50642
Glycolic acid nitrile solution
~55% in H2O
Sinônimo(s):
Formaldehyde cyanohydrin, Hydroxyacetonitrile
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About This Item
Fórmula linear:
HOCH2CN
Número CAS:
Peso molecular:
57.05
Beilstein:
605328
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
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contém
~0.5% phosphoric acid as stabilizer
concentração
~55% in H2O
índice de refração
n20/D 1.376
cadeia de caracteres SMILES
OCC#N
InChI
1S/C2H3NO/c3-1-2-4/h4H,2H2
chave InChI
LTYRAPJYLUPLCI-UHFFFAOYSA-N
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Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral
Código de classe de armazenamento
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
Classe de risco de água (WGK)
WGK 3
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G Arrhenius et al.
The Journal of organic chemistry, 62(16), 5522-5525 (1997-08-08)
A study of glycolonitrile polymerization has led to the isolation and characterization of two 2,5-dihydro-4-aminooxazoles, 4 and 5. Previous reports have misassigned these structures as s-triazines or pyrimidines. X-ray diffraction analysis of crystals of 4 and an acetylated oxazole derivative
Shijun Wu et al.
Biotechnology and bioengineering, 99(3), 717-720 (2007-09-06)
A key step in a chemoenzymatic process for the production of high-purity glycolic acid (GLA) is the enzymatic conversion of glycolonitrile (GLN) to ammonium glycolate using a nitrilase derived from Acidovorax facilis 72W. Protein engineering and over-expression of this nitrilase
Evidence for the microsomal metabolism of glycolonitrile.
J J Freeman et al.
Biochemical pharmacology, 36(1), 184-187 (1987-01-01)
Acceleration of HCN oligomerization by formaldehyde and related compounds: implications for prebiotic syntheses.
A W Schwartz et al.
Journal of molecular evolution, 18(5), 351-353 (1982-01-01)
P Eyer et al.
Archives of toxicology, 59(4), 266-271 (1986-12-01)
HI 6 has been shown to be efficacious in soman intoxication of laboratory animals by reactivation of acetylcholinesterase. To assess possible risks involved in the administration of HI 6 its degradation products were analyzed at pH 2.0, 4.0, 7.4, and
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