143936
Propionamide
97%
Synonym(s):
Propanamide, Propylamide
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About This Item
Linear Formula:
CH3CH2CONH2
CAS Number:
Molecular Weight:
73.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-172-1
MDL number:
Assay:
97%
Product Name
Propionamide, 97%
InChI key
QLNJFJADRCOGBJ-UHFFFAOYSA-N
InChI
1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5)
SMILES string
CCC(N)=O
assay
97%
bp
213 °C (lit.)
mp
76-79 °C (lit.)
solubility
alcohol: freely soluble
chloroform: freely soluble
diethyl ether: freely soluble
water: freely soluble
density
1.042 g/mL at 25 °C (lit.)
functional group
amide
Quality Level
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Application
Propionamide was used as adsorbent in the determination of adsorption isotherms of acetamide and propionamide on multi-wall carbon nanotube. It was used in a robust screening method to study biotransformations using (+)-γ-lactamase enzyme.
General description
Propionamide on γ-irradiation reacts with sulfur dioxide and this reaction has been studied by ESR spectroscopy, gas absorption measurements and X-ray diffraction.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Study of Adsorption Isotherms of Acetamide and Propionamide on Carbon Nanotube.
Vadi M and Moradi N.
Orient. J. Chem., 27(4), 1491-1491 (2011)
Richard H Stadler
Advances in experimental medicine and biology, 561, 157-169 (2006-01-28)
This paper summarizes the progress made to date on acrylamide research pertaining to analytical methods, mechanisms of formation, and mitigation research in the major food categories. Initial difficulties with the establishment of reliable analytical methods have today in most cases
M R Wilkins et al.
Journal of molecular biology, 289(3), 645-657 (1999-06-05)
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Dale W Sickles et al.
Toxicology and applied pharmacology, 222(1), 111-121 (2007-06-02)
The microtubule (MT) motor protein kinesin is a vital component of cells and organs expressing acrylamide (ACR) toxicity. As a mechanism of its potential carcinogenicity, we determined whether kinesins involved in cell division are inhibited by ACR similar to neuronal
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