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Fluphenazine Enanthate Dihydrochloride (125 Mg) CAS NO 3105-68-8


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CAS No.:3105-68-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fluphenazine Enanthate Dihydrochloride (125 Mg) is a high-purity pharmaceutical active ingredient (API) and a long-acting esterified derivative of the antipsychotic fluphenazine. This compound is critical for the formulation of depot injections, providing sustained therapeutic release for improved patient compliance in chronic treatment regimens. It is primarily required by pharmaceutical manufacturers and research institutions engaged in developing and producing advanced neuropsychiatric medications.

Application

  • Active Pharmaceutical Ingredient (API) for long-acting injectable antipsychotic formulations.
  • Pharmaceutical Intermediates in the synthesis of advanced neuroleptic drug products.
  • Reference Standard for quality control and analytical method development in pharmacopeial testing.
  • Clinical Research Material for studies on schizophrenia and other psychotic disorders.
  • Formulation Development for creating depot injection systems with controlled release profiles.
  • Regulatory Submission Batches used in the preparation of documentation for FDA, EMA, and other global health authority approvals.

Basic Information

Product Name Fluphenazine Enanthate Dihydrochloride (125 Mg)
CAS No. 3105-68-8
Molecular Formula C29H38F3N3O2S • 2HCl
Molecular Weight 622.6 g/mol (Free base: 549.7 g/mol)
Synonyms Fluphenazine Enanthate Dihydrochloride; Fluphenazine Heptanoate Dihydrochloride; Prolixin Enanthate Dihydrochloride; 4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol heptanoate ester dihydrochloride; SQ 10733; NSC-77370; Flufenazin enantat dihydrochlorid
EINECS 221-456-1

Quality Control

Our Fluphenazine Enanthate Dihydrochloride is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, suitable for pharmaceutical use. A Certificate of Analysis (COA) documenting results against relevant pharmacopeial standards (e.g., 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 (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item Specification
Appearance White or almost white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to 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) Total impurities ≤ 2.0% Any individual impurity ≤ 0.5%

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

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