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Postion:Product Catalog >Sofosbuvir Impurity 93
Sofosbuvir Impurity 93
  • Sofosbuvir Impurity 93
  • Sofosbuvir Impurity 93
  • Sofosbuvir Impurity 93

Sofosbuvir Impurity 93 NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000000000
Update Time: 2025-01-15

Product Details

Product Name: Sofosbuvir Impurity 93 CAS No.: 51496-03-8
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000000000 Release date: 2025/01/15
Sofosbuvir Impurity  51496-03-8
Article illustration

Sofosbuvir Impurity Reference Standards

Sofosbuvir, as a highly effective antiviral drug, plays a crucial role in drug research and development, production, and quality control. The Sofosbuvir impurity reference standards we provide have been carefully prepared and rigorously tested to ensure their accuracy and reliability.



Product Features:

  1. Comprehensive Range: Our product covers a wide range of Sofosbuvir impurities, including Impurity 1 to Impurity 41, to meet your needs at different research stages.

  2. High Purity: All impurity reference standards are purified using advanced techniques such as High Performance Liquid Chromatography (HPLC), with purities exceeding 95%.

  3. Structural Confirmation: Nuclear Magnetic Resonance (NMR) and Mass Spectrometry (MS) spectra are provided to ensure the accurate structure of the impurity reference standards.

  4. Quality Assurance: Each batch of impurity reference standards is accompanied by a detailed Certificate of Analysis (COA) to ensure product quality traceability.

Applications:

  • Drug Research and Development: Used for new drug screening, pharmacodynamics evaluation, and toxicology studies.

  • Production Monitoring: As a quality control standard in the production process to ensure product stability.

  • Regulatory Compliance: To meet the regulatory requirements of domestic and foreign drug regulatory agencies for drug impurity control.

  • 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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