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Principaux documents

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C55402

Sigma-Aldrich

4-Chloro-3-methylphenol

99%

Synonyme(s) :

4-Chloro-m-cresol, PCMC

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About This Item

Formule linéaire :
ClC6H3(CH3)OH
Numéro CAS:
59-50-7
Poids moléculaire :
142.58
Beilstein:
1237629
Numéro CE :
200-431-6
Numéro MDL:
MFCD00002323
Code UNSPSC :
12352100
ID de substance PubChem :
24892794
Nomenclature NACRES :
NA.22

Niveau de qualité

100

Essai

99%

Forme

solid

pb

235 °C (lit.)

Pf

63-65 °C (lit.)

Chaîne SMILES 

Cc1cc(O)ccc1Cl

InChI

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

Clé InChI

CFKMVGJGLGKFKI-UHFFFAOYSA-N

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Description générale

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).

Pictogrammes

CorrosionExclamation markEnvironment
GHS05,GHS07,GHS09

Mention d'avertissement

Danger

Mentions de danger

H302,H314,H317,H335,H410

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

244.4 °F - closed cup

Point d'éclair (°C)

118.0 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCF9933
BCCD4461
BCCC3096
BCCB3243
BCBZ5305

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Andrew P Ziman et al.
Biophysical journal, 99(8), 2705-2714 (2010-10-21)
Skeletal muscle stores Ca²(+) in the sarcoplasmic reticulum (SR) and releases it to initiate contraction, but the concentration of luminal Ca²(+) in the SR ([Ca²(+)](SR)) and the amount that is released by physiological or pharmacological stimulation has been difficult to
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
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
C D Sanmartin et al.
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Soluble amyloid-β peptide oligomers (AβOs), which are centrally involved in the pathogenesis of Alzheimer's disease, trigger Ca(2+) influx through N-methyl-D-aspartate receptors and stimulate reactive oxygen species generation in primary hippocampal neurons. We have previously reported that AβOs promote Ca(2+) release
Ramón Jiménez-Moreno et al.
Pflugers Archiv : European journal of physiology, 459(5), 725-735 (2010-01-14)
The endoplasmic/sarcoplasmic reticulum (ER/SR) plays a crucial role in cytoplasmic signalling in a variety of cells. It is particularly relevant to skeletal muscle fibres, where this organelle constitutes the main Ca2+ store for essential functions, such as contraction. In this
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Articles

US EPA Method 8041: GC Analysis of Phenols on Equity®-5

Separation of 2-Chlorophenol; 2,4-Dichlorophenol; 2,4,6-Tribromophenol; 2,4,6-Trichlorophenol; 2,4-Dinitrophenol; Pentafluorophenol; 2-Methylphenol, analytical standard; 2,3,4,6-Tetrachlorophenol; Pentachlorophenol; 4-Nitrophenol; 2-Bromophenol; 2,3,5,6-Tetrachlorophenol; 2,3,5-Trichlorophenol; 4-Chloro-3-methylphenol; 2,4,5-Trichlorophenol; 4-Methylphenol, analytical standard; 2,4-Dimethylphenol; 2-Nitrophenol; 3-Methylphenol, analytical standard; Phenol; 2-Methyl-4,6-dinitrophenol; 2,3,4-Trichlorophenol; 2,6-Dichlorophenol; 2,3,4,5-Tetrachlorophenol

Protocoles

GC Analysis of Phenols in Water on a 5% Phenyl Column after SPE using Supelclean™ ENVI-Chrom P

Separation of 2-Nitrophenol; Pentachlorophenol; 2-Bromophenol; Phenol; 4-Nitrophenol; 3-Methylphenol, analytical standard; 4-Chloro-3-methylphenol; 2,4-Dichlorophenol; 2,3,4,6-Tetrachlorophenol; 2-Methylphenol, analytical standard; 2,4,6-Trichlorophenol; 2,4-Dimethylphenol; 2-Chlorophenol

HPLC Analysis of Phenols on SUPELCOSIL™ LC-8

HPLC Analysis of Phenols on SUPELCOSIL™ LC-8

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