Dimethylformamide
Dimethylformamide sample and bottle
| |
Names | |
---|---|
IUPAC name
N,N-Dimethylformamide
| |
Other names
N,N-Dimethylmethanamide
DMF | |
Identifiers | |
Jmol-3D images | Image |
| |
Properties | |
C3H7NO | |
Molar mass | 73.10 g/mol |
Appearance | Colorless liquid |
Odor | None (fresh) Fishy, amoniacal (old) |
Density | 0.948 g/mL |
Melting point | −60.5 °C (−76.9 °F; 212.7 K) |
Boiling point | 152 to 154 °C (306 to 309 °F; 425 to 427 K) |
Miscible | |
Solubility | Miscible with ethanol, toluene |
Vapor pressure | 516 Pa |
Thermochemistry | |
Std enthalpy of
formation (ΔfH |
−240.6–−238.2 kJ mol−1 |
Hazards | |
Safety data sheet | LabChem |
Flash point | 58 °C |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
1.5 g kg−1 (dermal, rabbit) 2.8 g kg−1 (oral, rat) 3.7 g/kg (mouse, oral) 3.5 g/kg (rat, oral) |
LC50 (Median concentration)
|
3092 ppm (mouse, 2 hr) |
Related compounds | |
Related compounds
|
Formamide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
This article is a stub. Please help Sciencemadness Wiki by expanding it, adding pictures, and improving existing text.
|
Dimethylformamide or N,N-dimethylformamide is an organic compound with the formula (CH3)2NC(O)H.
Contents
Properties
Chemical
DMF penetrates most types of plastic and causes them to swell.
Physical
Dimethylformamide is an odorless, colorless liquid, miscible with water and most organic liquids. Technical grade or degraded samples often have a fishy smell due to impurities, such as dimethylamine.
Availability
DMF is sold by various chemical suppliers.
Preparation
Dimethylformamide can be synthesized from methyl formate and dimethylamine or by reaction of dimethylamine with carbon monoxide.
Projects
- Acyl halide synthesis
Handling
Safety
DMF has been linked to cancer in humans, and it is thought to cause birth defects.
Storage
In closed bottles, away from any acidic vapors. DMF will slowly break down to release dimethylamine.
Disposal
DMF should be mixed with a more flammable solvent and safely burned.
References
Relevant Sciencemadness threads
- Chemical pages without CAS Registry Number
- Articles without EBI source
- Chemical pages without ChemSpiderID
- Chemical pages without DrugBank identifier
- Articles without KEGG source
- Articles without InChI source
- Articles without UNII source
- Articles containing unverified chemical infoboxes
- Article stubs
- Chemical compounds
- Organic compounds
- Solvents
- Polar solvents
- Aprotic solvents
- Carcinogenic
- Liquids