Description

Caroverine Fumarate is a pharmaceutical-grade active pharmaceutical ingredient (API) and a selective calcium channel blocker. This compound is valued for its high purity and consistent quality, making it a critical component in the development and manufacturing of specialized therapeutic formulations. It is primarily utilized by pharmaceutical companies and research institutions focused on neurological and cardiovascular applications.

Application

• Active Pharmaceutical Ingredient (API) in neurological drug formulations.
• Key intermediate in the synthesis of advanced pharmaceutical compounds.
• Research and development of calcium channel blocking agents.
• Preclinical and clinical studies for potential therapeutic applications.
• Manufacturing of reference standards for analytical testing.
• Development of controlled-release drug delivery systems.

Basic Information

Product Name	Caroverine Fumarate
CAS No.	77515-03-8
Molecular Formula	C24H30N2O6
Molecular Weight	442.51 g/mol
Synonyms	1-(2-Diethylaminoethyl)-3-(p-methoxybenzyl)-1,2-dihydro-2-quinoxalinone fumarate; Caroverine Fumarate Salt; Fumaric acid - 1-(2-diethylaminoethyl)-3-[(4-methoxyphenyl)methyl]-2(1H)-quinoxalinone (1:1); Quinuclidinyl Benzilate (related class); Caroverine; 1-(2-Diethylaminoethyl)-3-(4-methoxybenzyl)-2(1H)-quinoxalinone fumarate
EINECS	Contact for details

Quality Control

Our Caroverine Fumarate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency, consistent with ICH guidelines. 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, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

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% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Maximum Impurity	≤ 0.5%
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.