Description

Zuclopenthixol is a high-purity pharmaceutical active ingredient belonging to the thioxanthene class of neuroleptic agents. This compound is critical for the development and manufacturing of antipsychotic medications, where consistent quality and purity are paramount for therapeutic efficacy and safety. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in neuropsychiatric drug development and formulation.

Application

• Active Pharmaceutical Ingredient (API) in the manufacture of antipsychotic medications.
• Reference standard for analytical method development and validation in quality control laboratories.
• Key intermediate in advanced pharmaceutical research for central nervous system (CNS) disorders.
• Biochemical research for studying dopamine receptor antagonism and related neurological pathways.
• Formulation studies for developing various dosage forms, including depot injections and oral tablets.

Basic Information

Product Name	Zuclopenthixol
CAS No.	1246833-58-8
Molecular Formula	C22H25ClN2OS
Molecular Weight	400.96 g/mol
Synonyms	(Z)-Clopenthixol; cis-Clopenthixol; Zuclopenthixolum; Zuclopentixol; NSC 75899; (Z)-2-[4-[3-(2-Chloro-9H-thioxanthen-9-ylidene)propyl]piperazin-1-yl]ethanol; (Z)-4-[3-(2-Chloro-9H-thioxanthen-9-ylidene)propyl]-1-piperazineethanol
EINECS	Contact for details

Quality Control

Our Zuclopenthixol is manufactured under strict quality management systems to ensure it meets the stringent requirements for pharmaceutical use. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via HPLC and other pharmacopeial methods. A Certificate of Analysis (COA) detailing all specifications and results is provided with every shipment to guarantee traceability and compliance with relevant standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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