Determination of Some 1,4-Benzodiazepines by Oxidative Coupling of their Acid-Induced Degradation Products
Bulletin des Sociétés Chimiques Belges
1, 4-benzodiazepines, acid hydrolysis, oxidative coupling, 3-methylbenzothiazolone hydrazone, dosage forms
Biochemistry | Chemistry | Medical Biochemistry | Medicinal and Pharmaceutical Chemistry
The oxidative coupling reaction of 3-methylbenzothiazolone hydrazone with aromatic amines was applied to the determination of five 1,4-benzodiazepine derivatives. The drugs were first hydrolyzed in acid medium and the liberated benzophenone derivatives were reacted with the chromogenic reagent in the presence of cerric ammonium sulphate to give a pink color. A linear correlation was found between the absorbance at λmax and concentration. The method was applied to the determination of these drugs in bulk powder and in pharmaceutical preparations. The procedure was extended to develop a stability-indicating method for these drugs.
El-Yazbi, Fawzy A.; Galal, Shereen M.; and Blaih, Salah (1993). Determination of Some 1,4-Benzodiazepines by Oxidative Coupling of their Acid-Induced Degradation Products. Bulletin des Sociétés Chimiques Belges 102(4), 233-237. doi: 10.1002/bscb.19931020403 Retrieved from https://digitalcommons.kent.edu/chempubs/38