Catégorie
Trimetazidine Dihydrochloride
Numéro CAS
STD - 5011-34-7 ;Imp-B-1257-19-8 ;
Autre numéro CAS
STD - 13171-25-0(Di HCl Salt)
Formule moléculaire
STD - C₁₄H₂₂N₂O₃ ; Imp-B-C₂₄H₃₄N₂O₆ ;
Masse moléculaire
STD - 266.34 g/mol ;Imp-B-446.6g/mol;
Synonyme

Trimetazidine Standard - 1-(2,3,4-Trimethoxybenzyl)piperazine;

Trimetazidine EP Impurity B - 1,4-Bis(2,3,4-Trimethoxybenzyl)piperazine ;Hexametazidine;

Mots-clés
Pharmaceutical Standards
Intermediates
Fine Chemicals
Amines
Aromatics
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.

Trimetazidine Peak Identification CRS (CAS No. 5011-34-7) and Impurity B (CAS No. 1257-19-8) from Manasa Life Sciences, a globally trusted manufacturer and supplier india pharmaceutical reference standards, are produced under stringent quality management systems to support pharmaceutical research, analytical laboratories, and regulatory compliance. Trimetazidine Standard (Molecular Formula: C₁₄H₂₂N₂O₃, Molecular Weight: 266.34 g/mol) and Trimetazidine Impurity B (Molecular Formula: C₂₄H₃₄N₂O₆, Molecular Weight: 446.6 g/mol) are extensively characterized for peak identification, HPLC reference standard applications, LC-MS/MS, Mass Spectrometry (MS), NMR spectroscopy, and comprehensive analytical profiling to ensure accurate impurity identification and chromatographic peak confirmation. Each batch is supported with detailed Certificate of Analysis (CoA), HPLC chromatograms, Mass spectra, NMR analysis reports, and complete analytical documentation, enabling reliable use in analytical method development, method validation, quality control (QC), analytical testing, stability studies, forced degradation studies, pharmaceutical R&D, and regulatory submissions. Manufactured following internationally recognized regulatory guidelines including ICH, USP, EP (European Pharmacopoeia), US FDA, and EMA expectations, Manasa Life Sciences delivers high-purity pharmaceutical reference standards with exceptional consistency, traceability, and global compliance, making them the preferred choice for pharmaceutical manufacturers and quality testing laboratories worldwide.