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61030

Sigma-Aldrich

p-Cresol

puriss. p.a., ≥99.0% (GC)

Synonym(s):

4-Methylphenol

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About This Item

Linear Formula:
CH3C6H4OH
CAS Number:
Molecular Weight:
108.14
Beilstein/REAXYS Number:
1305151
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.72 (vs air)

vapor pressure

1 mmHg ( 20 °C)

grade

puriss. p.a.

assay

≥99.0% (GC)

form

powder or crystals

autoignition temp.

1038 °F

expl. lim.

1 %
1.1 %, 150 °F

technique(s)

GC/MS: suitable

bp

202 °C (lit.)

mp

32-34 °C (lit.)
32-35 °C

density

1.034 g/mL at 25 °C (lit.)

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤10 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

storage temp.

2-8°C

SMILES string

Cc1ccc(O)cc1

InChI

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

InChI key

IWDCLRJOBJJRNH-UHFFFAOYSA-N

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General description

Cresols exist in three isomeric forms: o-, m- and p-cresol. They have phenolic odor.[1] p-cresol contamination in water samples has been determined by employing polyphenol oxidase at a graphite foil electrode.[2] Chemical changes involved during the adsorption of p-cresol on the activated carbon at 278, 298 and 323K have been investigated.[3] p-Cresol (4-Methylphenol) affords 4-methylcyclohexanol on hydrogenation in the presence of MoO3, MoO2, and MoS2 catalysts.[4] It affords 4-methyl-2-nitrophenol, via reaction with nitrogen dioxide in solution.[5]

Application

p-Cresol (4-Methylphenol) has been used in a study for the identification of volatile compounds from the meat samples aged for 4- and 8-days by gas chromatography-mass spectrometry.[6]

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 2

flash_point_f

186.8 °F - closed cup

flash_point_c

86 °C - closed cup


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Hydrodeoxygenation of 4-Methylphenol over Unsupported MoP, MoS2, and MoOx Catalysts?.
Whiffen VML and Smith KJ.
Energy and Fuels, 24(9), 4728-4737 (2010)
Adsorption of phenol, cresol isomers and benzyl alcohol from aqueous solution on activated carbon at 278, 298 and 323 K.
Ravi VP, et al.
Journal of Chemical Technology and Biotechnology, 71(2), 173-179 (1998)
The mechanism of nitration of phenol and 4-methylphenol by nitrogen dioxide in solution.
Coombes RG, et al.
Tetrahedron Letters, 35(34), 6373-6376 (1994)
The determination of p-cresol in chloroform with an enzyme electrode used in the organic phase.
Hall GF, et al.
Analytica Chimica Acta, 213, 113-119 (1988)
Eagleson M.
Concise Encyclopedia Chemistry, 276-276 (1994)

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