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Flupentixol CAS NO 56987-29-2
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CAS No.:56987-29-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Flupentixol is a potent thioxanthene derivative belonging to the class of typical antipsychotic agents. Its primary value lies in its dopaminergic receptor antagonism, making it a critical active pharmaceutical ingredient (API) for the formulation of neuroleptic medications. This compound is essential for pharmaceutical manufacturers and research institutions developing treatments for psychiatric conditions such as schizophrenia and other psychotic disorders. Flupentixol CAS NO 56987-29-2 is supplied under stringent quality controls to ensure consistency and efficacy in final drug products.
Application
- Active Pharmaceutical Ingredient (API): Primary use in the manufacture of antipsychotic and neuroleptic medications.
- Pharmaceutical Formulations: Used in the development of oral tablets, depot injections, and other dosage forms for long-term management of psychiatric disorders.
- Clinical Research: Serves as a reference standard and key intermediate in pharmacological studies and clinical trials investigating dopaminergic pathways.
- Generic Drug Production: A vital component for companies producing generic versions of established antipsychotic therapies.
- Biochemical Research: Utilized in neuroscience research to study receptor binding and the mechanisms of action of antipsychotic drugs.
Basic Information
| Product Name | Flupentixol |
| CAS No. | 56987-29-2 |
| Molecular Formula | C₂₃H₂₅F₃N₂OS |
| Molecular Weight | 434.52 g/mol |
| Synonyms | Flupentixol; Flupenthixol; Flupentixol Dihydrochloride; 2-Trifluoromethyl-9-[3-[4-(2-hydroxyethyl)piperazin-1-yl]propylidene]thioxanthene; Emergil; Depixol; Fluanxol; Cis(Z)-Flupentixol |
| EINECS | Contact for details |
Quality Control
Our Flupentixol is manufactured and tested to meet the highest standards of purity and consistency required for pharmaceutical applications. Quality assurance protocols are aligned with current Good Manufacturing Practices (cGMP). Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing key parameters such as identification, assay, and impurity profiles. We ensure compliance with relevant pharmacopoeial standards, and specifications can be tailored to meet specific customer requirements.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed in original packaging and protected from moisture and light exposure to maintain stability and potency.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥98.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% Any single 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.
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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.






