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| OtherNames = TNX; hexahydro-1,3,5-trinitroso-1,3,5-triazine; trinitrosotrimethylenetriamine |
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| OtherNames = {{ubl|TNX|Hexahydro-1,3,5-trinitroso-1,3,5-triazine|Trinitrosotrimethylenetriamine}} |
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'''R-salt''' ('''TNX''', ] '''hexahydro-1,3,5-trinitroso-1,3,5-triazine'''), is an ] that has been used as an ].<ref name="Wilkins">{{cite journal |doi=10.1002/prep.202400028 |title=A comprehensive study on the thermal properties and chemical characterization of 1,3,5-trinitroso-1,3,5-triazine (R-Salt) |date=2024 |last1=Wilkins |first1=Benjamin |last2=Sartain |first2=Hope T. |last3=Schneidereit |first3=Sheana |last4=Ostrow |first4=Benjamin |last5=Aparicio |first5=Joaquin |last6=Horan |first6=Andrew |last7=Pedersen |first7=Kevin |last8=Barber |first8=Jeffrey |last9=Perez |first9=Johnny |last10=Richard |first10=Marc |last11=Pollock |first11=Elizabeth |last12=Brady |first12=John |journal=Propellants, Explosives, Pyrotechnics |volume=49 |issue=6 }}</ref> It is a ], that less ] than other compounds of similar availability.<ref name="Wilkins"/> It has a similar structure to ]—TNX has ] groups as compared to the ] groups of RDX—but is less commonly used. It is also found as a decomposition product of RDX in the environment, such as after RDX detonation.<ref>{{cite journal |doi=10.1002/prep.201600149 |title=An Improved Process Towards Hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX) |date=2017 |last1=Rothstein |first1=Sarah A. |last2=Dubé |first2=Pascal |last3=Anderson |first3=Stephen R. |journal=Propellants, Explosives, Pyrotechnics |volume=42 |issue=2 |pages=126–130 }}</ref> Using chemistry similar to the synthesis of RDX, R-salt can be synthesized by reaction of ] with ] in the presence of an acid catalyst.<ref name="Wilkins"/> |
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'''R-salt''' ('''TNX''', ] '''hexahydro-1,3,5-trinitroso-1,3,5-triazine'''), is an ] that has been used as an ].<ref name="Wilkins">{{cite journal |doi=10.1002/prep.202400028 |title=A comprehensive study on the thermal properties and chemical characterization of 1,3,5-trinitroso-1,3,5-triazine (R-Salt) |date=2024 |last1=Wilkins |first1=Benjamin |last2=Sartain |first2=Hope T. |last3=Schneidereit |first3=Sheana |last4=Ostrow |first4=Benjamin |last5=Aparicio |first5=Joaquin |last6=Horan |first6=Andrew |last7=Pedersen |first7=Kevin |last8=Barber |first8=Jeffrey |last9=Perez |first9=Johnny |last10=Richard |first10=Marc |last11=Pollock |first11=Elizabeth |last12=Brady |first12=John |journal=Propellants, Explosives, Pyrotechnics |volume=49 |issue=6 }}</ref> It is a ], that is less ] than other compounds of similar availability.<ref name="Wilkins"/> It has a similar structure to ]—TNX has ] groups as compared to the ] groups of RDX—but is less commonly used. It is also found as a decomposition product of RDX in the environment, such as after RDX detonation.<ref>{{cite journal |doi=10.1002/prep.201600149 |title=An Improved Process Towards Hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX) |date=2017 |last1=Rothstein |first1=Sarah A. |last2=Dubé |first2=Pascal |last3=Anderson |first3=Stephen R. |journal=Propellants, Explosives, Pyrotechnics |volume=42 |issue=2 |pages=126–130 }}</ref> Using chemistry similar to the synthesis of RDX, R-salt can be synthesized by reaction of ] with ] in the presence of an acid catalyst.<ref name="Wilkins"/> |