Methyl nitrite

Methyl nitrite
Names
Preferred IUPAC name
Methyl nitrite
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.009.882
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PubChem CID
UNII
InChI
  • InChI=1S/CH3NO2/c1-4-2-3/h1H3 checkY
    Key: BLLFVUPNHCTMSV-UHFFFAOYSA-N checkY
  • InChI=1/CH3NO2/c1-4-2-3/h1H3
    Key: BLLFVUPNHCTMSV-UHFFFAOYAL
SMILES
  • O=NOC
Properties
Chemical formula
 CH3NO2
Molar mass 61.040 g·mol−1
Appearance Yellow gas[1]
Density 0.991 g/cm3[1]
Melting point −16 °C (3 °F; 257 K)[1]
Boiling point −12 °C (10 °F; 261 K)[1]
Thermochemistry[2]
Std enthalpy of
formation (ΔfH⦵298)
 -66.1 kJ/mol
Hazards
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Methyl nitrite is an organic compound with the chemical formula CH
3ONO. It is a gas, and is the simplest alkyl nitrite.

Structure

At room temperature, methyl nitrite exists as a mixture of cis and trans conformers. The cis conformer is 3.13 kJ mol−1, more stable than the trans form, with an energy barrier to rotation of 45.3 kJ mol−1.[3] The cis and trans structure have also been determined by microwave spectroscopy (see external links).

cis-methyl nitritetrans-methyl nitrite

Synthesis

Methyl nitrite can be prepared by the reaction of silver nitrite with iodomethane: Silver nitrite (AgNO2) exists in solution as the silver ion, Ag+ and the nitrite ion, NO2−. One of the lone pairs on an oxygen from nitrite ion attacks the methyl group (—CH3), releasing the iodide ion into solution.[4] Unlike silver nitrite, silver iodide is highly insoluble in water and thus forms a solid.[5] Note that nitrogen is a better nucleophile than oxygen and most nitrites would react via an SN2-like mechanism and the major product would be nitromethane. For example, sodium and potassium nitrite reacting with iodomethane would produce mostly nitromethane, with methyl nitrite as the minor product. However, the presence of the silver ion in solution has a stabilizing effect on the formation of carbocation intermediates, increasing the percent yield of methyl nitrite. In either case, some nitromethane and methyl nitrite are both formed.[4]

The figure shows the two gas-phase structures of methyl nitrite, as determined by IR and microwave spectroscopy.

Methyl nitrite free of nitromethane can be made by reacting iodomethane with nitrogen dioxide:

This compound is produced by the combustion of unleaded petrol, and might be a cause of the decline of insects, and hence that of the house sparrow and other songbirds in Europe.[6]

Methyl nitrite is also present in aged cigarette smoke. Here it is presumably formed from nitrous oxide (itself formed by autoxidation of nitric oxide) and methanol.[7]

Properties and uses

Methyl nitrite is an oxidizing agent and a heat-sensitive explosive; its sensitivity increases in presence of metal oxides. With inorganic bases it forms explosive salts. It forms explosive mixtures with air. It is used as a rocket propellant, a monopropellant.[8] It explodes more violently than ethyl nitrite. Lower alkyl nitrites may decompose and burst the container even when stored under refrigeration.[9]

Methyl nitrite is a toxic asphyxiating gas, a potent cyanotic agent. Exposure may result in methemoglobinemia.[10]

Methyl nitrite is used in chemical synthesis as a precursor and intermediate, e.g. during production of phenylpropanolamine.[10]

See also

  • Nitromethane
  • Organic chemistry
  • Nucleophilic substitution

References

  1. 1 2 3 4 Haynes, p. 3.382
  2. ↑ Haynes, p. 5.20
  3. ↑ Van Der Veken, B. J.; Maas, R.; Guirgis, G. A.; Stidham, H. D.; Sheehan, T. G.; Durig, James R. (1990). "Infrared spectrum, ab initio calculations, barriers to internal rotation and structural parameters for methyl nitrite". Journal of Physical Chemistry. 94 (10): 4029–39. doi:10.1021/j100373a028.
  4. 1 2 Pavia, Donald L.; Lampman, Gary M.; Kriz, George S. (2004). Organic Chemistry. Vol. 2. Mason, Ohio: Thompson Custom Publishing. ISBN 978-0-03-014813-2. OCLC 236055357.
  5. ↑ Darrell D. Ebbing; Steven D. Gammon (2005). General Chemistry (8th ed.). Boston: Houghton Mifflin. ISBN 978-0-618-39941-3.
  6. ↑ Summers-Smith, J. Denis (September 2007). "Is unleaded petrol a factor in urban House Sparrow decline?". British Birds. 100: 558. ISSN 0007-0335.
  7. ↑ Rodgman, Alan; Perfetti, Thomas A. (2016-04-19). The Chemical Components of Tobacco and Tobacco Smoke. ISBN 9781466515529.
  8. ↑ Methyl Nitrite. Cameochemicals.noaa.gov. Retrieved on 2019-03-10.
  9. ↑ Bretherick, L. (2016-10-27). Bretherick's Handbook of Reactive Chemical Hazards. ISBN 9781483162508.
  10. 1 2 METHYL NITRITE – National Library of Medicine HSDB Database. Toxnet.nlm.nih.gov. Retrieved on 2019-03-10.

Cited sources

  • Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). CRC Press. ISBN 978-1439855119.
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