35833
4-Chloro-2-methylphenol
PESTANAL®, analytical standard
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:
41116107
PubChem Substance ID:
NACRES:
NA.24
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
bp
220-225 °C (lit.)
mp
43-46 °C (lit.)
application(s)
agriculture
environmental
format
neat
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
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1
WGK
WGK 2
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Janne Juntunen et al.
Analytica chimica acta, 1127, 269-281 (2020-08-18)
Current theoretical, two compartment description of integrative passive sampling is renewed to establish a three-compartment model. The developed theoretical description includes external chemical conditions near the receiving phase, conditions inside the receiving phase and the chemically bonded compartments. New variable
Identification of 4-chloro-2-methylphenol as a soil degradation product of ring-labelled [14C]mecoprop.
A E Smith
Bulletin of environmental contamination and toxicology, 34(5), 656-660 (1985-05-01)
A follow-up study of cancer incidence among workers in manufacture of phenoxy herbicides in Denmark.
E Lynge
British journal of cancer, 52(2), 259-270 (1985-08-01)
The purpose of this cohort study is to shed further light on the potential carcinogenic effect indicated by a Swedish case control study of the 2,4-dichlorophenol and 4-chloro-ortho-cresol based phenoxy herbicides, unlikely to be contaminated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD). In the
K H Oh et al.
FEMS microbiology letters, 63(2-3), 141-146 (1991-04-15)
The concurrent bacterial degradation of 2-(2-methyl-4-chlorophenoxy)propionic acid and 2,4-dichlorophenoxyacetic acid was studied using a stirred tank reactor and a bacterial culture which had been originally derived by enrichment with MCPP. High pressure liquid chromatographic methodology was used to measure both
Degradation of 4-chloro-2-methylphenol by an activated sludge isolate and its taxonomic description.
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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