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Postion:Product Catalog >Organic Chemistry>Heterocyclic Compounds>Bilastine Impurity
Bilastine Impurity
  • Bilastine Impurity
  • Bilastine Impurity
  • Bilastine Impurity

Bilastine Impurity NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-06-18

Product Details

Product Name: Bilastine Impurity CAS No.: 51785-23-0
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/06/18
Bilastine Impurity 51785-23-0  in stock
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Bilastine impurity reference standards are crucial substances used in drug development, quality control, and project approval processes. These impurity reference standards cover various impurities that may exist in bilastine drugs, playing a vital role in ensuring the purity and stability of the drugs.





Product Information

  1. Product Name: Bilastine Impurity Reference Standards

  2. CAS Numbers: Including but not limited to 202189-78-4, 2069238-47-5 (specific CAS numbers vary depending on the type of impurity)

  3. Molecular Formula: C28H37N3O3 (the molecular formula of specific impurities may differ)

  4. Molecular Weight: 463.6117 (the molecular weight of specific impurities may differ)

  5. Purity: Generally above 98%, with some reaching over 99%

  6. Storage Conditions: Recommended to be stored in a low-temperature environment at 2-8°C to maintain stability

  7. Usage: Primarily used for impurity analysis, quality control, and new drug approval processes during drug development

Product Features

  1. Comprehensive Range: Offers a complete set of bilastine impurity reference standards to meet various needs in drug development

  2. High Purity: The purity of impurity reference standards is generally above 98%, ensuring the accuracy of analysis results

  3. Stable and Reliable: Undergoes strict quality control to ensure the stability and reliability of the impurity reference standards

Application Areas

Bilastine impurity reference standards are widely used in drug development, quality control departments of pharmaceutical companies, drug testing institutions, and new drug approval processes. They provide important reference standards for impurity analysis, purity detection, and stability studies during drug development.



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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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