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35833

Supelco

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:
1570-64-5
Molecular Weight:
142.58
Beilstein:
1906684
EC Number:
216-381-3
MDL number:
MFCD00002321
UNSPSC Code:
41116107
PubChem Substance ID:
329755226
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

H314,H331,H400

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK8906
BCBZ9091
SZBF223XV
SZBB305XV
SZB9314XV

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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
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
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)
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
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
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