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ARK2169

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Ethanolamin

Arzneimittelherstellung

Synonym(e):

2-Amino-ethanol, 2-Aminoethylalkohol, ETA, MEA, MEA 90, MEA-LCI, Monoethanolamin

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About This Item

Lineare Formel:
NH2CH2CH2OH
CAS-Nummer:
141-43-5
Molekulargewicht:
61.08
Beilstein:
505944
EG-Nummer:
205-483-3
MDL-Nummer:
MFCD00008183
UNSPSC-Code:
12352100
NACRES:
NA.21

Biologische Quelle

synthetic

Qualitätsniveau

500

Dampfdichte

2.1 (vs air)

Dampfdruck

0.2 mmHg ( 20 °C)

Assay

98.0-105.0% (Titrimetric)

Form

liquid

Selbstzündungstemp.

1436 °F

Expl.-Gr.

17 %

Brechungsindex

n20/D 1.454 (lit.)

bp

170 °C (lit.)
69-70 °C/10 mmHg

mp (Schmelzpunkt)

10-11 °C (lit.)

Dichte

1.012 g/mL at 25 °C (lit.)

Eignung

suitable for manufacturing use

Lagertemp.

room temp

SMILES String

NCCO

InChI

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

InChIKey

HZAXFHJVJLSVMW-UHFFFAOYSA-N

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Ersetzt durch

Produkt-Nr.
Beschreibung
Preisangaben

137133

Ethanolamin, EMPROVE® EXPERT, NF

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flammpunkt (°F)

195.8 °F - Pensky-Martens closed cup

Flammpunkt (°C)

91 °C - Pensky-Martens closed cup

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Analysenzertifikate (COA)

Lot/Batch Number

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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
Shingo Kobayashi et al.
Biochimica et biophysica acta, 1841(9), 1264-1271 (2014-05-17)
In eukaryotic cells, phospholipids are synthesized exclusively in the defined organelles specific for each phospholipid species. To explain the reason for this compartmental specificity in the case of phosphatidylcholine (PC) synthesis, we constructed and characterized a Saccharomyces cerevisiae strain that
Su Chul Jang et al.
Small (Weinheim an der Bergstrasse, Germany), 11(4), 456-461 (2014-09-10)
Evaluation of kinetic distribution and behaviors of nanoparticles in vivo provides crucial clues into their roles in living organisms. Extracellular vesicles are evolutionary conserved nanoparticles, known to play important biological functions in intercellular, inter-species, and inter-kingdom communication. In this study
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
Gemma C Langridge et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(3), 863-868 (2014-12-24)
Many bacterial pathogens are specialized, infecting one or few hosts, and this is often associated with more acute disease presentation. Specific genomes show markers of this specialization, which often reflect a balance between gene acquisition and functional gene loss. Within
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