Description

Desmethoxy Fluvoxamine is a key pharmaceutical intermediate and reference standard in the synthesis and analytical validation of active pharmaceutical ingredients (APIs). This compound is of significant importance for research and development within the pharmaceutical industry, particularly for the study of serotonin reuptake inhibitors. It is primarily needed by pharmaceutical manufacturers, analytical laboratories, and research institutions engaged in the development, quality control, and metabolic studies of neuropsychiatric therapeutics.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of Fluvoxamine and related serotonin reuptake inhibitor compounds.
• Reference Standard: Used for analytical method development, validation, and quality control (QC) testing in pharmaceutical manufacturing.
• Metabolite Studies: Serves as a reference compound in pharmacokinetic and metabolic pathway research for psychotropic drugs.
• Process Chemistry Research: Utilized in route scouting and optimization for the efficient production of active pharmaceutical ingredients (APIs).
• Impurity Profiling: Acts as a known impurity or degradation product standard to ensure drug substance purity and compliance with ICH guidelines.

Basic Information

Product Name	Desmethoxy Fluvoxamine
CAS No.	1217216-82-4
Molecular Formula	C14H19F3N2O
Molecular Weight	288.31 g/mol
Synonyms	5-Methoxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone O-(2-Aminoethyl)oxime; Desmethyl Fluvoxamine; Fluvoxamine Desmethoxy Impurity; Fluvoxamine Related Compound A; UNII-8B6QWG5J0F; 1-[4-(Trifluoromethyl)phenyl]-1-pentanone, 5-methoxy-, O-(2-aminoethyl)oxime
EINECS	Contact for details

Quality Control

Our Desmethoxy Fluvoxamine is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure high purity and consistency, meeting the stringent requirements for pharmaceutical intermediates and reference standards. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

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 impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C
Water Content (KF)	≤ 0.5%

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