Names | |
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Preferred IUPAC name
4-Methylphenol | |
Systematic IUPAC name
4-Methylbenzenol | |
Other names
4-Cresol
p-Cresol 4-Hydroxytoluene p-Cresylic acid 1-Hydroxy-4-methylbenzene | |
Identifiers | |
3D model (JSmol)
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1305151 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.003.090 |
EC Number |
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2779 | |
KEGG | |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C7H8O | |
Molar mass | 108.13 |
Appearance | colorless prismatic crystals |
Density | 1.0347 g/ml |
Melting point | 35.5 °C (95.9 °F; 308.6 K) |
Boiling point | 201.8 °C (395.2 °F; 474.9 K) |
2.4 g/100 ml at 40 °C 5.3 g/100 ml at 100 °C | |
Solubility in ethanol | miscible |
Solubility in diethyl ether | miscible |
Vapor pressure | 0.11 mmHg (25 °C)[1] |
−72.1×10−6 cm3/mol | |
Refractive index (nD)
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1.5395 |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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May be fatal if swallowed, inhaled, or absorbed through skin. |
GHS labelling: | |
Danger | |
H201, H311, H314, H351, H370, H372, H373, H401, H412 | |
P201, P202, P260, P264, P270, P273, P280, P281, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P307+P311, P308+P313, P310, P312, P314, P321, P322, P330, P361, P363, P405, P501 | |
NFPA 704 (fire diamond) | |
Flash point | 86.1 °C (187.0 °F; 359.2 K) |
Explosive limits | 1.1%–?[1] |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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207 mg/kg (oral, rat, 1969) 1800 mg/kg (oral, rat, 1944) 344 mg/kg (oral, mouse)[2] |
NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 5 ppm (22 mg/m3) [skin][1] |
REL (Recommended)
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TWA 2.3 ppm (10 mg/m3)[1] |
IDLH (Immediate danger)
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250 ppm[1] |
Safety data sheet (SDS) | External MSDS |
Related compounds | |
Related phenols
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o-cresol, m-cresol, phenol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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para-Cresol, also 4-methylphenol, is an organic compound with the formula CH3C6H4(OH). It is a colourless solid that is widely used intermediate in the production of other chemicals. It is a derivative of phenol and is an isomer of o-cresol and m-cresol.[3]