Description

Ethyl [3-(10,11-Dihydro-5H-Dibenz[B,F]Azepin-5-Yl)Propyl]Methylcarbamate is a high-purity pharmaceutical intermediate and active compound with significant research and development value. This compound is critical for ensuring the quality and consistency of downstream active pharmaceutical ingredients (APIs) and fine chemical synthesis. It is primarily utilized by pharmaceutical manufacturers, research institutions, and specialty chemical companies engaged in the development of advanced therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of complex active pharmaceutical ingredients (APIs) for central nervous system (CNS) applications.
• Research & Development: Used in medicinal chemistry for the discovery and optimization of new drug candidates, particularly in neurological and psychiatric research.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development, validation, and quality control testing in pharmaceutical laboratories.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis to introduce specific functional groups and molecular architectures.
• Biochemical Research: Utilized in studies investigating receptor binding, enzyme inhibition, and other pharmacological mechanisms.

Basic Information

Product Name	Ethyl [3-(10,11-Dihydro-5H-Dibenz[B,F]Azepin-5-Yl)Propyl]Methylcarbamate
CAS No.	27097-69-4
Molecular Formula	C21H26N2O2
Molecular Weight	338.45 g/mol
Synonyms	Ethyl [3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)propyl]methylcarbamate; Carbamazepine Ethyl Carbamate Derivative; 5H-Dibenz[b,f]azepine-5-propanamine, N-ethyl-N-methyl-, carbamate (ester); UNII-9V5Q8R4A4M; Ethyl Methylcarbamate Derivative of Carbamazepine; 27097-69-4; Ethyl 3-((methylamino)methyl)-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxylate (alternative IUPAC)
EINECS	Contact for details

Quality Control

Our Ethyl [3-(10,11-Dihydro-5H-Dibenz[B,F]Azepin-5-Yl)Propyl]Methylcarbamate is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) detailing all test results are provided and can be tailored to meet specific customer or regulatory requirements, supporting applications in GMP environments.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to exclude moisture. For long-term storage, consider using desiccants or an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline 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 impurity ≤ 0.5%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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