Triethyl phosphate
{{chembox
| Name = Triethyl phosphate
| ImageFile_Ref = {{chemboximage|correct|??}}
| ImageFile = Triethyl phosphate.png
| ImageSize = 180px
| ImageAlt = Skeletal formula of triethyl phosphate
| ImageFile1 = Triethyl-phosphate-3D-balls.png
| ImageSize1 = 180px
| ImageAlt1 = Ball-and-stick model of triethyl phosphate
| PIN = Triethyl phosphate
| OtherNames = Phosphoric acid triethyl ester
Phosphoric ester (archaic)
Flame retardant TEP{{cite web|url=https://pubchem.ncbi.nih.gov/compound/6535|title=Triethyl phosphate|access-date=2022-12-02|website=pubchem.ncbi.nih.gov}}
Tris(ethyl) phosphate
Triethoxyphosphine oxide
Ethyl phosphate (neutral)
|Section1={{Chembox Identifiers
| Abbreviations = TEP, Et3PO4
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6287
| InChI = 1/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3
| InChIKey = DQWPFSLDHJDLRL-UHFFFAOYAA
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C6H15O4P/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = DQWPFSLDHJDLRL-UHFFFAOYSA-N
| CASNo = 78-40-0
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = QIH4K96K7J
| PubChem = 6535
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB03347
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 45927
| SMILES = O=P(OCC)(OCC)OCC
}}
|Section2={{Chembox Properties
| Formula = C6H15O4P
| MolarMass = 182.15 g/mol
| Density = 1.072 g/cm3
| MeltingPtC =-56.5
| BoilingPtC = 215
| Solubility = Miscible
| MagSus = −125.3·10−6 cm3/mol
}}
|Section3={{Chembox Hazards
| MainHazards =
| NFPA-H = 2
| NFPA-F = 1
| NFPA-R = 0
| NFPA-S =
| FlashPtC = 107
| ExternalSDS = https://assets.thermofisher.com/DirectWebViewer/private/document.aspx?prd=ALFAA40001~~PDF~~MTR~~AGHS~~EN~~2024-03-27%2004:53:15~~Triethyl%20phosphate~~
}}
}}
Triethyl phosphate is an organic chemical compound with the formula (C2H5)3PO4 or OP(OEt)3. 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.[http://www.inchem.org/documents/sids/sids/78400.pdf Triethylphosphate], International Programme on Chemical Safety
History
It was studied for the first time by French chemist Jean Louis Lassaigne in the early 19th century.
See also
References
{{Reflist}}
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