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Postion:Product Catalog >Biochemical Engineering>Inhibitors>protein tyrosine kinase>Tepotinib Impurity
Tepotinib Impurity
  • Tepotinib Impurity
  • Tepotinib Impurity
  • Tepotinib Impurity

Tepotinib Impurity NEW

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

Product Details

Product Name: Tepotinib Impurity CAS No.: 1100598-32-0
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/22
Tepotinib Impurity1100598-32-0
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The Tepotinib Impurity Reference Standard is an important reagent in the field of scientific research. It aids researchers in conducting more in-depth studies and analyses of Tepotinib and its related impurities. Our Tepotinib Impurity Reference Standard undergoes strict quality control to ensure its purity and stability, meeting the high standards required for scientific experiments.


This reference standard is suitable for various scientific research experiments, including but not limited to drug analysis, impurity detection, and purity determination. By using our Tepotinib Impurity Reference Standard, researchers can gain a more accurate understanding of the changes in Tepotinib and its impurities during drug preparation and storage, providing valuable support for drug development and production.

Please note that this product is for research use only and is not for consumption. When storing, please keep it dry, away from light, and sealed under specified temperature conditions.


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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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