Description

Oxagrelate is a synthetic organic compound with significant pharmacological activity, primarily functioning as a thromboxane A2 synthase inhibitor. This mechanism of action makes it a valuable agent for research and development in the cardiovascular and hematological fields. It is a critical intermediate and active pharmaceutical ingredient (API) for researchers and manufacturers developing antiplatelet and antithrombotic therapies. The compound is essential for pharmaceutical R&D, clinical studies, and the production of specialized cardiovascular medications.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of advanced cardiovascular drugs.
• Thromboxane Synthase Inhibition Research: Used in biochemical and pharmacological studies to investigate platelet aggregation and vascular tone regulation.
• Antiplatelet Drug Development: A crucial component in the R&D pipeline for new anti-thrombotic and anti-ischemic medications.
• Reference Standard: Employed as a high-purity analytical standard in quality control laboratories for method development and validation.
• Clinical Research Material: Supplied for preclinical and clinical trial studies exploring treatments for thrombosis and related circulatory disorders.

Basic Information

Product Name	Oxagrelate
CAS No.	56611-65-5
Molecular Formula	C13H12N2O3
Molecular Weight	244.25 g/mol
Synonyms	Oxagrelate; OKY-046; (E)-3-[4-(1H-Imidazol-1-ylmethyl)phenyl]-2-propenoic Acid; (E)-3-[p-(Imidazol-1-ylmethyl)phenyl]acrylic Acid; 4-[(1H-Imidazol-1-yl)methyl]cinnamic Acid; OKY 046; NSC 351958
EINECS	Contact for details

Quality Control

Our Oxagrelate is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive analytical documentation, including a detailed Certificate of Analysis (COA) for each lot, which confirms identity, purity, and impurity profiles. The product is suitable for use under cGMP guidelines for pharmaceutical R&D and meets the stringent requirements for reference standard qualification.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from 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 impurity ≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤0.5%
Heavy Metals	≤20 ppm

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