Description

Trifluoperidol HCl is a high-purity pharmaceutical intermediate and research chemical of significant importance in neuropharmacology. This compound is valued for its critical role in the development and synthesis of antipsychotic agents used in neurological research. It is primarily required by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in central nervous system (CNS) drug discovery and development.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of potent antipsychotic medications and related neuroleptic compounds.
• Neurological Research: Used as a reference standard and active compound in preclinical studies investigating dopamine receptor antagonism and antipsychotic efficacy.
• Biochemical Assays: Employed in receptor binding studies and pharmacological screenings to understand mechanisms of action for CNS-active drugs.
• Fine Chemical Synthesis: Serves as a precursor for the development of novel derivatives with potential therapeutic applications in psychiatry.
• Academic Research: Utilized in university and institutional labs for teaching and advanced research in medicinal chemistry and psychopharmacology.
• Quality Control: Acts as a certified reference material (CRM) for analytical method development and validation in pharmaceutical quality assurance laboratories.

Basic Information

Product Name	Trifluoperidol Hydrochloride
CAS No.	2062-77-3
Molecular Formula	C₂₂H₂₄F₃NO₂ • HCl
Molecular Weight	427.89 g/mol
Synonyms	Trifluperidol Hydrochloride; 1-[4-(4-Fluorophenyl)-4-oxobutyl]-4-(4-hydroxy-4-(3-(trifluoromethyl)phenyl)piperidin-1-yl)pyridin-1-ium chloride; Triperidol HCl; Psicoperidol; R-2498; Flupredol; 4'-Fluoro-4-[4-hydroxy-4-(α,α,α-trifluoro-m-tolyl)piperidino]butyrophenone Hydrochloride
EINECS	Contact for details

Quality Control

Our Trifluoperidol HCl is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research and pharmaceutical applications. Each lot undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR spectroscopy, and stringent control of residual solvents and impurities. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting compliance with our rigorous specifications. We support cGMP standards for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Single Maximum Impurity	≤0.5%
Loss on Drying	≤1.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm

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