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Na€-(2,4-Dimethylphenyl) Vortioxetine CAS NO 1446751-00-3
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CAS No.:1446751-00-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Na€-(2,4-Dimethylphenyl) Vortioxetine is a key pharmaceutical intermediate in the synthesis of the antidepressant vortioxetine. This compound matters for its role in enabling the production of a high-value active pharmaceutical ingredient (API) with a complex molecular structure. It is primarily needed by pharmaceutical manufacturers, R&D laboratories, and fine chemical suppliers focused on central nervous system (CNS) drug development and generic API production.
Application
- Pharmaceutical Intermediate: Primary building block in the multi-step synthesis of the API Vortioxetine (Brintellix®/Trintellix®).
- Research & Development: Used in process chemistry research for developing new synthetic routes or optimizing existing manufacturing processes for vortioxetine.
- Reference Standard: Serves as a critical reference material for quality control and analytical method development in API production.
- Generic Drug Manufacturing: Essential for companies producing generic versions of vortioxetine after patent expiry, ensuring supply chain security.
- Chemical Synthesis: Utilized in academic and industrial labs studying serotonin receptor modulators and complex heterocyclic chemistry.
Basic Information
| Product Name | Na€-(2,4-Dimethylphenyl) Vortioxetine |
| CAS No. | 1446751-00-3 |
| Molecular Formula | C21H24N2OS |
| Molecular Weight | 352.50 g/mol |
| Synonyms | 1-[2-(2,4-Dimethylphenyl)sulfanylphenyl]piperazine; Vortioxetine Intermediate; Vortioxetine Impurity; Vortioxetine Related Compound; Lu AA21004 Intermediate; Brintellix Intermediate; Trintellix Intermediate; 2-((2,4-Dimethylphenyl)thio)phenylpiperazine |
| EINECS | Contact for details |
Quality Control
Our Na€-(2,4-Dimethylphenyl) Vortioxetine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing including HPLC, GC, and NMR to ensure high purity and consistency suitable for pharmaceutical synthesis. We provide full traceability and Certificates of Analysis (COA) compliant with cGMP standards for API intermediate production.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (HPLC) | Conforms |
| Identification (IR) | Conforms |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Meets ICH Q3C guidelines |
| Loss on Drying | ≤ 0.5% |
| 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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