Formoterol - NDSRI's

Formoterol Nitroso Impurity

  • CAT NUMBER DCTI-C-3651
  • CAS NUMBER NA
  • MOLECULAR FORMULA C19H23N3O5
  • MOLECULAR WEIGHT 373.41
References
FAQ's

Frequently Asked Questions

The purpose of synthesizing Formoterol impurities is to identify, characterize, and quantify the impurities present in Formoterol drug products. It assesses Formoterol's safety, efficacy, and quality while ensuring compliance with regulatory guidelines.

Formoterol impurities are typically detected and quantified using analytical methods such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS).

The polar solvent methanol helps in analyzing Formoterol and its impurities.

Formoterol impurities should be 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.

Back to Top
Product has been added to your cart