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Postion:Product Catalog >Etrasimod Impurity 17
Etrasimod Impurity 17
  • Etrasimod Impurity 17
  • Etrasimod Impurity 17
  • Etrasimod Impurity 17
  • Etrasimod Impurity 17
  • Etrasimod Impurity 17

Etrasimod Impurity 17 NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-06-18

Product Details

Product Name: Etrasimod Impurity 17 CAS No.: 567-15-7
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/18

Etrasimod Impurity 17;567-15-7


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WhatsAPP: +86 17320513646
E-mail: anna@molcoo.com

  • Etrasimod Impurity 17

  • Product Information

  • Product Code: E063017

  • English Name: Etrasimod Impurity 17

  • English Alias: 2,2'-bis(trifluoromethyl)-1,1'-biphenyl

  • CAS No.:567-15-7

  • Molecular Formula: C??H?F?

  • Molecular Weight: 290.20

  • Advantages

  • Purity & Structure: HPLC ≥99.0%, confirmed by X-ray and HRMS.

  • Stability: Stable for 36 months at -20℃, with <0.1% degradation in toluene.

  • Regulatory Compliance: Supports ICH Q3C guidelines for residual solvent control.

  • Applications

  • Impurity Profiling: Detects biphenyl impurities in Etrasimod via HPLC/LC-MS.

  • Synthesis Monitoring: Tracks biphenyl formation during trifluoromethylation coupling reactions.

  • Environmental Risk Assessment: Evaluates potential ecological impact of halogenated biphenyls.

  • Background Description

  • This impurity forms from oxidative coupling of trifluoromethylbenzene intermediates. As a persistent organic pollutant, it requires strict control in pharmaceutical manufacturing.
  • Research Status

  • Detection: UPLC-MS/MS with C18 column and gradient elution; LOD: 0.005 ng/mL.

  • Formation: Catalyzed by transition metals; using chelating agents reduces content by 85%.

  • Toxicity: OECD tests show low aquatic toxicity, but bioaccumulation potential is being evaluated.

NOTE!

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 17320513646
E-mail: anna@molcoo.com


NEW IN STOCK!

The Molcoo Laboratory added drug impurity reference standards, including Baricitinib, Piperazine, Benzylpenicillin, Tranilast and multiple N-Nitroso drug impurities! Now available for immediate delivery! 


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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