Description

(2-Fluoro-Benzyl)-Methyl-Piperidin-4-Yl-Amine Hydrochloride is a high-purity, advanced pharmaceutical intermediate with a defined molecular structure. This compound is critical for medicinal chemistry research and development, particularly in the synthesis of novel active pharmaceutical ingredients (APIs). It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the development of central nervous system (CNS) and other therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly for neurological and psychiatric disorders.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization processes in drug discovery.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in multi-step synthetic routes for complex target molecules.
• Biochemical Research: Employed as a reference standard or tool compound in pharmacological assays and target validation.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Utilized in university and institutional labs for organic synthesis methodology and new reaction development.

Basic Information

Product Name	(2-Fluoro-Benzyl)-Methyl-Piperidin-4-Yl-Amine Hydrochloride
CAS No.	1261235-83-9
Molecular Formula	C14H20ClFN2
Molecular Weight	270.78 g/mol
Synonyms	N-Methyl-N-[(2-fluorophenyl)methyl]-4-piperidinamine hydrochloride; 1-[(2-Fluorobenzyl)(methyl)amino]-4-piperidine hydrochloride; 4-[(2-Fluorobenzyl)(methyl)amino]piperidine hydrochloride; N-[(2-Fluorophenyl)methyl]-N-methyl-4-piperidinamine hydrochloride; (2-Fluorobenzyl)(methyl)(piperidin-4-yl)amine hydrochloride; 4-[(2-Fluorobenzyl)(methyl)amino]piperidine HCl; Contact for additional trade names.
EINECS	Contact for details

Quality Control

Our (2-Fluoro-Benzyl)-Methyl-Piperidin-4-Yl-Amine Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and tests for residual solvents and heavy metals to ensure it meets the high standards required for pharmaceutical R&D. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing all specifications and test results.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under inert atmosphere or in a desiccator after opening to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Residual Solvents (GC)	Meets ICH Q3C guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.