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Merck

15014

Ethanolamine

≥99%, liquid

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
NACRES:
NA.21
PubChem Substance ID:
57647200
UNSPSC Code:
12352100
EC Number:
205-483-3
MDL number:
MFCD00008183
Beilstein/REAXYS Number:
505944
Assay:
≥99%
Form:
liquid

Key Documents

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Product Name

Ethanolamine, ≥99%

InChI key

HZAXFHJVJLSVMW-UHFFFAOYSA-N

InChI

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

SMILES string

NCCO

vapor density

2.1 (vs air)

vapor pressure

0.2 mmHg ( 20 °C)

assay

≥99%

form

liquid

autoignition temp.

1436 °F

expl. lim.

17 %

impurities

≤0.5% water (Karl Fischer)

ign. residue

≤0.05% (as SO4)

Quality Level

200

bp

170 °C (lit.), 69-70 °C/10 mmHg

mp

10-11 °C (lit.)

density

1.012 g/mL at 25 °C (lit.)

cation traces

Fe: ≤10 mg/kg

functional group

amine, hydroxyl

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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

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Deleterious substance

pdsc

Class I Designated Chemical Substances

prtr

Group 4: Flammable liquids + Type 3 petroleums + Hazardous rank III + Water soluble liquid

fsl

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

15014-25ML:4548173333694 + 15014-VAR: + 15014-190KG:4548173248431 + 15014-1L:4548173248448 + 15014-BULK: + 15014-100ML:4548173333687 + 15014-2.5L:4548173248455 + 15014-210KG:4548173248462 + 15014-25KG:4548173248479 + 15014-4X2.5L:4548173248486 + 15014-6X1L:4548173248493

jan

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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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