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Sumatriptan

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Sumatriptan Succinate Impurity
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Sumatriptan Succinate Impurity

  • CAT Number DCTI-C-185
  • CAS Number 2144776-39-4
  • Molecular Formula C25H33N5O4S2
  • Molecular Weight 531.69
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References
FAQ's

References

  1. Oxford, Alexander William, Indole derivative, Glaxo Group Ltd., United Kingdom, US5037845A, August 6, 1991
  2. Oxford, J.; Lant, M. S., Development and validation of a liquid chromatographic-mass spectrometric assay for the determination of sumatriptan in plasma, Journal of Chromatography, Biomedical Applications, Volume: 496, Issue: 1, Pages: 137-46, 1989
  3. Dunne, Moira; Andrew, Peter, Fully automated assay for the determination of sumatriptan in human serum using solid-phase extraction and high-performance liquid chromatography with electrochemical detection, Journal of Pharmaceutical and Biomedical Analysis, Volume: 14, Issue: 6, Pages: 721-726, 1996

Frequently Asked Questions

The impurities in Sumatriptan are detected and quantified using various analytical techniques such as Reverse Phase High-Performance Liquid Chromatography (RP-HPLC).

Controlling the presence of impurities in Sumatriptan is crucial for ensuring that the drug is of high quality, safe, and effective. Further, they may harm various aspects of the drug's performance, such as its potency, stability, and overall shelf life.

Water or DMSO is the solvent used in analyzing many impurities in Sumatriptan.

Sumatriptan impurities are stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).

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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