Description

Lubazodone CAS NO 161178-21-8 is a high-purity pharmaceutical intermediate and research chemical. This compound is of significant interest for its role in the development of novel therapeutic agents, particularly within the central nervous system (CNS) domain. It is primarily utilized by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic research institutions engaged in medicinal chemistry and drug discovery programs.

Application

• Key intermediate in the synthesis of advanced pharmaceutical active ingredients (APIs).
• Research and development of potential psychotropic and neuroactive compounds.
• Pre-clinical and pharmacological studies within academic and industrial settings.
• Building block for custom synthesis and medicinal chemistry optimization projects.
• Reference standard for analytical method development and quality control in API manufacturing.

Basic Information

Product Name	Lubazodone
CAS No.	161178-21-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Lubazodone; 1-(4-Fluorophenyl)-4-((6-fluoropyridin-3-yl)methyl)piperazine; LBZ-1; BMS-820836 (developmental code); UNII-9K8F8T8V1T
EINECS	Contact for details

Quality Control

Our Lubazodone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including chromatographic purity assays and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical research and development. Certificates of Analysis (COA) detailing purity, impurities, and other critical parameters are available upon request.

Storage

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

Specification

Item	Specification
Appearance	White to off-white 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%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 1.0%

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