Description

Fluvoxamine is a selective serotonin reuptake inhibitor (SSRI) API, widely recognized for its therapeutic efficacy in managing major depressive disorder and obsessive-compulsive disorder. Its high purity and consistent quality are critical for ensuring the safety and efficacy of finished pharmaceutical formulations. This compound is essential for pharmaceutical manufacturers, research institutions, and developers of generic and branded medications.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of antidepressant and anti-anxiety medications.
• Generic Drug Manufacturing: Serves as the key active component in generic versions of fluvoxamine-based drugs.
• Clinical Research & Development: Utilized in preclinical and clinical studies for investigating new therapeutic applications of SSRIs.
• Reference Standard: Acts as a high-purity standard for analytical testing, quality control, and method validation in laboratories.
• Finished Dosage Forms: Incorporated into various dosage forms, including tablets and capsules.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for pharmaceutical production.

Basic Information

Product Name	Fluvoxamine
CAS No.	54739-18-3
Molecular Formula	C15H21F3N2O2
Molecular Weight	318.34 g/mol
Synonyms	Fluvoxamine Maleate; (E)-5-Methoxy-1-[4-(trifluoromethyl)phenyl]pentan-1-one O-2-Aminoethyl Oxime; DU-23000; Luvox (Trade Name); Fevarin; Faverin; Floxyfral
EINECS	Contact for details

Quality Control

Our Fluvoxamine is manufactured under strict quality management systems, targeting standards suitable for pharmaceutical applications. Each batch is subjected to comprehensive analytical testing, including identity, purity, and impurity profile verification. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to ensure full traceability and compliance with your quality requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry conditions to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Heavy Metals	≤ 20 ppm

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