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Merck
CN

135585

4-Chlorobenzoic acid

99%

Synonym(s):

4-CBA, p-Chlorobenzoic acid

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About This Item

Linear Formula:
ClC6H4CO2H
CAS Number:
Molecular Weight:
156.57
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-805-9
Beilstein/REAXYS Number:
907196
MDL number:
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Product Name

4-Chlorobenzoic acid, 99%

InChI

1S/C7H5ClO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)

InChI key

XRHGYUZYPHTUJZ-UHFFFAOYSA-N

SMILES string

OC(=O)c1ccc(Cl)cc1

assay

99%

form

powder

mp

238-241 °C (lit.)

solubility

methanol: soluble 1%, clear, colorless to faintly yellow

functional group

carboxylic acid
chloro

Quality Level

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Application

4-Chlorobenzoic acid can be used:
  • As a ligand to synthesize luminescent lanthanide complexes for bio-labeling or fiber communication applications.
  • To prepare organotin(IV) chlorobenzoates exhibiting anticorrosion properties.
  • As a ligand to synthesize di-n-butyl(4-chlorobenzoxy)(4-chlorobenzohydroxamato)tin(IV).

General description

4-Chlorobenzoic acid is a degradation product of indomethacin. It is degraded by Acinetobacter sp. strain ST-1 and causes its dehalogenation to yield 4-hydroxybenzoic acid under both aerobic and anaerobic conditions.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

460.4 °F - closed cup

flash_point_c

238 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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The Synthesis, characterization and comparative anticorrosion study of some organotin (IV) 4-chlorobenzoates
Kurniasih H, et al.
Orient. J. Chem., 31(4), 2377-2383 (2015)
Synthesis, structure and fluorescence of Er (III) complexes with benzoic acid and 4-chlorobenzoic acid
Luo X, et al.
Inorganica chimica acta, 446, 169-175 (2016)
Aliyeh Hasanzadeh et al.
Scientific reports, 9(1), 13780-13780 (2019-09-26)
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Heather O'Neal Tugaoen et al.
The Science of the total environment, 613-614, 1331-1338 (2017-10-04)
A key barrier to implementing photocatalysis is delivering light to photocatalysts that are in contact with aqueous pollutants. Slurry photocatalyst systems suffer from poor light penetration and require post-treatment to separate the catalyst. The alternative is to deposit photocatalysts on
S M Lindenauer et al.
Biomedical engineering, 11(9), 301-306 (1976-09-01)
Knitted Dacron cloth fabricated into tubes has gained widespread acceptance as an arterial prosthesis. Continued research and development in the field of vascular prostheses is required because existing materials are not ideal. This paper relates general developments in vascular prosthesis

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