Description

Zicronapine Fumarate is a high-purity active pharmaceutical ingredient (API) and chemical intermediate of significant interest in advanced pharmaceutical research and development. This compound is valued for its specific pharmacological activity and serves as a critical building block in the synthesis of novel therapeutic agents. It is primarily utilized by pharmaceutical companies, contract research organizations (CROs), and academic institutions engaged in the discovery and development of new central nervous system (CNS) medications.

Application

• Pharmaceutical API Intermediate: A key starting material or intermediate in the multi-step synthesis of novel antipsychotic drug candidates.
• Preclinical & Clinical Research: Used in pharmacological studies, bioavailability testing, and formulation development for experimental therapies.
• Reference Standard: Serves as an analytical standard for quality control and method validation in pharmaceutical laboratories.
• Chemical Synthesis: Employed in medicinal chemistry for structure-activity relationship (SAR) studies and molecular optimization.
• Academic Research: Utilized in university and institutional labs for neuroscience and neuropharmacology research projects.

Basic Information

Item	Details
Product Name	Zicronapine Fumarate
CAS No.	170381-17-6
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Zicronapine Fumarate Salt; Zicronapine Hydrogen Fumarate; (E)-But-2-enedioic acid;Zicronapine compound; ORG-5222 (as fumarate); Potential antipsychotic agent ORG-5222 fumarate
EINECS	Contact for details

Quality Control

Our Zicronapine Fumarate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and support our products with a detailed Certificate of Analysis (COA) that includes results from advanced techniques such as HPLC, NMR, and mass spectrometry. Our quality commitment aligns with cGMP principles for pharmaceutical ingredients, ensuring reliability for your critical research and development work.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The container should be kept tightly sealed to protect the contents from moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms
Identification (IR)	Conforms to reference spectrum
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.