a complex consisting of an organic base in association with hydrogen chloride
English Journal
Sensitive spectrofluorimetric and spectrophotometric methods for the determination of thonzylamine hydrochloride in pharmaceutical preparations based on coupling with dimethylbarbituric acid in presence of dicyclohexylcarbodiimide.
Sabry SM, Abdel-Hay MH, Barary MH, Belal TS.SourceDepartment of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, University of Alexandria, Egypt.
Journal of pharmaceutical and biomedical analysis.J Pharm Biomed Anal.2000 Mar;22(2):257-64.
Two sensitive and selective spectrophotometric and spectrofluoimetric procedures were developed for the determination of thonzylamine hydrochloride (THAH) in tablets and nasal drops. The methods are based on König reaction which resulted in an orange-yellow fluorescent product. The orange-yellow pr
[4-[Benzyl-(2-dimethylaminoethyl)amino]pyrimidine compounds with selective antagonistic activity against H1-histamine receptors].
Mossini F, Maggiali C, Morini G, Impicciatore M, Morini G, Molina E.AbstractThis paper describes the synthesis of 2- and 4-[benzyl-(2-dimethylaminoethyl)amino]pyrimidine compounds and their antihistaminic properties studied on isolated guinea-pig ileum. Calculated pA2 values show that the antihistaminic activity of 4-[p.methoxybenzyl-(2-dimethylaminoethyl)amino]pyrimidine is specific and potent (8-10 times higher than that of thonzylamine).
Il Farmaco; edizione scientifica.Farmaco Sci.1984 Mar;39(3):189-99.
This paper describes the synthesis of 2- and 4-[benzyl-(2-dimethylaminoethyl)amino]pyrimidine compounds and their antihistaminic properties studied on isolated guinea-pig ileum. Calculated pA2 values show that the antihistaminic activity of 4-[p.methoxybenzyl-(2-dimethylaminoethyl)amino]pyrimidine i
Carbon-13 magnetic resonance spectroscopy of drugs II: antihistamines.
Chang CJ, Peck GE.AbstractThe natural abundance carbon-13 magnetic resonance spectra of a series of antihistamines (pheniramine, chlorpheniramine, methapyrilene, tripelennamine, pyrilamine, and thonzylamine) were detemined using the pulse Fourier transform technique. The chemical shifts were assigned with the aid of long-range carbon-13-hydrogen coupling constants.
Journal of pharmaceutical sciences.J Pharm Sci.1976 Jul;65(7):1019-23.
The natural abundance carbon-13 magnetic resonance spectra of a series of antihistamines (pheniramine, chlorpheniramine, methapyrilene, tripelennamine, pyrilamine, and thonzylamine) were detemined using the pulse Fourier transform technique. The chemical shifts were assigned with the aid of long-ran
… times dilution.) <BR>The serum samples, containing a fixed amount (200 ng-2μg/tube) of the internal standard (thonzylaminehydrochloride) were alkalinized with 0.1N NaOH at a pH above 7.8. …
… Fluorometric determination of thonzylaminehydrochloride (I) with o-aminothiophenol (II) was investigated. … The ether layer is washed twice with 5 ml of water, 1 ml of 0.5% II-hydrochloride is added, ether is evaporated, and 5 ml of 30% (w/v) H_2SO_4 is added to the residue. …
Thonzylamine Hydrochloride is a medicine available in a number of countries worldwide. A list of US medications equivalent to Thonzylamine Hydrochloride is available on the Drugs.com website. ... Drugs.com provides accurate and ...
THONZYLAMINE HYDROCHLORIDE behaves as a weak organic acid. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0.