Hydrazoic acid
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
| Properties: | |
|---|---|
| Image:Hydrogen-azide-2D-dimensions.png | |
| Image:Hydrogen-azide-3D-vdW.png | |
| IUPAC name | hydrogen azide |
| Identifiers | |
| CAS number | |
| SMILES | N=N=N |
| Properties | |
| Molecular formula | HN3 |
| Molar mass | 43.03 g/mol |
| Melting point |
−80 °C (193.15 K) |
| Boiling point |
37 °C (310.15 K) |
| Acidity (pKa) | 4.6 to 4.7 |
| Structure | |
| Molecular shape | Linear |
| Hazards | |
| Main hazards | Highly toxic, explosive. |
| R-phrases | R1, R2 |
| Related Compounds | |
| Other anions | Hydrogen chloride |
| Other cations | Sodium azide |
| Related acids | Hydrochloric acid hydrocyanic acid |
| Related compounds | Hydrazine |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Hydrazoic acid, HN3, is a colorless, volatile, and extremely explosive liquid at room temperature and pressure.
Contents |
Applications
Hydrazoic acid is used primarily for preservation of stock solutions, and as a reagent.
History
It was first isolated in 1890 by Theodor Curtius (Berichte, 1890, 23, p. 3023).
Chemistry
It is soluble in water, and the solution dissolves many metals (e.g. zinc, iron) with liberation of hydrogen and formation of salts (azides, formerly also called azoimides or hydrazoates).
All the salts are explosive and readily interact with the alkyl iodides. In its properties it shows some analogy to the halogen acids, since it forms poorly soluble lead, silver and mercurous salts (in water). 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 4.6-4.7).
Production
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.
Toxicity
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.
References
- Dictionary of inorganic and organometallic compounds, Chapman & Hall
External links
This article incorporates text from the Encyclopædia Britannica Eleventh Edition, a publication now in the public domain.cs:Kyselina azidovodíková de:Stickstoffwasserstoffsäureit:Acido azotidrico lv:Slāpekļūdeņražskābe nl:Waterstofazidesk:Kyselina azidovodíková
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
