Description

1-(3-(4-Chlorobenzoyl)Piperidin-1-Yl)Ethanone is a high-purity, advanced pharmaceutical intermediate characterized by its specific piperidine-based molecular architecture. This compound is of significant commercial value for its role in the synthesis of complex active pharmaceutical ingredients (APIs) and other fine chemicals. It is primarily sought after by research institutions, pharmaceutical development companies, and fine chemical manufacturers engaged in medicinal chemistry and process R&D.

Application

• Pharmaceutical Intermediate: A key building block in the research and synthesis of novel drug candidates, particularly those targeting neurological and metabolic disorders.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization processes in drug discovery pipelines.
• API Synthesis: Serves as a critical precursor in the multi-step manufacturing processes of complex Active Pharmaceutical Ingredients.
• Chemical Reference Standard: Employed as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
• Biochemical Research: Utilized in the development of enzyme inhibitors and receptor modulators for biochemical assays.
• Fine Chemical Production: Acts as a specialized intermediate for creating other complex, high-value organic compounds.

Basic Information

Product Name	1-(3-(4-Chlorobenzoyl)Piperidin-1-Yl)Ethanone
CAS No.	1216763-69-7
Molecular Formula	C14H16ClNO2
Molecular Weight	265.74 g/mol
Synonyms	1-[3-(4-Chlorobenzoyl)piperidin-1-yl]ethanone; 1-(3-(4-Chlorobenzoyl)piperidin-1-yl)ethan-1-one; Ethanone, 1-[3-(4-chlorobenzoyl)-1-piperidinyl]-; 1-(3-(p-Chlorobenzoyl)piperidino)ethyl ketone; 1216763-69-7; 4'-Chloro-3-piperidin-1-ylpropiophenone derivative; 3-(4-Chlorobenzoyl)-1-acetylpiperidine
EINECS	Contact for details

Quality Control

Our 1-(3-(4-Chlorobenzoyl)Piperidin-1-Yl)Ethanone is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to confirm identity and purity. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for critical research and development applications.

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 nature, the container must be kept tightly sealed to exclude moisture. Keep away from heat, sparks, and open flame.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
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.