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Safety Information

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:
505944
EC Number:
205-483-3
MDL number:
MFCD00008183
UNSPSC Code:
12352100
PubChem Substance ID:
57647200
NACRES:
NA.21

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)

refractive index

n20/D 1.454 (lit.)

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

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

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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.

PDSCL

Deleterious substance

PRTR

Class I Designated Chemical Substances

FSL

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

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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SAFC

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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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