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Kinetics of base catalyzed racemization of ibuprofen enantiomers
- Source :
- International journal of pharmaceutics. 196(1)
- Publication Year :
- 2000
-
Abstract
- The kinetics of base catalyzed racemization of ibuprofen enantiomers has been studied in DMSO-water mixed medium. The dynamic equilibrium rate of keto-enol tautomerism leading to racemization of ibuprofen enantiomers, is proportional to the concentrations of base catalyst and substrate. A kinetic model capable of predicting the time course of racemization, under different base and substrate concentrations, is established and experimentally verified.
- Subjects :
- Chemistry
Kinetics
Anti-Inflammatory Agents, Non-Steroidal
Pharmaceutical Science
Substrate (chemistry)
Water
Stereoisomerism
Ibuprofen
Hydrogen-Ion Concentration
Tautomer
Catalysis
chemistry.chemical_compound
Models, Chemical
Sodium hydroxide
Predictive Value of Tests
Organic chemistry
Sodium Hydroxide
Dimethyl Sulfoxide
Enantiomer
Racemization
Subjects
Details
- ISSN :
- 03785173
- Volume :
- 196
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- International journal of pharmaceutics
- Accession number :
- edsair.doi.dedup.....652f23ab5425f9006e6df8f2e02510c1