|Jmol 3D model||Interactive image|
|Molar mass||43.03 g/mol|
|Appearance||colorless, highly volatile liquid|
|Melting point||−80 °C (−112 °F; 193 K)|
|Boiling point||37 °C (99 °F; 310 K)|
|Solubility||soluble in alkali, alcohol, ether|
|Acidity (pKa)||4.6 |
|Main hazards||Highly toxic, explosive, reactive|
|S-phrases||S33, S36/37, S38|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Hydrazoic acid, also known as hydrogen azide or azoimide, is a compound with the chemical formula HN3. It is a colorless, volatile, and explosive liquid at room temperature and pressure. It is a compound of nitrogen and hydrogen, and is therefore a pnictogen hydride. It was first isolated in 1890 by Theodor Curtius. The acid has few applications, but its conjugate base, the azide ion, is useful in specialized processes.
Hydrazoic acid is soluble in water. Undiluted hydrazoic acid is dangerously explosive with a standard enthalpy of formation ΔfHo (l, 298K) = +264 kJmol−1). When dilute, the gas and aqueous solutions (<10%) can be safely handled.
The acid is usually formed by acidification of an azide salt like sodium azide. Normally solutions of sodium azide in water contain trace quantities of hydrazoic acid in equilibrium with the azide salt, but introduction of a stronger acid can convert the primary species in solution to hydrazoic acid. The pure acid may be subsequently obtained by fractional distillation as an extremely explosive colorless liquid with an unpleasant smell.
- NaN3 + HCl → HN3 + NaCl
- N2H5+ + HNO2 → HN3 + H+ + 2 H2O
In its properties hydrazoic acid shows some analogy to the halogen acids, since it forms poorly soluble (in water) lead, silver and mercury(I) salts. The metallic salts all crystallize in the anhydrous form and decompose on heating, leaving a residue of the pure metal. It is a weak acid (pKa = 4.75.) Its heavy metal salts are explosive and readily interact with the alkyl iodides. Azides of heavier alkali metals (excluding lithium) or alkaline earth metals are not explosive, but decompose in a more controlled way upon heating, releasing spectroscopically-pure N
2 gas. Solutions of hydrazoic acid dissolve many metals (e.g. zinc, iron) with liberation of hydrogen and formation of salts, which are called azides (formerly also called azoimides or hydrazoates).
Dissolution in the strongest acids produces explosive salts containing the H
ion, for example:
- HN=N=N + HSbCl
6 → [H
The decomposition of hydrazoic acid, triggered by shock, friction, spark, etc. goes as follows:
3 → H
2 + 3N
Hydrazoic acid is volatile and highly toxic. It has a pungent smell and its vapor can cause violent headaches. The compound acts as a non-cumulative poison.
2-Furonitrile, a pharmaceutical intermediate and potential artificial sweetening agent has been prepared in good yield by treating furfural with a mixture of hydrazoic acid (HN3) and perchloric acid in the presence of magnesium perchlorate in the benzene solution at 35 °C.
The all gas-phase iodine laser (AGIL) mixes gaseous hydrazoic acid with chlorine to produce excited nitrogen chloride, which is then used to cause iodine to lase; this avoids the liquid chemistry requirements of COIL lasers.
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- Furman, David; Dubnikova, Faina; van Duin, Adri C. T.; Zeiri, Yehuda; Kosloff, Ronnie (2016-03-10). "Reactive Force Field for Liquid Hydrazoic Acid with Applications to Detonation Chemistry". The Journal of Physical Chemistry C. 120 (9): 4744–4752. doi:10.1021/acs.jpcc.5b10812. ISSN 1932-7447.
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- B. Bandgar; Makone, S. (2006). "Organic reactions in water. Transformation of aldehydes to nitriles using NBS under mild conditions". Synthetic Communications. 36 (10): 1347–1352. doi:10.1080/00397910500522009.