Direkt zum Inhalt
Merck

147400

Sigma-Aldrich

N-Ethylacetamid

99%

Synonym(e):

Acetamidoethane, N-Acetylethylamine

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Lineare Formel:
CH3CONHC2H5
CAS-Nummer:
Molekulargewicht:
87.12
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

99%

Form

liquid

Brechungsindex

n20/D 1.433 (lit.)

bp

90-92 °C/8 mmHg (lit.)

Dichte

0.924 g/mL at 25 °C (lit.)

Funktionelle Gruppe

amide

SMILES String

CCNC(C)=O

InChI

1S/C4H9NO/c1-3-5-4(2)6/h3H2,1-2H3,(H,5,6)

InChIKey

PMDCZENCAXMSOU-UHFFFAOYSA-N

Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich

Allgemeine Beschreibung

N-Ethylacetamide is a suitable nylon model for mechanistic studies of dye fading.

Anwendung

N-Ethylacetamide was used to investigate propylene carbonate and a mixture of N-methylformamide and N-ethylacetamide by broadband dielectric and mechanical shear spectroscopy. It was used in determination of reaction products of OH-oxidation of N-methylpyrrolidone under atmospheric conditions.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

224.6 °F - closed cup

Flammpunkt (°C)

107 °C - closed cup


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Kunden haben sich ebenfalls angesehen

Jolanta Świergiel et al.
Physical chemistry chemical physics : PCCP, 13(9), 3911-3916 (2011-01-07)
The impedance spectroscopy studies performed for two strongly hydrogen-bonded liquid amides: N-methylpropionamide (NMP, CH(3)·NH·CO·C(2)H(5)) and N-ethylacetamide (NEA, C(2)H(5)·NH·CO·CH(3)) have shown that the two centers of the peptide linkage, -NH·CO-, active in the C=OH-N hydrogen bonds formation, exhibit quite different sensibilities
Catalin Gainaru et al.
The Journal of chemical physics, 137(6), 064508-064508 (2012-08-18)
Propylene carbonate and a mixture of two secondary amides, N-methylformamide and N-ethylacetamide, are investigated by means of broadband dielectric and mechanical shear spectroscopy. The similarities between the rheological and the dielectric responses of these liquids and of the previously investigated
Tetsuya Tatsukawa et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 26(18), 4820-4825 (2006-05-05)
AMPA receptor (AMPAR) internalization provides a mechanism for long-term depression (LTD) in both hippocampal pyramidal neurons and cerebellar Purkinje cells (PCs). Cerebellar LTD at the parallel fiber (PF)-PC synapse is the underlying basis of motor learning and requires AMPAR activation
Li-Min Wang et al.
The Journal of chemical physics, 123(5), 054516-054516 (2005-08-20)
Dielectric relaxation dynamics of secondary amides is explored in their supercooled state near the glass transition temperature Tg by investigating N-ethylacetamide and its mixtures with N-methylformamide. All the samples are found to exhibit giant dielectric permittivities, reaching over 500 in
R Buchet et al.
Biophysical chemistry, 22(4), 249-254 (1985-10-01)
It is shown that a striking parallelism exists between the anesthetic potency of general halocarbon anesthetics and their influence on the hydrogen bond association constants in N-H...O=C type hydrogen bonds, important for shaping the ion channels. It is further shown

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.