Description

Prasugrel CAS NO 150322-43-3 is a potent thienopyridine-class antiplatelet agent, a key active pharmaceutical ingredient (API) used in the prevention of thrombotic cardiovascular events. Its primary value lies in its irreversible inhibition of the P2Y12 adenosine diphosphate receptor on platelets, offering a more consistent and rapid onset of action compared to earlier generation drugs. This high-purity pharmaceutical intermediate is essential for manufacturers of finished dosage forms, particularly in the production of medications for patients with acute coronary syndrome undergoing percutaneous coronary intervention.

Application

• Pharmaceutical API Synthesis: Primary use as the active ingredient in the manufacture of antiplatelet tablets for cardiovascular disease prevention.
• Cardiovascular Drug Formulation: Critical component in the production of medications designed to reduce the rate of heart attack, stroke, and cardiovascular death in high-risk patients.
• Clinical Research & Development: Serves as a reference standard and key material in R&D for novel anti-thrombotic therapies and combination drug studies.
• Generic Drug Manufacturing: A vital raw material for companies producing bioequivalent versions of established antiplatelet therapies.
• Hospital & Compounding Pharmacy Use: Used in specialized settings for formulating patient-specific dosages where commercial formulations are unsuitable.

Basic Information

Product Name	Prasugrel
CAS No.	150322-43-3
Molecular Formula	C20H20FNO3S
Molecular Weight	373.44 g/mol
Synonyms	Prasugrel; 5-[(1RS)-2-Cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetate; CS-747; LY640315; Effient (Trade Name); Efient; Prasugrel Hydrochloride (Salt Form); 2-Acetoxy-5-(α-cyclopropylcarbonyl-2-fluorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridin
EINECS	Contact for details

Quality Control

Our Prasugrel is manufactured under strict quality management systems, targeting specifications suitable for pharmaceutical applications. Quality is assured through comprehensive analytical testing, including HPLC for purity and impurity profiling, residual solvent analysis, and stringent control of related substances. A Certificate of Analysis (COA) is provided with each batch, detailing compliance with agreed specifications. We support development and commercial projects requiring ICH stability data and can supply material manufactured in alignment with cGMP principles.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (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 using desiccants.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 2.0%
Water Content (KF)	NMT 1.0%
Residue on Ignition	NMT 0.1%
Heavy Metals	NMT 20 ppm

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