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Abundance and diversity of octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)-metabolizing bacteria in UXO-contaminated marine sediments

โœ Scribed by Jian-Shen Zhao; Dominic Manno; Jalal Hawari

Book ID
109302885
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
175 KB
Volume
59
Category
Article
ISSN
0168-6496

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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

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.