Description

Lusaperidone CAS NO 214548-46-6 is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) of significant importance in modern medicinal chemistry. This compound serves as a critical building block in the research and development of novel therapeutic agents, particularly within the central nervous system (CNS) domain. It is essential for pharmaceutical manufacturers, contract research organizations (CROs), and academic research institutions engaged in the synthesis of advanced drug candidates.

Application

• Pharmaceutical Intermediate: Primary use as a key synthetic precursor in the production of advanced antipsychotic and neuropsychiatric drug candidates.
• Active Pharmaceutical Ingredient (API) Development: Serves as the core chemical entity in the formulation and clinical development of new therapeutic compounds.
• Research & Development (R&D): Utilized in medicinal chemistry research for structure-activity relationship (SAR) studies and the discovery of new bioactive molecules.
• Reference Standard: Acts as a high-purity analytical standard for quality control, method development, and regulatory submissions in pharmaceutical analysis.
• Process Chemistry: Employed in scale-up and optimization studies for the commercial manufacturing of pharmaceutical products.

Basic Information

Product Name	Lusaperidone
CAS No.	214548-46-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Lusaperidone; 214548-46-6; (3aR,4S,7R,7aS)-2-[(2R,4R)-4-(2,3-Difluorophenyl)-2-methylpiperazin-1-yl]-4,7-methano-2H-isoindole-1,3(3aH,4H,7H,7aH)-dione; UNII-4V7P2K3Q2K; 4V7P2K3Q2K; BDBM50135425; CHEMBL3186395; HY-101966; SCHEMBL15516799; AKOS025310923; AS-58300; CS-0476647; NS-00061392; P11142; STK682111; ZINC000004143756
EINECS	Contact for details

Quality Control

Our Lusaperidone is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. The product undergoes rigorous analytical testing, including HPLC, NMR, and MS, to confirm identity, purity, and the absence of critical impurities. Certificates of Analysis (COA) detailing all specifications and test results are provided with each shipment to support your quality assurance and regulatory compliance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%
Total Impurities	≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Water Content (KF)	≤ 0.5%
Heavy Metals	≤ 20 ppm

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