Description

6,11-Dihydro-N,n-Dimethyl-5H-Dibenz[B,E]Azepine-11-(1-Propanamine) is a specialized organic compound belonging to the dibenzazepine class, serving as a key intermediate in advanced pharmaceutical synthesis. Its value lies in its precise molecular architecture, which is critical for constructing active pharmaceutical ingredients (APIs) with specific neurological or therapeutic targets. This high-purity intermediate is essential for research institutions and pharmaceutical manufacturers engaged in the development and production of innovative central nervous system (CNS) drugs and other specialty medicines. The compound is supplied with full traceability and documentation to support rigorous quality control and regulatory compliance in drug development pipelines.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel dibenzazepine-based active pharmaceutical ingredients (APIs).
• Neurological Drug Research: Used in R&D for developing potential therapeutics targeting CNS disorders.
• Organic Synthesis Reference Standard: Serves as a high-purity reference material for analytical method development and validation.
• Process Chemistry: Employed in scale-up and optimization studies for new drug manufacturing processes.
• Academic & Contract Research: Utilized in university and CRO laboratories for medicinal chemistry and pharmacological studies.

Basic Information

Product Name	6,11-Dihydro-N,n-Dimethyl-5H-Dibenz[B,E]Azepine-11-(1-Propanamine)
CAS No.	39051-51-9
Molecular Formula	C20H26N2
Molecular Weight	294.44 g/mol
Synonyms	11-(3-(Dimethylamino)propyl)-6,11-dihydro-5H-dibenzo[b,e]azepine; 11-(3-Dimethylaminopropyl)-6,11-dihydro-5H-dibenzo[b,e]azepine; 6,11-Dihydro-11-(3-(dimethylamino)propyl)-5H-dibenzo[b,e]azepine; 5H-Dibenzo[b,e]azepine-11(6H)-propanamine, N,N-dimethyl-; 39051-51-9; Dibenzo[b,e]azepine derivative; Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our 6,11-Dihydro-N,n-Dimethyl-5H-Dibenz[B,E]Azepine-11-(1-Propanamine) is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure identity, purity, and consistency, meeting the high standards required for pharmaceutical intermediate applications. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing specifications such as assay, related substances, and residual solvents. We support our clients' regulatory needs with full traceability and documentation.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials and sources of ignition. For long-term storage, consider under an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white powder or crystalline solid
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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