Nitrotriazolone
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Names | |
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Preferred IUPAC name
5-Nitro-1,2-dihydro-3H-1,2,4-triazin-3-one | |
Identifiers | |
3D model (JSmol)
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Abbreviations | NTO |
ChemSpider | |
ECHA InfoCard | 100.012.050 ![]() |
EC Number |
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MeSH | C420648 |
PubChem CID
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UN number | 0490 |
CompTox Dashboard (EPA)
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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). | |
Infobox references | |
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[]
- ^ "Nitrotriazolone". PubChem. National Institutes of Health. Archived from the original on 17 November 2016. Retrieved 16 November 2016.
- ^ High-performance Computing. The Laboratory. 1993. Archived from the original on 2021-01-25. Retrieved 2019-08-20.
- ^ 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.
- ^ 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.
- ^ 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.
Categories:
- Explosive chemicals
- Nitro compounds
- Explosives stubs