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MilliporeSigma

143936

Sigma-Aldrich

Propionamide

97%

Synonym(s):

Propanamide, Propylamide

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About This Item

Linear Formula:
CH3CH2CONH2
CAS Number:
79-05-0
Molecular Weight:
73.09
EC Number:
201-172-1
MDL number:
MFCD00008039
UNSPSC Code:
12352100
PubChem Substance ID:
24848618
NACRES:
NA.22

Key Documents

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Quality Level

200

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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1 of 4

This Item
8.21046751235136905
Propionamide 97%

Sigma-Aldrich

143936

Propionamide

Propionamide for synthesis

Sigma-Aldrich

8.21046

Propionamide

Propiolamide 97%

Sigma-Aldrich

751235

Propiolamide

4-Methoxybenzyl alcohol 98%

Sigma-Aldrich

136905

4-Methoxybenzyl alcohol

assay

97%

assay

-

assay

97%

assay

98%

solubility

alcohol: freely soluble, diethyl ether: freely soluble, chloroform: freely soluble, water: freely soluble

solubility

-

solubility

-

solubility

alcohol: freely soluble, diethyl ether: freely soluble, water: insoluble

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

bp

213 °C (lit.)

bp

-

bp

-

bp

259 °C (lit.)

mp

76-79 °C (lit.)

mp

75-78 °C

mp

57-62 °C

mp

22-25 °C (lit.)

density

1.042 g/mL at 25 °C (lit.)

density

-

density

-

density

1.113 g/mL at 25 °C (lit.)

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[1].

Application

Propionamide was used as adsorbent in the determination of adsorption isotherms of acetamide and propionamide on multi-wall carbon nanotube[2]. It was used in a robust screening method to study biotransformations using (+)-γ-lactamase enzyme[3].

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000487594
0000487594
0000391695
0000360373
0000361664

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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)
The availability of genome sequences, affordable mass spectrometers and high-resolution two-dimensional gels has made possible the identification of hundreds of proteins from many organisms by peptide mass fingerprinting. However, little attention has been paid to how information generated by these
J D Stone et al.
Toxicology and applied pharmacology, 161(1), 50-58 (1999-11-24)
Neurofilament modification and accumulation, occurring in toxicant-induced neuropathies, has been proposed to compromise fast axonal transport and contribute to neurological symptoms or pathology. The current study compares the effects of the neurotoxicants acrylamide (ACR) and 2,5-hexanedione (2,5-HD) on the quantity
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
View All Related Papers

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