p-Cresol
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| Names | |
|---|---|
| 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: | |
  
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| 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]
Production
[edit]Together with many other compounds, p-cresol is conventionally extracted from coal tar, the volatilized materials obtained in the roasting of coal to produce coke. This residue contains a few percent by weight of phenol and cresols. Industrially, p-cresol is currently prepared mainly by a two-step route beginning with the sulfonation of toluene:[4]
- CH3C6H5 + H2SO4 → CH3C6H4SO3H + H2O
Basic hydrolysis of the sulfonate salt gives the sodium salt of the cresol:
- CH3C6H4SO3H + 2 NaOH → CH3C6H4OH + Na2SO3 + H2O
Other methods for the production of p-cresol include chlorination of toluene followed by hydrolysis. In the cymene-cresol process, toluene is alkylated with propene to give p-cymene, which can be oxidatively dealkylated in a manner similar to the cumene process.[3]
Applications
[edit]p-Cresol is consumed mainly in the production of antioxidants, such as butylated hydroxytoluene (BHT). The monoalkylated derivatives undergo coupling to give an extensive family of diphenol antioxidants. These antioxidants are valued because they are relatively low in toxicity and nonstaining.[3][5][6]
Natural occurrences
[edit]In humans
[edit]p-Cresol is produced by bacterial fermentation of protein in the human large intestine. It is excreted in feces and urine,[7] and is a component of human sweat that attracts female mosquitoes.[8][9]
p-Cresol is a constituent of tobacco smoke.[10]
In other species
[edit]p-Cresol is a major component in pig odor.[11] Temporal glands secretion examination showed the presence of phenol and p-cresol during musth in male elephants.[12][13] It is one of the very few compounds to attract the orchid bee Euglossa cyanura and has been used to capture and study the species.[14] p-Cresol is a component found in horse urine during estrus that can elicit the Flehmen response.[15]
References
[edit]- ^ a b c d e NIOSH Pocket Guide to Chemical Hazards. "#0156". National Institute for Occupational Safety and Health (NIOSH).
- ^ "Cresol (o, m, p isomers)". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c Fiege H (2000). "Cresols and Xylenols". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_025. ISBN 3-527-30673-0.
- ^ W. W. Hartman (1923). "p-Cresol". Organic Syntheses. 3: 37. doi:10.15227/orgsyn.003.0037.
- ^ "meta- and para-Cresols" (PDF). International Programme on Chemical Safety (IPCS INCHEM). April 2005. Archived from the original (PDF) on 8 December 2017. Retrieved 4 November 2022.
- ^ "p-Cresol - Hazardous Agents". Haz-Map: Information on Hazardous Chemicals and Occupational Diseases. Retrieved 4 November 2022.
- ^ Hamer HM, De Preter V, Windey K, Verbeke K (January 2012). "Functional analysis of colonic bacterial metabolism: relevant to health?". American Journal of Physiology. Gastrointestinal and Liver Physiology. 302 (1): G1-9. doi:10.1152/ajpgi.00048.2011. PMC 3345969. PMID 22016433.
- ^ Hallem EA, Nicole Fox A, Zwiebel LJ, Carlson JR (January 2004). "Olfaction: mosquito receptor for human-sweat odorant". Nature. 427 (6971): 212–213. Bibcode:2004Natur.427..212H. doi:10.1038/427212a. PMID 14724626. S2CID 4419658.
- ^ Linley JR (October 1989). "Laboratory tests of the effects of p-cresol and 4-methylcyclohexanol on oviposition by three species of Toxorhynchites mosquitoes". Medical and Veterinary Entomology. 3 (4): 347–52. doi:10.1111/j.1365-2915.1989.tb00241.x. PMID 2577519. S2CID 1641506.
- ^ Talhout R, Schulz T, Florek E, van Benthem J, Wester P, Opperhuizen A (February 2011). "Hazardous compounds in tobacco smoke". International Journal of Environmental Research and Public Health. 8 (2): 613–28. doi:10.3390/ijerph8020613. PMC 3084482. PMID 21556207.
- ^ Borrell, Brendan (5 March 2009). "Why study pig odor?". Scientific American. Archived from the original on 20 March 2021. Retrieved 9 March 2009.
- ^ Rasmussen LE, Perrin TE (October 1999). "Physiological correlates of musth: lipid metabolites and chemical composition of exudates". Physiology & Behavior. 67 (4): 539–49. doi:10.1016/S0031-9384(99)00114-6. PMID 10549891. S2CID 21368454.
- ^ Ananth D (May 2000). "Musth in elephants". Zoos' Print Journal. 15 (5): 259–62. doi:10.11609/jott.zpj.14.4.259-62.
- ^ Williams NH, Whitten WM (June 1983). "Orchid Floral Fragrances and Male Euglossine Bees: Methods and Advances in the Last Sesquidecade". Biological Bulletin. 164 (3): 355–95. doi:10.2307/1541248. JSTOR 1541248. Archived from the original on 5 June 2020. Retrieved 10 November 2021.
- ^ Būda V, Mozūraitis R, Kutra J, Borg-Karlson AK (July 2012). "p-Cresol: a sex pheromone component identified from the estrous urine of mares". Journal of Chemical Ecology. 38 (7): 811–3. doi:10.1007/s10886-012-0138-2. PMID 22592336. S2CID 14558317.