推薦產品
![4,7-二溴苯并[c]-1,2,5-噻二唑 95%](/deepweb/assets/sigmaaldrich/product/structures/711/964/3fd3ffd1-5916-468e-a743-22f1611b5a33/640/3fd3ffd1-5916-468e-a743-22f1611b5a33.png)
包含
~0.5% phosphoric acid as stabilizer
濃度
~55% in H2O
折射率
n20/D 1.376
SMILES 字串
OCC#N
InChI
1S/C2H3NO/c3-1-2-4/h4H,2H2
InChI 密鑰
LTYRAPJYLUPLCI-UHFFFAOYSA-N
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訊號詞
Danger
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
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)
Evidence for the microsomal metabolism of glycolonitrile.
J J Freeman et al.
Biochemical pharmacology, 36(1), 184-187 (1987-01-01)
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
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