Category
Bacitracin
CAS Number
144572-52-1
Molecular Formula
C₆₄H₉₄N₁₆O₁₇S
Molecular Weight
1391.6 g/mol
Synonym

4,10-anhydro[N-[[2-[(2S)-2-methyl-1-oxobutyl]-1,3-thiazol-4-yl]carbonyl]-L-leucyl-D-α-glutamyl-L-valyl-L-lysyl-D-ornithyl-L-valyl-D-phenylalanyl-L-histidyl-D-α-aspartyl-L-asparagine] (as per EP) ; 

Keywords
High-Quality Pharmaceutical Reference Standards
Impurities
Metabolites.
Pharmaceutical Standards
Fine Chemicals
Amino Acid Derivatives
Peptides
Antibiotic
Impurities Manufacturer in India
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.

Manasa Life Sciences is a reliable manufacturer and supplier of Bacitracin EP Impurity K, offering a high-purity pharmaceutical reference standard with CAS No. 144572-52-1, molecular formula C₆₄H₉₄N₁₆O₁₇S, and molecular weight 1391.6 g/mol. We provide Bacitracin EP Impurity K with complete analytical testing reports, including Certificate of Analysis (COA), structural characterization data, and regulatory documentation aligned with ICH, EMA, EP, and USP guidelines. This impurity standard is suitable for related substance identification, chromatographic method development, analytical method validation, degradation product profiling, stability-indicating studies, and pharmaceutical quality control. With a strong commitment to quality, accuracy, and regulatory compliance, Manasa Life Sciences serves as a trusted partner for Bacitracin degradation impurities, peptide antibiotic impurity standards, pharmacopeial reference standards, EP-compliant impurity standards, USP-grade reference materials, and regulatory-grade analytical documentation for global pharmaceutical research and quality assurance.