Description

11-(3-Methylamino-1-Azetidinyl)Dibenzo[B,E]Thiepin is a high-purity, advanced pharmaceutical intermediate characterized by its unique dibenzothiepin core fused with an azetidine ring system. This compound matters as a critical building block in the research and development of novel therapeutic agents, particularly within the central nervous system (CNS) and neuropharmacology domains. Pharmaceutical R&D laboratories and fine chemical manufacturers need it for synthesizing potential drug candidates targeting specific receptor pathways. Its precise molecular architecture enables the exploration of new structure-activity relationships.

Application

• Pharmaceutical Intermediate: Serves as a key precursor in the synthesis of novel psychotropic and neuroactive drug candidates.
• Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization programs.
• Preclinical Studies: Employed in the development of compounds for potential application in treating CNS disorders.
• Reference Standard: Acts as a high-purity analytical standard for quality control and method development in analytical laboratories.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Utilized in university and institutional labs for pharmacological and biochemical research.

Basic Information

Item	Details
Product Name	11-(3-Methylamino-1-Azetidinyl)Dibenzo[B,E]Thiepin
CAS No.	73927-84-1
Molecular Formula	C19H20N2S
Molecular Weight	308.44 g/mol
Synonyms	11-(3-Methylaminoazetidin-1-yl)dibenzo[b,e]thiepin; Dibenzo[b,e]thiepin, 11-(3-(methylamino)-1-azetidinyl)-; 11-(3-Methylamino-1-azetidinyl)dibenzo[b,e]thiepin; 73927-84-1; UNII-7V4A8U16MB; 7V4A8U16MB; SCHEMBL218422; BDBM50389395; AKOS005258209
EINECS	Contact for details

Quality Control

Every batch of 11-(3-Methylamino-1-Azetidinyl)Dibenzo[B,E]Thiepin is manufactured under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical quality attributes. Our commitment to quality supports compliance with cGMP guidelines for pharmaceutical intermediates, ensuring reliability for your most demanding R&D and scale-up processes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). The product should be kept under an inert atmosphere if long-term stability is required. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms
Identification (IR)	Conforms
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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