High Purity Cefixime Impurity CAS 80554-17-8: A Key Pharmaceutical Intermediate for Quality Control
Essential for ensuring the quality and safety of Cefixime-based medications.
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(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-methoxy-2-oxoethoxy)iminoacetic Acid
This high-purity pharmaceutical impurity, Cefixime Impurity CAS 80554-17-8, is a critical reference standard. It plays a vital role in the pharmaceutical industry for drug development, rigorous quality control, and meeting stringent regulatory compliance requirements for Cefixime. Produced with expertise, it ensures the reliability of analytical testing in pharmaceutical research.
- Discover the essential role of Cefixime Impurity CAS 80554-17-8 in pharmaceutical quality control, ensuring the safety and efficacy of Cefixime medications.
- Leverage high-purity Cefixime impurity reference standards for accurate analytical method development and validation in pharmaceutical research.
- Source crucial pharmaceutical intermediates necessary for robust drug development processes and meeting regulatory compliance for Cefixime.
- Benefit from the expertise of Anhui Keynovo Biotech Co., Ltd. in providing reliable pharmaceutical impurity reference materials for the industry.
Advantages of Using This Product
Ensures Medication Safety
Utilizing this specific Cefixime impurity reference standard guarantees accurate identification and quantification of impurities, directly contributing to the safety profile of pharmaceutical products.
Supports Regulatory Approval
The availability of well-characterized pharmaceutical intermediates like this Cefixime impurity is fundamental for successful ANDA and DMF filings, streamlining regulatory processes.
Enhances Quality Control
Incorporating this reference standard into your QC protocols allows for precise method validation, ensuring consistent quality throughout the pharmaceutical manufacturing lifecycle of Cefixime.
Key Applications
Pharmaceutical Research
Crucial for understanding the behavior and impact of impurities during the development phases of new drug formulations.
Quality Control (QC)
Essential for routine testing to confirm that Cefixime drug products meet predefined purity and quality standards.
Method Validation
Used to validate analytical methods, ensuring their accuracy, precision, and reliability for impurity detection and quantification.
Regulatory Compliance
Serves as a critical component for meeting stringent regulatory guidelines set by health authorities worldwide for pharmaceutical products.