share

Dibenzepine Hcl CAS NO 315-80-0


Unit Price:

CAS No.:315-80-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Dibenzepine Hcl is a pharmaceutical-grade active pharmaceutical ingredient (API) and a tricyclic compound of significant chemical interest. This compound is valued for its high purity and consistent quality, which are critical for research and development applications in medicinal chemistry. It is primarily utilized by pharmaceutical R&D laboratories, academic research institutions, and chemical manufacturers focused on neuropharmacology and psychotropic drug development.

Application

  • Pharmaceutical Intermediate: Serves as a key building block in the synthesis of complex tricyclic psychotropic agents and related therapeutic compounds.
  • Medicinal Chemistry Research: Used as a reference standard or starting material in the study of structure-activity relationships (SAR) for central nervous system (CNS) targets.
  • Biochemical Research: Employed in in-vitro studies to investigate pharmacological mechanisms and receptor binding profiles.
  • Analytical Standard: Functions as a high-purity certified reference material (CRM) for quality control and method validation in analytical laboratories.
  • Academic Studies: Utilized in university laboratories for advanced organic synthesis projects and pharmacological education.

Basic Information

Product Name Dibenzepine Hcl
CAS No. 315-80-0
Molecular Formula C18H21N3O • HCl
Molecular Weight 331.84 g/mol (Free base: 295.38 g/mol)
Synonyms Dibenzepin Hydrochloride; 10,11-Dihydro-5-methyl-10-[2-(methylamino)ethyl]-5H-dibenzo[b,e][1,4]diazepin-11-one Hydrochloride; Noveril (trade name); NSC 108164; 5H-Dibenzo[b,e][1,4]diazepin-11(10H)-one, 10,11-dihydro-5-methyl-10-[2-(methylamino)ethyl]-, hydrochloride; Dibenzepine Hydrochloride
EINECS 206-261-4

Quality Control

Our Dibenzepine Hcl is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling, to ensure it meets stringent specifications for pharmaceutical research. A Certificate of Analysis (COA) detailing the results of tests such as HPLC, IR, and residual solvent analysis is provided with every shipment to guarantee traceability and compliance with your quality requirements.

Storage

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

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥98.0% (on anhydrous basis)
Water Content (KF) ≤1.0%
Residue on Ignition ≤0.1%
Related Substances (HPLC) Total impurities ≤2.0% Any single impurity ≤0.5%
Heavy Metals ≤20 ppm

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.