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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Ticagrelor Impurity
Ticagrelor Impurity
  • Ticagrelor Impurity
  • Ticagrelor Impurity
  • Ticagrelor Impurity
  • Ticagrelor Impurity
  • Ticagrelor Impurity

Ticagrelor Impurity NEW

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

Product Details

Product Name: Ticagrelor Impurity CAS No.: 2518331-26-3
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/12/16

Ticagrelor Impurity 

Article illustration


Product Information

  • Product Code:T004162

  • English Name:Ticagrelor Impurity 162

  • English Alias:4-chloro-5-nitro-2-(propylthio)pyrimidine

  • CAS No.:2518331-26-3

  • Molecular Formula:C₇H₈ClN₃O₂S

  • Molecular Weight:233.68

Advantages

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

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.3% in acetonitrile-water solution within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of Impurity 162 in Ticagrelor API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors Impurity 162 formation during Ticagrelor synthesis, reducing generation by >40% by adjusting nitration temperature (e.g., 0-5℃) and reaction time.

  • Method Validation:Serves as a standard for developing impurity detection methods, verifying UPLC resolution (≥3.0) and LOD (0.01 ng/mL).

Background Description

Ticagrelor, a P2Y12 receptor antagonist, is used for treating acute coronary syndromes. Impurity 162, as a process-related impurity of Ticagrelor, may originate from side products of chlorination, nitration, and thioalkylation during pyrimidine ring synthesis. Its chloro, nitro, and propylthio groups may affect drug stability and efficacy. With stricter FDA and EMA requirements for cardiovascular drug impurities, studying Impurity 162 is crucial for ensuring drug quality.

Research Status

  • Detection Technology:UPLC-MS/MS with C18 column (1.7μm) and 0.1% formic acid-acetonitrile gradient elution achieves separation within 5 minutes, with LOD of 0.005 ng/mL for trace impurity analysis.

  • Formation Mechanism:Formed by nitration and chlorination of 2-propylthiopyrimidine; optimizing reaction sequence (chlorination before nitration) and catalyst type (e.g., ferric chloride instead of strong acids) inhibits side reactions.

  • Safety Evaluation:In vitro cytotoxicity shows IC₅₀ of 192.5 μM against HUVEC cells (Ticagrelor IC₅₀=15.6 μM), with lower toxicity than the main drug but requiring strict content control. Long-term stability testing is ongoing to monitor degradation under different humidity, light, and temperature 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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