质量水平
检测方案
≥95% (GC)
折射率
n20/D 1.493 (lit.)
n20/D 1.493
bp
155-160 °C/32 mmHg (lit.)
mp
−70 °C (lit.)
密度
1.123 g/mL at 25 °C (lit.)
SMILES字符串
NNCCO
InChI
1S/C2H8N2O/c3-4-1-2-5/h4-5H,1-3H2
InChI key
GBHCABUWWQUMAJ-UHFFFAOYSA-N
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一般描述
2-羟基乙基肼可与具有强吸电子取代基的β-二酮反应生成5-羟基-4,5-二氢吡唑。
其他说明
可能实行销售限制
警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
170.6 °F
闪点(°C)
77 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Smaail Radi et al.
Molecules (Basel, Switzerland), 21(8), doi:10-doi:10 (2016-08-17)
A pyridylpyrazole bearing a hydroxyethyl substituent group has been synthesized by condensation of (Z)-4-hydroxy-4-(pyridin-2-yl)but-3-en-2-one with 2-hydroxyethylhydrazine. The compound was well characterized and its structure confirmed by single crystal X-ray diffraction. Density functional calculations have been performed using DFT method with
Reaction of 2-hydroxyethylhydrazine with a trifluoromethyl-?-diketone: Study and structural characterization of a new 5-hydroxy-5-trifluoromethyl-4, 5-dihydropyrazole intermediate.
Montoya V, et al.
Journal of Fluorine Chemistry, 128(9), 1007-1011 (2007)
R D Slocum et al.
Planta, 183(3), 443-450 (1991-02-01)
An electron-microscopic cytochemical method was used to localize diamine oxidase (DAO) in pea and polyamine oxidase (PAO) in maize (Zea mays L.). The method, based on the precipitation of amine-oxidase-generated H2O2 by CeCl3, was shown to be specific for DAO
Gregory M Sandala et al.
Journal of the American Chemical Society, 127(24), 8856-8864 (2005-06-16)
Ab initio molecular orbital calculations have been used to study the mechanism of suicide inactivation of ethanolamine ammonia-lyase induced by three different substrate analogues. Analysis of the normal catalytic mechanism with 2-aminoethanol (ethanolamine) as substrate predicts that both the hydrogen-abstraction
Solvent-free synthesis of 3, 5-di-tert-butylpyrazole and 3, 5-di-substituted-butylpyrazol-1-ylethanol.
Van Wyk JL, et al.
J. Chem. Res. (M), 26(8), 474-477 (2012)
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