Skip to Content
Merck
CN
All Photos(3)

Documents

135585

Sigma-Aldrich

4-Chlorobenzoic acid

99%

Synonym(s):

4-CBA, p-Chlorobenzoic acid

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
ClC6H4CO2H
CAS Number:
74-11-3
Molecular Weight:
156.57
Beilstein:
907196
EC Number:
200-805-9
MDL number:
MFCD00002531
UNSPSC Code:
12352100
PubChem Substance ID:
24848211
NACRES:
NA.22

Quality Level

100

Assay

99%

form

powder

mp

238-241 °C (lit.)

solubility

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

SMILES string

OC(=O)c1ccc(Cl)cc1

InChI

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

InChI key

XRHGYUZYPHTUJZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

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.

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).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 2

Flash Point(F)

460.4 °F

Flash Point(C)

238 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Mariana Lanzarini-Lopes et al.
Chemosphere, 188, 304-311 (2017-09-10)
Electrochemical oxidation (EO) is an advanced oxidation process for water treatment to mineralize organic contaminants. While proven to degrade a range of emerging pollutants in water, less attention has been given to quantify the effect of operational variables such applied
Synthesis and crystal structure of a mixed-ligand compound di-n-butyl (4-chlorobenzoxy)(4-chlorobenzohydroxamato) tin (IV)
Shang X, et al.
Journal of Organometallic Chemistry, 690(17), 3997-4000 (2005)
Q Q Cai et al.
Water research, 183, 116119-116119 (2020-07-15)
Fluidized bed reactor Fenton (FBR-Fenton) process was adopted for reverse osmosis concentrate (ROC) treatment with three types of carriers, including sand, zeolite and granular activated carbon (GAC). Adsorption studies demonstrated that GAC achieved the best adsorption performance (maximum COD removal
Ruiyang Xiao et al.
Environmental pollution (Barking, Essex : 1987), 257, 113498-113498 (2019-11-26)
Carbamazepine (CBZ), a widely detected pharmaceutical in wastewaters, cannot currently be treated by conventional activated sludge technologies, as it is highly resistant to biodegradation. In this study, the degradation kinetics and reaction mechanisms of CBZ by hydroxyl radical (OH) and
Kikuo Kobayashi et al.
The Journal of general and applied microbiology, 43(2), 105-108 (1997-04-01)
Acinetobacter sp. strain ST-1, isolated from garden soil, can mineralize 4-chlorobenzoic acid (4-CBA). The bacterium degrades 4-CBA, starting with dehalogenation to yield 4-hydroxybenzoic acid (4-HBA) under both aerobic and anaerobic conditions, suggesting that the dehalogenating enzyme in the strain is
View All Related Papers

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