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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:
Assay:
99%
Form:
liquid
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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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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Photostability of Anthraquinone and Azo Dyes in N-Ethylacetamide (Nylon Model).
Chang IY and Miller IK.
Journal of the Society of Dyers and Colourists, 102(2), 46-53 (1986)
Aurélie Leverrier et al.
Phytochemistry, 72(11-12), 1443-1452 (2011-05-10)
An in vitro biological screening of Malaysian plants allowed the selection of several species with a significant binding affinity for the antiapoptotic protein Bcl-xL. The chemical investigation of Endiandra kingiana led to the isolation of a series of polyketides named
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
Raphaela Kannengießer et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 16(9), 1906-1911 (2015-04-29)
The gas-phase structures and parameters describing acetyl methyl torsion of N-ethylacetamide are determined with high accuracy, using a combination of molecular beam Fourier-transform microwave spectroscopy and quantum chemical calculations. Conformational studies at the MP2 level of theory yield four minima
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
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