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Cefadroxil

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N-Phenylglycyl cefadroxil
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N-Phenylglycyl cefadroxil

  • CAT Number DCTI-C-1220
  • CAS Number 147103-95-5(free base)
  • Molecular Formula C26H25F3N4O9S (TFA Salt) C24H24N4O7S (Free base)
  • Molecular Weight 626.56 (TFA Salt) 512.54 (Free base)
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N-Phenylglycyl delta-3 cefadroxil
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N-Phenylglycyl delta-3 cefadroxil

  • CAT Number DCTI-C-1237
  • CAS Number NA
  • Molecular Formula C24H24N4O7S
  • Molecular Weight 512.54
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References
FAQ's

References

  1. Crast, Leonard B., Jr.; Gottstein, William J., “Production of p-hydroxy cephalexin”, Bristol-Myers Co., United States, US3985741A, October 12, 1976
  2. Lindgren, Klas, “Determination of cefadroxil in serum by high-performance liquid chromatography with cephradine as internal standard”, Journal of Chromatography, Biomedical Applications, Volume: 413, Pages: 347-50, 1987
  3. Hsu, Mei-Chich; Chang, Ya-Wen; Lee, Yu-Tzer,”Column liquid chromatography and microbiological assay compared for determination of cefadroxil preparations”, Journal of Chromatography, Volume: 609, Issue: 1-2, Pages: 181-6, 1992

Frequently Asked Questions

The analytical methods used for the detection of impurities in Cefadroxil include high-performance liquid chromatography (HPLC), liquid chromatography mass spectrometry (LC-MS), etc.

Impurities in Cefadroxil can affect its safety by causing adverse effects in patients, such as allergic reactions, toxicity, and organ damage.

Impurities in Cefadroxil can affect the bioavailability of the drug by altering its pharmacokinetic properties, such as absorption, distribution, metabolism, and excretion.

The removal of Impurities in Cefadroxil may be by various purification techniques, such as recrystallization, column chromatography, and preparative HPLC.

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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