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Ranolazine
References
FAQ's
References
- Kluge, Arthur Frederick; Clark, Robin Douglas; Strosberg, Arthur Martin; Pascal, Jean Claude; Whiting, Roger Lewis, Cardioselective aryloxy- and arylthio- hydroxypropylene-piperazinyl acetanilides which affect calcium entry, Syntex (U.S.A.), Inc., United States, US4567264A, Jan 28, 1986
- Delee, E.; Le Garrec, L.; Jullien, I.; Beranger, S.; Pascal, J. C.; Pinhas, H., Direct HPLC resolution of beta-aminoalcohol (tazifylline, ranolazine, sotalol) enantiomers, Chromatographia, Volume: 24, Pages: 357-9, 1987
Frequently Asked Questions
Which solvent helps in the analysis of Ranolazine impurities?
Methanol is the solvent for analyzing many Ranolazine impurities.
What are the temperature conditions required to store Ranolazine impurities?
Ranolazine impurities should be stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).
How are Ranolazine impurities eliminated or removed?
Ranolazine impurities can be eliminated or removed through appropriate purification steps such as chromatography, crystallization, or recrystallization. Additionally, degradation impurities can be removed by following cGMP practices.
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