59283-76-0

Usage

Uses

Used in Chemical Synthesis:
2-Hydroxylamino-4,6-dinitrotoluene is used as an intermediate in the synthesis of various chemical compounds, particularly those with potential applications in the pharmaceutical and explosives industries. Its unique structure allows for further functionalization and modification, making it a versatile building block for the development of new molecules.
Used in Explosives Industry:
In the explosives industry, 2-hydroxylamino-4,6-dinitrotoluene is used as a precursor for the production of certain types of explosives. Its high energy content and reactivity make it a valuable component in the formulation of powerful explosive materials.
Used in Pharmaceutical Research:
2-Hydroxylamino-4,6-dinitrotoluene is used as a research compound in the pharmaceutical industry, where it can be further modified to develop new drugs with potential therapeutic applications. Its unique chemical structure may offer novel mechanisms of action or improved pharmacological properties compared to existing drugs.
Used in Environmental Remediation:
2-Hydroxylamino-4,6-dinitrotoluene can be utilized in the development of environmental remediation technologies, particularly for the treatment of soil and water contaminated with nitroaromatic compounds. Its reactivity and affinity for such contaminants make it a promising candidate for the design of novel remediation strategies.
Used in Material Science:
In the field of material science, 2-hydroxylamino-4,6-dinitrotoluene can be employed in the development of new materials with specific properties, such as high-energy density materials or materials with unique mechanical, electrical, or thermal characteristics. Its chemical structure and reactivity can be harnessed to create novel materials with a wide range of applications.

InChI:InChI=1/C7H7N3O5/c1-4-6(8-11)2-5(9(12)13)3-7(4)10(14)15/h2-3,8,11H,1H3

Upstream product

• 118-96-7 2,4,6-Trinitrotoluene 
• 164534-18-3 [ring-14C]-2,4,6-trinitrotoluene 

Downstream Products

• 35212-01-2 4,4',6,6'-tetranitro-2,2'-azoxytoluene 
• 1009620-09-0 N-(2-methyl-3,5-dinitrophenyl)-4-methyl-3,5-dinitroaniline 
• 185376-54-9 2,4-dihydroxylamino-6-nitrotoluene 

Relevant academic research and scientific papers

OYE flavoprotein reductases initiate the condensation of TNT-derived intermediates to secondary diarylamines and nitrite

Polynitroaromatic explosives such as 2,4,6-trinitrophenol (picric acid) and 2,4,6-trinitrotoluene (TNT) are toxic and recalcitrant environmental pollutants. They persist in the environment due to the highly inactivated π system of their aromatic rings, wh

The crystal structures of three primary products from the selective reduction of 2,4,6-trinitrotoluene

The crystal structures of three primary products from the selective reduction of 2,4,6-trinitrotoluene (TNT) have been determined by synchrotron X-ray powder diffraction (2-amino-4,6-dinitrotoluene) and single crystal X-ray diffraction (4-amino-2,6-dinitr

Enzymatic Reduction of 2,4,6-Trinitrotoluene and Related Nitroarenes: Kinetics Linked to One-Electron Redox Potentials

At military bases and munitions factories 2,4,6-trinitrotoluene (TNT) is a common soil and groundwater contaminant. Although the reduction of nitro groups in TNT and related nitroarenes has been extensively investigated, few researchers have studied the l

Reductive transformation of bound trinitrophenyl residues and free TNT during a bioremediation process analyzed by immunoassay

To follow the fate of bound metabolites of TNT in soil, a synthetic trinitrophenyl residue covalently linked to humic acids was used as model compound. A selective monoclonal antibody was able to detect chemical changes of the nitro groups of the bound re

Bamberger rearrangement during TNT metabolism by Clostridium acetobutylicum

Studies were conducted to isolate and identify polar and oxygen- sensitive intermediates of 2,4,6-trinitrotoluene (TNT) transformation by Clostridium acetobutylicum. Studies conducted in anaerobic cell extracts demonstrated that a polar product formed fro