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Merck

50640

Sigma-Aldrich

乙醇腈 溶液

~70% in H2O

别名:

氰基甲醇, 甲醛氰醇

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About This Item

线性分子式:
HOCH2CN
CAS号:
分子量:
57.05
Beilstein:
605328
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

包含

~0.5% phosphoric acid as stabilizer

品質等級

濃度

~70% in H2O

折射率

n20/D 1.389

密度

1.076 g/mL at 20 °C

SMILES 字串

OCC#N

InChI

1S/C2H3NO/c3-1-2-4/h4H,2H2

InChI 密鑰

LTYRAPJYLUPLCI-UHFFFAOYSA-N

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一般說明

The product is a 70% solution of glycolic acid nitrile in water. Glycolic acid nitrile, also known as hydroxyacetonitrile is the simplest cyanohydrin. The microwave spectra of hydroxyacetonitrile have been recorded in gas-phase and its rotational constants have been calculated. Ice containing formaldehyde and hydrogen cyanide react under astrophysical-like conditions to form hydroxyacetonitrile.

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3


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其他客户在看

Slide 1 of 2

1 of 2

Rotational isomerism and barriers to internal rotation in hydroxyacetonitrile from microwave spectroscopy.
Cazzoli G, et al.
J. Chem. Soc., Faraday II, 69, 569-578 (1973)
Hydroxyacetonitrile (HOCH2CN) formation in astrophysical conditions. competition with the aminomethanol, a glycine precursor.
Danger G, et al.
The Astrophysical Journal, 756(1), 11-11 (2012)
Microwave and Quantum-Chemical Study of Conformational Properties and Intramolecular Hydrogen Bonding of 2-Hydroxy-3-Butynenitrile (HC=CCH(OH)C=N).
M?llendal H, et al.
The Journal of Physical Chemistry A, 119(4), 634-640 (2015)
Formation of hydroxyacetonitrile (HOCH2CN) and polyoxymethylene (POM)-derivatives in comets from formaldehyde (CH2O) and hydrogen cyanide (HCN) activated by water.
Danger G, et al.
Physical Chemistry Chemical Physics, 16(8), 3360-3370 (2014)
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

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