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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Ivabradine Impurity 34
Ivabradine Impurity 34
  • Ivabradine Impurity 34
  • Ivabradine Impurity 34
  • Ivabradine Impurity 34

Ivabradine Impurity 34 NEW

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

Product Details

Product Name: Ivabradine Impurity 34 CAS No.: 304464-97-9
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/18
Ivabradine Impurity 304464-97-9
Article illustration


Ivabradine Impurity Reference Standards

Product Details:

Ivabradine, as an important pharmaceutical ingredient, its impurity reference standards play a crucial role in drug research and development, quality control, and production processes. Our Ivabradine impurity reference standards feature high purity, high stability, and precise chemical structures, making them widely applicable in drug analysis, impurity detection, and quality standard formulation.


Product Features:

  1. High Purity: Prepared using advanced manufacturing techniques to ensure a purity level of over 99%.

  2. Accurate Structure: Rigorously synthesized and structurally identified to ensure complete consistency with the target impurity.

  3. Stable and Reliable: Stored under appropriate conditions to maintain stability and reliability over extended periods.

Applications:

  1. Drug Research and Development: Serves as an essential reference material in the drug development process, assessing drug purity and impurity content.

  2. Quality Control: Monitors and controls impurity levels in drugs during production, ensuring drug quality meets standards.

  3. Quality Standard Formulation: Provides accurate impurity reference standards for formulating drug quality standards, ensuring drug safety and efficacy.


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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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