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332925

Sigma-Aldrich

4-Chlorobenzenesulfonic acid

technical grade, 90%

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About This Item

Linear Formula:
ClC6H4SO3H
CAS Number:
98-66-8
Molecular Weight:
192.62
EC Number:
202-690-0
MDL number:
MFCD00065342
UNSPSC Code:
12352100
PubChem Substance ID:
24860090
NACRES:
NA.22

grade

technical grade

Assay

90%

impurities

<3.5% H2SO4

bp

149 °C/22 mmHg (lit.)

functional group

chloro
sulfonic acid

SMILES string

OS(=O)(=O)c1ccc(Cl)cc1

InChI

1S/C6H5ClO3S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H,8,9,10)

InChI key

RJWBTWIBUIGANW-UHFFFAOYSA-N

General description

4-Chlorobenzenesulfonic acid is the major polar by-product formed during the chemical synthesis of 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT).[1]

Application

4-Chlorobenzenesulfonic acid was employed as anion dopants for the matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS) of neutral oligosaccharides.[2]

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
09307BD
06002CU
02725AY
00431JZ
07306KY

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A W Wong et al.
Analytical chemistry, 72(7), 1419-1425 (2000-04-14)
Alkylsulfonates are examined as anion dopants for the matrix-assisted laser desorption/ionization-mass spectrometry (MALDI-MS) of neutral oligosaccharides. The anion dopants allow neutral oligosaccharides to be examined in the same mixture as acidic oligosaccharides. The alkylsulfonate dopants interact strongly with the oligosaccharide
Rafael Blasco et al.
Environmental microbiology, 10(6), 1591-1600 (2008-03-12)
Pseudomonas aeruginosa RW41 is the first bacterial strain, which could be isolated by virtue of its capability to mineralize 4-chlorobenzenesulfonic acid (4CBSA), the major polar by-product of the chemical synthesis of 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT). This capability makes the isolate a promising

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