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Trinitroethylorthoformate

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Trinitroethylorthoformate
Names
Systematic IUPAC name
Tris(2,2,2-trinitroethyl)orthoformate
Other names
  • TNEOF
Identifiers
3D model (JSmol)
  • InChI=1S/C7H7N9O21/c17-8(18)5(9(19)20,10(21)22)1-35-4(36-2-6(11(23)24,12(25)26)13(27)28)37-3-7(14(29)30,15(31)32)16(33)34/h4H,1-3H2
  • C([N+]([O-])=O)([N+]([O-])=O)([N+]([O-])=O)COC(OCC([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O)OCC([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O
Properties
C7H7N9O21
Molar mass 553.174
Appearance Colorless crystals
Melting point 128 °C (262 °F; 401 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Trinitroethylorthoformate also known as TNEOF is an explosive with excellent chemical stability. It does not have hygroscopicity, does not dissolve in water, and does not react with acids. It decomposes in aqueous sodium hydroxide solution to release formaldehyde odor. The explosion point of TNEOF is 229 ° C, though it begins to decompose at 190 ° C. Its explosion heat is 6.3076 J/g and specific volume is 682 L/kg

Synthesis

Trinitroethanol is reacted with chloroform under a catalyst of FeCl3.

File:TNEOFSynthesis.png

References

1. Liu, Jiping (2015). Liquid Explosives. Springer. p.8. ISBN 9783662458464.