Names | |
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Systematic IUPAC name Trimethylstibane | |
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CAS Number | |
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ChemSpider | |
ECHA InfoCard | 100.008.933 |
EC Number |
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MeSH | trimethylantimony |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
Chemical formula | C 3SbH 9 |
Molar mass | 166.86 g mol |
Appearance | Colourless liquid |
Density | 1.523 g cm (at 15°C) |
Melting point | −62 °C (−80 °F; 211 K) |
Boiling point | 81 °C (178 °F; 354 K) |
Thermochemistry | |
Std enthalpy of formation (ΔfH298) |
24-26 kJ mol |
Std enthalpy of combustion (ΔcH298) |
-2.896--2.946 MJ mol |
Related compounds | |
Related compounds | Trimethylamine Trimethylphosphine Trimethylarsine Triphenylstibine Trimethylbismuth |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
Trimethylstibine is an organoantimony compound with the formula Sb(CH3)3. It is a colorless pyrophoric and toxic liquid. It is synthesized by treatment of antimony trichloride and methyl Grignard reagent. It is produced by anaerobic bacteria in antimony-rich soils. In contrast to trimethylphosphine, trimethylstibine is a weaker Lewis base. It is used in the production of some III-V semiconductors.
References
- "trimethylantimony - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information. 26 March 2005. Descriptors Computed from Structure. Retrieved 25 September 2011.
- Wiberg, Nils; Wiberg, Egon; Holleman, A. F. (2001), Inorganic Chemistry, Academic Press, p. 766, ISBN 0-12-352651-5, retrieved 2009-07-17
- Sabina C. Grund, Kunibert Hanusch, Hans J. Breunig, Hans Uwe Wolf "Antimony and Antimony Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2006, Wiley-VCH, Weinheim. doi:10.1002/14356007.a03_055.pub2
- Craig, P. J. (2003), Organometallic Compounds in the Environment (2 ed.), Wiley and Sons, p. 295, ISBN 978-0-471-89993-8, retrieved 2009-07-17
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Antimony compounds | |||
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Sb(III) |
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Sb(III,V) | |||
Sb(V) |
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