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{{Chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 434654119
| ImageFile = Dimethyl-telluride-2D.svg
| ImageFile_Ref = {{chemboximage|correct|??}}
| ImageSize = 244
| ImageName = Skeletal formula of dimethyl telluride with all implicit hydrogens shown
| ImageFile1 = Dimethyl-telluride-3D-balls.png
| ImageFile1_Ref = {{chemboximage|correct|??}}
|
| ImageName1 = Ball and stick model of dimethyl telluride
| PIN = (Methyltellanyl)methane
| OtherNames = Dimethyltellurium<ref name = "dimethyl telluride (CHEBI:4613)">{{Cite web|title = dimethyl telluride (CHEBI:4613)|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=4613|work = Chemical Entities of Biological Interest (ChEBI)|publisher = European Bioinformatics Institute|at = IUPAC Names|accessdate = 19 September 2011|___location = UK|date = 25 September 2006}}</ref> (additive)<br>Dimethyltellane
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 593-80-6
| PubChem = 68977
| ChemSpiderID = 62199
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| EINECS = 209-809-5
| KEGG = C02677
| KEGG_Ref = {{keggcite|changed|kegg}}
| MeSHName = dimethyltelluride
| ChEBI = 4613
| ChEBI_Ref = {{ebicite|changed|EBI}}
| Beilstein = 1696849
| Gmelin = 1480
|
| StdInChI = 1S/C2H6Te/c1-3-2/h1-2H3
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = YMUZFVVKDBZHGP-UHFFFAOYSA-N
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
}}
|Section2={{Chembox Properties
| C=2 | H=6 | Te=1
| Appearance = Pale yellow, translucent liquid
| Odor = Garlic
| MeltingPtC = -10
| BoilingPtC = 82
}}
|Section3={{Chembox Related
| OtherFunction_label = [[chalcogen]]ides
| OtherFunction = [[Dimethyl oxide]] (dimethyl ether)<br />
[[Dimethyl sulfide]]<br />[[Dimethyl selenide]]
| OtherCompounds = [[Hydrogen telluride]]<br />
[[Diphenyl telluride]]
}}
}}
'''Dimethyl telluride''' is an [[organotelluride]] compound, formula ([[methyl|CH<sub>3</sub>]])<sub>2</sub>[[tellurium|Te]], also known by the abbreviation DMTe.
This was the first material used to grow [[epitaxy|epitaxial]] [[cadmium telluride]] and [[HgCdTe|mercury cadmium telluride]] using [[MOVPE|metalorganic vapour phase epitaxy]].<ref>{{ cite journal |author1=Tunnicliffe, J. |author2=Irvine, S. J. C. |author3=Dosser, O. D. |author4=Mullin, J. B. | title = A new MOVPE technique for the growth of highly uniform CMT | journal = Journal of Crystal Growth | year = 1984 | volume = 68 | issue = 1 | pages = 245–253 | doi = 10.1016/0022-0248(84)90423-8 | bibcode = 1984JCrGr..68..245T }}</ref><ref>{{ cite journal |author1=Singh, H. B. |author2=Sudha, N. | title = Organotellurium precursors for metal organic chemical vapour deposition (MOCVD) of mercury cadmium telluride (MCT) | journal = [[Polyhedron (journal)|Polyhedron]] | year = 1996 | volume = 15 | issue = 5–6 | pages = 745–763 | doi = 10.1016/0277-5387(95)00249-X }}</ref>
Dimethyl telluride as a product of microbial metabolism was first discovered in 1939.<ref>{{ cite journal |author1=Bird, M. L. |author2=Challenger, F. | title = Formation of organometalloidal and similar compounds by microorganisms. VII. Dimethyl telluride | journal = [[Journal of the Chemical Society]] | year = 1939 | volume = 1939 | pages = 163–168 | doi = 10.1039/JR9390000163}}</ref>
It is produced by some fungi and bacteria (''[[Penicillium brevicaule]]'', [[Penicillium chrysogenum|''P. chrysogenum'']], and ''[[Penicillium notatum|P. notatum]]'' and the bacterium ''[[Pseudomonas fluorescens]]'').<ref>{{ cite journal |author1=Basnayake, R. S. T. |author2=Bius, J. H. |author3=Akpolat, O. M. |author4=Chasteen, T. G. | title = Production of dimethyl telluride and elemental tellurium by bacteria amended with tellurite or tellurate | journal = [[Applied Organometallic Chemistry]] | year = 2001 | volume = 15 | issue = 6 | pages = 499–510 | doi = 10.1002/aoc.186 | doi-access = free }}</ref>
The toxicity of DMTe is unclear. It is produced by the body when [[tellurium]] or one of its compounds are ingested. It is noticeable by the garlic smelling breath it gives those exposed, similar to the effect of [[Dimethyl sulfoxide|DMSO]]. Tellurium is known to be [[toxic]].<ref>{{ cite journal |author1=Chasteen, T. G. |author2=Bentley, R. | title = Biomethylation of Selenium and Tellurium: Microorganisms and Plants | journal = [[Chemical Reviews]] | year = 2003 | volume = 103 | issue = 1 | pages = 1–26 | doi = 10.1021/cr010210+ | pmid = 12517179 }}</ref>
==References==
{{Reflist}}
{{refbegin}}
* {{ cite journal |author1=Liu, M. |author2=Turner, R. J. |author3=Winstone, T. L. |author4=Saetre, A. |author5=Dyllick-Brenzinger, M. |author6=Jickling, G. |author7=Tari, L. W. |author8=Weiner, J. H. |author9=Taylor, D. E. | title = ''Escherichia coli'' TehB Requires S-Adenosylmethionine as a Cofactor to Mediate Tellurite Resistance | journal = Journal of Bacteriology | year = 2000 | volume = 182 | issue = 22 | pages = 6509–6513 | doi = 10.1128/JB.182.22.6509-6513.2000 | pmid = 11053398 | pmc = 94800 | url = }}
* {{ cite journal | title = Vacuum ultraviolet absorption spectra of dimethyl sulfide, dimethyl selenide, and dimethyl telluride |author1=Scott, J. D. |author2=Causley, G. C. |author3=Russell, B. R. | journal = The Journal of Chemical Physics | volume = 59 | issue = 12 | pages = 6577–6586 | year = 1973 | doi = 10.1063/1.1680037 |bibcode = 1973JChPh..59.6577S }}
* {{ cite journal |author1=Gharieb, M. M. |author2=Kierans, M. |author3=Gadd, G. M. |author3-link=Geoffrey Michael Gadd | title = Transformation and tolerance of tellurite by filamentous fungi: accumulation, reduction, and volatilization | journal = [[Mycological Research]] | year = 1999 | volume = 103 | issue = 3 | pages = 299–305 | doi = 10.1017/S0953756298007102 }}
{{refend}}
==External links==
*
{{tellurides}}
[[Category:Tellurides]]
[[Category:
[[Category:Foul-smelling chemicals]]
[[Category:Substances discovered in the 1930s]]
[[Category:Tellurium(II) compounds]]
[[Category:Methyl compounds]]
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