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Merck
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Documenti

C55208

Sigma-Aldrich

4-Chloro-2-methylphenol

97%

Sinonimo/i:

4-Chloro-o-cresol

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About This Item

Formula condensata:
ClC6H3(CH3)OH
Numero CAS:
1570-64-5
Peso molecolare:
142.58
Beilstein:
1906684
Numero CE:
216-381-3
Numero MDL:
MFCD00002321
Codice UNSPSC:
12352100
ID PubChem:
24892793
NACRES:
NA.22

Saggio

97%

Forma fisica

crystals

P. eboll.

220-225 °C (lit.)

Punto di fusione

43-46 °C (lit.)

Stringa SMILE

Cc1cc(Cl)ccc1O

InChI

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

Informazioni sul gene

rat ... Ar(24208)

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Avvertenze

Danger

Indicazioni di pericolo

H314,H331,H400

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

172.4 °F - closed cup

Punto d’infiammabilità (°C)

78 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificati d'analisi (COA)

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4-Chloro-3-methylphenol analytical standard

Supelco

48519

4-Chloro-3-methylphenol

4-Chlorophenol ≥99%

Sigma-Aldrich

185787

4-Chlorophenol

Chloroacetic acid ACS reagent, ≥99.0%

Sigma-Aldrich

402923

Chloroacetic acid

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)
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
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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