Description

Prasugrel Hydrobromide is a high-purity active pharmaceutical ingredient (API) and a key intermediate in the synthesis of the antiplatelet drug Prasugrel. This compound is critical for ensuring the efficacy and safety of the final pharmaceutical formulation. It is primarily required by pharmaceutical manufacturers, research institutions, and CDMOs (Contract Development and Manufacturing Organizations) engaged in the development and production of cardiovascular medications.

Application

• Active Pharmaceutical Ingredient (API) for the production of Prasugrel, a potent antiplatelet medication.
• Pharmaceutical Intermediate in the multi-step synthesis of Prasugrel-based finished dosage forms (e.g., tablets).
• Reference Standard for quality control and analytical method development in pharmaceutical laboratories.
• Research & Development of new cardiovascular therapies and drug delivery systems.
• Process Chemistry for scale-up and optimization of Prasugrel manufacturing routes.
• Regulatory Submission Batches for generating stability and clinical trial materials.

Basic Information

Product Name	Prasugrel Hydrobromide
CAS No.	1060616-79-6
Molecular Formula	C20H20BrFNO3S
Molecular Weight	469.35 g/mol
Synonyms	5-[(1RS)-2-Cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl acetate hydrobromide; Prasugrel HBr; Prasugrel Hydrobromide Salt; (RS)-Prasugrel Hydrobromide; LY640315 Hydrobromide; CS-747 Hydrobromide; Effient Intermediate
EINECS	Contact for details

Quality Control

Our Prasugrel Hydrobromide is manufactured under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical applications, with specifications typically aligned with ICH guidelines. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

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

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)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5% Any single impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤0.5%
Residue on Ignition	≤0.1%

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