Misplaced Pages

Orthoformic acid

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Hypothetical molecule with the formula HC(OH)3 "Methanetriol" redirects here. Not to be confused with Methanethiol.
Orthoformic acid
Stereo skeletal formula of orthoformic acid
Names
Preferred IUPAC name Methanetriol
Other names Orthoformic acid
Trihydroxymethane
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CH4O3/c2-1(3)4/h1-4HKey: RLAHWVDQYNDAGG-UHFFFAOYSA-N
  • InChI=1/CH4O3/c2-1(3)4/h1-4HKey: RLAHWVDQYNDAGG-UHFFFAOYAS
SMILES
  • OC(O)O
Properties
Chemical formula HC(OH)3
Molar mass 64.040 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Orthoformic acid or methanetriol is a chemical compound with the formula HC(OH)3. In this molecule, the central carbon atom is bound to one hydrogen and three hydroxyl groups.

Orthoformic acid was long held to be a hypothetical chemical compound, as it was expected to decompose instantly into formic acid and water, making it too unstable to isolate or observe. However, observation was shown to be possible in 2024, when it was identified by mass spectrometry. This involved the electron-irradiation of a frozen mixture of methanol and oxygen.

Esters

Main article: Ortho ester

Methanetriol esters, known as orthoformates or ortho esters, are well known and commercially available. Like acetals, they are stable towards bases but easily hydrolyzed in acidic conditions to the alcohol and an ester of formic acid. They are used as mild dehydrating agents. Especially well known are trimethyl orthoformate, triethyl orthoformate, and triisopropyl orthoformate.

See also

References

  1. "Methanetriol - PubChem". NCBI. Retrieved 22 April 2013.
  2. Bohm, Stanislav; Antipova, Diana; Kuthan, Josef (15 October 1996). "Study of methanetriol decomposition mechanisms". International Journal of Quantum Chemistry. 60 (2): 649–655. doi:10.1002/(SICI)1097-461X(1996)60:2<649::AID-QUA3>3.0.CO;2-X.
  3. >Marks, Joshua H.; Bai, Xilin; Nikolayev, Anatoliy A.; Gong, Qi’ang; Zhu, Cheng; Kleimeier, N. Fabian; Turner, Andrew M.; Singh, Santosh K.; Wang, Jia; Yang, Jiuzhong; Pan, Yang; Yang, Tao; Mebel, Alexander M.; Kaiser, Ralf I. (17 April 2024). "Methanetriol─Formation of an Impossible Molecule". Journal of the American Chemical Society. doi:10.1021/jacs.4c02637.
  4. Sah, Peter P. T.; Ma, Tsu Sheng (July 1932). "ESTERS OF ORTHOFORMIC ACID". Journal of the American Chemical Society. 54 (7): 2964–2966. doi:10.1021/ja01346a048.
  5. H. W. Post (1943), "The Chemistry of the Aliphatic Orthoesters", Reinhold, 188 pages
Categories: