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Overview
Ceftazidime EP Impurity H is a specified degradation product monitored in pharmaceutical manufacturing to ensure compliance with European Pharmacopoeia standards. This reference standard is critical for validating the purity of the active pharmaceutical ingredient during synthesis and storage. Molecular Formula: C18H18N6O7S2; CAS No.: 80615-95-4.
Application
- Quality Control: Used as analytical reference standards for HPLC method validation.
- Stability Testing: Employed to identify and quantify impurities formed under stress conditions.
- R&D: Supports process optimization by tracking specific byproducts in synthetic routes.
Precautions
- Storage: Maintain at -20°C in airtight containers protected from light and moisture.
- Handling: Use appropriate PPE; avoid inhalation or skin contact due to potential allergenic properties.
- Regulatory: Strictly limit usage to laboratory analysis; not for clinical administration.