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HHTDD

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HHTDD
Names
IUPAC name 2,6-dioxo-1,3,4,5,7,8-hexanitrodecahydro-1H,5H-diimidazopyrazine
Identifiers
3D model (JSmol)
ChemSpider
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H4N12O14/c19-5-9(15(25)26)1-2(10(5)16(27)28)8(14(23)24)4-3(7(1)13(21)22)11(17(29)30)6(20)12(4)18(31)32/h1-4HKey: ZFBXJPJQJKATGM-UHFFFAOYSA-N
  • InChI=1/C6H4N12O14/c19-5-9(15(25)26)1-2(10(5)16(27)28)8(14(23)24)​4-3(7(1)13(21)22)11(17(29)30)6(20)12(4)18(31)32/h1-4HKey: ZFBXJPJQJKATGM-UHFFFAOYAE
SMILES
  • O=C2N((=O)=O)C3C(N2(=O)=O)N((=O)=O)C1C(N3(=O)=O)N((=O)=O)C(=O)N1(=O)=O
Properties
Chemical formula C6H4N12O14
Molar mass 468.168
Explosive data
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

HHTDD is a powerful but moisture sensitive explosive compound. It is essentially an open analogue of the cyclic nitroamine cage compounds such as CL-20. While it is highly explosive, with a velocity of detonation even higher than that of CL-20, HHTDD readily decomposes in the presence of even trace amounts of water, making it unsuitable for any practical applications.

See also

References

  1. Vedachalam, Murugappa; Ramakrishnan, Vayalakkavoor T.; Boyer, Joseph H.; Dagley, Ian J.; Nelson, Keith A.; Adolph, Horst G.; Gilardi, Richard; George, Clifford; Flippen-Anderson, Judith L. (1991). "Facile synthesis and nitration of cis-syn-cis-2,6-dioxodecahydro-1H,5H-diimidazopyrazine". The Journal of Organic Chemistry. 56 (10): 3413–3419. doi:10.1021/jo00010a043.


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