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E9508

Sigma-Aldrich

Ethanolamine

≥98%

Synonyme(s) :

2-Aminoéthanol, Alcool 2-aminoéthylique

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About This Item

Formule linéaire :
NH2CH2CH2OH
Numéro CAS:
Poids moléculaire :
61.08
Numéro Beilstein :
505944
Numéro CE :
Numéro MDL:
Code UNSPSC :
12161700
ID de substance PubChem :
Nomenclature NACRES :
NA.25

Densité de vapeur

2.1 (vs air)

Niveau de qualité

Pression de vapeur

0.2 mmHg ( 20 °C)

Pureté

≥98%

Forme

liquid

Température d'inflammation spontanée

1436 °F

Limite d'explosivité

17 %

Indice de réfraction

n20/D 1.454 (lit.)

pH

12.1 (20 °C, 100 g/L)

pKa (25 °C)

9.5(lit.)

Point d'ébullition

170 °C (lit.)
69-70 °C/10 mmHg

Pf

10-11 °C (lit.)

Densité

1.012 g/mL at 25 °C (lit.)

Chaîne SMILES 

NCCO

InChI

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

Clé InChI

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Catégories apparentées

Application


  • 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).

Pictogrammes

CorrosionExclamation mark

Mention d'avertissement

Danger

Classification des risques

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

Organes cibles

Respiratory system

Code de la classe de stockage

8A - Combustible, corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

195.8 °F - Pensky-Martens closed cup

Point d'éclair (°C)

91 °C - Pensky-Martens closed cup

Équipement de protection individuelle

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


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Les clients ont également consulté

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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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