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Postion:Product Catalog >Ambrisentan Impurity
Ambrisentan Impurity
  • Ambrisentan Impurity
  • Ambrisentan Impurity
  • Ambrisentan Impurity

Ambrisentan Impurity NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-04-27

Product Details

Product Name: Ambrisentan Impurity CAS No.: 178306-47-3
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/04/27
Ambrisentan Impurity 178306-47-3
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Ambrisentan Impurity Reference Standard
Utilized in pharmaceutical R&D, quality control, and regulatory submissions as an analytical standard to detect and quantify impurities in drug substances, ensuring drug safety and efficacy.




  • High Purity Assurance:Synthesized and purified under rigorous protocols to ensure single-component impurities.

  • Regulatory Compliance:Adheres to USP, EP, BP pharmacopeia standards, supporting global regulatory filings.

  • Stability:Stable for up to 3 years when stored at -20°C.


  • Storage:Store at -20°C, protected from light and moisture.

  • Shipping:Transported under cryogenic conditions (dry ice or cold chain) to maintain stability.

    application area :

    • Impurity profiling in new drug development

    • Process optimization and quality control in drug manufacturing

    • Generic drug bioequivalence studies


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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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