Description

Seratrodast is a selective thromboxane A2 receptor antagonist, a high-purity active pharmaceutical ingredient (API) critical for advanced pharmaceutical research and development. Its primary value lies in its targeted mechanism of action, which is essential for developing therapeutic agents. This compound is primarily needed by pharmaceutical manufacturers and research institutions focused on respiratory and inflammatory conditions.

Application

• Primary use as an Active Pharmaceutical Ingredient (API) in pharmaceutical formulations.
• Key component in respiratory disease research, particularly for asthma and related inflammatory conditions.
• Utilized in preclinical and clinical studies to investigate thromboxane-mediated pathways.
• Reference standard for analytical method development and quality control in pharmaceutical labs.
• Intermediate in the synthesis of novel therapeutic agents targeting specific receptors.
• Used in pharmacological research to study anti-inflammatory and anti-allergic effects.

Basic Information

Product Name	Seratrodast
CAS No.	112665-43-7
Molecular Formula	C₂₂H₂₈N₂O₆
Molecular Weight	416.47 g/mol
Synonyms	AA-2414; (±)-7-Phenyl-7-(2-hydroxyethoxy)-6-oxoheptanoic Acid; 7-(3,5,6-Trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoic Acid; Seratrodastum; ABT-001; Seratrodast (USAN); CC-1004
EINECS	Contact for details

Quality Control

Our Seratrodast is manufactured under strict quality systems to ensure it meets the high standards required for pharmaceutical applications. Each batch undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. Certificates of Analysis (COA) documenting compliance with agreed specifications are available upon request.

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 nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5% 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.