Prasugrel
Prasugrel (CAS: 150322-43-3), with the empirical formula C20H20FNO3S and a molecular weight of 373.44 g/mol, is a potent antiplatelet medication. It functions as a P2Y12 receptor antagonist, crucial in preventing thrombotic events. This compound is primarily utilised in clinical settings for patients with acute coronary syndrome undergoing percutaneous coronary intervention, demonstrating its significant role in cardiovascular therapies.
- IUPAC
- 5-[2-Cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetate,CS 747,CS-747,Effient,Efient,LY640315
- Synonyms
- 5-[2-Cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetateCS 747CS-747EffientEfientLY640315

Antiplatelet Therapy
Prasugrel acts as an irreversible inhibitor of the P2Y12 adenosine diphosphate (ADP) receptor on platelets. This action prevents ADP-mediated platelet activation and aggregation, contributing to the prevention of blood clots.
Cardiovascular Disease Management
It is prescribed to reduce the risk of thrombotic cardiovascular events, such as heart attack and stroke, in patients with unstable angina or myocardial infarction who are scheduled for percutaneous coronary intervention (PCI).
Research Chemical
As a well-characterised compound, Prasugrel serves as a valuable tool in research laboratories investigating platelet function, thrombosis, and related cardiovascular mechanisms.
| Molecular weight | 373.44 |
|---|---|
| Empirical formula | C20H20FNO3S |
| Assay | ≥98% (HPLC) |
| Form | powder |
| Colour | white to beige |
| Solubility | DMSO: >5 mg/mL (warmed at 60 °C) |
| Storage temperature | 2-8°C |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Prasugrel primarily used for?
+
Prasugrel is primarily used as an antiplatelet medication to prevent blood clots in patients with acute coronary syndrome undergoing percutaneous coronary intervention.
What are the CAS number and empirical formula for Prasugrel?
+
The CAS number for Prasugrel is 150322-43-3, and its empirical formula is C20H20FNO3S.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Prasugrel with a purity of ≥98% (HPLC). This product is intended for research and development purposes and is not supplied as USP, BP, EP, or pharmacopoeia grade.
How should Prasugrel be stored and handled?
+
Prasugrel should be stored at 2-8°C. Handle with appropriate personal protective equipment in a well-ventilated area. Refer to the Safety Data Sheet for detailed handling and hazard information.
Can I get a quote or sample for Prasugrel?
+
Yes, you can request a quote or sample for Prasugrel by contacting our sales team through the website or by direct inquiry.
Is Prasugrel a controlled substance?
+
Based on the provided data, Prasugrel is not listed as a controlled substance.
How is Prasugrel packed, shipped, and exported?
+
Prasugrel is carefully packed to ensure stability during transit and is available for export globally by Tech Serve Solutions.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis