Description

Fluphenazine Dimaleate is a high-purity pharmaceutical active ingredient (API) and a key intermediate in the synthesis of potent antipsychotic medications. Its primary value lies in its critical role as a precursor for the production of long-acting neuroleptic formulations, ensuring reliable and controlled therapeutic delivery. This compound is essential for pharmaceutical manufacturers and research institutions focused on developing and producing treatments for psychiatric and neurological disorders, where precise chemical integrity is paramount for efficacy and safety.

Application

• Pharmaceutical API Synthesis: Primary use as an active pharmaceutical ingredient in the manufacture of antipsychotic drugs.
• Long-Acting Injectable Formulations: Key precursor for depot injections, such as fluphenazine decanoate, enabling sustained drug release.
• Neurological Research: Used in preclinical and clinical research to study dopamine receptor antagonism and related pathways.
• Reference Standard: Serves as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical labs.
• Chemical Intermediate: Utilized in further organic synthesis to create novel derivatives for pharmacological evaluation.

Basic Information

Product Name	Fluphenazine Dimaleate
CAS No.	3093-66-1
Molecular Formula	C₃₂H₃₄F₃N₃O₈S
Molecular Weight	665.69 g/mol
Synonyms	Fluphenazine Maleate; 4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol dimaleate; Prolixin Dimaleate; Fluphenazine Di(hydrogen maleate); PMS-Fluphenazine; Anatensol; Dapotum; Lyogen; Moditen; Pacinol; Permitil; SQ 4918; Trancin
EINECS	221-426-5

Quality Control

Our Fluphenazine Dimaleate is manufactured under strict quality systems to meet the exacting standards of the pharmaceutical industry. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC and other validated methods. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, ensuring compliance with relevant pharmacopeial guidelines (e.g., USP, EP) and cGMP principles.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Specific Rotation	Contact for details

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