Description

Cibenzoline Succinate is a pharmaceutical salt form of the antiarrhythmic agent cibenzoline. This compound is critical for ensuring the stability, bioavailability, and manufacturability of the final drug product. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of cardiac rhythm management medications.

Application

• Active Pharmaceutical Ingredient (API) for antiarrhythmic drug formulations.
• Pharmaceutical Intermediates in the synthesis of complex drug substances.
• Clinical Research and development of new cardiovascular therapies.
• Reference Standard for quality control and analytical method development in pharmaceutical laboratories.
• Pre-clinical Studies investigating cardiac electrophysiology and pharmacology.

Basic Information

Product Name	Cibenzoline Succinate
CAS No.	100678-32-8
Molecular Formula	C22H30N2O4
Molecular Weight	386.49 g/mol
Synonyms	Cibenzoline Hydrogen Succinate; Cifenline Succinate; 1-(2,2-Diphenylcyclopropyl)-4-(2,2,2-trifluoroethyl)piperazine Succinate; 2-(2,2-Diphenylcyclopropyl)-4,5-dihydro-1H-imidazole Succinate; Cibenol Succinate; Pracizoline Succinate; Ro 22-7796
EINECS	Contact for details

Quality Control

Our Cibenzoline Succinate 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 pharmaceutical-grade standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

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% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%

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