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Dimethylformamide, DMF is an organic compound with the chemical formula H C O N(CH 3) 2. Its structure is HC(=O)−N( −CH 3 ) 2 . Commonly abbreviated as DMF (although this initialism is sometimes used for dimethylfuran , or dimethyl fumarate ), this colourless liquid is miscible with water and the majority of organic liquids.
DMF has a number of attractions as a biofuel.It has an energy density 40% greater than that of ethanol, making it comparable to gasoline (petrol). It is also chemically stable and, being insoluble in water, does not absorb moisture from the atmosphere.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
Dimethyl fumarate (DMF) is the methyl ester of fumaric acid and is named after the earth smoke plant (Fumaria officinalis). [8] Dimethyl fumarate combined with three other fumaric acid esters (FAEs) is solely licensed in Germany as an oral therapy for psoriasis (brand name Fumaderm ). [ 9 ]
The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: . CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −
DMF may refer to: Science and technology. Chemistry. Dimethylformamide, a common solvent; Dimethyl fumarate, a small molecule anti-inflammatory human medicine;
Propanephosphonic acid anhydride (PPAA, T3P) is an anhydride of propanephosphonic acid.Its structure is a cyclic trimer, with a phosphorus–oxygen core and propyl groups and additional oxygens attached. [1]