Category
Aprotinin
CAS Number
NA
Molecular Formula
C279H424N82O77S7
Molecular Weight
331.54 g/mol
Synonym

Aprotinin-(1-56)-peptide ; Des-Gly57, Ala58-Aprotinin ;Bovine Pancreatic Trypsin Inhibitor ;

Keywords
Impurities Manufacturer in India
Impurities manufacturer and Suppliers in Hyderabad india
Impurities
Slide_1
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.

Aprotinin EP Impurity A (CAS No.: N/A; Molecular Formula: C₂₇₉H₄₂₄N₈₂O₇₇S₇; Molecular Weight: 331.54 g/mol) is a high-purity Aprotinin related substance, protein impurity marker, and pharmaceutical reference material designed for protein impurity characterization, peptide mapping, molecular characterization, purity profiling, degradation assessment, process-related variant evaluation, chromatographic analysis, bioanalytical testing, and quality control. Manasa Life Sciences, a trusted biological reference standard manufacturer and pharmaceutical analytical material supplier in Hyderabad, India, provides Aprotinin EP Impurity A reference standards, Aprotinin related compounds, protein impurity standards, biopharmaceutical reference materials, peptide/protein analytical standards, process-related impurity markers, degradation product references, and characterization materials for pharmaceutical, biotechnology, CRO, and research laboratories worldwide. These analytical materials support drug substance characterization, batch-to-batch quality assessment, impurity monitoring, method development, method validation, and stability-indicating studies and are supplied with Certificate of Analysis (COA), MSDS, SDS, and relevant technical documentation, supporting applicable GMP, GDP, ICH, USFDA, USP, EP, and EMA quality and regulatory requirements.