Description

Fluindione is a synthetic anticoagulant belonging to the 4-hydroxycoumarin vitamin K antagonist class. This high-purity active pharmaceutical ingredient (API) is critical for the development and production of specialized anticoagulant medications. It is primarily utilized by pharmaceutical manufacturers and research institutions in the life sciences sector for therapeutic applications and advanced biochemical studies.

Application

• Pharmaceutical API: Primary active ingredient in the formulation of anticoagulant and antithrombotic drugs.
• Biochemical Research: Used as a reference standard and tool compound in studies of blood coagulation pathways and vitamin K metabolism.
• Veterinary Medicine: Potential application in the development of anticoagulant treatments for animals.
• Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control and analytical method development in laboratories.

Basic Information

Product Name	Fluindione
CAS No.	957-56-2
Molecular Formula	C16H10FO3
Molecular Weight	278.25 g/mol
Synonyms	2-(4-Fluorophenyl)-1,3-indandione; 2-(p-Fluorophenyl)indane-1,3-dione; Previscan (trade name); Fluindiona; Fluindionum; Pefluindione; LM 320
EINECS	213-500-8

Quality Control

Our Fluindione is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. A detailed Certificate of Analysis (COA), including results for identity, purity, and related substances, is provided with every shipment to guarantee traceability and compliance.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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