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Postion:Product Catalog >Cilastatin Impurity
Cilastatin Impurity
  • Cilastatin Impurity
  • Cilastatin Impurity
  • Cilastatin Impurity

Cilastatin Impurity NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000000
Update Time: 2024-12-20
Related documents: MSDS NMR IR COA

Product Details

Product Name: Cilastatin Impurity CAS No.: 1114-50-7
Min. Order: 10mg Purity: 98
Supply Ability: 100000000 Release date: 2024/12/20
Cilastatin: Cilastatin Cilastatin: Cilastatin Impurity
Cilastatin: custom synthesis impurities

We understand that impurities are not just about the purity of a drug; they directly relate to patient safety and efficacy. Therefore, we are dedicated to the research and control of Cilastatin impurities, utilizing advanced detection technologies to precisely identify and remove every trace of impurities that may compromise drug quality.

Through a rigorous quality control system, we ensure that each batch of Cilastatin meets the highest standards, providing patients with a safe, effective, and reliable treatment option. We firmly believe that only by having zero tolerance for impurities can we uphold the dignity and value of every life.

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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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