Names | |
---|---|
Other names Methylphosphane | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChemSpider | |
PubChem CID | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | CH3PH2 |
Molar mass | 48.02 |
Appearance | colorless gas |
Boiling point | −17.1 °C (1.2 °F; 256.0 K) |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | toxic |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
Methylphosphine is the simplest organophosphorus compound with the formula CH3PH2, often written MePH2. It is a malodorous gas that condenses to a colorless liquid. It can be produced by methylation of phosphide salts:
- KPH2 + MeI → MePH2 + KI
Reactions
The compound exhibits the properties characteristic of a primary phosphine, i.e., a compound of the type RPH2. It can be oxidized to methylphosphonous acid:
- MePH2 + O2 → MeP(H)O2H
It protonates to give the phosphonium ion:
- MePH2 + H → MePH3
With strong bases, it can be deprotonated to give methylphosphide derivatives:
- MePH2 + KOH → K + H2O
References
- W. L. Jolly “Methylphosphine” Inorganic Syntheses 1968, volume 11, p. 124. doi:10.1002/9780470132425.ch25