Acetamide
![]() Freshly prepared acetamide in a jar
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Names | |
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IUPAC name
Acetamide
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Systematic IUPAC name
Ethanamide | |
Properties | |
C2H5NO | |
Molar mass | 59.068 g/mol |
Appearance | Colorless solid |
Odor | Odorless (pure) "Mouse"-like (impure) |
Density | 1.159 g/cm3 (20 °C) |
Melting point | 81.16 °C (178.09 °F; 354.31 K) |
Boiling point | 221.2 °C (430.2 °F; 494.3 K) (decomposes) |
200 g/100 ml | |
Solubility | Soluble in benzene, chloroform, ethanol, glycerol, isopropanol, methanol, pyridine Slightly soluble in diethyl ether, toluene |
Solubility in ethanol | 50 g/100 ml |
Solubility in pyridine | 16.6 g/100 ml |
Vapor pressure | 0.0182 mmHg at 25 °C |
Hazards | |
Safety data sheet | Sigma-Aldrich |
Flash point | 126 °C (259 °F; 399 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
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7,000 mg/kg (rat, oral) |
Related compounds | |
Related compounds
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Formamide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Acetamide or ethanamide is an organic compound with the chemical formula CH3CONH2. It is the simplest amide derived from acetic acid.
Contents
[hide]Properties
Chemical
Dehydration of acetamide in the presence of catalyst yields acetonitrile.
Physical
Acetamide is a colorless solid, very soluble in water.
Availability
It is sold by chemical suppliers.
Preparation
Acetamide can be produced in the laboratory by dehydrating ammonium acetate.
A simpler route involves refluxing urea with glacial acetic acid.[1]
Ammonolysis of ethyl acetate is also another route.
Alternatively acetamide can be obtained in excellent yield via ammonolysis of acetylacetone under conditions commonly used in reductive amination.
Projects
- Make acetonitrile
Handling
Safety
Acetamide doesn't appear to be very toxic.
Storage
Acetamide should be kept in closed glass or PE bottles.
Disposal
Can be neutralized with a strong oxidizing mixture.