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11-Piperazinyldibenz[B,F][1,4]Oxazepine CAS NO 21636-40-8


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CAS No.:21636-40-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

11-Piperazinyldibenz[B,F][1,4]Oxazepine is a high-purity, heterocyclic organic compound of significant interest in advanced chemical synthesis. This specialized intermediate is valued for its unique molecular scaffold, which is crucial for research and development in targeted therapeutic areas. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the development of novel active pharmaceutical ingredients (APIs) and other complex organic molecules.

Application

  • Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel psychotropic and neurological drug candidates.
  • Research Chemical: Used in academic and industrial R&D for structure-activity relationship (SAR) studies and medicinal chemistry programs.
  • Fine Chemical Synthesis: Employed in the multi-step synthesis of complex heterocyclic compounds for various high-value applications.
  • Reference Standard: Can be supplied as a certified reference material for analytical method development and quality control in API manufacturing.
  • Biochemical Research: Investigated for its potential interactions with specific receptor systems in pharmacological studies.

Basic Information

Product Name 11-Piperazinyldibenz[B,F][1,4]Oxazepine
CAS No. 21636-40-8
Molecular Formula C19H19N3O
Molecular Weight 305.38 g/mol
Synonyms 11-(1-Piperazinyl)dibenz[b,f][1,4]oxazepine; 11-Piperazin-1-yldibenzo[b,f][1,4]oxazepine; Loxapine Impurity; Loxapine Related Compound; 8-Chloro-6-(4-methylpiperazin-1-yl)benzo[b][1,5]benzoxazepine (related structure); Dibenzo[b,f][1,4]oxazepine, 11-(1-piperazinyl)-; DBFO-Pip
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Quality Control

Every batch of 11-Piperazinyldibenz[B,F][1,4]Oxazepine is manufactured under a strict quality management system and undergoes comprehensive analytical testing to ensure identity, purity, and consistency. Our standard pharmaceutical-grade material is characterized by HPLC, NMR, and MS. A detailed Certificate of Analysis (COA) is provided with each shipment, and we support compliance with ICH guidelines for impurities.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). The compound may be hygroscopic (moisture-sensitive); keep the container tightly sealed under an inert atmosphere if specified.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Single Maximum Unknown Impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C
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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