Category
Albendazole
CAS Number
80983-36-4
Molecular Formula
C₁₀H₁₃N₃S
Molecular Weight
207.3 g/mol
Synonym

5-(Propylsulphanyl)-1H-benzimidazol-2-amine; Desmethoxycarbonyl Albendazole; 5-(Propylthio)-1H-benzimidazol-2-amine; Albendazole Amine; 5-(Propylsulphanyl)-1H-benzimidazol-2-amine; (5-Propylthiobenzimidazol-2-amine); Albendazole Related Compound A;

Keywords
sulphur and selenium compounds
Fine Chemicals
Aromatics
Pharmaceutical Standards
Metabolites.
Impurities
Heterocycles
Intermediates
Impurities manufacturer and Suppliers in Hyderabad india
Impurities Manufacturer in 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.

Albendazole EP Impurity A (CAS No. 80983-36-4) is a high-purity pharmaceutical reference impurity with the molecular formula C₁₀H₁₃N₃S and a molecular weight of 207.3 g/mol. It is extensively used as a certified analytical reference standard for pharmaceutical impurity profiling, HPLC method development, LC-MS analysis, mass spectrometry, NMR characterization, analytical method validation, quality control (QC), quality assurance (QA), stability studies, and pharmaceutical research and development (R&D). Manasa Life Sciences is a trusted and reliable manufacturer of Albendazole EP Impurity A in India, supported by an experienced team of research scientists and advanced analytical laboratories to ensure high purity, batch-to-batch consistency, and reliable performance. The impurity is manufactured and characterized in accordance with applicable ICH, European Pharmacopoeia (EP), United States Pharmacopeia (USP), EMA, GLP, GDP, and ISO quality management guidelines, making it suitable for regulated pharmaceutical applications. Every batch is supplied with comprehensive technical documentation, including Certificate of Analysis (COA), analytical reports, HPLC chromatograms, LC-MS and Mass Spectrometry data, NMR spectra, product specifications, Safety Data Sheet (SDS/MSDS), and supporting quality documentation, providing complete traceability and regulatory compliance. Manasa Life Sciences is committed to delivering high-quality pharmaceutical reference standards, impurity standards, and analytical research materials for global pharmaceutical manufacturers, contract research organizations (CROs), analytical testing laboratories, and academic research institutions.