Category
Bacitracin
CAS Number
NA
Molecular Formula
C₆₇H₁₀₃N₁₇O₁₆S
Molecular Weight
1434.7 g/mol
Synonym

4,10-anhydro[N-[[(4R)-2-[(1S,2S)-1-amino-2-methylpent4-en-1-yl]-4,5-dihydro-1,3-thiazol-4-yl]carbonyl]-L-leucylD-α-glutamyl-L-isoleucyl-L-lysyl-D-ornithyl-L-isoleucylD-phenylalanyl-L-histidyl-D-α-aspartyl-L-asparagine] (bacitracin J3)

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
Pharmaceutical Standards
Fine Chemicals
sulphur and selenium compounds
Amino Acid Derivatives
Impurities
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 leading manufacturer and supplier of Bacitracin EP Impurity Q, providing a high-purity pharmaceutical reference standard with CAS No. NA, molecular formula C₆₇H₁₀₃N₁₇O₁₆S, and molecular weight 1434.7 g/mol. We supply Bacitracin EP Impurity Q with complete analytical testing reports, including Certificate of Analysis (COA), structural characterization data, and regulatory documentation compliant with ICH, EMA, EP, and USP guidelines. This impurity standard is widely used for related substance identification, chromatographic method development, analytical method validation, degradation product profiling, stability-indicating studies, and pharmaceutical quality control. With a strong focus on quality, accuracy, and regulatory compliance, Manasa Life Sciences is a trusted source 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.