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Oseltamivir Nitroso Impurity 1

  • CAT NUMBER DCTI-C-2366
  • CAS NUMBER NA
  • MOLECULAR FORMULA C18H32N2O5
  • MOLECULAR WEIGHT 356.46
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Oseltamivir Nitroso Impurity 2

  • CAT NUMBER DCTI-C-2367
  • CAS NUMBER NA
  • MOLECULAR FORMULA C24H41N3O4
  • MOLECULAR WEIGHT 435.61
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References
FAQ's

References

  1. Willard Lew, Choung U. Kim, Hongtao LiuMatthew A. Williams, Carbocyclic compounds, Gilead Sciences, Inc, US5866601A, February 2, 1999
  2. Narasimhan, Balasubramanian; Abida, Khan; Srinivas, Kona, Stability indicating RP-HPLC method development and validation for oseltamivir API, Chemical & Pharmaceutical Bulletin, Volume: 56, Issue: 4, Pages: 413-417, 2008

Frequently Asked Questions

Reverse-phase high-performance liquid chromatography method helps detect and analyze the degradation impurities in Oseltamivir.

Impurities in Oseltamivir can affect the drug’s efficacy by decreasing its potency or interfering with its mechanism of action.

Acetonitrile or Methanol are the solvents used in analyzing many Oseltamivir impurities.

Oseltamivir 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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