| Identification | More | [Name]
N-Methylpropionamide | [CAS]
1187-58-2 | [Synonyms]
N-METHYLPROPIONAMIDE
n-methyl-propanamid
N-Methylpropanamide
N-methyl-Propanamide
n-methyl-propionamid
N-Methylpropionic acid amide
n-methylpropionicacidamide
N-Methylpropionsaureamid
Propionamide, N-methyl- | [EINECS(EC#)]
214-699-7 | [Molecular Formula]
C4H9NO | [MDL Number]
MFCD00009300 | [Molecular Weight]
87.12 | [MOL File]
1187-58-2.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS LIQUID | [Melting point ]
-43 °C (lit.) | [Boiling point ]
146 °C/90 mmHg (lit.) | [density ]
0.931 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.436(lit.)
| [Fp ]
222 °F
| [storage temp. ]
Store at room temperature | [form ]
clear liquid | [pka]
16.61±0.46(Predicted) | [color ]
Colorless | [Specific Gravity]
0.93 | [Specific Heat Capacity]
Cp(liquid):179J/(g·K),at 25℃ | [BRN ]
1737640 | [InChI]
1S/C4H9NO/c1-3-4(6)5-2/h3H2,1-2H3,(H,5,6) | [InChIKey]
QJQAMHYHNCADNR-UHFFFAOYSA-N | [SMILES]
CCC(=O)NC | [CAS DataBase Reference]
1187-58-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Propanamide, N-methyl-(1187-58-2) | [EPA Substance Registry System]
1187-58-2(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
UE4515000
| [F ]
3 | [TSCA ]
TSCA listed | [HS Code ]
2924.19.8000 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS LIQUID | [Uses]
N-Methylpropionamide has been used to investigate amide-induced phase separation of hexafluoro-2-propanol-water mixtures. | [Purification Methods]
The amide is a colourless, odourless, neutral liquid at room temperature with a high dielectric constant. The amount of water present can be determined directly by Karl Fischer titration, GLC and NMR have been used to detect unreacted propionic acid. Commercial material of high quality is available, probably from the condensation of anhydrous methylamine with 50% excess of propionic acid. Rapid heating to 120-140o with stirring favours the reaction by removing water either directly or as the ternary xylene azeotrope. The quality of the distillate improves during the distillation. N-Methylpropionamide can be dried over CaO. Water and unreacted propionic acid are removed as their xylene azeotropes. It is then distilled in a vacuum. Material used as an electrolyte solvent (specific conductance less than 10-6 ohm-1 cm -1) is obtained by fractional distillation under reduced pressure, and storage over BaO or molecular sieves because it readily absorbs moisture from the atmosphere on prolonged storage. [Hoover Pure Appl Chem 37 581 1974, Recommended Methods for Purification of Solvents and Tests for Impurities, Coetzee Ed., Pergamon Press, 1982, Beilstein 4 IV 183.] |
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