4-nitro-2,4-diazabutanal

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2003-2015
012320032015

Papers overview

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2015
2015
Alkaline hydrolysis mechanism of possible environmental contaminant RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) was… (More)
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2015
2015
In this work, we developed and characterized a novel nitrogen-fixing aerobic microbial consortium for the complete detoxification… (More)
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2010
2010
AIM The goal of this study was to compare the degradation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by three Rhodococcus… (More)
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2009
2009
The transformation of explosives, including hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), by xenobiotic reductases XenA and XenB… (More)
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2005
2005
Biodegradation of the Hexahydro-l,3,5-Trinitro-l,3,5-Triazine Ring Cleavage Product 4-Nitro-2,4-Diazabutanal by Phanerochaete… (More)
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2004
2004
Initial denitration of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by Rhodococcus sp. strain DN22 produces CO2 and the dead-end… (More)
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2004
2004
Cyclic nitramine explosives, RDX, HMX, and CL-20 are hydrophobic pollutants with very little aqueous solubility. In sediment and… (More)
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2004
2004
Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) was degraded in reed canary grass leaves exposed to simulated sunlight to primary… (More)
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2003
2003
Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX, I) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) hydrolyze at pH > 10… (More)
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2003
2003
Enzyme catalyzed biotransformation of the energetic chemical octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX) is not known… (More)
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