5SO2Cl
CAS Number:
Molecular Weight:
176.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-636-6
Beilstein/REAXYS Number:
606926
MDL number:
eCl@ss:
39092406
Assay:
96%
vapor pressure
0.04 mmHg ( 20 °C)
Quality Level
assay
96%
refractive index
n20/D 1.551 (lit.)
bp
251-252 °C (lit.)
mp
13-15 °C (lit.)
solubility
alcohol: soluble, cold water: insoluble, diethyl ether: soluble
density
1.384 g/mL at 25 °C (lit.)
SMILES string
ClS(=O)(=O)c1ccccc1
InChI
1S/C6H5ClO2S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H
InChI key
CSKNSYBAZOQPLR-UHFFFAOYSA-N
General description
Benzenesulfonyl chloride reacts with Grignard reagent from N-unsubstituted indoles to form oxindoles or substituted indoles. It is the derivatization reagent for the determination of various amines in waste water and surface water at the sub-ppb level by gas chromatography-mass spectrometry.
Application
Benzenesulfonyl chloride may be used in thiamine assay for determination of thiamine in different food products.
Still not finding the right product?
Explore all of our products under Benzenesulfonyl chloride
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
260.6 °F
flash_point_c
127 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Unusual reactions of magnesium indolates with benzenesulfonyl chloride.
Wenkert E, et al.
The Journal of Organic Chemistry, 52(15), 3404-3409 (1987)
A G Soliman
Journal - Association of Official Analytical Chemists, 64(3), 616-622 (1981-05-01)
A semiautomated procedure was used to measure the fluorescence of sample extracts before and after the addition of benzenesulfonyl chloride (BSC). Addition of BSC inhibited thiochrome formation and provided a more representative blank based on the fluorescence of all the
Analysis of primary and secondary aliphatic amines in waste water and surface water by gas chromatography-mass spectrometry after derivatization with 2, 4-dinitrofluorobenzene or benzenesulfonyl chloride.
Sacher F, et al.
Journal of Chromatography A, 764(1), 85-93 (1997)