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4-[(3,4-Difluorophenoxy)Methyl]Piperidinehydrochloride CAS NO 1050509-63-1
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CAS No.:1050509-63-1
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
4-[(3,4-Difluorophenoxy)Methyl]Piperidinehydrochloride is a high-purity, advanced pharmaceutical intermediate with the CAS number 1050509-63-1. This compound is critical for the synthesis of complex active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) and other therapeutic agents. It is primarily required by research institutions and pharmaceutical manufacturers engaged in drug discovery, process development, and commercial-scale production.
Application
- Pharmaceutical Intermediate: Key building block in the synthesis of novel drug candidates, especially for neurological and psychiatric disorders.
- Active Pharmaceutical Ingredient (API) Development: Used in research and process chemistry for constructing complex molecular scaffolds.
- Medicinal Chemistry Research: Serves as a versatile precursor for structure-activity relationship (SAR) studies and lead optimization.
- Contract Manufacturing (CMO/CDMO): Supplied to contract organizations for cGMP-compliant production of clinical trial materials and commercial APIs.
- Chemical Reference Standard: Used as a high-purity standard for analytical method development and quality control in pharmaceutical labs.
Basic Information
| Product Name | 4-[(3,4-Difluorophenoxy)Methyl]Piperidinehydrochloride |
| CAS No. | 1050509-63-1 |
| Molecular Formula | C12H15ClF2NO |
| Molecular Weight | 262.70 g/mol |
| Synonyms | 4-[(3,4-Difluorophenoxy)methyl]piperidine hydrochloride; 1-[(3,4-Difluorophenoxy)methyl]piperidin-4-ium chloride; 4-[(3,4-Difluorophenoxy)methyl]piperidine HCl; Piperidine, 4-[(3,4-difluorophenoxy)methyl]-, hydrochloride; 1050509-63-1; 4-(3,4-Difluorophenoxymethyl)piperidine hydrochloride |
| EINECS | Contact for details |
Quality Control
Our 4-[(3,4-Difluorophenoxy)Methyl]Piperidinehydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, to ensure compliance with stringent pharmaceutical-grade specifications. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment. We support development and commercial projects requiring ICH stability data and can supply material suitable for cGMP manufacturing.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption, which may affect stability and handling properties.
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% |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Total impurities ≤ 2.0%; Any single impurity ≤ 0.5% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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