Triethyl phosphate
Skeletal formula of triethyl phosphate | |
Ball-and-stick model of triethyl phosphate | |
Names | |
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IUPAC name
Triethyl phosphate
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Other names
Ethyl phosphate; Triethylphosphate; Tris(ethyl) phosphate; Triethoxyphosphine oxide
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Identifiers | |
78-40-0 ![]() |
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Abbreviations | TEP, Et3PO4 |
ChEBI | CHEBI:45927 ![]() |
ChemSpider | 6287 ![]() |
DrugBank | DB03347 ![]() |
Jmol 3D model | Interactive image |
PubChem | 6535 |
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Properties | |
C6H15O4P | |
Molar mass | 182.15 g/mol |
Density | 1.072 g/cm3 |
Melting point | −56.5 °C (−69.7 °F; 216.7 K) |
Boiling point | 215 °C (419 °F; 488 K) |
Miscible | |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Triethyl phosphate is a chemical compound with the formula (C2H5)3PO4. It is a colorless liquid. It is the triester of ethanol and phosphoric acid and can be called "phosphoric acid, triethyl ester".
Its primary uses are as an industrial catalyst (in acetic anhydride synthesis), a polymer resin modifier, and a plasticizer (e.g. for unsaturated polyesters). In smaller scale it is used as a solvent for e.g. cellulose acetate, flame retardant, an intermediate for pesticides and other chemicals, stabilizer for peroxides, a strength agent for rubber and plastic including vinyl polymers and unsaturated polyesters, etc.[2]
Triethyl phosphate is also a common intermediate in the manufacture of pesticides.
History
It was studied for the first time by French chemist Jean Louis Lassaigne in the early 19th century.
See also
References
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- ↑ Triethylphosphate, International Programme on Chemical Safety