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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
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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
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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).
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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,[1] 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.