Hexanitroethane

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Hexanitroethane
File:Hexanitroethane.png
File:Hexanitroethane-3D-vdW.png
Names
Preferred IUPAC name
Hexanitroethane
Identifiers
3D model (JSmol)
ChemSpider
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EC Number
  • 213-042-1
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  • InChI=1S/C2N6O12/c9-3(10)1(4(11)12,5(13)14)2(6(15)16,7(17)18)8(19)20 checkY
    Key: CCAKQXWHJIKAST-UHFFFAOYSA-N checkY
  • InChI=1/C2N6O12/c9-3(10)1(4(11)12,5(13)14)2(6(15)16,7(17)18)8(19)20
    Key: CCAKQXWHJIKAST-UHFFFAOYAX
  • C(C([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-])([N+](=O)[O-])([N+](=O)[O-])[N+](=O)[O-]
Properties
C2N6O12
Molar mass 300.0544
Melting point 135 °C (275 °F; 408 K)
Related compounds
Related compounds
Nitroethane
Tetranitromethane
Trinitromethane
Hexanitrobenzene
Octanitrocubane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hexanitroethane (HNE) is an organic compound with chemical formula C2N6O12 or (O2N)3C-C(NO2)3. It is a solid matter with a melting point of 135 °C.

Hexanitroethane is used in some pyrotechnic compositions as a nitrogen-rich oxidizer, e.g. in some decoy flare compositions and some propellants. Like hexanitrobenzene, HNE has been investigated as a gas source for explosively pumped gas dynamic lasers.[citation needed]

A composition of HNE as oxidizer with boron as fuel is being investigated as a new explosive.[1]

Preparation

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The first synthesis was described by Wilhelm Will in 1914, using the reaction between the potassium salt of tetranitroethane with nitric acid.[2]

C2(NO2)4K2 + 4 HNO3 → C2(NO2)6 + 2 KNO3 + 2 H2O

A practicable method for industrial use starts with furfural,[3] which first undergoes oxidative ring-opening by bromine to mucobromic acid.[4] In the following step, mucobromic acid is reacted with potassium nitrite at just below room temperature to form the dipotassium salt of 2,3,3-trinitropropanal. The final product is obtained by nitration with nitric acid and sulfuric acid at −60 °C.

File:Hexanitroethane synthesis.svg

Properties

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The thermal decomposition of hexanitroethane has been detected at 60 °C upwards in both the solid and solution phases.[5] Above 140 °C, this can occur explosively.[6] The decomposition is first order and is significantly faster in solution than in the solid. For the solid, the following reaction can be formulated:[5]

C2(NO2)6 → 3 NO2 + NO + N2O + 2 CO2

For the decomposition in solution, tetranitroethylene is first formed and can be trapped and detected as a Diels–Alder adduct, for example with anthracene or cyclopentadiene.[7][8]

File:Hexanitroethane reactions01.svg

References

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  1. ^ Compatibility Testing of Hexanitroethane with Boron Archived September 30, 2007, at the Wayback Machine
  2. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ US 3101379, "Synthesis of hexanitroethane", issued Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value). 
  4. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
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Further reading

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  • Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
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