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Merck

135585

Sigma-Aldrich

4-Chlorbenzoesäure

99%

Synonym(e):

4-CBA, p-Chlorobenzoic acid

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About This Item

Lineare Formel:
ClC6H4CO2H
CAS-Nummer:
Molekulargewicht:
156.57
Beilstein:
907196
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

99%

Form

powder

mp (Schmelzpunkt)

238-241 °C (lit.)

Löslichkeit

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)

InChIKey

XRHGYUZYPHTUJZ-UHFFFAOYSA-N

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Allgemeine Beschreibung

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.

Anwendung

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).

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

460.4 °F - closed cup

Flammpunkt (°C)

238 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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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
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