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Merck
CN

54340

Sigma-Aldrich

2-羟乙基肼

≥95% (GC)

别名:

2-肼基乙醇

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About This Item

线性分子式:
HOCH2CH2NHNH2
CAS号:
分子量:
76.10
Beilstein:
1731669
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥95% (GC)

折射率

n20/D 1.493 (lit.)
n20/D 1.493

沸点

155-160 °C/32 mmHg (lit.)

mp

−70 °C (lit.)

密度

1.123 g/mL at 25 °C (lit.)

官能团

amine
hydrazine
hydroxyl

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

象形图

Skull and crossbonesHealth hazard

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

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

170.6 °F - closed cup

闪点(°C)

77 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

Lot/Batch Number

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A new method for the synthesis of 1, 4, 5-oxadiazocines and its application in the structure modification of natural products.
Liu W, et al.
Tetrahedron Letters, 46(46), 8009-8012 (2005)
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)
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)
C Andriamampandry et al.
Journal of neurochemistry, 56(6), 1845-1850 (1991-06-01)
The sequential methylation of ethanolamine and its phosphorylated derivatives has been studied with chick neurons in culture in the presence of several pharmacological agents. Incubation with [3H]ethanolamine in the presence of monomethylethanolamine and dimethylethanolamine indicated that in these neurons the

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