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215201

Sigma-Aldrich

2-Hydroxyethylhydrazine

technical grade, 90%

Synonym(s):

2-Hydrazinoethanol

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About This Item

Linear Formula:
HOCH2CH2NHNH2
CAS Number:
109-84-2
Molecular Weight:
76.10
Beilstein/REAXYS Number:
1731669
EC Number:
203-711-6
MDL number:
MFCD00007623
UNSPSC Code:
12352100
PubChem Substance ID:
24852878

grade

technical grade

assay

90%

refractive index

n20/D 1.493 (lit.)

bp

155-160 °C/32 mmHg (lit.)

mp

−70 °C (lit.)

density

1.123 g/mL at 25 °C (lit.)

SMILES string

NNCCO

InChI

1S/C2H8N2O/c3-4-1-2-5/h4-5H,1-3H2

Inchi Key

GBHCABUWWQUMAJ-UHFFFAOYSA-N

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pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

170.6 °F - closed cup

flash_point_c

77 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
08622DJ
01418JH
08031EH
09003PD
12826ED

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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
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
Guoxing Su et al.
Journal of plant physiology, 162(12), 1297-1303 (2006-01-21)
In order to analyze the relationship between polyamine oxidative degradation induced by light and the Lignin synthesis in cell walls, the activities of diamine oxidases and peroxidase, the contents of H2O2 and lignin, and the growth of hypocotyls in soybean
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
A M Timperio et al.
Xenobiotica; the fate of foreign compounds in biological systems, 33(2), 153-167 (2003-03-08)
1 Furazolidone, a drug widely used in human and veterinary medicine, exhibits inhibition of monoamine oxidase activity, as observed in the tissues of a number of different animal species, including man. The aim of the current study was to determine
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