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15014

Sigma-Aldrich

Ethanolamine

≥99%

Synonym(s):

2-Aminoethanol, 2-Aminoethyl alcohol, ETA, MEA, MEA 90, MEA-LCI, Monoethanolamine

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About This Item

Linear Formula:
NH2CH2CH2OH
CAS Number:
141-43-5
Molecular Weight:
61.08
Beilstein/REAXYS Number:
505944
EC Number:
205-483-3
MDL number:
MFCD00008183
UNSPSC Code:
12352100
PubChem Substance ID:
57647200
NACRES:
NA.21

Quality Level

200

assay

≥99%

form

liquid

impurities

≤0.5% water (Karl Fischer)

ign. residue

≤0.05% (as SO4)

refractive index

n20/D 1.454 (lit.)

cation traces

Fe: ≤10 mg/kg

SMILES string

NCCO

InChI

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

InChI key

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Application

  • Catalytic performance and acidic analysis of chloroaluminate ionic liquid: Explores the effects of ethanolamine on the catalytic properties of ionic liquids in oil synthesis (Hu et al., 2024).

Other Notes

The article number 15014-4X2.5L will be discontinued. Please order the single bottle 15014-2.5L which is physically identical with the same exact specifications.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 2

flash_point_f

195.8 °F - Pensky-Martens closed cup

flash_point_c

91 °C - Pensky-Martens closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6610
STBK6611
STBK2829
STBJ7304
STBJ5243

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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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