Hexanitrohexaazaisowurtzitane

Hexanitrohexaazaisowurtzitane

Names
IUPAC name 2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane
Other names CL-20
Identifiers
CAS Number	135285-90-4 Y
3D model (Jmol)	Interactive image Interactive image
Abbreviations	CL-20, HNIW
ChEBI	CHEBI:77327 N
ChemSpider	8064994 Y 9223599 (3R,9R)-dodec Y 9594121 (3R,5S,9R,11S)- dodec Y
ECHA InfoCard	100.114.169
PubChem	9889323 11048432 (3R,9R)-dodec 11419235 (3R,5S,9R,11S)- dodec
InChI InChI=1S/C6H6N12O12/c19-13(20)7-1-2-8(14(21)22)5(7)6-9(15(23)24)3(11(1)17(27)28)4(10(6)16(25)26)12(2)18(29)30/h1-6H Y Key: NDYLCHGXSQOGMS-UHFFFAOYSA-N Y
SMILES o:n(:o)N1C2C3N(C4C(N3n(:o):o)N(C(C1N4n(:o):o)N2n(:o):o)n(:o):o)n(:o):o [O-][N+](=O)N1C2C3N(C4C(N3[N+]([O-])=O)N(C(C1N4[N+]([O-])=O)N2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O
Properties
Chemical formula	C 6N 12H 6O 12
Molar mass	438.1850 g mol−1
Density	2.044 g cm−3
Explosive data
Detonation velocity	9.38 km s−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Hexanitrohexaazaisowurtzitane /ˈhɛksɑːˈnaɪtroʊˈhɛksɑːˌæzɑːˌaɪsoʊˈvʊərtsɪteɪn/, also called HNIW and CL-20, is a nitroamine explosive with the formula C₆H₆N₁₂O₁₂. The structure of CL-20 was first proposed in 1979 by Dalian Institute of Chemical Physics.^[1] In 1980s, CL-20 was developed by the China Lake facility, primarily to be used in propellants. It has a better oxidizer-to-fuel ratio than conventional HMX or RDX. It produces 20% more energy than traditional HMX-based propellants, and is widely superior to conventional high-energy propellants and explosives.

Industrial production of CL-20 was achieved in China in 2011, and it was soon fielded in propellant of solid rockets.^[2] While most development of CL-20 has been fielded by the Thiokol Corporation, the US Navy (through ONR) has also been interested in CL-20 for use in rocket propellants, such as for missiles, as it has lower observability characteristics such as less visible smoke.^[3]

CL-20 has not yet been fielded in any production weapons system, but is undergoing testing for stability, production capabilities, and other weapons characteristics.

Synthesis

Synthesis of CL20

First, benzylamine (1) is condensed with glyoxal (2) under acidic and dehydrating conditions to yield the first intermediate compound.(3). Four benzyl groups selectively undergo hydrogenolysis using palladium on carbon and hydrogen. The amino groups are then acetylated during the same step using acetic anhydride as the solvent. (4). Finally, compound 4 is reacted with nitronium tetrafluoroborate and nitrosonium tetrafluoroborate, resulting in HNIW.^[4]

Cocrystal product with HMX

In August 2012, Onas Bolton et al. published results showing that a cocrystal of 2 parts CL-20 and 1 part HMX had similar safety properties to HMX, but with a greater firing power closer to CL-20. ^[5][6]

Cocrystal product with TNT

In August 2011, Adam Matzger and Onas Bolton published results showing that a cocrystal of CL-20 and TNT had twice the stability of CL-20—safe enough to transport, but when heated to 136 C the cocrystal may separate into liquid TNT and a crystal form of CL-20 with structural defects that is somewhat less stable than CL-20.^[7][8]

See also

• 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
• 4,4’-Dinitro-3,3’-diazenofuroxan (DDF)
• Heptanitrocubane (HNC)
• HHTDD
• Octanitrocubane (ONC)
• Iceane (Wurtzitane)
• RE factor

References

Further reading

• Bolton, Onas; Adam J. Matzger (September 12, 2011). "Improved Stability and Smart-Material Functionality Realized in an Energetic Cocrystal". Angewandte Chemie. 123 (38): 9122–9125. doi:10.1002/ange.201104164. Retrieved 8 July 2012. 
• Lowe, Derek (11 November 2011) "Things I won't work with: Hexanitrohexaazaisowurtzitane"