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C85751

Sigma-Aldrich

p-Crésol

99%

Synonyme(s) :

4-méthylphénol

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About This Item

Formule linéaire :
CH3C6H4OH
Numéro CAS:
106-44-5
Poids moléculaire :
108.14
Numéro Beilstein :
1305151
Numéro CE :
203-398-6
Numéro MDL:
MFCD00002376
Code UNSPSC :
12352002
ID de substance PubChem :
329775178
Nomenclature NACRES :
NA.21

Densité de vapeur

3.72 (vs air)

Niveau de qualité

200

Pression de vapeur

1 mmHg ( 20 °C)

Pureté

99%

Forme

(Liquid, Solid, or Crystalline Solid)

Température d'inflammation spontanée

1038 °F

Limite d'explosivité

1 %
1.1 %, 150 °F

Point d'ébullition

202 °C (lit.)

Pf

32-34 °C (lit.)

Densité

1.034 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cc1ccc(O)cc1

InChI

1S/C7H8O/c1-6-2-4-7(8)5-3-6/h2-5,8H,1H3

Clé InChI

IWDCLRJOBJJRNH-UHFFFAOYSA-N

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Description générale

p-Cresol, also known as 4-methylphenol, is an organic compound frequently utilized as an intermediate to synthesis various chemicals. It belongs to the phenol family and is an isomer of o-cresol and m-cresol.

Application


  • Detoxification of sewage sludge by natural attenuation and implications for its use as a fertilizer on agricultural soils.: This article discusses the role of p-Cresol in the detoxification processes of sewage sludge, considering its implications for safe agricultural use, addressing environmental and health concerns (Mazzeo DEC et al., 2016).

  • Characterization of livestock odors using steel plates, solid-phase microextraction, and multidimensional gas chromatography-mass spectrometry-olfactometry.: This research characterizes the complex odors of livestock environments, highlighting the role of p-Cresol in odor profiles, which could help improve management practices and mitigate odor emissions (Bulliner EA et al., 2006).

Pictogrammes

Skull and crossbonesCorrosion
GHS06,GHS05

Mention d'avertissement

Danger

Mentions de danger

H301 + H311,H314,H412

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B

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)

186.8 °F - closed cup

Point d'éclair (°C)

86 °C - closed cup

Certificats d'analyse (COA)

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K Akasaka et al.
Journal of chromatography, 617(2), 205-211 (1993-08-11)
Cholesterol ester (ChE) and triacylglycerol (TG) hydroperoxides in human plasma were determined by high-performance liquid chromatography with postcolumn detection with diphenyl-1-pyrenylphosphine. Human plasma was extracted once with n-hexane. 2,6-Di-tert.-butyl-4-methylphenol and N-stearylcinnamide were added to human plasma before extraction as an
Fangxin Hu et al.
Analytica chimica acta, 724, 40-46 (2012-04-10)
In this paper, the reduced graphene oxide and multiwall carbon nanotubes hybrid materials (RGO-MWNTs) were prepared and a strategy for detecting environmental contaminations was proposed on the basis of RGO-MWNTs modified electrode. The hybrid materials were characterized by the scanning
Yu-Sen Peng et al.
Toxicology, 302(1), 11-17 (2012-07-21)
High serum levels of p-cresol have been associated with cardiovascular diseases. This study investigated the effects of p-cresol on gap junctions in neonatal cultured cardiomyocytes. p-Cresol reduced the spontaneous contraction rates of cardiomyocytes, and caused irregular cardiomyocyte beating. Junctional connexin
H A M Mutsaers et al.
Biochimica et biophysica acta, 1832(1), 142-150 (2012-09-29)
During chronic kidney disease (CKD), drug metabolism is affected leading to changes in drug disposition. Furthermore, there is a progressive accumulation of uremic retention solutes due to impaired renal clearance. Here, we investigated whether uremic toxins can influence the metabolic
Donatella Boschi et al.
Journal of medicinal chemistry, 49(10), 2886-2897 (2006-05-12)
The synthesis and study of the antioxidant and vasodilator properties of a new class of phenols able to release nitric oxide are described. The products were designed through a symbiotic approach using selected phenols and selected nitrooxy and furoxan NO-donors
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