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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Rosuvastatin EP Impurity A
Rosuvastatin EP Impurity A
  • Rosuvastatin EP Impurity A
  • Rosuvastatin EP Impurity A
  • Rosuvastatin EP Impurity A

Rosuvastatin EP Impurity A NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 20g
Update Time: 2024-12-26
Related documents: COA IR MSDS NMR

Product Details

Product Name: Rosuvastatin EP Impurity A CAS No.: 1714147-47-3
Min. Order: 10mg Purity: 98%+
Supply Ability: 20g Release date: 2024/12/26

Professional R&D, Quality Assurance

Our R&D team boasts years of experience in developing Rosuvastatin impurity reference standards, dedicated to providing customers with the highest quality products. Through rigorous quality control testing, we ensure that each batch meets international standards and customer requirements.

Comprehensive Services, Meeting Needs

Beyond providing high-quality Rosuvastatin impurity reference standards, we also offer comprehensive service support. From product consultation, purchasing guidance, to after-sales support, we always put customers first, meeting your various needs.

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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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