3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||43.025 g·mol−1|
|Appearance||Colorless liquid or gas (boiling point near room temperature)|
|Density||1.14 g/cm3 (20 °C)|
|Melting point||−86 °C (−123 °F; 187 K)|
|Boiling point||23.5 °C (74.3 °F; 296.6 K)|
|Solubility||Soluble in benzene, toluene, diethyl ether|
|Occupational safety and health (OHS/OSH):|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Isocyanic acid is a chemical compound with the structural formula HNCO, which is often written as H−N=C=O. It is a colourless, volatile and poisonous substance, with a boiling point of 23.5 °C. It is the predominant tautomer of cyanic acid (H−O−C≡N).
The derived anion of isocyanic acid is the same as the derived anion of cyanic acid, and that anion is [N=C=O]−, which is called cyanate. The related functional group −N=C=O is isocyanate; it is distinct from cyanate (−O−C≡N), fulminate (−O−N+≡C−), and nitrile oxide (−C≡N+−O−).
Isocyanic acid was discovered in 1830 by Justus von Liebig and Friedrich Wöhler.
Isocyanic acid is the simplest stable chemical compound that contains carbon, hydrogen, nitrogen, and oxygen, the four most commonly found elements in organic chemistry and biology. It is the only fairly stable one of the four linear isomers with molecular formula HOCN that have been synthesized, the others being cyanic acid (cyanol, H−O−C≡N) and the elusive fulminic acid (H−C≡N+−O−) and isofulminic acid H−O−N+≡C−.
Although the electronic structure according to valence bond theory can be written as H−N=C=O, the vibrational spectrum has a band at 2268.8 cm−1 in the gas phase, which clearly indicates a carbon–nitrogen triple bond. Thus the canonical form H−N+≡C−O− is the major resonance structure.
The pure compound has a melting point of −86.8 °C and a boiling point of 23.5 °C, so it is volatile at ambient temperatures.
In aqueous solution it is a weak acid, having a pKa of 3.7:
Isocyanic acid hydrolyses to carbon dioxide and ammonia:
At sufficiently high concentrations, isocyanic acid oligomerizes to give the trimer cyanuric acid and cyamelide, a polymer. These species usually are easily separated from liquid- or gas-phase reaction products. Cyanuric acid itself decomposes on further heating back to isocyanic acid.
Dilute solutions of isocyanic acid are stable in inert solvents, e.g. ether and chlorinated hydrocarbons.
Isocyanic acid reacts with amines to give ureas (carbamides):
This reaction is called carbamylation.
HNCO adds across electron-rich double bonds, such as vinylethers, to give the corresponding isocyanates.
Isocyanic acid, HNCO, is a Lewis acid whose free energy, enthalpy and entropy changes for its 1:1 association with a number of bases in carbon tetrachloride solution at 25 °C have been reported. The acceptor properties of HNCO are compared with other Lewis acid in the ECW model.
The tautomer, known as cyanic acid, HOCN, in which the oxygen atom is protonated, is unstable to decomposition, but in solution it is present in equilibrium with isocyanic acid to the extent of about 3%. The vibrational spectrum is indicative of the presence of a triple bond between the nitrogen and carbon atoms.
Low-temperature photolysis of solids containing HNCO creates the tautomer cyanic acid H−O−C≡N, also called hydrogen cyanate. Pure cyanic acid has not been isolated, and isocyanic acid is the predominant form in all solvents. Sometimes information presented for cyanic acid in reference books is actually for isocyanic acid.
Isocyanic acid can be made by protonation of the cyanate anion, such as from salts like potassium cyanate, by either gaseous hydrogen chloride or acids such as oxalic acid.
HNCO also can be made by the high-temperature thermal decomposition of the trimer cyanuric acid:
In the reverse of the famous synthesis of urea by Friedrich Wöhler,
isocyanic acid is produced and rapidly trimerizes to cyanuric acid.
Isocyanic acid has been detected in many kinds of interstellar environments.
Isocyanic acid is also present in various forms of smoke, including smog and cigarette smoke. It was detected using mass spectrometry, and easily dissolves in water, posing a health risk to the lungs.