Dalbavancin Impurity A40926: Understanding CAS 102961-72-8
Explore the critical role of Dalbavancin Impurity A40926 in pharmaceutical research and quality assurance.
Get a Quote & SampleProduct Core Value
Dalbavancin Impurity A40926
Dalbavancin Impurity A40926 (CAS 102961-72-8) is a vital chemical compound primarily recognized for its role as a reference standard in the pharmaceutical industry. Its significance lies in its close structural relationship to dalbavancin, a potent lipoglycopeptide antibiotic. This impurity is crucial for detailed pharmaceutical impurity analysis and understanding the degradation pathways of dalbavancin, thereby contributing to the overall quality control in drug development and manufacturing.
- Explore the precise chemical structure of Dalbavancin Impurity A40926 to ensure accurate identification in pharmaceutical development.
- Utilize this compound for rigorous quality control in pharmaceutical manufacturing, ensuring the purity of dalbavancin.
- Understand the synthesis and degradation pathways of dalbavancin by studying this critical impurity.
- Adhere to stringent regulatory standards for pharmaceutical impurities by employing reliable reference materials like Dalbavancin Impurity A40926.
Key Advantages
Enhanced Purity Analysis
Leverage Dalbavancin Impurity A40926 for precise pharmaceutical impurity analysis, ensuring the highest standards of drug purity and safety.
Process Optimization
Gain insights into dalbavancin synthesis and degradation pathways, facilitating the optimization of production processes and improving yields.
Regulatory Compliance
Meet strict regulatory requirements by using validated reference standards for impurity profiling in drug submissions and quality checks.
Key Applications
Pharmaceutical Research
Essential for laboratories focusing on drug discovery and development, particularly those investigating glycopeptide antibiotics like dalbavancin.
Quality Control
Utilized in quality control departments to verify the purity and integrity of dalbavancin batches, ensuring compliance with pharmacopeial standards.
Chemical Synthesis Studies
Serves as a reference point in studies aimed at understanding and optimizing the chemical synthesis routes for complex antibiotic molecules.
Analytical Method Development
A crucial standard for developing and validating analytical methods, such as HPLC, used to detect and quantify impurities in pharmaceutical products.