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Postion:Product Catalog >Ilaprazole Impurity 117
Ilaprazole Impurity 117
  • Ilaprazole Impurity 117
  • Ilaprazole Impurity 117
  • Ilaprazole Impurity 117

Ilaprazole Impurity 117 NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-01-18

Product Details

Product Name: Ilaprazole Impurity 117 CAS No.: 172152-59-9
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/18
Ilaprazole Impurity  172152-59-9
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Ilaprazole Impurity Reference Standards

Ilaprazole impurity reference standards play a crucial role in the fields of drug research and development, quality control, and pharmaceutical testing. As a highly effective therapeutic drug, the purity and stability of Ilaprazole are essential for ensuring drug efficacy and patient safety. To comprehensively evaluate and control the quality of Ilaprazole products, accurate identification and quantitative analysis of its impurities are particularly important.

Our Ilaprazole impurity reference standards cover a variety of key impurities, including but not limited to Ilaprazole Impurity 1 to Ilaprazole Impurity 31. These impurity reference standards have undergone rigorous quality control to ensure their purity and chemical structure comply with international and industry standards. By using these impurity reference standards, drug researchers and quality control personnel can more accurately identify and quantitatively analyze the impurity components in Ilaprazole products, thereby ensuring the quality and safety of the drugs.


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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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