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24940

Sigma-Aldrich

4-Chloro-3-methylphenol

≥98.0% (HPLC)

Sinonimo/i:

4-Chloro-m-cresol, PCMC

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About This Item

Formula condensata:
ClC6H3(CH3)OH
Numero CAS:
59-50-7
Peso molecolare:
142.58
Beilstein:
1237629
Numero CE:
200-431-6
Numero MDL:
MFCD00002323
Codice UNSPSC:
12352100
ID PubChem:
57648100
NACRES:
NA.22

Saggio

≥98.0% (HPLC)

Forma fisica

pellets

P. eboll.

235 °C (lit.)

Punto di fusione

63-65 °C (lit.)

Solubilità

methanol: soluble 1 g/10 mL, clear, colorless
water: soluble

Stringa SMILE

Cc1cc(O)ccc1Cl

InChI

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

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Descrizione generale

4-Chloro-3-methylphenol is an organic compound belonging to the class of monochlorinated m-cresol. It is used as an organic building block in chemical synthesis.

Applicazioni

4-Chloro-3-methylphenol has been used in paint formulations.

Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H317,H335,H410

Classi di pericolo

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

Organi bersaglio

Respiratory system

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)

244.4 °F - closed cup

Punto d’infiammabilità (°C)

118.0 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
BCCF6517
BCBT2623
BCBT2622
BCBS2206V
BCBR3387V

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A Peñalver et al.
Journal of chromatography. A, 839(1-2), 253-260 (1999-05-18)
Three pesticides usually added to paint formulations, Irgarol 1051, dichlofluanid and 4-chloro-3-methylphenol, were determined by solid-phase microextraction (SPME) with 85-micron polyacrylate fibers and gas chromatography-mass spectrometry. The parameters affecting the SPME process (the pH, the addition of salt to the
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.
Neuro-degenerative diseases, 10(1-4), 34-37 (2012-01-31)
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
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