Literature DB >> 21948

Oxidation kinetics of phenothiazine and 10-methylphenothiazine in acidic medium.

H Roseboom, J H Perrin.   

Abstract

The rate of phenothiazine degradation in an acidic oxygen-saturated medium was studied. 3H-Phenothiazine-3-one and phenothiazine 5-oxide are produced by parallel reactions, and 7-(10'-phenothiazinyl)-3H-phenothiazine-3-one is produced in a more complex manner. The overall phenothiazine degradation rate appears to be pH independent up to pH 7.0. The degradation kinetics of 10-methylphenothiazine were studied after isolation and identification of its degradation products, 10-methylphenothiazine 5-oxide and 3H-phenothiazine-3-one. The main degradation product is 10-methylphenothiazine 5-oxide; but at low pH values and high temperatures, more 3H-phenothiazine-3-one is formed. The degradation rate of 10-methylphenothiazine is pH independent up to pH 7.

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Year:  1977        PMID: 21948     DOI: 10.1002/jps.2600661010

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Electrochemically Induced Mesomorphism Switching in a Chlorpromazine Hydrochloride Lyotropic Liquid Crystal.

Authors:  Robert D Crapnell; Huda S Alhasan; Lee I Partington; Yan Zhou; Ziauddin Ahmed; Amal A Altalhi; Thomas S Varley; Nadiyah Alahmadi; Georg H Mehl; Stephen M Kelly; Nathan S Lawrence; Frank Marken; Jay D Wadhawan
Journal:  ACS Omega       Date:  2021-02-05
  1 in total

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