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Toxicity of Octahydro-1,3,5,7-Tetranitro-1,3,5,7-Tetrazocine (HMX) in Three Vertebrate Species

โœ Scribed by Mark S. Johnson; Craig A. McFarland; Matthew A. Bazar; Michael J. Quinn; Emily May LaFiandra; Larry G. Talent


Publisher
Springer
Year
2009
Tongue
English
Weight
271 KB
Volume
58
Category
Article
ISSN
0090-4341

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๐Ÿ“œ SIMILAR VOLUMES


New adducts of octahydro-1,3,5,7-tetrani
โœ W. Selig ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 1012 KB

## Abstract A new series of relatively stable adducts of octahydroโ€1,3,5,7โ€tetranitroโ€1,3,5,7โ€tetrazocine (HMX) with derivatives of pyridineโ€Nโ€oxide were prepared. In addition, relative stable new adducts of HMX were prepared with 5โ€membered, 6โ€membered, and condensedโ€ring heterocyclic compounds. M

Studies on octahydro-1,3,5,7-tetranitro-
โœ C. P. Achuthan; C. I. Jose ๐Ÿ“‚ Article ๐Ÿ“… 1990 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 403 KB

## Abstract Various methods of preparation of the different polymorphs of HMX have been evaluated. Infrared and Raman spectra have been used to differentiate the polymorphs and understand their conformational behaviour. Possible conformation of the ฮณ form has been suggested.

Synthesis of 14C-labeled octahydro-1,3,5
โœ Chi-Yu Huang; Robert A. Mah; Shane S. Que Hee ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 293 KB ๐Ÿ‘ 1 views

The \({ }^{14} \mathrm{C}\)-uniformly labeled (UL) explosive, octahydro-1,3,5,7-tetranitro-1,3,5,7tetrazocine (HMX) was synthesized in \(40 \%\) yield by nitrolysis of \({ }^{14} \mathrm{C}\)-labeled hexamethylenetetramine (hexamine) in the presence of boron trifluoride diethyl etherate as catalyst.