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Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report errors or [[use
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{{distinguish|cresol}}
{{distinguish|cresol}}
{{chembox
{{chembox
| verifiedrevid = 415896086
| verifiedrevid = 448765425
|ImageFileL1=creosol.png
| ImageFileL1=creosol.png
|ImageSizeL1=100px
| ImageSizeL1=100px
|ImageFileR1=creosolm.gif
| ImageFileR1=Creosol ball-and-stick.png
|ImageSizeR1=150px
| ImageSizeR1=150px
|IUPACName=2-Methoxy-4-methylphenol
| PIN=2-Methoxy-4-methylphenol
|OtherNames=4-Methylguaiacol
| OtherNames=4-Methylguaiacol; Valspice
|Section1={{Chembox Identifiers
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 21105936
| ChemSpiderID = 21105936
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII_Ref = {{fdacite|correct|FDA}}
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| StdInChIKey = PETRWTHZSKVLRE-UHFFFAOYSA-N
| StdInChIKey = PETRWTHZSKVLRE-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo=93-51-6
| CASNo=93-51-6
| PubChem=7144
| PubChem=7144
| SMILES = Oc1ccc(C)cc1OC
| SMILES = Oc1ccc(C)cc1OC
}}
}}
|Section2={{Chembox Properties
|Section2={{Chembox Properties
| Formula=C<sub>8</sub>H<sub>10</sub>O<sub>2</sub>
| Formula=C<sub>8</sub>H<sub>10</sub>O<sub>2</sub>
| MolarMass=138.16 g/mol
| MolarMass=138.16 g/mol
| Appearance=Colorless to yellowish aromatic liquid
| Appearance=Colorless to yellowish aromatic liquid
| Density=1.0966 g/cm<sup>3</sup> (20 °C) <ref name="Baird2019">{{cite journal |last1=Baird |first1=Zachariah Steven |last2=Uusi-Kyyny |first2=Petri |last3=Pokki |first3=Juha-Pekka |last4=Pedegert |first4=Emilie |last5=Alopaeus |first5=Ville |title=Vapor Pressures, Densities, and PC-SAFT Parameters for 11 Bio-compounds |journal=International Journal of Thermophysics |date=6 Nov 2019 |volume=40 |issue=11 |page=102 |doi=10.1007/s10765-019-2570-9|bibcode=2019IJT....40..102B |doi-access=free }}</ref>
| Density=1.092 g/cm<sup>3</sup>
| MeltingPtC=5.5
| MeltingPtC=5.5
| BoilingPtC=220
| BoilingPtC=221 <ref name="Baird2019" />
| RefractIndex = 1.5373 (20 °C) <ref name="Baird2019" />
| Solubility=Slightly soluble
| Solubility=Slightly soluble
| SolubleOther = Miscible
| SolubleOther = Miscible
| Solvent = [[ethanol]], [[diethyl ether|ether]], [[benzene]]
| Solvent = [[ethanol]], [[diethyl ether|ether]], [[benzene]]
|
}}
}}
|Section3={{Chembox Hazards
|Section3={{Chembox Hazards
| MainHazards=
| MainHazards=
| FlashPt=
| FlashPt=
| AutoignitionPt =
| Autoignition=
}}
}}
}}
}}


'''Creosol''' is an ingredient of [[creosote]]. Compared with phenol, creosol is a less toxic disinfectant.
'''Creosol''' is a chemical compound with the molecular formula C<sub>8</sub>H<sub>10</sub>O<sub>2</sub>. It is one of the components of [[creosote]]. Compared with [[phenol]], creosol is a less toxic [[disinfectant]].


==Sources ==
== Sources ==
Sources of creosol include:
* Coal tar creosote
* [[Coal tar]] creosote
* Wood creosote
* Wood creosote
* Reduction product of [[vanillin]] using zinc powder in strong hydrochloric acid
* Reduction product of [[vanillin]] using [[zinc]] powder in strong [[hydrochloric acid]] ([[Clemmensen reduction]])
* Found as glycosides in green vanilla beans<ref>Identification of glucosides in green beans of Vanilla planifolia Andrews and kinetics of vanilla β-glucosidase, ''Food Chemistry'', Volume 85, Issue 2, April 2004, Pages 199-205</ref>
* Found as [[glycoside]]s in green [[vanilla bean]]s<ref>{{Cite journal | title = Identification of glucosides in green beans of Vanilla planifolia Andrews and kinetics of vanilla β-glucosidase | journal = Food Chemistry | volume = 85 | issue = 2 | year = 2004 | pages = 199–205 | doi = 10.1016/S0308-8146(03)00293-0 | last1 = Dignum | first1 = Mark J.W. | last2 = Van Der Heijden | first2 = Rob | last3 = Kerler | first3 = Josef | last4 = Winkel | first4 = Chris | last5 = Verpoorte | first5 = Rob}}</ref>
* It is also found in [[tequila]].<ref>Characterization of volatile compounds from ethnic Agave alcoholic beverages by gas chromatography-mass spectrometry. León-Rodríguez, A. de, Escalante-Minakata, P., Jiménez-García, M. I., Ordoñez-Acevedo, L. G., Flores Flores, J. L. and Barba de la Rosa, A. P., Food Technology and Biotechnology, 2008, Volume 46, Number 4, pages 448-455 ([http://www.cabdirect.org/abstracts/20083308167.html;jsessionid=82FF23BBEEED2B409045ED15966551B1 abstract] {{Webarchive|url=https://web.archive.org/web/20140313195245/http://www.cabdirect.org/abstracts/20083308167.html;jsessionid=82FF23BBEEED2B409045ED15966551B1 |date=2014-03-13 }})</ref>


==Reactions==
==Reactions==
Creosol reacts with hydrogen halide to give a catechol.
Creosol reacts with [[hydrogen halide]]s to give a [[catechol]].
[[Image:creosolr.gif]]
:[[Image:creosolr.gif]]


==See also==
==See also==
* [[Vanillin]], a related phenol
* [[vanillin]]


==References==
==References==
{{reflist}}
{{reflist}}

==External links==
{{commonscat-inline|Creosol}}


[[Category:Antiseptics]]
[[Category:Antiseptics]]
[[Category:Phenol ethers]]
[[Category:Phenol ethers]]
[[Category:Phenols]]
[[Category:Alkylphenols]]

[[cs:Kreosol]]
[[pl:Kreozol]]