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Postion:Product Catalog >Suzetrigine Impurity 8
Suzetrigine Impurity 8
  • Suzetrigine Impurity 8
  • Suzetrigine Impurity 8
  • Suzetrigine Impurity 8
  • Suzetrigine Impurity 8
  • Suzetrigine Impurity 8

Suzetrigine Impurity 8 NEW

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

Product Details

Product Name: Suzetrigine Impurity 8 CAS No.: 2875066-46-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/07/31
Molecular formula: C16H17F5O4

Suzetrigine Impurity 8;2875066-46-7

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


  • Product Information

  • Product No.:S054008

  • English Name:Suzetrigine Impurity 8

  • English Alias:(3S,4S,5R)-3-(3,4-difluoro-2-methoxyphenyl)-4,5-dimethyl-5-(trifluoromethyl)tetrahydrofuran-2-yl acetate

  • CAS No.:2875066-46-7

  • Molecular Formula:C₁₆H₁₇F₅O₄

  • Molecular Weight:368.30

  • Advantages

  • High purity, suitable for drug impurity analysis and quality control, meeting the strict requirements of the pharmaceutical industry for impurity reference standards.

  • Well-defined structure confirmed by spectroscopic data (such as NMR, MS), ensuring the reliability of experimental results.

  • Applications

  • Used as a drug impurity reference standard for the quality research, stability investigation, and impurity limit verification of Suzetrigine bulk drugs and formulations.

  • Supports impurity traceability analysis in the drug research and development stage, helping to evaluate the impact of production processes on impurity formation.

  • Background Description

  • Suzetrigine is a drug under development, and impurity control is crucial to ensure the safety and effectiveness of the drug. As a related substance that may be generated during the synthesis or storage of Suzetrigine, this impurity needs to be qualitatively and quantitatively analyzed by reference standards to ensure that the drug meets the requirements of pharmacopoeias and regulations.
  • Research Status

  • Current research on this impurity mainly focuses on the field of pharmaceutical analysis. Detection methods such as high-performance liquid chromatography (HPLC) and mass spectrometry (MS) are used to establish its testing procedures, and its toxicity and potential risks are evaluated during drug development. Relevant studies are committed to improving the quality standards of Suzetrigine and promoting the clinical application process of the drug.

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



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