Trimethyl phosphate
Names | |
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Preferred IUPAC name
Trimethyl phosphate | |
Other names | |
Identifiers | |
512-56-1 | |
3D model (Jmol) | Interactive image |
Abbreviations | TMP |
ChEBI | CHEBI:46324 |
ChemSpider | 10101 |
ECHA InfoCard | 100.007.405 |
PubChem | 10541 |
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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 | |
EU classification (DSD) |
Harmful substances or preparations (Xn) |
R-phrases | R22,R36/37/38 |
S-phrases | S36/37,S45 |
NFPA 704 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
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
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
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
It is used as a color inhibitor for fibers (e.g. polyester) and other polymers.
Safety considerations
With an LD50 of 2g/kg for rats, trimethylphosphate is expected to have low acute toxicity.[3]
References
- ↑ D. E. C. Corbridge "Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology" 5th Edition Elsevier: Amsterdam 1995. ISBN 0-444-89307-5.
- ↑ William A. Sheppard (1973). "m-Trifluoromethyl-N,N-dimethylaniline". Org. Synth.; Coll. Vol., 5, p. 1085
- ↑ J. Svara, N. Weferling, T. Hofmann "Phosphorus Compounds, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2006. doi:10.1002/14356007.a19_545.pub2