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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Mupirocin EP Impurity E
Mupirocin EP Impurity E
  • Mupirocin EP Impurity E
  • Mupirocin EP Impurity E
  • Mupirocin EP Impurity E

Mupirocin EP Impurity E NEW

Price Get Latest Price
Package 10mg 30mg 100mg
Min. Order: 10mg
Supply Ability: 100000
Update Time: 2025-01-16

Product Details

Product Name: Mupirocin EP Impurity E CAS No.: 71087-96-2
Min. Order: 10mg Purity: 95%+
Supply Ability: 100000 Release date: 2025/01/16
Mupirocin EP Impurity E
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Product Name:Mupirocin Impurity Reference Standards

Product Overview:Mupirocin Impurity Reference Standards are reference materials specifically designed for drug research and development, quality control, and regulatory submissions. These impurity reference standards cover a wide range of impurities that may be present in Mupirocin drugs, including but not limited to EP Impurity A, B, C, D, E, etc. They are rigorously prepared and purified to ensure high purity and stability, accurately reflecting the impurity characteristics of Mupirocin drugs.


Application Areas

  1. Drug Research and Development:During the drug research and development phase, Mupirocin Impurity Reference Standards can be used to assess the purity and stability of new compounds, helping researchers identify and remove potential harmful impurities.

  2. Quality Control:In the drug production process, using Mupirocin Impurity Reference Standards ensures that the impurity content of the product meets relevant regulations and standards, thereby improving product quality and safety.

  3. Regulatory Submissions:During drug registration and approval processes, Mupirocin Impurity Reference Standards can serve as critical evidence demonstrating that the impurity content in the drug is within acceptable limits, facilitating the smooth approval of the drug.

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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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