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5-[3-(Diethylamino)-1-Oxopropyl]-10,11-Dihydro-5H-Dibenz[B,F]Azepine CAS NO 16488-05-4
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CAS No.:16488-05-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
5-[3-(Diethylamino)-1-Oxopropyl]-10,11-Dihydro-5H-Dibenz[B,F]Azepine CAS NO 16488-05-4 is a high-purity, specialized organic compound belonging to the dibenzazepine class. This chemical is a critical advanced pharmaceutical intermediate valued for its role in the synthesis of complex active pharmaceutical ingredients (APIs). It is primarily required by research institutions, fine chemical manufacturers, and pharmaceutical companies engaged in the development and production of therapeutic agents.
Application
- Key Intermediate in Pharmaceutical Synthesis: Serves as a crucial building block in the multi-step synthesis of tricyclic antidepressant and neuroactive drug candidates.
- Research & Development (R&D): Used in medicinal chemistry for structure-activity relationship (SAR) studies and the discovery of new bioactive molecules targeting the central nervous system.
- Process Chemistry & Scale-Up: Employed in process optimization and pilot-scale production for new chemical entities (NCEs) before commercial manufacturing.
- Reference Standard: Supplied as a high-purity compound for analytical method development, validation, and quality control in pharmaceutical laboratories.
Basic Information
| Product Name | 5-[3-(Diethylamino)-1-Oxopropyl]-10,11-Dihydro-5H-Dibenz[B,F]Azepine |
| CAS No. | 16488-05-4 |
| Molecular Formula | C21H26N2O |
| Molecular Weight | 322.45 g/mol |
| Synonyms | 10,11-Dihydro-5-[3-(diethylamino)propionyl]-5H-dibenz[b,f]azepine; 5-[3-(Diethylamino)propionyl]-10,11-dihydro-5H-dibenz[b,f]azepine; 5-(3-Diethylaminopropionyl)-10,11-dihydro-5H-dibenzo[b,f]azepine; Desipramine Impurity; Desmethylimipramine Related Compound; DMI Intermediate |
| EINECS | Contact for details |
Quality Control
We supply this intermediate under a rigorous quality management system. Each batch is produced and tested to meet exacting standards suitable for pharmaceutical R&D and synthesis. Certificates of Analysis (COA) are provided, detailing purity, identity, and impurity profiles as determined by advanced analytical techniques including HPLC, GC, and NMR. Our commitment ensures batch-to-batch consistency and traceability for your critical development work.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (typically 15-25°C). Keep away from heat and incompatible materials. Due to its light-sensitive nature, containers should be opaque or stored in dark conditions.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| Loss on Drying | ≤ 0.5% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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