Category
Canagliflozin
CAS Number
1589590-87-3
Molecular Formula
C₂₄H₂₅FO₅S
Molecular Weight
444.52 g/mol
Synonym

 Canagliflozin alpha-Isomer Impurity; (2R,3R,4R,5S,6R)-2-(3-((5-(4-Fluorophenyl)thiophen-2-yl)methyl)-4-methylphenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol; Canagliflozin α-Isomer ;

Keywords
Aromatics
Heterocycles
sulphur and selenium compounds
Impurities
Impurities manufacturer and Suppliers in Hyderabad india
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Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Canagliflozin α-Isomer (CAS No. 1589590-87-3), represented by the molecular formula C₂₄H₂₅FO₅S and a molecular weight of 444.52 g/mol, is a critical epimeric impurity that must be carefully monitored and controlled during the development, manufacturing, and quality assessment of Canagliflozin to ensure compliance with stringent ICH, USFDA, EMA, USP, and EP regulatory guidelines. High-purity Canagliflozin α-Isomer Reference Standards are essential for impurity profiling, analytical method development, method validation, quality control testing, stability studies, and regulatory submissions. Comprehensive characterization using advanced analytical techniques including HPLC, LC-MS, NMR, and IR spectroscopy ensures accurate identification, purity determination, and structural confirmation. Manasa Life Sciences, a global manufacturer and supplier based in Hyderabad, provides research-grade Canagliflozin α-Isomer Analytical Standards supported by complete documentation, including Certificate of Analysis (COA), GMP and GDP compliance documentation, MSDS, SDS, chromatographic data, and spectral reports, enabling pharmaceutical companies, CROs, research laboratories, and quality control facilities worldwide to meet regulatory requirements while maintaining product safety, efficacy, and quality.