Methoxymethanol

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Methoxymethanol
Names
Preferred IUPAC name
Methoxymethanol
Other names
Formaldehyde methyl hemiacetal
Identifiers
3D model (JSmol)
1900186
ChEBI
ChemSpider
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EC Number
  • 224-722-2
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UNII
  • InChI=1S/C2H6O2/c1-4-2-3/h3H,2H2,1H3
    Key: VHWYCFISAQVCCP-UHFFFAOYSA-N
  • COCO
Properties
C2H6O2
Molar mass 62.068 g·mol−1
Density 0.948
Hazards
GHS labelling:
GHS02: FlammableGHS07: Exclamation markGHS08: Health hazard
Warning
H226, H302, H371
P210, P233, P240, P241, P242, P243, P260, P264, P270, P280, P301+P312, P303+P361+P353, P309+P311, P330, P370+P378, P403+P235, P405, P501
Flash point 39.9 °C (103.8 °F; 313.0 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Methoxymethanol is a chemical compound which is both an ether and an alcohol, a hemiformal.[1] The structural formula can be written as CH3OCH2OH. It has been discovered in space.[2]

Formation

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Methoxymethanol forms spontaneously when a water solution of formaldehyde and methanol are mixed.[3][1] or when formaldehyde is bubbled through methanol.[4]

In space methoxymethanol can form when methanol radicals (CH2OH or CH3O) react. These are radiolysis products derived when ultraviolet light or cosmic rays hit frozen methanol.[3]

Methanol can react with carbon dioxide and hydrogen at 80°C and some pressure with a ruthenium or cobalt catalyst, to yield some methoxymethanol.[5]

Properties

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Different conformations of the molecule are Gauche-gauce (Gg), Gauche-gauce' (Gg'), and Trans-gauche (Tg).[6]

References

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