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E9508

Sigma-Aldrich

Ethanolamine

≥98%

Sinônimo(s):

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

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About This Item

Fórmula linear:
NH2CH2CH2OH
Número CAS:
141-43-5
Peso molecular:
61.08
Beilstein:
505944
Número CE:
205-483-3
Número MDL:
MFCD00008183
Código UNSPSC:
12161700
ID de substância PubChem:
329799085
NACRES:
NA.25

Nível de qualidade

300

Ensaio

≥98%

forma

liquid

índice de refração

n20/D 1.454 (lit.)

pH

12.1 (20 °C, 100 g/L)

pKa (25 °C)

9.5(lit.)

cadeia de caracteres SMILES

NCCO

InChI

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

chave InChI

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Aplicação


  • New Functionalized Di-substituent Imidazolium Ionic Liquids as Superior Faster Absorbents for Carbon Dioxide Gas.: This research highlights the development of novel imidazolium ionic liquids, where ethanolamine plays a crucial role in enhancing their efficiency as fast absorbents for carbon dioxide removal, presenting a potential impactful application in environmental science and engineering (Shawish et al., 2024).

  • Role of ethanolamine utilization and bacterial microcompartment formation in Listeria monocytogenes intracellular infection.: This study explores how Listeria monocytogenes utilizes ethanolamine and forms bacterial microcompartments, offering insights into bacterial pathogenesis and potential targets for antibiotic development (Chatterjee et al., 2024).

  • (13)C-Stable isotope resolved metabolomics uncovers dynamic biochemical landscape of gut microbiome-host organ communications in mice.: Research here utilizes ethanolamine in stable isotope-resolved metabolomics to map the dynamic biochemical interactions between the gut microbiome and host organs, advancing our understanding of microbial contributions to host metabolism (Xiao et al., 2024).

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

195.8 °F - Pensky-Martens closed cup

Ponto de fulgor (°C)

91 °C - Pensky-Martens closed cup

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
MKCQ8983
MKCQ8642
MKCP8696
MKCP8654
MKCP6930

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Ethanolamine EMPROVE® EXPERT, Ph. Eur., BP, NF

SAFC

1.37044

Ethanolamine

Diethanolamine reagent grade, ≥98.0%

Sigma-Aldrich

D8885

Diethanolamine

Yacine Bounab et al.
Nature protocols, 15(9), 2920-2955 (2020-08-14)
Characterization of immune responses is currently hampered by the lack of systems enabling quantitative and dynamic phenotypic characterization of individual cells and, in particular, analysis of secreted proteins such as cytokines and antibodies. We recently developed a simple and robust
Florent Arbogast et al.
Autophagy, 15(2), 280-294 (2018-09-11)
The involvement of macroautophagy/autophagy proteins in B-cell receptor (BCR) trafficking, although suspected, is not well understood. We show that ATG5 (autophagy related 5) contributes to BCR polarization after stimulation and internalization into LAMP1 (lysosomal-associated membrane protein 1)+ and major histocompatibility
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
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