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Postion:Product Catalog >Analytical Chemistry>Standard>Standard Substance>Ciclosporin EP Impurity G
Ciclosporin EP Impurity G
  • Ciclosporin EP Impurity G
  • Ciclosporin EP Impurity G
  • Ciclosporin EP Impurity G

Ciclosporin EP Impurity G NEW

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

Product Details

Product Name: Ciclosporin EP Impurity G CAS No.: 63775-96-2
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/18
Ciclosporin EP Impurity G
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Cyclosporine Impurity Reference Standards

Cyclosporine impurity reference standards are crucial for drug development and quality control. Cyclosporine is a widely used immunosuppressant for preventing rejection reactions in allogeneic organ transplantations. To ensure the safety and efficacy of the drug, accurate detection and quantitative analysis of cyclosporine and its impurities are essential.



Our cyclosporine impurity reference standards cover a variety of cyclosporine impurities, including but not limited to Cyclosporine Impurity A, B, C, D, and more. These impurity reference standards have undergone rigorous quality control and purity testing to ensure they meet international and industry standards.

With cyclosporine impurity reference standards, you can:

  1. Accurate Identification: By comparing with impurity reference standards, accurately identify impurity components in the drug.

  2. Quantitative Analysis: Utilize impurity reference standards for quantitative analysis to ensure that the impurity content in the drug is within an acceptable range.

  3. Quality Control: Use impurity reference standards for quality control during drug production and development to ensure product quality is stable and reliable.

We are committed to providing high-quality cyclosporine impurity reference standards to meet our customers' needs in drug development and quality control.



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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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