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Postion:Product Catalog >Amorolfine Impurity
Amorolfine Impurity
  • Amorolfine Impurity
  • Amorolfine Impurity
  • Amorolfine Impurity

Amorolfine Impurity NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 10000000000
Update Time: 2024-12-26
Related documents: NMR MSDS COA IR

Product Details

Product Name: Amorolfine Impurity CAS No.: 142347-84-0
Min. Order: 10mg Purity: 95%+
Supply Ability: 10000000000 Release date: 2024/12/26

Amorolfine Impurity    CAS:142347-84-0  

Article illustration

Our testing and analysis laboratory is equipped with a variety of foreign imported testing equipment such as LC-MS, liquid phase, TGA, infrared, etc., to escort research and development. At the same time, it also provides customers with faster, more true and accurate product quality confirmation. For impurities with different properties, MOLCOO provides accurate impurity adaptation environment (-80°C, -20°C, 2-8°C), and uses different adapted reagent bottles to ensure the stable storage of impurity controls in various environments. Worry-free after-sales! If there is a problem with the quality of the sample, we promise to return it quickly and refund unconditionally!

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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