N-Nitrobis(2-hydroxyethyl)-amine dinitrate

• Formula: C₄H₈N₄O₈
• Molecular weight: 240.1283
• IUPAC Standard InChI: InChI=1S/C4H8N4O8/c9-6(10)5(1-3-15-7(11)12)2-4-16-8(13)14/h1-4H2 Copy

  
• IUPAC Standard InChIKey: NZDNCDGEHXHPCO-UHFFFAOYSA-N Copy
• CAS Registry Number: 4185-47-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Ethanol, 2,2'-nitroiminodi-, dinitrate; Diethanolnitramine dinitrate; Diethanol-N-nitramine dinitrate; DINA; 2,2'-Dinitrato-N-nitrodiethylamine; sym-Dinitroxydiethylnitramine; Ethanol, 2,2'-(nitroimino)bis-, dinitrate; Nitrodiethanolamine dinitrate; N-Nitrodiethanolamine dinitrate; 2,2'-Nitroiminobis(ethylnitrate); 2,2'-Nitroiminodiethanol nitrate; 2,2'-(Nitroimino)ethanol dinitrate; DINA (explosive); Ethanol, 2,2'-(nitroimino)bis-, dinitrate (ester)
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• Information on this page:
  • Condensed phase thermochemistry data
  • Mass spectrum (electron ionization)
  • References
  • Notes
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Condensed phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Mass spectrum (electron ionization)

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

References

Go To: Top, Condensed phase thermochemistry data, Mass spectrum (electron ionization), Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Simmons, 1994
Simmons, R.L., Thermochemistry of NENA plasticizers, Int. Annu. Conf. ICT, 25th, 1994, 1-10. [all data]

Sosnova, Voskoboinikov, et al., 1962
Sosnova, G.S.; Voskoboinikov, M.; Brusnikina, V.M.; Lapshina, Z.Ya.; Novikov, S.S.; Apin, A.Ya., Comparative data on the physiocochemical properties of some liquid explosive substances, Bull. Acad. Sci. USSR, Div. Chem. Sci., 1962, 325-326. [all data]

Tavernier and Lamouroux, 1955
Tavernier, P.; Lamouroux, M., Determinations calorimetriques relatives a douze substances organiques susceptibles d'utilisation dans les poudres, Mem. Poudres, 1955, 37, 197-206. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Medard and Thomas, 1954
Medard, L.; Thomas, M., Chaleurs de combustion de vingt-quatre substances explosives ou apparentees a des explosifs, Mem. Poudres, 1954, 36, 97-127. [all data]

Medard, 1954
Medard, L., Tables thermochimiques a l'usage des techniciens des substances explosives, Mem. Artillerie Fr. Sci. Tech. Armement, 1954, 28, 415-492. [all data]

Handrick, 1956
Handrick, G.R., Report of the study of pure explosive compounds. Part IV. Calculation of heat of combustion of organic compounds from structural features and calculation of power of high explosives, Rpt. C-58247 for the Office of the Chief of Ordnance, contract DA-19-020-ORD-47 by the Arthur D. Little, Inc., Cambridge, MA, 1956, 467-573. [all data]

Notes

Go To: Top, Condensed phase thermochemistry data, Mass spectrum (electron ionization), References

• Symbols used in this document:
  

  ΔcH°liquid	Enthalpy of combustion of liquid at standard conditions
  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔfH°liquid	Enthalpy of formation of liquid at standard conditions
  ΔfH°solid	Enthalpy of formation of solid at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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