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Merck

35833

4-Chloro-2-methylphenol

PESTANAL®, analytical standard

Synonyme(s) :

4-Chloro-o-cresol

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A propos de cet article

Formule linéaire :
ClC6H3(CH3)OH
Numéro CAS:
1570-64-5
Poids moléculaire :
142.58
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755226
EC Number:
216-381-3
Beilstein/REAXYS Number:
1906684
MDL number:
MFCD00002321

Principaux documents

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Nom du produit

4-Chloro-2-methylphenol, PESTANAL®, analytical standard

InChI key

RHPUJHQBPORFGV-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1cc(Cl)ccc1O

grade

analytical standard

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

Quality Level

100

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Catégories apparentées

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

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.

Legal Information

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

signalword

Danger

Hazard Classifications

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

Classe de stockage

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

ppe

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK8906
BCBZ9091

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Consulter la Bibliothèque de documents

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 E Andersen
Dermatosen in Beruf und Umwelt. Occupation and environment, 33(4), 132-136 (1985-01-01)
Guinea pig maximization tests (GPMT) with chlorocresol were performed to ascertain whether the sensitization rate was affected by minor changes in the Freund's complete adjuvant (FCA) emulsion used. Three types of emulsion were evaluated: the oil phase was mixed with
Tatsunori Takayasu et al.
Journal of analytical toxicology, 32(2), 187-191 (2008-03-13)
We report a fatal intoxication case by the ingestion of an herbicide, 2-methyl-4-chlorophenoxyacetic acid (MCPA). A 23-year-old male was found dead in his car. The forensic autopsy revealed no remarkable morphological changes. However, in a toxicological screening test, MCPA was
A Struk et al.
The Journal of physiology, 515 ( Pt 1), 221-231 (1999-02-02)
1. The effect of 5 microM 4-chloro-m-cresol (4-CmC) on voltage-controlled Ca2+ release was studied in cut muscle fibres of the frog loaded with internal solutions containing 15 mM EGTA. Fibres were voltage clamped using a double Vaseline gap system, and
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
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