Trimethyl phosphate
| Names | |
|---|---|
| Preferred IUPAC name
Trimethyl phosphate | |
| Other names
Phosphoric acid trimethyl ester
Methyl phosphate, tribasic Trimethoxyphosphine oxide Trimethyl orthophosphate fraction | |
| Identifiers | |
3D model (JSmol)
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| Abbreviations | TMP |
| 1071731 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
| 49926 | |
PubChem CID
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| RTECS number |
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| (CH3O)3PO | |
| Molar mass | 140.08 |
| Appearance | Colorless liquid |
| Melting point | −46 °C (−51 °F; 227 K) |
| Boiling point | 197 °C (387 °F; 470 K) |
| good | |
| Hazards | |
| GHS labelling: | |
| GHS05: CorrosiveGHS07: Exclamation markGHS08: Health hazard | |
| Danger | |
| H302, H315, H318, H319, H340, H350, H351, H361, H373 | |
| P201, P202, P260, P264, P270, P280, P281, P301+P312, P302+P352, P305+P351+P338, P308+P313, P310, P314, P321, P330, P332+P313, P337+P313, P362, P405, P501 | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Trimethyl phosphate is the trimethyl ester of phosphoric acid. It is a colourless, nonvolatile liquid. It has some specialized uses in the production of other compounds.[1]
Production
[edit | edit source]Trimethyl phosphate is prepared by treating phosphorus oxychloride with methanol in the presence of an amine base:
- POCl3 + 3 CH3OH + 3 R3N → PO(OCH3)3 + 3 R3NH+Cl−
It is a tetrahedral molecule that is a weakly polar solvent.
Applications
[edit | edit source]Trimethyl phosphate is a mild methylating agent, useful for dimethylation of anilines and related heterocyclic compounds.[2] The method is complementary to the traditional Eschweiler-Clarke reaction in cases where formaldehyde engages in side reactions.
Trimethyl phosphate is used as a solvent for aromatic halogenations and nitrations as required for the preparation of pesticides and pharmaceuticals.
Other applications
[edit | edit source]It is used as a color inhibitor for fibers (e.g. polyester) and other polymers. Trimethyl phosphate is used as a simulant for chemical weapon nerve agents.[citation needed]
Safety considerations
[edit | edit source]With an LD50 of 2g/kg for rats, trimethylphosphate is expected to have low acute toxicity.[3]
References
[edit | edit source]- ^ D. E. C. Corbridge "Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology" 5th Edition Elsevier: Amsterdam 1995. Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)..
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).; Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)..
- ^ J. Svara, N. Weferling, T. Hofmann "Phosphorus Compounds, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2006. Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).