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Postion:Product Catalog >Ribociclib Impurity 14
Ribociclib Impurity 14
  • Ribociclib Impurity 14
  • Ribociclib Impurity 14
  • Ribociclib Impurity 14

Ribociclib Impurity 14 NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-01-22

Product Details

Product Name: Ribociclib Impurity 14 CAS No.: 2460732-08-3
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/22
Ribociclib Impurity 2460732-08-3
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Ribociclib Impurity Reference Standards

Ribociclib impurity reference standards play a vital role in drug research and development, quality control, and pharmaceutical testing. Ribociclib, a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor, is primarily used for the treatment of patients with HR-positive, HER2-negative breast cancer. To ensure the quality and safety of Ribociclib products, precise identification and quantitative analysis of its impurities are essential steps.

Our Ribociclib impurity reference standards cover a variety of key impurities, including but not limited to Ribociclib N-Oxide and N-desmethyl Ribociclib. These impurity reference standards have been meticulously prepared and undergone rigorous quality control to ensure their purity, chemical structure, and stability comply with international and industry standards.

By utilizing Ribociclib impurity reference standards, drug researchers and quality control personnel can more accurately identify and quantitatively analyze impurity components in pharmaceutical products, thereby effectively monitoring the production process and ensuring the quality and safety of the final products.

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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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