Draft:Methylarsine
Submission declined on 30 March 2026 by Graeme Bartlett (talk).
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Comment: Also there are a number of invalid statements, such as arsine being a base, and the appearance muddles this with arsenic. Our Greek article suggests that it is a gas PubChem being an aggregator does not prove notability or even if it exists. Graeme Bartlett (talk) 21:21, 30 March 2026 (UTC)
| Names | |
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| IUPAC name
Methylarsane[1]
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| Properties | |
| CH3AsH2 | |
| Molar mass | 91.973 g·mol−1 |
| Appearance | Colorless gas[2] |
| Odor | Intense garlic[2] |
| Melting point | −143 °C (−225 °F; 130 K)[3] |
| Boiling point | 2 °C (36 °F; 275 K)[2][3] |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards
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Arsenic poisoning |
| Related compounds | |
Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Methylarsine is an organoarsenic compound with the formula CH3AsH2. It is a colorless highly poisonous gas with a strong garlic odor.[2][4] It is the simplest organic arsine. It is the arsenic analogue of methylamine CH3NH2 and methylphosphine CH3PH2.
Methylarsine, being a compound of arsenic, carries the risk of arsenic poisoning.[1]
Synthesis
Methylarsine can be synthesized by reacting methyl chloride with potassium dihydrogen arsenide.[3]
- CH3Cl + KAsH2 → CH3AsH2 + KCl
Methylarsine can also be synthesized by reduction of methylarsonic acid by sodium borohydride.[5] It can also be prepared by reduction of methylarsine dichloride (CH3AsCl2) by lithium aluminium hydride.[2]
Occurrence
Methylarsine is found in some marine biological systems. It arises as a product of volatilization of methylarsonic acid by microbial activity in the environment.[6][4]
Reactions
Methylarsine reacts with potassium metal in liquid ammonia to give potassium hydrogen methylarsenide (CH3AsH−K+).[3]
- 2 CH3AsH2 + 2 K → 2 CH3AsHK + H2
References
- ^ a b "Methylarsine". pubchem.ncbi.nlm.nih.gov. Retrieved 30 March 2026.
- ^ a b c d e https://www.sciencedirect.com/science/article/abs/pii/S0022286020303628
- ^ a b c d https://pubs.acs.org/doi/abs/10.1021/ja01289a084
- ^ a b https://www.sciencedirect.com/science/article/abs/pii/S0003267099008922
- ^ https://link.springer.com/article/10.1007/s00216-011-5503-4
- ^ https://www.sciencedirect.com/science/article/abs/pii/S0025326X20308110
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