Description

3-Chloro-4-(4-Methyl-Piperidin-1-Yl)-Phenylamine is a high-purity, advanced pharmaceutical intermediate characterized by its specific piperidine-substituted aniline structure. This compound is of significant commercial value for its role as a critical building block in the synthesis of complex active pharmaceutical ingredients (APIs). It is primarily sought after by research institutions and manufacturers in the pharmaceutical and agrochemical sectors for developing new therapeutic agents and specialty chemicals. Our supply ensures consistent quality and reliable availability for global R&D and production needs.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates, particularly in central nervous system (CNS) and oncology research.
• Agrochemical Synthesis: Used in the development of advanced pesticides and herbicides due to its functionalized aromatic amine core.
• Chemical Research & Development: Serves as a versatile building block for organic chemists exploring new heterocyclic compounds and molecular libraries.
• Material Science: Potential application in the synthesis of specialty polymers and advanced organic electronic materials.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	3-Chloro-4-(4-Methyl-Piperidin-1-Yl)-Phenylamine
CAS No.	626208-15-9
Molecular Formula	C12H17ClN2
Molecular Weight	224.73 g/mol
Synonyms	1-(5-Amino-2-chlorophenyl)-4-methylpiperidine; 3-Chloro-4-(4-methyl-1-piperidinyl)aniline; 2-Chloro-5-(4-methylpiperidin-1-yl)aniline; 626208-15-9; 3-Chloro-4-(4-methylpiperidino)aniline; Benzenamine, 3-chloro-4-(4-methyl-1-piperidinyl)-; 4-(4-Methylpiperidin-1-yl)-3-chloroaniline
EINECS	Contact for details

Quality Control

Our 3-Chloro-4-(4-Methyl-Piperidin-1-Yl)-Phenylamine is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and GC-MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all specified parameters. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical synthesis workflows.

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 (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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