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%
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.)
Quality Level
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
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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.
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)
Reactions of Gases with Irradiated Organic Solids: III. Reactions of Propionamide, n-Butyramide, Isobutyramide, Methacrylamide, Valeramide, and Stearamide with Sulfur Dioxide.
Perotti A, et al.
Mol. Cryst. Liq. Cryst., 9(1), 323-342 (2969)
Nobuhito Yukuhiro et al.
Brain research, 1027(1-2), 59-66 (2004-10-21)
We investigated the effects of (S)-N-[2-(1,6,7,8-tetrahydro-2H-indeno-[5,4]furan-8-yl)ethyl]propionamide (ramelteon, TAK-375), a novel MT1/MT2 receptor agonist, on nocturnal sleep in freely moving monkeys and compared these results with those of melatonin and zolpidem. Treatment with ramelteon (0.03 and 0.3 mg/kg, p.o.) significantly shortened
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
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
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