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Postion:Product Catalog >Bempedoic Acid Impurity
Bempedoic Acid Impurity
  • Bempedoic Acid Impurity
  • Bempedoic Acid Impurity
  • Bempedoic Acid Impurity
  • Bempedoic Acid Impurity
  • Bempedoic Acid Impurity

Bempedoic Acid 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: Bempedoic Acid Impurity CAS No.: 2943-42-2
Min. Order: 10mg Purity: 99%+ HPLC
Supply Ability: 1000 Release date: 2025/12/16

Bempedoic Acid Impurity;2943-42-2

Article illustration


Product Information

  • Product Code:B079029

  • English Name:Bempedoic Acid Impurity 29

  • English Alias:S-p-tolyl 4-methylbenzenesulfonothioate

  • CAS No.:2943-42-2

  • Molecular Formula:C??H??O?S?

  • Molecular Weight:278.39

Advantages

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

  • Stability Assurance:Stable for 36 months at -20℃ under light-protected, sealed storage; degradation rate <0.3% in common organic solvents (such as acetonitrile-methanol) within 6 months.

Applications

  • Quality Control Testing:Used for UPLC-MS/MS detection of Impurity 29 in Bempedoic Acid API and formulations, controlling content to meet ICH Q3A standards (single impurity limit ≤0.1%).

  • Process Optimization Research:Monitors Impurity 29 formation during Bempedoic Acid synthesis, reducing generation by >40% by adjusting sulfonothioylation temperature (e.g., 20-30℃) 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

Bempedoic Acid, an ATP citrate lyase inhibitor, is used for treating hypercholesterolemia. Impurity 29, as a process-related impurity of Bempedoic Acid, may originate from side products of sulfonothioylation during synthesis. Its sulfonothioate and methyl groups may affect drug stability and efficacy. With stricter requirements from global regulatory agencies for lipid-lowering drug impurities, studying Impurity 29 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 6 minutes, with LOD of 0.005 ng/mL for trace impurity analysis.

  • Formation Mechanism:Formed by reaction of p-tolyl mercaptan with p-toluenesulfonyl chloride under alkaline conditions (e.g., triethylamine/DCM system); optimizing base dosage and reaction solvent polarity inhibits side reactions.

  • Safety Evaluation:In vitro cytotoxicity shows IC?? of 198.7 μM against HepG2 cells (Bempedoic Acid IC??=15.2 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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