Preferred IUPAC name
Systematic IUPAC name
Other names
75-12-7 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:48431 YesY
ChEMBL ChEMBL266160 YesY
ChemSpider 693 YesY
ECHA InfoCard 100.000.766
KEGG C00488 YesY
PubChem 713
Molar mass 45.04 g/mol
Appearance Colorless, oily liquid[2]
Density 1.133 g/cm3
Melting point 2 to 3 °C (36 to 37 °F; 275 to 276 K)
Boiling point 210 °C (410 °F; 483 K)
Vapor pressure 0.08 mmHg at 20 °C
Acidity (pKa) 23.5 (in DMSO)[3]
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point 154 °C (309 °F; 427 K) (closed cup)
US health exposure limits (NIOSH):
PEL (Permissible)
REL (Recommended)
TWA 10 ppm (15 mg/m3) [skin][2]
IDLH (Immediate danger)
Related compounds
Related compounds
Carbamic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Formamide, also known as methanamide, is an amide derived from formic acid. It is a clear liquid which is miscible with water and has an ammonia-like odor. It is chemical feedstock for the manufacture of sulfa drugs, other pharmaceuticals, herbicides, pesticides and the manufacture of hydrocyanic acid. It has been used as a softener for paper and fiber. It is a solvent for many ionic compounds. It has also been used as a solvent for resins and plasticizers.[4]

Formamide will begin to partially decompose into carbon monoxide and ammonia at 180 °C together with traces of hydrogen cyanide (HCN) and water. In the presence of solid acid catalysts, formamide yields HCN in high yield:[5]

low temperature: HC(O)NH2 → CO + NH3
high temperature, acid-catalyzed: HC(O)NH2 → HCN + H2O


Historical production

In the past, formamide was produced by treating formic acid with ammonia, which produces ammonium formate, which in turn yield formamide upon heating:[6]


Formamide is also generated by aminolysis of ethyl formate:[7]


Modern production

The current industrial process for the manufacture of formamide involves either the carbonylation of ammonia:[4]


An alternative two-stage process involves the aminolysis of methyl formate, which is formed from carbon monoxide and methanol:

HCO2CH3 + NH3 → HC(O)NH2 + CH3OH


Formamide is used in the industrial production of hydrogen cyanide. It is also used as a solvent for processing various polymers such as polyacrylonitrile.[5]

Niche or laboratory applications

Formamide is a constituent of cryoprotectant vitrification mixtures used for cryopreservation of tissues and organs.

Formamide is also used as an RNA stabiliser in gel electrophoresis by deionizing RNA. In capillary electrophoresis, it is used for stabilizing (single) strands of denatured DNA.

Another use is to add it in sol-gel solutions in order to avoid cracking during sintering.

Formamide, in its pure state, has been used as an alternative solvent for the electrostatic self-assembly of polymer nanofilms.[8]

Formamide is used to prepare primary amines directly from ketones via their N-formyl derivatives, using the Leuckart reaction.

Hypothetical biochemistry

Formamide has also been proposed as an alternative solvent to water, perhaps with the ability to support life with alternative biochemistries to that currently found on Earth. It can be formed by the reaction of hydrogen cyanide and water, has a large dipole moment, and dissolves almost everything that will dissolve in water.[9]

RNA base creation

Formamide has been shown to create guanine at 130 °C in the presence of ultra violet light.[10]


Formamide is moderately irritating to the eyes, skin and mucous membranes.[11] Inhalation of large amounts of formamide vapor may require medical attention.[12][13] It is also a teratogen.[14] Formamide has been shown to exhibit hematoxicity in animals and is considered hazardous by prolonged exposure through inhalation, oral intake and dermal absorption.[15] Formamide should never be handled without proper safety attire including gloves and goggles.


  1. Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 841. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The traditional name ‘formamide’ is retained for HCO-NH2 and is the preferred IUPAC name.
  2. 1 2 3 4 "NIOSH Pocket Guide to Chemical Hazards #0295". National Institute for Occupational Safety and Health (NIOSH).
  3. F. G. Bordwell; J. E. Bartmess; J. A. Hautala (1978). "Alkyl effects on equilibrium acidities of carbon acids in protic and dipolar aprotic media and the gas phase". J. Org. Chem. 43 (16): 3095–3101. doi:10.1021/jo00410a001.
  4. 1 2 Hohn, A. (1999). "Formamide". In Kroschwitz, Jacqueline I. Kirk-Othmer Concise Encylclopedia of Chemical Technology (4th ed.). New York: John Wiley & Sons, Inc. pp. 943–944. ISBN 978-0471419617.
  5. 1 2 Bipp, H.; Kieczka, H. (2005), "Formamides", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a12_001.pub2
  6. Lorin, M. (1864). "Preparation of Formamide by means of Formiates and Oxalates". The Chemical News and Journal of Physical Science. IX: 291. Retrieved 14 June 2014.
  7. Phelps, I.K.; Deming, C.D. (1908). "The Preparation of Formamide from Ethyl Formate and Ammonium Hydroxide". The Chemical News and Journal of Physical Science. XCVII: 86–87. Retrieved 14 June 2014.
  8. Vimal K. Kamineni; Yuri M. Lvov; Tabbetha A. Dobbins (2007). "Layer-by-Layer Nanoassembly of Polyelectrolytes Using Formamide as the Working Medium". Langmuir. 23 (14): 7423–7427. doi:10.1021/la700465n. PMID 17536845.
  9. Committee On The Limits Of Organic Life In Planetary Systems (2007). The Limits of Organic Life in Planetary Systems. Washington, DC: The National Academies Press. p. 74. ISBN 0-309-66906-5. Retrieved 2012-08-29.
  10. "Origin of Life: Adding UV Light Helps Form 'Missing G' of RNA Building Blocks". Science Daily. June 14, 2010.
  11. TOXNet Formamide HSDB: Formamide
  12. Warheit DB1, Kinney LA, Carakostas MC, Ross PE (1989). "Inhalation toxicity study of formamide in rats". Fundamental and Applied Toxicology. 13 (4): 702–713. doi:10.1093/toxsci/13.4.702. PMID 2620791.
  13. MSDS for formamide,
  14. Lab use of formamide, University of Bath
  15. ECHA Formamide
This article is issued from Wikipedia - version of the 10/11/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.