Description

(4-(2-(4-Methylpiperazin-1-yl)ethoxy)phenyl)methanamine is a high-purity pharmaceutical intermediate and building block of significant commercial importance. Its molecular structure, featuring a piperazine ring linked via an ethoxy chain to a benzylamine group, makes it a versatile synthon for the development of active pharmaceutical ingredients (APIs). This compound is primarily sought by research institutions and manufacturers in the pharmaceutical and fine chemical sectors for the synthesis of novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of complex drug molecules, particularly those targeting neurological and oncological pathways.
• Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and the discovery of new chemical entities.
• API Synthesis: Serves as a critical precursor in the multi-step manufacturing process of final Active Pharmaceutical Ingredients.
• Chemical Reference Standard: Employed as a high-purity standard for analytical method development and quality control in pharmaceutical labs.
• Bioconjugation & Probe Development: The primary amine functionality allows for conjugation, useful in creating biochemical probes and labeled compounds.

Basic Information

Product Name	(4-(2-(4-Methylpiperazin-1-yl)ethoxy)phenyl)methanamine
CAS No.	128540-39-6
Molecular Formula	C14H23N3O
Molecular Weight	249.35 g/mol
Synonyms	1-[2-[4-(Aminomethyl)phenoxy]ethyl]-4-methylpiperazine; 4-(2-(4-Methyl-1-piperazinyl)ethoxy)benzylamine; 4-[2-(4-Methylpiperazin-1-yl)ethoxy]benzylamine; Benzylamine, 4-[2-(4-methyl-1-piperazinyl)ethoxy]-; UNII-9J8N7E8692; 9J8N7E8692; 4-(2-(4-Methylpiperazin-1-yl)ethoxy)benzenemethanamine
EINECS	Contact for details

Quality Control

Our (4-(2-(4-Methylpiperazin-1-yl)ethoxy)phenyl)methanamine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis, to ensure it meets the stringent requirements for pharmaceutical R&D and manufacturing. A Certificate of Analysis (COA) detailing all specifications and test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residual Solvents (GC)	Meets ICH guidelines

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