Methyldichlorophosphine
Methyldichlorophosphine (alternatively known as dichloro(methyl)phosphane and methyl phosphonous dichloride) is an organophosphorus compound with the chemical formula CH3PCl2. It is a colorless, corrosive, flammable, and highly reactive liquid with a pungent odor.
![]() | |
| Names | |
|---|---|
| Preferred IUPAC name
Methylphosphonous dichloride | |
| Other names
Methyl phosphonous dichloride, Dichloromethylphosphine | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider | |
| EC Number |
|
PubChem CID |
|
| UN number | 2845 |
| |
| |
| Properties | |
| CH3Cl2P | |
| Molar mass | 116.91 g·mol−1 |
| Appearance | Colorless liquid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Preparation
Methyldichlorophosphine is produced by alkylation of phosphorus trichloride with methyl iodide followed by reduction of the resulting phosphonium salt with iron powder: [1] The compound is an intermediate for the synthesis of other chemicals for instance dimethylphenylphosphine:
- CH3I + PCl3 + AlCl3 → [CH3PCl3]+AlCl3I−
- [CH3PCl3]+AlCl3I− + Fe → CH3PCl2 + FeClI + AlCl3
Uses
Methyldichlorophosphine belongs to the group of halophosphines, some of which are used as intermediates in the production of plant protection agents, stabilizers for plastics, and catalysts. It is a precursor of the herbicide Glufosinate. It is also used in the production of flameproofing compounds.[2]
Safety
It is also toxic if inhaled, can cause burns upon contact with the skin and eyes, and releases fumes of hydrochloric acid in moist environments.[3]
References
- Robert Engel, JaimeLee Iolani Cohen (2004). Synthesis of Carbon–Phosphorus Bonds. CRC. ISBN 0-8493-1617-0.
{{cite book}}: CS1 maint: uses authors parameter (link) - "Phosphorus Compounds, Organic", Ullmann's Encyclopedia of Industrial Chemistry (7th ed.), 2007, doi:10.1002/14356007.a19_545.pub2
- Pubchem. "Dichloro(methyl)phosphane". pubchem.ncbi.nlm.nih.gov. Retrieved 19 April 2018.
