374768
Glycolonitrile
55 wt. % in H2O
Synonym(s):
Glycolic acid nitrile solution, Formaldehyde cyanohydrin, Hydroxyacetonitrile
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
HOCH2CN
CAS Number:
Molecular Weight:
57.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
605328
Form:
liquid
InChI
1S/C2H3NO/c3-1-2-4/h4H,2H2
SMILES string
OCC#N
InChI key
LTYRAPJYLUPLCI-UHFFFAOYSA-N
form
liquid
concentration
55 wt. % in H2O
impurities
3 mol methyl alcohol
refractive index
n20/D 1.375
density
1.045 g/mL at 25 °C
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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)
T Arrhenius et al.
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life, 24(1), 1-17 (1994-02-01)
The sources and speciation of reduced carbon and nitrogen inferred for the early Archean are reviewed in terms of current observations and models, and known chemical reactions. Within this framework hydrogen cyanide and cyanide ion in significant concentration would have
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service