Description

Ozagrel-015 is a high-purity pharmaceutical intermediate and research chemical, identified by CAS NO 1332370-00-9. This compound is a critical building block in the synthesis of advanced active pharmaceutical ingredients (APIs), valued for its specific chemical reactivity and structural role. It is essential for R&D laboratories and manufacturing facilities in the pharmaceutical and fine chemical sectors that require reliable, high-quality raw materials for process development and scale-up.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of thromboxane A2 synthase inhibitors and related therapeutic agents.
• Research & Development: Used in academic and industrial laboratories for pharmacological studies and the development of new chemical entities.
• API Synthesis: Serves as a crucial building block in multi-step synthetic routes for producing complex active pharmaceutical ingredients.
• Biochemical Research: Employed in studies investigating platelet aggregation, thrombosis, and related cardiovascular pathways.
• Reference Standard: Utilized as an analytical standard for quality control and method validation in pharmaceutical analysis.
• Fine Chemical Production: Integrated into the manufacture of specialized, high-value organic compounds for various industrial applications.

Basic Information

Product Name	Ozagrel-015
CAS No.	1332370-00-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Ozagrel Impurity 15; Ozagrel Related Compound 15; Ozagrel EP Impurity I; (E)-3-[4-(1H-Imidazol-1-ylmethyl)phenyl]-2-propenoic Acid; Ozagrel Intermediate; Ozagrel Metabolite; Antiplatelet Agent Intermediate; TXA2 Synthase Inhibitor Intermediate
EINECS	Contact for details

Quality Control

Our Ozagrel-015 is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all relevant specifications. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (typically 15-25°C). Keep the container sealed to protect from moisture. Follow standard laboratory safety practices for handling chemical powders.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH limits
Loss on Drying	≤ 1.0%

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