Creosol: Difference between revisions
Appearance
Content deleted Content added
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 |
Ozzie10aaaa (talk | contribs) m Cleaned up using AutoEd |
||
(26 intermediate revisions by 21 users not shown) | |||
Line 1: | Line 1: | ||
{{distinguish|cresol}} |
{{distinguish|cresol}} |
||
{{chembox |
{{chembox |
||
| verifiedrevid = |
| verifiedrevid = 448765425 |
||
|ImageFileL1=creosol.png |
| ImageFileL1=creosol.png |
||
|ImageSizeL1=100px |
| ImageSizeL1=100px |
||
|ImageFileR1= |
| ImageFileR1=Creosol ball-and-stick.png |
||
|ImageSizeR1=150px |
| ImageSizeR1=150px |
||
| |
| PIN=2-Methoxy-4-methylphenol |
||
|OtherNames=4-Methylguaiacol |
| OtherNames=4-Methylguaiacol; Valspice |
||
|Section1={{Chembox Identifiers |
|Section1={{Chembox Identifiers |
||
| |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
||
| ChemSpiderID = 21105936 |
| ChemSpiderID = 21105936 |
||
| UNII_Ref = {{fdacite|correct|FDA}} |
| UNII_Ref = {{fdacite|correct|FDA}} |
||
Line 20: | Line 20: | ||
| 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 |
||
| |
| SMILES = Oc1ccc(C)cc1OC |
||
}} |
}} |
||
|Section2={{Chembox Properties |
|Section2={{Chembox Properties |
||
| |
| Formula=C<sub>8</sub>H<sub>10</sub>O<sub>2</sub> |
||
| |
| MolarMass=138.16 g/mol |
||
| |
| 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 |
||
| |
| BoilingPtC=221 <ref name="Baird2019" /> |
||
| RefractIndex = 1.5373 (20 °C) <ref name="Baird2019" /> |
|||
| |
| 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= |
||
| |
| FlashPt= |
||
| AutoignitionPt = |
|||
| Autoignition= |
|||
}} |
}} |
||
}} |
}} |
||
'''Creosol''' is |
'''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 |
* 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: |
[[Category:Alkylphenols]] |
||
[[cs:Kreosol]] |
|||
[[pl:Kreozol]] |