Trimethyl phosphate

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Trimethyl phosphate
Ball-and-stick model of trimethyl phosphate Trimethyl-phosphate-3D-balls.png
Ball-and-stick model of 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)
AbbreviationsTMP
1071731
ChEBI
ChemSpider
ECHA InfoCard 100.007.405 OOjs UI icon edit-ltr-progressive.svg
49926
PubChem CID
RTECS number
  • TC8225000
UNII
  • InChI=1S/C3H9O4P/c1-5-8(4,6-2)7-3/h1-3H3 Yes check.svgY
    Key: WVLBCYQITXONBZ-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C3H9O4P/c1-5-8(4,6-2)7-3/h1-3H3
    Key: WVLBCYQITXONBZ-UHFFFAOYAV
  • O=P(OC)(OC)OC
Properties
(CH3O)3PO
Molar mass 140.08
AppearanceColorless liquid
Melting point −46 °C (−51 °F; 227 K)
Boiling point 197 °C (387 °F; 470 K)
good
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg GHS-pictogram-silhouette.svg
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)
NFPA 704.svgHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

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]

Contents

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. Trimethyl phosphate is used as a simulant for chemical weapon nerve agents.[ citation needed ]

Safety considerations

With an LD50 of 2g/kg for rats, trimethylphosphate is expected to have low acute toxicity. [3]

References

  1. ↑ D. E. C. Corbridge "Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology" 5th Edition Elsevier: Amsterdam 1995. ISBN   0-444-89307-5.
  2. ↑ William A. Sheppard (1973). "m-Trifluoromethyl-N,N-dimethylaniline". Organic Syntheses ; Collected Volumes, vol. 5, p. 1085.
  3. ↑ 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
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