Dimethyltelluride

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Dimethyltelluride
Image:Dimethyltelluride.png
Systematic name Dimethyltelluride
Appearance Pale yellow, very strong smell
Chemical formula (CH3)2Te
Molar mass 157.68 g/mol
Density x.xxx g/cm³
Melting point -10ºC
Boiling point 82ºC
CAS number [593-80-6]
SMILES xxxxx
Disclaimer and references

Dimethyltelluride is an organotelluride compound, formula (CH3)2Te, also known by the abbreviation DMTe.

This was the first material used to grow epitaxial cadmium telluride and mercury cadmium telluride using metalorganic vapour phase epitaxy.[1][2] CAS registry number [593-80-6].

Dimethyltelluride as a product of microbial metabolism was first discovered in 1939.[3] Dimethyltelluride is produced by some fungi and bacteria (Penicillium brevicaule, P. chrysogenum, and P. notatum and the bacterium Pseudomonas fluorescens).[4]

It is highly toxic to humans. It is produced by the body when tellurium or one of its compounds are ingested. It is noticeable by its garlic-like smell. Anyone who has been working with or exposed to tellurium and exhibits this garlic-like smell on the breath, sweat or in the urine should remove themselves from the area. Tellurium is known to be toxic.[5]

[edit] See also

[edit] References

  1. ^ J. Tunnicliffe, S. J. C. Irvine, O. D. Dosser, J. B. Mullin (1984). "A new MOVPE technique for the growth of highly uniform CMT". J. Cryst. Growth. 68 (1): 245-253. DOI:10.1016/0277-5387(95)00249-X. 
  2. ^ H. B. Singh, N. Sudha (1996). "Organotellurium precursors for metal organic chemical vapour deposition (MOCVD) of mercury cadmium telluride (MCT)". Polyhedron 15 (5-6): 745-763. DOI:10.1016/0277-5387(95)00249-X. 
  3. ^ M. L. Bird, F. Challenger (1939). "Formation of organometalloidal and similar compounds by microorganisms. VII. Dimethyl telluride". Journal of the Chemical Society 163-168: 299-305. DOI:10.1039/JR9390000163. 
  4. ^ R. S. T. Basnayake, J. H. Bius, O. M. Akpolat, T. G. Chasteen (1939). "Production of dimethyl telluride and elemental tellurium by bacteria amended with tellurite or tellurate". Applied Organometallic Chemistry 15 (6): 499 - 510. DOI:10.1002/aoc.186. 
  5. ^ T. G. Chasteen, R. Bentley (2003). "Biomethylation of Selenium and Tellurium: Microorganisms and Plants". Chemical Reviews 103 (1): 1-26. DOI:10.1021/cr010210+. 
  • Vacuum ultraviolet absorption spectra of dimethylsulfide, dimethylselenide, and dimethyltelluride, J. D. Scott, G. C. Causley, and B. R. Russell, The Journal of Chemical Physics, Vol. 59, Iss. 12, pp. 6577-6586 (1973) DOI:10.1063/1.1680037
  • M. M. Gharieb, M. Kierans, G. M. Gadd (1999). "Transformation and tolerance of tellurite by filamentous fungi: accumulation, reduction, and volatilization". Mycological Research 103: 299-305. DOI:10.1017/S0953756298007102. 

[edit] External links

  • Epichem (Commercial supplier datasheet)