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Merck
CN

110167

Ethanolamine

≥99%, liquid, ReagentPlus®

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:
Molecular Weight:
61.08
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
205-483-3
Beilstein/REAXYS Number:
505944
MDL number:
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Product Name

Ethanolamine, ReagentPlus®, ≥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)

product line

ReagentPlus®

assay

≥99%

form

liquid

autoignition temp.

1436 °F

expl. lim.

17 %

refractive index

n20/D 1.454 (lit.)

bp

170 °C (lit.)
69-70 °C/10 mmHg

mp

10-11 °C (lit.)

solubility

water: miscible 1000 g/L at 20 °C

density

1.012 g/mL at 25 °C (lit.)

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Other Notes

This product has been replaced by 15014-ALDRICH | Ethanolamine, ≥99% | NH2CH2CH2OH

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

CorrosionExclamation mark

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 Information

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Fast one-step synthesis of N-doped carbon dots by pyrolyzing ethanolamine.
Dong X, et al.
Journal of Material Chemistry C, 2(36), 7477-7481 (2014)
Surface reactions of brominated arenes as a model for the formation of chlorinated dibenzodioxins and-furans in incineration: inhibition by ethanolamine.
Lippert T, et al.
Environmental Science & Technology, 25(8), 1485-1489 (1991)
Aqueous solvation and functionalization of weak-acid polyelectrolyte thin films.
Peez RF, et al.
Langmuir, 14(15), 4232-4237 (1998)
Fong-Fu Hsu et al.
Journal of the American Society for Mass Spectrometry, 13(5), 558-570 (2002-05-22)
Negative-ion electrospray ionization tandem quadrupole mass spectrometry provides a useful method for the structural characterization of ceramides. Fragment ions referring to the identities of the fatty acid substituent and of the long chain base of the molecules are readily available
Cristina Mayor-Ruiz et al.
Nature chemical biology, 16(11), 1199-1207 (2020-08-05)
Targeted protein degradation is a new therapeutic modality based on drugs that destabilize proteins by inducing their proximity to E3 ubiquitin ligases. Of particular interest are molecular glues that can degrade otherwise unligandable proteins by orchestrating direct interactions between target

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