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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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
SMILES string
CCNC(C)=O
InChI
1S/C4H9NO/c1-3-5-4(2)6/h3H2,1-2H3,(H,5,6)
InChI key
PMDCZENCAXMSOU-UHFFFAOYSA-N
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General description
N-Ethylacetamide is a suitable nylon model for mechanistic studies of dye fading.
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.
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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
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
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)
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
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
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