Chemistry:HHTDD
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Names | |
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Preferred IUPAC name
1,3,4,5,7,8-Hexanitrooctahydrodiimidazo[4,5-b:4′,5′-e]pyrazine-2,6(1H,3H)-dione | |
Other names
Hexanitrohexaazatricyclododecanedione
DTNGU Naza/Namsorguyl/uryl HnHaza/amTcDglcDuryl | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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Properties | |
C6H4N12O14 | |
Molar mass | 468.168 g·mol−1 |
Explosive data | |
Detonation velocity | 9700 m/s |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Tracking categories (test):
HHTDD (hexanitrohexaazatricyclododecanedione) 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.[1]
See also
- TNGU
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 4,4’-Dinitro-3,3’-diazenofuroxan (DDF)
- Heptanitrocubane
- Octanitrocubane
- RE factor
References
- ↑ Vedachalam, Murugappa; Ramakrishnan, Vayalakkavoor T.; Boyer, Joseph H.; Dagley, Ian J.; Nelson, Keith A.; Adolph, Horst G.; Gilardi, Richard; George, Clifford et al. (1991). "Facile synthesis and nitration of cis-syn-cis-2,6-dioxodecahydro-1H,5H-diimidazo[4,5-b:4',5'-e]pyrazine". The Journal of Organic Chemistry 56 (10): 3413–3419. doi:10.1021/jo00010a043.
![]() | Original source: https://en.wikipedia.org/wiki/HHTDD.
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