Trinitroethylorthocarbonate
Names
Preferred IUPAC name
1,1,1-Trinitro-2-[tris(2,2,2-trinitroethoxy)methoxy]ethane
Other names
  • TNEOC
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C9H8N12O28/c22-10(23)5(11(24)25,12(26)27)1-46-9(47-2-6(13(28)29,14(30)31)15(32)33,48-3-7(16(34)35,17(36)37)18(38)39)49-4-8(19(40)41,20(42)43)21(44)45/h1-4H2
    Key: JPTHXHQVODRICI-UHFFFAOYSA-N
  • C(C([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-])OC(OCC([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-])(OCC([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-])OCC([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-]
Properties
C9H8N12O28
Molar mass 732.219 g·mol−1
Appearance Colorless crystals
Melting point 161 °C (322 °F; 434 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Trinitroethylorthocarbonate also known as TNEOC is an oxidizer with excellent chemical stability. Its explosion point is 238 °C, and it begins to be decomposed at 200 °C. Its explosion heat is 5.797 J/g and specific volume is 694 L/kg.[1] Its structure is closely related to that of trinitroethylorthoformate (TNEOF). Both are highly explosive and very shock-sensitive, and may be dissolved in nitroalkanes to reduce their shock-sensitivity.[1]

Synthesis

Trinitroethanol reacts with carbon tetrachloride under a catalyst of FeCl3.

References

  1. 1 2 Liu, Jiping (2015). Liquid Explosives. Springer. pp. 5, 6, 8, 136, 309. ISBN 9783662458471. Retrieved 26 March 2016.


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