furtrethonium iodide Chemical Properties

Melting point:

116-117° (Weilmuenster, Jordan); mp 118-120° (Khromov-Borisov)

storage temp. 

-196°C

Safety Information

Toxicity

LD50 intraperitoneal in mouse: 50mg/kg

furtrethonium iodide Usage And Synthesis

Originator

Furmethide,SKF,US,1944

Manufacturing Process

Furfuryl dimethyl amine is first produced, This may conveniently be accomplished by employing the Leuckart synthesis known to those skilled in the art, which involves the use of an aldehyde or a ketone, and formate of ammonia or an amine, or corresponding formamide derived by dehydration of formate of ammonia or an amine.
For example, 5 mols of dimethyl amine and 5 mols of formic acid and water are distilled to 135°C; distilling off most of the water. To the remaining liquid, consisting for the most part of the formyl derivative of dimethyl amine, 1 mol of furfural mixed with 1 mol of formic acid is slowly added with heating, the temperature being maintained at 150°C to 170°C, until the reaction is complete. The mixture is then distilled into a receiver. The course of this reaction may be illustrated as follows:
Part of the formic acid used in the above reaction functions to react with the dimethyl amine liberated in the reaction.
After the furfural has all been added and the reaction has subsided, the residue is cooled, diluted with water, made strongly alkaline and distilled until all volatile substances are removed, The distillate is then made acid with formic acid and distilled with steam as long as nonbasic substances are carried over by the steam. The residue is then made strongly basic with caustic soda and the volatile amines again distilled with steam. The distillate is then treated with strong alkali and then extracted with ether to extract the base. The extract is dried by the addition of caustic potash, the ether removed and the residual amine purified by distillation. Furfuryl dimethyl amine boils over the range 145°C to 150°C.
To obtain the quaternary salt, furfuryl dimethyl amine so prepared is dissolved in dry benzene and to the solution is added slightly more than one equivalent of methyl iodide. Inducement of crystallization of the quaternary salt which separates may be effected as, for example, by scratching the side of the vessel containing the mixture or seeding with a small quantity of the crystalline quaternary salt.

Therapeutic Function

Cholinergic

furtrethonium iodide(541-64-0)Related Product Information

• THIFLUZAMIDE
• Dinotefuran
• 5-METHYLFURMETHIODIDE
• RARECHEM AM UF B024
• RARECHEM AM UF B017
• furtrethonium iodide