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Postion:Product Catalog >Minocycline EP Impurity A
Minocycline EP Impurity A
  • Minocycline EP Impurity A
  • Minocycline EP Impurity A
  • Minocycline EP Impurity A

Minocycline EP Impurity A NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-01-17

Product Details

Product Name: Minocycline EP Impurity A CAS No.: 43168-51-0
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/17
Minocycline EP Impurity A
Article illustration

Product Name: Minocycline Impurity Reference Standard

Product Details:

The Minocycline Impurity Reference Standard serves as an important reference material for drug research and development, production, and registration. This product undergoes rigorous quality control to ensure high purity and stability, enabling accurate identification and quantitative analysis of impurities in Minocycline drugs.


Application Areas:

  • Drug Research and Development: In the process of drug R&D, the Minocycline Impurity Reference Standard can be used to evaluate the purity and stability of drugs, ensuring that the quality of the drugs meets relevant regulatory requirements.

  • Drug Production: During drug production, the use of the Minocycline Impurity Reference Standard can effectively monitor the impurity content in the production process, improving the qualification rate and safety of the drugs.

  • Drug Registration: In the process of drug registration, the Minocycline Impurity Reference Standard can serve as key evidence to demonstrate that the impurity content in the drugs meets relevant standards, facilitating smooth approval.


Article illustration


Company Profile Introduction

1. Drug standards and drug impurity reference substances: provide more than 20,000 kinds of spot impurity reference substances, with sufficient supply and same-day delivery. We have a professional R&D team and comprehensive quality control testing to ensure product quality and reliability. 2. Customized synthesis of impurities and new molecules: Quickly respond to the customized needs of CDE impurities, stably supply impurities that have established quality standards, and provide customized synthesis services for new compounds in the research and development of innovative drugs. 3. Preparation and separation of unknown impurities: With a professional impurity preparation and separation technical team and SFC preparation and separation instruments, we can solve the problems of impurity preparation in complex projects. 4. Process development of new drug intermediates: provide the supply of new drugs and new molecular impurities, process optimization services, as well as the screening and impurity analysis of commercialization routes. 5. Peptide synthesis: Provide customized peptide synthesis services, and cover all kinds of degradation impurities and process impurities generated in the research and development of peptide drugs. At the same time, it provides comprehensive structural confirmation data and customized testing services.

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