Description

2-Oxo Ticlopidine Hcl is a key pharmaceutical intermediate and chemical building block. This compound is of significant importance for the synthesis of active pharmaceutical ingredients (APIs) and advanced research in medicinal chemistry. It is primarily required by pharmaceutical manufacturers, R&D laboratories, and fine chemical producers engaged in developing and scaling up novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of advanced pharmaceutical compounds and active ingredients.
• Research & Development: Used in medicinal chemistry research for the discovery and optimization of new drug candidates.
• API Synthesis: Serves as a building block in the multi-step manufacturing process of complex Active Pharmaceutical Ingredients (APIs).
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
• Chemical Synthesis: Utilized in organic synthesis for constructing complex molecular frameworks in fine chemical production.
• Biochemical Research: Applied in biochemical studies to investigate structure-activity relationships and metabolic pathways.

Basic Information

Product Name	2-Oxo Ticlopidine Hcl
CAS No.	83427-55-8
Molecular Formula	C14H15ClNOS•HCl
Molecular Weight	316.26 g/mol
Synonyms	2-Oxo Ticlopidine Hydrochloride; 5-[(2-Chlorophenyl)methyl]-4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2(3H)-one Hydrochloride; Ticlopidine Impurity; Ticlopidine Related Compound; Ticlopidine EP Impurity B; Ticlopidine Hydrochloride Impurity; 2-Oxo Ticlopidine; 2-Keto Ticlopidine HCl
EINECS	Contact for details

Quality Control

Our 2-Oxo Ticlopidine Hcl is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. The product undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to meet exacting standards for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment to support your quality assurance and regulatory needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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