147400
N-Ethylacetamide
99%
Synonym(s):
Acetamidoethane, N-Acetylethylamine
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About This Item
Linear Formula:
CH3CONHC2H5
CAS Number:
Molecular Weight:
87.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-896-7
MDL number:
Product Name
N-Ethylacetamide, 99%
InChI key
PMDCZENCAXMSOU-UHFFFAOYSA-N
InChI
1S/C4H9NO/c1-3-5-4(2)6/h3H2,1-2H3,(H,5,6)
SMILES string
CCNC(C)=O
assay
99%
form
liquid
refractive index
n20/D 1.433 (lit.)
bp
90-92 °C/8 mmHg (lit.)
density
0.924 g/mL at 25 °C (lit.)
functional group
amide
Quality Level
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Application
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.
General description
N-Ethylacetamide is a suitable nylon model for mechanistic studies of dye fading.
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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
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
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
New On-line Mass Spectrometer for Identification of Reaction Products in the Aqueous Phase: Application to the OH-oxidation of N-methylpyrrolidone under Atmospheric Conditions.
Poulain L, et al.
Environmental Simulation Chambers: Application to Atmospheric Chemical Processes, 83-96 (2006)
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