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Nitrotriazolone

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Nitrotriazolone[1]
Names
Preferred IUPAC name
5-nitro-1,2-dihydro-1,2,4-triazol-3-one
Identifiers
3D model (JSmol)
Abbreviations NTO
ChemSpider
ECHA InfoCard 100.012.050 Edit this at Wikidata
EC Number
  • 213-254-4
MeSH C420648
UN number 0490
  • InChI=1S/C2H2N4O3/c7-2-3-1(4-5-2)6(8)9/h(H2,3,4,5,7)
    Key: QJTIRVUEVSKJTK-UHFFFAOYSA-N
  • C1(=NC(=O)NN1)[N+](=O)[O-]
Properties
C2H2N4O3
Molar mass 130.063 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Nitrotriazolone (NTO) is a high explosive developed in the weapons program, [2] first identified in 1905, but research into its explosive properties was not fully undertaken until the 1980s, [3] used by the US Army in munitions.[4]

Nitrotriazolone is being progressively made use of in novel explosive formulations.[5]

References

  1. ^ "Nitrotriazolone". PubChem. National Institutes of Health. Archived from the original on 17 November 2016. Retrieved 16 November 2016.
  2. ^ High-performance Computing. The Laboratory. 1993. Archived from the original on 2021-01-25. Retrieved 2019-08-20.
  3. ^ Jai Prakash Agrawal (20 November 2015). High Energy Materials: Propellants, Explosives and Pyrotechnics. Wiley. pp. 124–. ISBN 978-3-527-80268-5. Archived from the original on 25 January 2021. Retrieved 20 August 2019.
  4. ^ Winstead, Bob (26 October 2011). "Nitrotriazolone: An Environmental Odyssey" (PDF). NDIA Systems Engineering Conference. Archived (PDF) from the original on 13 December 2016. Retrieved 16 November 2016.
  5. ^ Shree Nath Singh (4 August 2013). Biological Remediation of Explosive Residues. Springer Science & Business Media. pp. 285–. ISBN 978-3-319-01083-0. Archived from the original on 25 January 2021. Retrieved 20 August 2019.