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Supelco

4-Chlor-2-methylphenol

PESTANAL®, analytical standard

Synonym(e):

4-Chlor-o-kresol

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About This Item

Lineare Formel:
ClC6H3(CH3)OH
CAS-Nummer:
1570-64-5
Molekulargewicht:
142.58
Beilstein:
1906684
EG-Nummer:
216-381-3
MDL-Nummer:
MFCD00002321
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329755226

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

220-225 °C (lit.)

mp (Schmelzpunkt)

43-46 °C (lit.)

Anwendung(en)

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

InChIKey

RHPUJHQBPORFGV-UHFFFAOYSA-N

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Anwendung

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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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 2

Flammpunkt (°F)

172.4 °F - closed cup

Flammpunkt (°C)

78 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCBZ9091
SZBF223XV
SZBB305XV
SZB9314XV
SZE9314X

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Die Dokumentenbibliothek aufrufen

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
Serge Chiron et al.
Chemosphere, 74(4), 599-604 (2008-11-11)
A field monitoring campaign for pesticides and their transformation intermediates was carried out in the Rhône delta (Southern France). It was evidenced the following transformation sequence: MCPA-->4-chloro-2-methylphenol (CMP)-->4-chloro-2-methyl-6-nitrophenol (CMNP). Interestingly CMP disappeared about as quickly as MCPA, while CMNP was
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
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)
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