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Biotransformation Routes of Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine by Municipal Anaerobic Sludge

โœ Scribed by Hawari, Jalal; Halasz, Annamaria; Beaudet, Sylvie; Paquet, Louise; Ampleman, Guy; Thiboutot, Sonia

Book ID
127216501
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
79 KB
Volume
35
Category
Article
ISSN
0013-936X

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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)
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## 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)
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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.