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C55402

Sigma-Aldrich

4-Chloro-3-methylphenol

99%

Synonym(s):

4-Chloro-m-cresol, PCMC

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About This Item

Linear Formula:
ClC6H3(CH3)OH
CAS Number:
Molecular Weight:
142.58
Beilstein:
1237629
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

solid

bp

235 °C (lit.)

mp

63-65 °C (lit.)

SMILES string

Cc1cc(O)ccc1Cl

InChI

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

InChI key

CFKMVGJGLGKFKI-UHFFFAOYSA-N

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General description

4-Chloro-3-methylphenol, also known as p-chlorocresol or chloroxylenol, is commonly used as a building block in the synthesis of organic compounds. It can be utilized to synthesize various biologically active compounds, including pharmaceuticals and agrochemicals. (2) Additionally, it serves as a potent disinfectant and antiseptic and is also used as a preservative in medicinal products.

Application

  • Compression of mono-4 chloro, 3-methylphenyl phosphate ester and di-4 chloro, 3-methylphenyl phosphate ester through kinetic study: This study discusses a method using 4-chloro-3-methylphenol and POCl3 taken in a 2:1 ratio, exploring their kinetic behaviors (AR Teli, AA Khan, SH Dar, A Rashid, 2017).
  • Commercially Important Chlorinated Phenols: Reviews the usage of 4-chloro-3-methylphenol among other chlorinated phenols in various industrial applications (K Smith, G El-Hiti).

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C - Skin Sens. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

244.4 °F - closed cup

Flash Point(C)

118.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthetic and natural phenols
Tyman et al.
Elsevier's Integrated Review Biochemistry (Second Edition) (1996)
Synthesis and insecticidal activity evaluation of virtually screened phenylsulfonamides
Gang et al.
Journal of Agricultural and Food Chemistry, 68, 11665-11671 (2020)
Synthesis and biological evaluation of novel aryloxyacetic acid hydrazide derivatives as anticancer agents
Sevil et al.
Synthetic Communications, 51, 2634-2643 (2021)
Niels Ørtenblad et al.
The Journal of physiology, 589(Pt 3), 711-725 (2010-12-08)
Glucose is stored as glycogen in skeletal muscle. The importance of glycogen as a fuel during exercise has been recognized since the 1960s; however, little is known about the precise mechanism that relates skeletal muscle glycogen to muscle fatigue. We
Ian McLaren et al.
Avian pathology : journal of the W.V.P.A, 40(1), 33-42 (2011-02-19)
Two experimental models of Salmonella contamination were used in an attempt to mimic the conditions of disinfectant use on farms. A wet model, for conditions such as boot dips, used disinfectant application to a slurry of poultry faeces inoculated with

Protocols

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

Analytical standard separation of various phenols for research and industrial applications.

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