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Ranolazine - NDSRI's
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N-Nitroso Ranolazine Impurity B

  • CAT NUMBER DCTI-C-3713
  • CAS NUMBER NA
  • MOLECULAR FORMULA C14H20N4O2
  • MOLECULAR WEIGHT 276.34
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N-Nitroso Ranolazine Impurity A

  • CAT NUMBER DCTI-C-3712
  • CAS NUMBER NA
  • MOLECULAR FORMULA C14H21N3O4
  • MOLECULAR WEIGHT 295.34
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References
FAQ's

References

  1. 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
  2. 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

Methanol is the solvent for analyzing many 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).

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.

Note: Products protected by valid patents by a manufacturer are not offered for sale in countries having patent protection. The sale of such products constitutes a patent infringement, and its liability is at the buyer's risk.

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