Trimethylarsine
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| Names | |||
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| Preferred IUPAC name
Trimethylarsane | |||
Other names
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| Identifiers | |||
3D model (JSmol) |
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| 1730780 | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.008.925 | ||
| EC Number |
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| 141657 | |||
| MeSH | Trimethylarsine | ||
PubChem CID |
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| RTECS number |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C3H9As | |||
| Molar mass | 120.027 g·mol−1 | ||
| Appearance | Colourless liquid | ||
| Density | 1.124 g cm−3 | ||
| Melting point | −87.3 °C (−125.1 °F; 185.8 K) | ||
| Boiling point | 56 °C (133 °F; 329 K) | ||
| Slightly soluble | |||
| Solubility in other solvents | organic solvents | ||
| Structure | |||
| Trigonal pyramidal | |||
| 0.86 D | |||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Flammable | ||
| GHS labelling: | |||
| Danger | |||
| H301, H331, H410 | |||
| Flash point | −25 °C (−13 °F; 248 K) | ||
| Safety data sheet (SDS) | External MSDS | ||
| Related compounds | |||
Related compounds |
Cacodylic acid Triphenylarsine Pentamethylarsenic Trimethylphosphine Trimethylamine | ||
| Supplementary data page | |||
| Trimethylarsine (data page) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Trimethylarsine (abbreviated TMA or TMAs) is the chemical compound with the formula (CH3)3As, commonly abbreviated AsMe3 or TMAs. This organic derivative of arsine has been used as a source of arsenic in microelectronics industry, a building block to other organoarsenic compounds, and serves as a ligand in coordination chemistry. It has distinct "garlic"-like smell. Trimethylarsine had been discovered as early as 1854.