share

Ketipramine Fumarate CAS NO 17243-32-2


Unit Price:

CAS No.:17243-32-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Ketipramine Fumarate is a high-purity pharmaceutical intermediate and active ingredient. It is a critical compound valued for its role in the synthesis and development of advanced therapeutic agents. This product is essential for research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development of new chemical entities and generic pharmaceuticals.

Application

  • Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for central nervous system (CNS) applications.
  • Research & Development: Used in preclinical and clinical research for investigating new therapeutic pathways and drug efficacy.
  • Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
  • Generic Drug Manufacturing: Employed in the production of established generic pharmaceutical formulations requiring this specific fumarate salt.
  • Chemical Synthesis: Utilized in organic synthesis for creating more complex molecular structures in fine chemical production.

Basic Information

Product Name Ketipramine Fumarate
CAS No. 17243-32-2
Molecular Formula Contact for details
Molecular Weight Contact for details
Synonyms Ketipramine hydrogen fumarate; 5H-Dibenz[b,f]azepine-5-propanamine, 10,11-dihydro-N,N-dimethyl-, (2E)-2-butenedioate (1:1); Ketipramine (fumarate); 10,11-Dihydro-N,N-dimethyl-5H-dibenz[b,f]azepine-5-propanamine fumarate
EINECS Contact for details

Quality Control

Our Ketipramine Fumarate is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with detailed chromatographic and spectroscopic data, including HPLC purity, residual solvent analysis, and identification by IR and NMR. Our quality standards are designed to meet the rigorous demands of pharmaceutical R&D and manufacturing.

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). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

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%
Related Substances (HPLC) Total impurities ≤2.0%
Loss on Drying ≤1.0%
Residue on Ignition ≤0.1%
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.