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Anaerobic transformation of octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) by ovine rumen microorganisms

โœ Scribed by Sudeep Perumbakkam; A.M. Craig

Book ID
119357647
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
295 KB
Volume
163
Category
Article
ISSN
0923-2508

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๐Ÿ“œ SIMILAR VOLUMES

New adducts of octahydro-1,3,5,7-tetrani
New adducts of octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)
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

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Studies on octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) polymorphism
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## 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
Synthesis of 14C-labeled octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)
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.