Chemistry:Ethyl azide
From HandWiki
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| Names | |
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| Preferred IUPAC name
Azidoethane | |
| Other names
Ethane, azido-; 1-Azidoethane
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| Properties | |
| CH 3CH 2N 3 | |
| Molar mass | 71.083 g·mol−1 |
| Appearance | liquid |
| Boiling point | 50 |
| Explosive data | |
| Shock sensitivity | High |
| Friction sensitivity | High |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
266.872 |
| Hazards | |
| Main hazards | Harmful, Explosive |
| Related compounds | |
Related compounds
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Hydrazoic acid, Chlorine azide, Methyl azide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Ethyl azide (CH
3CH
2N
3) is an explosive compound sensitive to rapid heating, shock or impact. It has exploded when heated to room temperature.[1][2] When heated to decomposition it emits toxic fumes of NO {x}.[3][4]
It is irritating to eyes, respiratory system and skin.
Uses
Ethyl azide is used for organic synthesis.
References
- ↑ Campbell, H. C.; Rice, O. K. (1935). "The Explosion of Ethyl Azide". Journal of the American Chemical Society 57 (6): 1044–1050. doi:10.1021/ja01309a019.
- ↑ Rice, O. K.; Campbell, H. C. (1939). "The Explosion of Ethyl Azide in the Presence of Diethyl Ether". The Journal of Chemical Physics 7 (8): 700–709. doi:10.1063/1.1750516. Bibcode: 1939JChPh...7..700R.
- ↑ Rice, O. K. (1940). "The Role of Heat Conduction in Thermal Gaseous Explosions". The Journal of Chemical Physics 8 (9): 727–733. doi:10.1063/1.1750808. Bibcode: 1940JChPh...8..727R.
- ↑ Costa Cabral, B. J.; Costa, M. L.; Almoster Ferreira, M. A. (2010). "ChemInform Abstract: Molecular Structure and Ionization Energies of Azides: An ab initio Study of Hydrazoic Acid, Methyl Azide and Ethyl Azide". ChemInform 24 (37): no. doi:10.1002/chin.199337053.
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