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Silodosin

Silodosin Impurities & Reference Standards

Silodosin is an established active pharmaceutical ingredient (API) with broad application in pharmaceutical formulation, drug substance manufacturing, and quality control. Silodosin related substances / impurity reference standards support HPLC method validation, forced degradation studies, and regulatory documentation consistent with ICH, USP, BP, and EP requirements. Our Silodosin reference standards are provided with full documentation — Certificate of Analysis (CoA), HPLC chromatographic data, and spectral characterization — to support pharmaceutical R&D and GMP manufacturing.


Associated Impurities

Racemic KAM-1 of Silodosin

  • CAS No: 1338365-54-0
  • Mol. F.: C22H25N3O2

Racemic Silodosin

  • CAS No: 160970-64-9
  • Mol. F.: C25H32F3N3O4

Racemic Stage 1- of Silodosin

  • CAS No: 885340-11-4
  • Mol. F.: C32H34F3N3O4

Silodosin (S)-Isomer

  • CAS No: 160970-54-7
  • Mol. F.: C25H32F3N3O4

Silodosin Dehydro Impurity

  • CAS No: 175870-21-0
  • Mol. F.: C25H30F3N3O4

Silodosin Impurity

  • CAS No: 160969-02-8
  • Mol. F.: C10H11F3O3

Silodosin Ksm – II

  • CAS No: 160969-03-9
  • Mol. F.:
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