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Tetrazocines, octahydro

Monteil-Rivera F, L Paquet, A Halasz, MT Montgomery, J Hawari (2005) Reduction of octahydro-l,3,5,7-tetra-nitro-l,3,5,7-tetrazocine by zero-valent iron product distribution. Environ Sci Technol 39 9725-9731. [Pg.44]

Reed Canary Grass Phalaris arundinacea) was grown in liquid culture and exposed to RDX that was metabolized to the potentially toxic 4-nitro-2,4-diazabutanal (Just and Schnoor 2004). This metabolite is also produced from RDX by strains of Rhodococcus sp. and from the homologous octahydro-l,3,5,7-tetranitro-l,3,5,7-tetrazocine (HMX) by Phanerochaete chrysosporium. [Pg.99]

HMG-CoA reductase inhibitors (Statins), 5 137, 138-140t, 142-143 HMX (High Melting eXplosive octahydro-1,3,5,7- tetranitro-l,3,5,7-tetrazocine), 70 735-736... [Pg.440]

Energetic Materials. 2. Deuterium Isotope Effects and Isotopic Scrambling in Condensed-Phase Decomposition of Octahydro-l,3,5,7-tetranitro-l,3,5,7-tetrazocine. [Pg.187]

These are common abbreviations for the following TNT 2,4,6-trinitrotoluene AN ammonium nitrate PETN pentaerythritol tetranitrate HMX octahydro-l,3,5,7,-tetranitro-l,3,4,5-tetrazocine RDX hexahydro-l,3,5-trinitro-s-triazine HMTD hexamethylene triperoxide diamine TATP triacetone triperoxide. [Pg.37]

Melting explosive octahydro-l,3,5.7-tetranitro-l,3,5,7-tetrazocine) and i N-dimethylhydrazine. These compounds are sometimes present at quite high levels in soils and groundwater on military bases and production sites. Bioremediation is a promising new technology for treating sites contaminated with such compounds. [Pg.209]

The high explosive octahydro-l,3,5,7-tetranitro-l,3,5,7-tetrazocine (HMX, Fig. 1) is the energetic material in a number of high performance military explosive and propellant formulations [3], HMX exhibits three crystal polymorphs at ambient pressure denoted J3- [4,5], a- [6], and <5-FlMX [7] and listed in terms of stability with increasing temperature. At temperature T 550 K the crystalline structure become unstable and HMX begins to melt. The liquid phase of HMX is very unstable and therefore no direct measurements of... [Pg.279]


See other pages where Tetrazocines, octahydro is mentioned: [Pg.259]    [Pg.259]    [Pg.25]    [Pg.585]    [Pg.604]    [Pg.676]    [Pg.1198]    [Pg.1276]    [Pg.1690]    [Pg.141]    [Pg.220]    [Pg.332]    [Pg.851]    [Pg.355]    [Pg.141]    [Pg.49]    [Pg.195]    [Pg.388]    [Pg.35]    [Pg.594]    [Pg.49]    [Pg.883]    [Pg.186]    [Pg.226]    [Pg.403]    [Pg.260]    [Pg.16]    [Pg.82]    [Pg.132]    [Pg.21]    [Pg.187]    [Pg.387]    [Pg.47]    [Pg.355]    [Pg.49]   


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Tetrazocines

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