Description

4-Amino-1-(4-Phenylpiperazin-1-Yl)Butan-1-One Dihydrochloride is a high-purity, synthetically derived organic salt of significant interest in advanced chemical research and development. This compound serves as a critical pharmaceutical intermediate and a versatile building block for the synthesis of complex molecules. It is primarily needed by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers engaged in developing new therapeutic agents and specialty chemicals.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel active pharmaceutical ingredients (APIs), particularly those targeting neurological and psychiatric disorders.
• Medicinal Chemistry Research: Used as a core scaffold or building block for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• Chemical Synthesis: Serves as a versatile reagent for constructing complex piperazine-containing molecular architectures in fine chemical and agrochemical research.
• Biochemical Research: Employed in the development of biochemical probes and tool compounds for studying receptor-ligand interactions and signal transduction pathways.
• Reference Standard: Utilized as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	4-Amino-1-(4-Phenylpiperazin-1-Yl)Butan-1-One Dihydrochloride
CAS No.	1311316-75-2
Molecular Formula	C14H22N3O • 2HCl
Molecular Weight	329.27 g/mol (Free base: 248.35 g/mol)
Synonyms	1-(4-Aminobutyl)-4-phenylpiperazine dihydrochloride; 4-Phenyl-1-[4-(aminobutyl)]piperazine dihydrochloride; 4-Amino-1-(4-phenyl-1-piperazinyl)-1-butanone dihydrochloride; N-(4-Aminobutyl)-N'-phenylpiperazine dihydrochloride; Butan-1-one, 4-amino-1-(4-phenyl-1-piperazinyl)-, dihydrochloride; ABPP Dihydrochloride
EINECS	Contact for details

Quality Control

Our 4-Amino-1-(4-Phenylpiperazin-1-Yl)Butan-1-One Dihydrochloride is manufactured under a strict quality management system. Every batch undergoes rigorous analytical testing including HPLC, NMR, and mass spectrometry 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 the standards expected for pharmaceutical-grade intermediates used in GLP and GMP environments.

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). This product is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider storing under an inert atmosphere such as argon or nitrogen.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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