share

Cangrelor CAS NO 163706-06-7


Unit Price:

CAS No.:163706-06-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Cangrelor CAS NO 163706-06-7 is a potent, direct-acting, and reversible P2Y12 platelet receptor antagonist. This compound is of significant commercial and clinical interest as a fast-acting, intravenous antiplatelet agent. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of cardiovascular therapeutics, particularly for use in percutaneous coronary intervention (PCI) to prevent thrombotic complications.

Application

  • Active Pharmaceutical Ingredient (API) for injectable antiplatelet medications.
  • Cardiovascular Research as a reference standard for studying P2Y12 receptor inhibition and platelet aggregation.
  • Pharmaceutical Development for formulating new rapid-onset anti-thrombotic drugs.
  • Clinical Trial Material for studies investigating acute coronary syndrome management.
  • Biochemical Research tool for exploring purinergic signaling pathways.
  • Quality Control as a high-purity reference compound for analytical method development and validation.

Basic Information

Product Name Cangrelor
CAS No. 163706-06-7
Molecular Formula C17H25Cl2F3N5O12P3S2
Molecular Weight 776.33 g/mol
Synonyms AR-C69931MX; AR-C69931; Cangrelor Tetrasodium; (1R,2S,3R,5R)-3-[6-Amino-2-(methylthio)-9H-purin-9-yl]-5-(2-chloro-6-fluorobenzyloxy)-2-(hydroxymethyl)-4-cyclopentene-1-methyl Dihydrogen (Chloromethylene)bis(phosphonate) Tetrasodium Salt; N6-(2-Methylthioethyl)-2-(3,3,3-trifluoropropylthio)-5'-adenylic Acid Monohydride (Rp)-Dichloromethylene-bis(phosphonic Acid) Ester Tetrasodium Salt
EINECS Contact for details

Quality Control

Our Cangrelor is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and assay, identification by spectroscopic methods (IR, NMR, MS), and stringent control of related substances and residual solvents. Certificates of Analysis (COA) detailing all specifications and test results are provided and available upon request to ensure compliance with your quality and regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under inert conditions or in a desiccator to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Water Content (KF) ≤ 5.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
Heavy Metals ≤ 20 ppm

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

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

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.