Description

Ticlopidine is a potent thienopyridine-class antiplatelet agent, primarily recognized for its role in preventing thrombotic events. Its value lies in its specific mechanism of action, irreversibly inhibiting ADP-induced platelet aggregation, which is critical for managing and preventing arterial clotting. This compound is essential for the pharmaceutical industry, serving as the active pharmaceutical ingredient (API) in medications designed for patients at risk of stroke, myocardial infarction, or with peripheral arterial disease. Global suppliers and manufacturers of cardiovascular drugs rely on high-purity Ticlopidine to ensure the efficacy and safety of their final formulations.

Application

• Primary use as an Active Pharmaceutical Ingredient (API) in antiplatelet and antithrombotic medications.
• Formulation of oral solid dosage forms, such as tablets, for the prevention of stroke and transient ischemic attacks (TIAs).
• Research and development of new cardiovascular therapies and combination drug products.
• Production of reference standards and impurities for quality control and analytical testing in pharmaceutical laboratories.
• Use in biochemical research to study platelet aggregation pathways and ADP receptor (P2Y12) antagonists.
• Potential intermediate in the synthesis of related thienopyridine derivatives for pharmacological evaluation.

Basic Information

Product Name	Ticlopidine
CAS No.	55142-85-3
Molecular Formula	C14H14ClNS
Molecular Weight	263.79 g/mol
Synonyms	5-[(2-Chlorophenyl)methyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridine; Ticlopidine Hydrochloride (salt form); Ticlodone; Ticlodix; Tiklid; Ticlo; Antigreg; Panaldine; PCR 3789; Ticlopidina; Ticlopidin
EINECS	259-516-7

Quality Control

Our Ticlopidine is manufactured and tested under a strict quality management system to meet the exacting standards of the global pharmaceutical industry. We adhere to relevant pharmacopeial guidelines, including USP and EP monographs where applicable, ensuring identity, purity, strength, and composition. Each batch is supported by a comprehensive Certificate of Analysis (COA) detailing all critical quality attributes. Our commitment to cGMP compliance and rigorous analytical validation provides our B2B clients with the supply reliability and documentation necessary for their regulatory submissions and production processes.

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 low-humidity environment to prevent degradation. For long-term storage, consider the use of desiccants.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5%
Microbial Limits	Meets Ph. Eur. / USP criteria

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