143936
Propionamide
97%
Synonym(s):
Propanamide, Propylamide
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About This Item
Linear Formula:
CH3CH2CONH2
CAS Number:
Molecular Weight:
73.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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
SMILES string
CCC(N)=O
InChI
1S/C3H7NO/c1-2-3(4)5/h2H2,1H3,(H2,4,5)
InChI key
QLNJFJADRCOGBJ-UHFFFAOYSA-N
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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.
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
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)
David Crich et al.
The Journal of organic chemistry, 74(9), 3389-3393 (2009-04-25)
Beta-thiolactones monosubstituted in the 3-position by alkyl and carbamoyl groups undergo nucleophilic ring opening by arenethiolates through a process involving an S(N)2-type attack at the 4-position leading to 3-arylthiopropionates substituted in the 2-position. These thiocarboxylates can be trapped in situ
R X Xu et al.
Biochemistry, 33(4), 907-916 (1994-02-01)
The oxidation of Co(II) bleomycin A2 by dioxygen leads to two products, HO2-Co(III) bleomycin A2 (form I) and Co(III) bleomycin A2 (form II). 1H NMR chemical shift assignments for protons of both forms have been made by two-dimensional NMR spectral
Tiia Kuuranne et al.
Drug metabolism and disposition: the biological fate of chemicals, 36(3), 571-581 (2007-12-19)
Selective androgen receptor modulators (SARM) are a prominent group of compounds for being misused in sports owing to their advantageous anabolic properties and reduced side effects. To target the preventive doping control analysis in relevant compounds, the challenge is to
Mohamed Mohamed Naseer Ali et al.
Carbohydrate research, 344(3), 355-361 (2008-12-26)
GlcNAcbetaAsn linkage is conserved in the N-glycoproteins of all eukaryotes. l-Glutamine (Gln), which is a one carbon higher homolog of Asn, is never glycosylated. X-ray crystallographic study of several beta-1-N-acetamido- and propionamido derivatives of monosaccharides has earlier shown that the
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