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Postion:Product Catalog >Etrasimod Impurity 9
Etrasimod Impurity 9
  • Etrasimod Impurity 9
  • Etrasimod Impurity 9
  • Etrasimod Impurity 9
  • Etrasimod Impurity 9
  • Etrasimod Impurity 9

Etrasimod Impurity 9 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 9 CAS No.: 2305626-60-0
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/06/18

Etrasimod Impurity 9;2305626-60-0


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

  • Etrasimod Impurity 9

  • Product Information

  • Product Code: E063009

  • English Name: Etrasimod Impurity 9

  • English Alias: (E)-ethyl 2-(7-(benzyloxy)-1,2-dihydrocyclopenta[b]indol-3(4H)-ylidene)acetate

  • CAS No.:2305626-60-0

  • Molecular Formula: C??H??NO?

  • Molecular Weight: 347.41

  • Advantages

  • Structural Validation: Confirmed by X-ray crystallography, NMR, and HPLC (≥99.0%).

  • Stability: Stable for 24 months at 2-8℃, with <0.5% degradation in ethanol.

  • Regulatory Compliance: Supports ICH Q3D guidelines for genotoxic impurity assessment.

  • Applications

  • Impurity Profiling: Used in LC-MS for Etrasimod impurity analysis, meeting USP/EP standards.

  • Synthesis Monitoring: Tracks benzyloxy indole condensation side reactions to optimize deprotection steps.

  • Safety Assessment: Evaluates potential genotoxicity via Ames tests and cytotoxicity assays.

  • Background Description

  • This impurity forms during Etrasimod synthesis from benzyloxy protection/deprotection steps. As a potential genotoxic impurity, it requires strict control in drug development for inflammatory disease treatment.
  • Research Status

  • Detection: UPLC-MS/MS with phenyl-hexyl column and gradient elution; LOD: 0.001 ng/mL.

  • Formation Mechanism: Results from benzyloxy group migration; using catalytic hydrogenation reduces generation by 70%.

  • Toxicity: Ames test shows no mutagenicity, but chronic toxicity studies in rodents are in progress


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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