Description

Zuclopenthixol Acetate CAS NO 85721-05-7 is a high-purity pharmaceutical active ingredient belonging to the thioxanthene class of neuroleptic agents. It is a critical intermediate in the synthesis of long-acting antipsychotic medications, valued for its consistent quality and reliable performance. This compound is essential for pharmaceutical manufacturers and research institutions engaged in the development and production of neuropsychiatric therapeutics.

Application

• Active Pharmaceutical Ingredient (API) in the manufacture of long-acting injectable antipsychotic formulations.
• Pharmaceutical Intermediate for the synthesis of Zuclopenthixol Decanoate and other ester derivatives.
• Reference Standard for analytical method development and quality control in pharmaceutical laboratories.
• Research & Development of novel neuroleptic drugs and delivery systems within academic and institutional settings.
• Clinical Trial Material for studies investigating new indications or formulations of antipsychotic therapies.

Basic Information

Product Name	Zuclopenthixol Acetate
CAS No.	85721-05-7
Molecular Formula	C24H27ClN2O2S
Molecular Weight	442.99 g/mol
Synonyms	cis-Zuclopenthixol Acetate; (Z)-Clopenthixol Acetate; (Z)-2-[4-[3-(2-Chloro-9H-thioxanthen-9-ylidene)propyl]-1-piperazinyl]ethyl Acetate; NSC 339024; Zuclopenthixol 21-Acetate; Clopixol Acetate (associated); α-Clopenthixol Acetate
EINECS	Contact for details

Quality Control

Our Zuclopenthixol Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, suitable for pharmaceutical applications. A Certificate of Analysis (COA) detailing results for assay, related substances, residual solvents, and other critical parameters 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 product is hygroscopic (moisture-sensitive) and light-sensitive; ensure containers are sealed immediately after use to minimize exposure to atmospheric moisture and light.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm
Loss on Drying	≤ 0.5%

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