| Weight | 57.052 g/mol |
|---|---|
| Formula | C2H3NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
GLYCOLONITRILE (107-16-4)
hydroxyacetonitrile · cyanohydrin formaldehyde
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- Bioproduction of Glycolic Acid from Glycolonitrile with a New Bacterial Isolate of Alcaligenes sp. ECU0401 (Applied Biochemistry and Biotechnology, 2010)
- Separation of glycolic acid from glycolonitrile hydrolysate by reactive extraction with tri-n-octylamine (Separation and Purification Technology, 2006)
- Archean geochemistry of formaldehyde and cyanide and the oligomerization of cyanohydrin. (Origins of Life and Evolution of Biospheres, 1994)
- HYDROXYACETONITRILE (HOCH2CN) FORMATION IN ASTROPHYSICAL CONDITIONS. COMPETITION WITH THE AMINOMETHANOL, A GLYCINE PRECURSOR (The Astrophysical Journal, 2012)
- Matrix reactions of oxygen atoms with methyl cyanide: infrared spectra of hydroxyacetonitrile and acetonitrile N-oxide (The Journal of Physical Chemistry, 1989)
- Evidence for the microsomal metabolism of glycolonitrile. (Biochemical Pharmacology, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H227: Combustible liquid
Warning Flammable liquids - Category 4 - H310: Fatal in contact with skin
Danger Acute toxicity, dermal - Category 1, 2 - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - hydroxyacetonitrile
- cyanohydrin formaldehyde
-
SMILESC(C#N)O
-
InChIKeyLTYRAPJYLUPLCI-UHFFFAOYSA-N
- Pubchem - GLYCOLONITRILE
- Wikipedia - hydroxyacetonitrile
Glycolonitrile, also called hydroxyacetonitrile or formaldehyde cyanohydrin, is the organic compound with the formula HOCH2CN. It is the simplest cyanohydrin and it is derived from formaldehyde. It is a colourless liquid that dissolves in water and ether.
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