2-Dimethylaminoethylazide
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Names | |||
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Preferred IUPAC name
2-Azido-N,N-dimethylethan-1-amine | |||
Other names
(2-Azidoethyl)(dimethyl)amine | |||
Identifiers | |||
3D model (JSmol) |
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ChemSpider | |||
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Properties | |||
C4H10N4 | |||
Molar mass | 114.15 g·mol−1 | ||
Appearance | Colorless liquid | ||
Density | 993.0 | ||
Melting point | −68.9 °C (−92.0 °F; 204.2 K) | ||
Boiling point | 135 °C (275 °F; 408 K) | ||
Solubility | ethers, alcohols | ||
Thermochemistry | |||
Std enthalpy of formation (ΔfH |
+586 cal/g | ||
Hazards | |||
Flash point | 29.4 °C (84.9 °F; 302.5 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
verify (what is ?) | |||
Infobox references | |||
2-Dimethylaminoethylazide (DMAZ) is a liquid fuel being investigated for use as a spacecraft propellent to replace the toxic, carcinogenic monomethylhydrazine.[1] It is a member of the competitive impulse non-carcinogenic hypergol (CINCH) family which were assessed as a replacement for hydrazine-derived propellants.[2][3]
References
- ↑ Mellor, B. (2004). "A Preliminary Technical Review of DMAZ: A Low-Toxicity Hypergolic Fuel". Proceedings of the 2nd International Conference on Green Propellants for Space Propulsion: 22. Bibcode:2004ESASP.557E..22M.
- ↑ "Army Develops New Fuel". Spacedaily.com. February 23, 2000. Retrieved July 12, 2014.
- ↑ Michael J. McQuaid (April 2004). "The Structure of Secondary 2-Azidoethanamines: A Hypergolic Fuel vs. a Nonhypergolic Fuel" (PDF). ARL-TR-3176. Army Research Laboratory.
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