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E0135

Sigma-Aldrich

Ethanolamine

liquid, BioReagent, suitable for cell culture, ≥98%

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:
12161700
PubChem Substance ID:
24894363
NACRES:
NA.21

vapor density

2.1 (vs air)

Quality Level

300

vapor pressure

0.2 mmHg ( 20 °C)

product line

BioReagent

Assay

≥98%

form

liquid

autoignition temp.

1436 °F

expl. lim.

17 %

concentration

16.6 M

technique(s)

cell culture | mammalian: suitable

refractive index

n20/D 1.454 (lit.)

pKa (25 °C)

9.5(lit.)

bp

170 °C (lit.)
69-70 °C/10 mmHg

mp

10-11 °C (lit.)

density

1.012 g/mL at 25 °C (lit.)

SMILES string

NCCO

InChI

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

InChI key

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Related Categories

Application

A medium supplement used as a precursor for phospholipid biosynthesis.

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT5468
MKCQ7138
MKCR1570
MKCP2368
MKCN0201

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Soeren Lukassen et al.
The EMBO journal, 39(10), e105114-e105114 (2020-04-05)
The SARS-CoV-2 pandemic affecting the human respiratory system severely challenges public health and urgently demands for increasing our understanding of COVID-19 pathogenesis, especially host factors facilitating virus infection and replication. SARS-CoV-2 was reported to enter cells via binding to ACE2
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
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
Jenny Fitting et al.
mAbs, 7(2), 390-402 (2015-03-12)
The current standard treatment for acute myeloid leukemia (AML) is chemotherapy based on cytarabine and daunorubicine (7 + 3), but it discriminates poorly between malignant and benign cells. Dose-limiting off‑target effects and intrinsic drug resistance result in the inefficient eradication
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
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