Isocyanic acid

























































































Isocyanic acid

Isocyansäure.svg

Isocyanic acid 3D balls.png
Names

IUPAC name
Isocyanic acid

Other names
Carbimide[1]

Identifiers

CAS Number


  • 75-13-8 ☑Y


  • 420-05-3 (cyanic acid) ☒N

3D model (JSmol)

  • Isocyanic acid: Interactive image

  • Cyanic acid: Interactive image

ChEBI

  • CHEBI:29202 ☑Y

ChemSpider

  • 6107 ☑Y

ECHA InfoCard
100.109.068


PubChem CID
  • 6347




Properties

Chemical formula

 HNCO

Molar mass
 43.03 g/mol
Appearance
 Colorless liquid or gas (b.p. near room temperature)

Density
 1.14 g/cm3 (20 °C)

Melting point
 −86 °C (−123 °F; 187 K)[2]

Boiling point
 23.5 °C (74.3 °F; 296.6 K)

Solubility in water

 Dissolves

Solubility
 Soluble in benzene, toluene, ether

Conjugate base
Cyanate
Hazards
Main hazards
 Poisonous

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).


☒N verify (what is ☑Y☒N ?)

Infobox references

Isocyanic acid is a chemical compound with the formula HNCO, discovered in 1830 by Liebig and Wöhler.[3] This colourless substance is volatile and poisonous, with a boiling point of 23.5 °C. 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.




Contents






  • 1 Preparation and reactions


  • 2 Isomers: Cyanic acid and fulminic acid


  • 3 See also


  • 4 References


  • 5 Further reading


  • 6 External links





Preparation and reactions


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.[4]


H+ + NCO- → HNCO

HNCO also can be made by the high-temperature thermal decomposition of cyanuric acid, a trimer.


C3H3N3O3 → 3 HNCO

Isocyanic acid hydrolyses to carbon dioxide and ammonia:


HNCO + H2O → CO2 + NH3

At sufficiently high concentrations, isocyanic acid oligomerizes to give cyanuric acid and cyamelide, a polymer. These species usually are easily separated from liquid- or gas-phase reaction products. Dilute solutions of isocyanic acid are stable in inert solvents, e.g. ether and chlorinated hydrocarbons.[5]


Isocyanic acid reacts with amines to give ureas (carbamides):


HNCO + RNH2 → RNHC(O)NH2.

This reaction is called carbamylation.


HNCO adds across electron-rich double bonds, such as vinylethers, to give the corresponding isocyanates.


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.[6]



Isomers: Cyanic acid and fulminic acid


Low-temperature photolysis of solids containing HNCO has been shown to make H-O-C≡N, known as cyanic acid or hydrogen cyanate; it is a tautomer of isocyanic acid.[7] Pure cyanic acid has not been isolated, and isocyanic acid is the predominant form in all solvents.[5] Sometimes information presented for cyanic acid in reference books is actually for isocyanic acid.[citation needed]


Cyanic and isocyanic acids are isomers of fulminic acid (H-C=N-O), an unstable compound.[8]



See also



  • Cyanate

  • Thiocyanic acid



References





  1. ^ Cyanamide also has this name, and for which it is more systematically correct


  2. ^ Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, .mw-parser-output cite.citation{font-style:inherit}.mw-parser-output q{quotes:"""""""'""'"}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}
    ISBN 0-07-049439-8


  3. ^ Liebig, J.; Wöhler, F. (1830). "Untersuchungen über die Cyansäuren". Ann. Phys. 20 (11): 394. Bibcode:1830AnP....96..369L. doi:10.1002/andp.18300961102.


  4. ^ Fischer, G.; Geith, J.; Klapötke, T. M.; Krumm B. (2002). "Synthesis, Properties and Dimerization Study of Isocyanic Acid" (PDF). Z. Naturforsch. 57b (1): 19–25.


  5. ^ ab A. S. Narula, K. Ramachandran “Isocyanic Acid” in Encyclopedia of Reagents for Organic Synthesis, 2001, John Wiley & Sons, New York. doi:10.1002/047084289X.ri072m Article Online Posting Date: April 15, 2001.


  6. ^ Preidt, Robert. "Chemical in Smoke May Pose Health Risk". MyOptumHealth. AccuWeather. Retrieved 14 September 2011.


  7. ^ Jacox, M.E.; Milligan, D.E. (1964). "Low-Temperature Infrared Study of Intermediates in the Photolysis of HNCO and DNCO". Journal of Chemical Physics. 40 (9): 2457–2460. Bibcode:1964JChPh..40.2457J. doi:10.1063/1.1725546.


  8. ^ Kurzer, Frederick (2000). "Fulminic Acid in the History of Organic Chemistry". Journal of Chemical Education. 77 (7): 851–857. Bibcode:2000JChEd..77..851K. doi:10.1021/ed077p851.




Further reading



  • Handbook of Chemistry and Physics, 65th. Edition, CRC Press (1984)


External links




  • Walter, Wolfgang (1997). Organic Chemistry: A Comprehensive Degree Text and Source Book. Chichester: Albion Publishing. p. 364. ISBN 978-1-898563-37-2. Retrieved 2008-06-21.


  • Cyanic acid from NIST Chemistry WebBook (accessed 2006-09-09)











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