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Postion:Product Catalog >Pentoxifylline Impurity
Pentoxifylline Impurity
  • Pentoxifylline Impurity
  • Pentoxifylline Impurity
  • Pentoxifylline Impurity
  • Pentoxifylline Impurity
  • Pentoxifylline Impurity

Pentoxifylline Impurity NEW

Price Get Latest Price
Package 10mg 50mg 100mg
Min. Order: 10mg
Supply Ability: 1000
Update Time: 2025-12-16

Product Details

Product Name: Pentoxifylline Impurity CAS No.: 10226-28-5
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/12/16

Pentoxifylline Impurity

Article illustration


Product Information

  • Product Code:P060024

  • English Name:Pentoxifylline Impurity 24

  • English Alias:ethyl 6-methyl-3,4-dihydro-2H-pyran-5-carboxylate

  • CAS No.:10226-28-5

  • Molecular Formula:C?H??O?

  • Molecular Weight:170.21

Advantages

  • High-Purity Reference Standard:Confirmed by HPLC (≥99.0%), NMR (1H, 13C), IR, and elemental analysis, suitable for Pentoxifylline impurity analysis and quality control.

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.5% in methanol-water solution within 6 months.

Applications

  • Quality Control Testing:Used for HPLC and LC-MS detection of Impurity 24 in Pentoxifylline API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors Impurity 24 formation during Pentoxifylline synthesis, reducing generation by >40% by adjusting cyclization temperature (e.g., 50-60℃) and reaction time.

  • Method Validation:Serves as a standard for developing impurity detection methods, verifying HPLC resolution (≥2.0) and LOD (0.05 ng/mL).

Background Description

Pentoxifylline is a peripheral vasodilator used to improve cerebrovascular and peripheral circulatory disorders. Impurity 24, as a process-related impurity of Pentoxifylline, may originate from alkylation side reactions of the pyran ring or raw material residues during synthesis. Its pyran ring and ester group may affect drug stability and efficacy. With stricter EMA enforcement of EP standards, studying such impurities is crucial for drug registration and manufacturing.

Research Status

  • Detection Technology:HPLC-DAD with C18 column (5μm) and methanol-water (30:70) isocratic elution achieves separation within 8 minutes, with LOD of 0.02 ng/mL for routine impurity analysis.

  • Formation Mechanism:Formed by reaction of ethyl acetoacetate with methylacrolein under acidic conditions (e.g., acetic acid catalysis); optimizing catalyst dosage and solvent polarity (e.g., ethanol-water system) inhibits side reactions.

  • Safety Evaluation:In vitro cytotoxicity shows IC?? of 215.3 μM against HUVEC cells (Pentoxifylline IC??=28.7 μM), with low toxicity but requiring ≤0.1% limit. Long-term stability testing is ongoing to monitor degradation under different pH conditions.

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


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! 



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