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Merck

09-0590

Sigma-Aldrich

Ethanolamin

JIS special grade, ≥99.0%

Synonym(e):

2-Amino-ethanol, 2-Aminoethylalkohol, ETA, MEA, MEA 90, MEA-LCI, Monoethanolamin

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About This Item

Lineare Formel:
NH2CH2CH2OH
CAS-Nummer:
Molekulargewicht:
61.08
Beilstein:
505944
MDL-Nummer:
UNSPSC-Code:
12352116
PubChem Substanz-ID:

Qualität

JIS special grade

Dampfdichte

2.1 (vs air)

Dampfdruck

0.2 mmHg ( 20 °C)

Assay

≥99.0%

Form

liquid

Selbstzündungstemp.

1436 °F

Expl.-Gr.

17 %

Verfügbarkeit

available only in Japan

Brechungsindex

n20/D 1.454 (lit.)

bp

170 °C (lit.)
69-70 °C/10 mmHg

mp (Schmelzpunkt)

10-11 °C (lit.)

Dichte

1.012 g/mL at 25 °C (lit.)

SMILES String

NCCO

InChI

1S/C2H7NO/c3-1-2-4/h4H,1-3H2

InChIKey

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Piktogramme

CorrosionExclamation mark

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flammpunkt (°F)

185.0 °F

Flammpunkt (°C)

85 °C


Analysenzertifikate (COA)

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J E Vance
Biochimica et biophysica acta, 1045(2), 128-134 (1990-07-16)
Monolayer cultures of rat hepatocytes have been examined for their ability to secrete ethanolamine plasmalogen as a component of nascent lipoproteins. In culture medium from these cells, ethanolamine plasmalogen comprises approx. 20-30% of total ethanolamine glycerophospholipids when measured either as
H Perschak et al.
Human neurobiology, 6(3), 191-194 (1987-01-01)
Concentrations of putative neuroactive substances glutamate, aspartate, gamma-aminobutyric acid, glycine, proline and ethanolamine were determined in ventricular cerebrospinal fluid collected in patients suffering from Parkinson's disease, pain syndromes or cerebellar tremor. Values are similar to those given in the literature
Gabriel da Silva
The journal of physical chemistry. A, 116(45), 10980-10986 (2012-09-22)
The alkanolamine 2-aminoethanol (NH(2)CH(2)CH(2)OH), otherwise known as monoethanolamine (MEA), is a widely used solvent for carbon capture, yet relatively little is known about its atmospheric chemistry. The hydroxyl radical initiated oxidation of MEA is thought to predominantly form the α-aminoalkyl
Danielle A Garsin
Nature reviews. Microbiology, 8(4), 290-295 (2010-03-18)
Ethanolamine is a compound that can be readily derived from cell membranes and that some bacteria can use as a source of carbon and/or nitrogen. The complex biology and chemistry of this process has been under investigation since the 1970s
Ye-Jin Hwang et al.
Advanced materials (Deerfield Beach, Fla.), 27(31), 4578-4584 (2015-07-03)
By controlling the polymer/polymer blend self-organization rate, all-polymer solar cells composed of a high-mobility, crystalline, naphthalene diimide-selenophene copolymer acceptor and a benzodithiophene-thieno[3,4-b]thiophene copolymer donor are achieved with a record 7.7% power conversion efficiency and a record short-circuit current density (18.8

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