Description

1-[4-(Ethylsulfonyl)Phenyl]Homopiperazine Hydrochloride is a high-purity, advanced pharmaceutical intermediate characterized by its specific sulfonyl and piperazine-based structure. This compound is critical for the research and development of novel therapeutic agents, particularly in the fields of central nervous system (CNS) and oncology drug discovery. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers seeking reliable, high-quality building blocks for complex synthesis.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates, particularly for CNS-targeted therapies.
• Chemical Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in multi-step synthetic routes for potential active ingredients.
• Biochemical Research: Employed in the development of enzyme inhibitors or receptor modulators due to its heterocyclic structure.
• Custom Synthesis: A starting material for contract manufacturing organizations (CMOs) producing specialized compounds for clients.
• Reference Standard: Used as an analytical standard for quality control and method development in pharmaceutical analysis.

Basic Information

Product Name	1-[4-(Ethylsulfonyl)Phenyl]Homopiperazine Hydrochloride
CAS No.	1170944-34-9
Molecular Formula	C13H19N2O2S·HCl
Molecular Weight	312.83 g/mol
Synonyms	1-[4-(Ethylsulfonyl)phenyl]hexahydro-1H-1,4-diazepine hydrochloride; 1-(4-Ethylsulfonylphenyl)homopiperazine hydrochloride; Homopiperazine, 1-[4-(ethylsulfonyl)phenyl]-, hydrochloride; 1-(4-Ethanesulfonylphenyl)homopiperazine HCl; 1170944-34-9; 1-(4-(Ethylsulfonyl)phenyl)hexahydro-1H-1,4-diazepine HCl
EINECS	Contact for details

Quality Control

Our 1-[4-(Ethylsulfonyl)Phenyl]Homopiperazine Hydrochloride is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including HPLC for assay and impurity profiling, to meet the stringent requirements of pharmaceutical R&D. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting identity, purity, and related substances.

Storage

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

Specification

Item	Specification
Appearance	White to off-white 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%
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.