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C55208

Sigma-Aldrich

4-Chloro-2-methylphenol

97%

Synonym(s):

4-Chloro-o-cresol

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About This Item

Linear Formula:
ClC6H3(CH3)OH
CAS Number:
Molecular Weight:
142.58
Beilstein:
1906684
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

crystals

bp

220-225 °C (lit.)

mp

43-46 °C (lit.)

SMILES string

Cc1cc(Cl)ccc1O

InChI

1S/C7H7ClO/c1-5-4-6(8)2-3-7(5)9/h2-4,9H,1H3

InChI key

RHPUJHQBPORFGV-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

172.4 °F - closed cup

Flash Point(C)

78 °C - closed cup

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’.

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Ian Harrison et al.
Chemosphere, 53(5), 539-549 (2003-09-02)
Natural attenuation of mecoprop has been studied by determining changes in enantiomeric fraction in different redox environments down gradient from a landfill in the Lincolnshire limestone. Such changes could be due to differential metabolism of the enantiomers, or enantiomeric inversion.
K Nickel et al.
Journal of bacteriology, 179(21), 6674-6679 (1997-11-14)
Cell extracts of Sphingomonas herbicidovorans MH grown on (R)-mecoprop contained an enzyme activity that selectively converted (R)-mecoprop to 4-chloro-2-methylphenol, whereas extracts of cells grown on (S)-mecoprop contained an enzyme activity selective for the S enantiomer. Both reactions were dependent on
Saúl E Bustamante et al.
Journal of hazardous materials, 365, 725-732 (2018-11-26)
We have prepared polymeric films as easy-to-handle sensory materials for the colorimetric detection and quantification of phenol derivatives (phenols) in water. Phenols in water resources result from their presence in pesticides and fungicides, among other goods, and are harmful ecotoxins.
Effects of chlorocresol (4-chloro-2-methyl phenol) administered during the fertilization and cleavage phases of Xenopus laevis.
C Vismara et al.
Bulletin of environmental contamination and toxicology, 55(2), 195-200 (1995-08-01)
U Lechner et al.
Biodegradation, 6(2), 83-92 (1995-06-01)
The Gram-negative strain S1, isolated from activated sludge, metabolized 4-chloro-2-methylphenol by an inducible pathway via a modified ortho-cleavage route as indicated by a transiently secreted intermediate, identified as 2-methyl-4-carboxymethylenebut-2-en-4-olide by gas chromatography/mass spectrometry. Beside 4-chloro-2-methylphenol only 2,4-dichlorophenol and 4-chlorophenol were

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