Description

Fluphenazine Octanoate is a long-acting ester derivative of the potent antipsychotic agent fluphenazine, designed for depot injection formulations. This compound is critical for providing sustained therapeutic effects, improving patient compliance in long-term treatment regimens. It is an essential active pharmaceutical ingredient (API) for manufacturers developing controlled-release injectable medications targeting chronic psychotic disorders.

Application

• Primary Active Pharmaceutical Ingredient (API) in long-acting depot injectable antipsychotic medications.
• Formulation of sustained-release pharmaceutical products for the management of schizophrenia and other psychotic conditions.
• Used in clinical research and development of novel neuroleptic delivery systems.
• Manufacturing of generic pharmaceutical products requiring a reliable source of high-purity fluphenazine octanoate.
• Reference standard material for analytical testing and quality control in pharmaceutical laboratories.

Basic Information

Product Name	Fluphenazine Octanoate
CAS No.	97671-70-0
Molecular Formula	C₃₂H₄₄F₃N₃O₂S
Molecular Weight	591.77 g/mol
Synonyms	Fluphenazine Octanoate; Fluphenazine Enanthate (common misnomer for the octanoate ester); Prolixin Decanoate (related trade name); 2-[4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]piperazin-1-yl]ethyl octanoate; Flufenazin Octanoat; Fluphenazinum Octanoas; SQ 10733; NSC 77370
EINECS	Contact for details

Quality Control

Our Fluphenazine Octanoate is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for pharmaceutical use, including identity, purity, and impurity profiles. A Certificate of Analysis (COA) documenting compliance with relevant pharmacopeial standards (such as USP/EP) is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (typically 15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Individual impurity: NMT 0.5% Total impurities: NMT 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	NMT 1.0%
Heavy Metals	NMT 20 ppm

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