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Postion:Product Catalog >Topiramate Impurity 22
Topiramate Impurity 22
  • Topiramate Impurity 22
  • Topiramate Impurity 22
  • Topiramate Impurity 22
  • Topiramate Impurity 22
  • Topiramate Impurity 22

Topiramate Impurity 22 NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-07-31

Product Details

Product Name: Topiramate Impurity 22 CAS No.: 25018-67-1
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
Molecular formula: C8H10Br2N2

Topiramate Impurity;25018-67-1

Article illustration

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com


  • Product Information

  • Product Code: T053022

  • English Name: Topiramate Impurity 22

  • English Alias: (3aR,4'S,7S,7aS)-2,2,2',2'-tetramethyltetrahydrospiro[[1,3]dioxolo[4,5-c]pyran-6,4'-[1,3]dioxolan]-7-ol

  • CAS No.: 25018-67-1

  • Molecular Formula: C??H??O?

  • Molecular Weight: 260.28

  • Advantages

  • As an impurity reference standard for Topiramate, it features a clear structure and high purity, which is essential for pharmaceutical quality control and impurity analysis to ensure drug safety and consistency.

  • The defined stereoconfiguration (3aR,4'S,7S,7aS) makes it suitable for analytical scenarios requiring precise structural characterization.

  • Applications

  • Primarily used for impurity research, methodological validation (such as development and validation of HPLC, LC-MS, etc.), and formulation of pharmaceutical quality standards for Topiramate raw materials and preparations.

  • Serves as a reference standard to evaluate the generation and control of impurities in the production process, assisting in optimizing the synthetic route.

  • Background Description

  • Topiramate is a broad-spectrum antiepileptic drug that exerts its effect by blocking sodium channels and enhancing γ-aminobutyric acid (GABA) activity. In the research, development, and production of drugs, impurity control is a key link to ensure drug quality. As a related impurity of Topiramate, Topiramate Impurity 22 may be generated from raw material residues, reaction by-products, or degradation during synthesis, requiring qualitative and quantitative analysis.
  • Research Status

  • Current research on Topiramate impurities mainly focuses on the separation, identification, and toxicity assessment of impurities. The stereostructure of this impurity is relatively complex, and studying its limit standards and detection methods in drugs is the current focus of quality control. With the development of pharmaceutical analysis technologies, highly sensitive and high-resolution analytical methods (such as ultra-high-performance liquid chromatography-mass spectrometry) have been widely used for the precise detection of such impurities, and related studies help improve the quality standards of Topiramate drugs.

We can also customize related analogues and modified peptides including HPLC, MS, 1H-NMR, MS, HPLC, IR, UV, COA, MSDS.
This product is intended for laboratory use only!

WhatsAPP: +86 17386083646
E-mail: anna@molcoo.com




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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