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Vicagrel CAS NO 1314081-53-2


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CAS No.:1314081-53-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Vicagrel CAS NO 1314081-53-2 is a novel, potent antiplatelet agent and a promising active pharmaceutical ingredient (API). It functions as a selective and irreversible P2Y12 receptor antagonist, offering a significant therapeutic profile for cardiovascular protection. This compound is primarily targeted at the pharmaceutical industry for the research, development, and manufacturing of next-generation anti-thrombotic medications.

Application

  • Pharmaceutical API: Core active ingredient in the formulation of antiplatelet drugs for the prevention of atherothrombotic events.
  • Cardiovascular Drug Development: Key intermediate or final API in R&D pipelines for treating conditions like acute coronary syndrome (ACS) and post-percutaneous coronary intervention (PCI).
  • Biochemical Research: Used as a reference standard or tool compound in pharmacological studies of platelet aggregation and P2Y12 receptor pathways.
  • Generic Drug Manufacturing: Serves as the critical component for producing generic versions of advanced antiplatelet therapies upon patent expiry.
  • Preclinical & Clinical Trial Material: Supplied under GMP guidelines for use in non-clinical safety assessments and clinical studies.

Basic Information

Product Name Vicagrel
CAS No. 1314081-53-2
Molecular Formula C20H22ClN3O3S
Molecular Weight 419.92 g/mol
Synonyms Vicagrel; 2-(2-(2-Chloro-6-fluorobenzyl)oxy)-5-(methoxycarbonyl)phenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine; (2-(2-((2-Chloro-6-fluorobenzyl)oxy)-5-(methoxycarbonyl)phenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine); Ticagrelor analogue; P2Y12 receptor antagonist
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Quality Control

Our Vicagrel is manufactured under strict quality management systems. Each batch is subjected to rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specified parameters. Production can be aligned with GMP (Good Manufacturing Practice) standards for pharmaceutical applications upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item Specification
Appearance White to off-white powder
Identification (HPLC/IR) Conforms to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Loss on Drying ≤ 1.0%
Heavy Metals ≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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