Keywords

• 9H-Purine,2-amino-6-chloro-9-b-D-ribofuranosyl- (6CI,7CI,8CI)
• Regadenoson Impurity
• 2-Amino-6-chloro-9-b-D-ribofuranosylpurine

Quick Details

• ProName: Regadenoson Impurity 30
• CasNo: 2004-07-1
• Molecular Formula: C10H12ClN5O4
• Appearance: White to off white powder
• Application: experiment research
• DeliveryTime: prompt delivery
• PackAge: Food bags, aluminum foil bags
• Port: Shenzhen/hongkong
• ProductionCapacity: 5000 Gram/Year
• Purity: 99%+ HPLC
• Storage: cool and dry
• Transportation: DHL,EMS,TNT,UPS,EMS,by air,by sea;
• LimitNum: 10 Milligram
• Moisture Content: 0.1%
• Impurity: 0.1%

Superiority

• Advantages

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

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

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Details

Regadenoson Impurity;2004-07-1

Product Information

• Product Code：R013030

• English Name：Regadenoson Impurity 30

• English Alias：(2R,3R,4S,5R)-2-(2-amino-6-chloro-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol

• CAS No.：2004-07-1

• Molecular Formula：C??H??ClN?O?

• Molecular Weight：301.69

Advantages

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

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

Applications

• Quality Control Testing：Used for UPLC-MS/MS detection of Impurity 30 in Regadenoson API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

• Process Optimization Research：Monitors impurity formation during Regadenoson synthesis, reducing generation by >35% by adjusting amination temperature (e.g., 60-70℃) and pH.

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

Background Description

Regadenoson, a selective A2A adenosine receptor agonist, is used for myocardial perfusion imaging to diagnose coronary heart disease. Impurity 30, a process-related impurity in its synthesis, may originate from chlorination of purine rings or glycosylation side reactions. Its amino, chlorine, and polyol groups may affect drug water solubility, stability, and receptor binding. Strict impurity control for cardiovascular drugs is critical to medication safety, making research on this impurity essential 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 6 minutes, with LOD of 0.005 ng/mL for trace impurity analysis.

• Formation Mechanism：Formed by nucleophilic substitution of 2,6-dichloropurine with glycosyl compounds in ammonia solution; optimizing reaction temperature and ammonia concentration inhibits side reactions.

• Safety Evaluation：In vitro cytotoxicity shows IC?? of 178.5 μM against H9c2 cardiac cells (Regadenoson IC??=8.7 μM), with lower toxicity than the main drug but requiring strict content control. Long-term stability testing is ongoing to monitor degradation under high temperature (40℃) and high humidity (75%RH) conditions.