timonacic sodium Usage And Synthesis

Originator

Hepaldine,Riker,France,1964

Manufacturing Process

Cysteine is first dissolved in distilled water which has been freed of oxygen by boiling. Formaldehyde of 30% (w/v) concentration is added while stirring and the temperature of the mixture rises, while the thiazolidine carboxylic acid begins crystallizing. The stirring is continued for 2 hours after which ethyl alcohol of 95% (w/v) concentration is added to induce further crystallization. The mixture is left to stand for 24 hours at 4°C. The mixture is then filtered with retention of a crude product, which is purified by recrystallization from boiling distilled water. The crystals are then dried at about 40°C. The free acid is then converted to the sodium salt with NaOH.

Therapeutic Function

Hepatoprotectant, Choleretic

timonacic sodium(35041-11-3)Related Product Information

• Sulbenicillin sodium
• Piperacillin sodium salt
• Carbenicillin disodium
• Ampicillin sodium
• OXACILLIN SODIUM
• Cloxacillin benzathine
• Flucloxacillin sodium
• Sodium cloxacillin monohydrate
• Penicillin G sodium salt
• Dicloxacillin sodium
• LABOTEST-BB LT00244831
• Cloxacillin-13C4 SodiuM Salt
• apalcillin sodium
• LABOTEST-BB LT00244816
• Nafcillin sodium salt monohydrate
• timonacic sodium