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| Names | |
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| Systematic IUPAC name
Trimethylstibane[1] | |
| Identifiers | |
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3D model (JSmol) |
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| ChemSpider |
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| ECHA InfoCard | 100.008.933 
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| EC Number |
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| MeSH | trimethylantimony |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C 3SbH 9 | |
| Molar mass | 166.86 g mol−1 |
| Appearance | Colourless liquid |
| Density | 1.523 g cm−3 (at 15°C) |
| Melting point | −62 °C (−80 °F; 211 K) |
| Boiling point | 81 °C (178 °F; 354 K) |
| Thermochemistry | |
Std enthalpy of |
24-26 kJ mol−1 |
Std enthalpy of |
-2.896--2.946 MJ mol−1 |
| 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 [77 °F], 100 kPa). | |
Trimethylstibine is an organoantimony compound with the formula Sb(CH3)3. It is a colorless pyrophoric and toxic liquid.[2] It is synthesized by treatment of antimony trichloride and methyl Grignard reagent.[3] It is produced by anaerobic bacteria in antimony-rich soils.[4] In contrast to trimethylphosphine, trimethylstibine is a weaker Lewis base. It is used in the production of some III-V semiconductors.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
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| Antimonides |
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| Sb(III) |
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| Sb(III,V) |
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| Sb(V) |
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