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3-[(2-Phenoxyethoxy)Methyl]Piperidinehydrochloride CAS NO 1220021-43-1


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CAS No.:1220021-43-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

3-[(2-Phenoxyethoxy)Methyl]Piperidinehydrochloride is a high-purity, specialized organic compound primarily used as a key intermediate in advanced pharmaceutical synthesis. Its molecular structure, featuring a piperidine core with a phenoxyethoxy methyl side chain, makes it a valuable building block for creating complex active pharmaceutical ingredients (APIs). This compound is essential for research and development chemists and manufacturers in the life sciences sector who require reliable, high-quality intermediates for drug discovery and production processes.

Application

  • Pharmaceutical Intermediate: A critical building block in the synthesis of novel therapeutic agents, particularly in central nervous system (CNS) and other specialty drug candidates.
  • Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and the development of new chemical entities.
  • Active Pharmaceutical Ingredient (API) Synthesis: Serves as a precursor in multi-step synthetic routes for the manufacture of complex APIs.
  • Chemical Reference Standard: Employed as a high-purity standard for analytical method development and quality control in pharmaceutical laboratories.
  • Agrochemical Research: Potential intermediate in the development of new crop protection agents and pesticides.

Basic Information

Product Name 3-[(2-Phenoxyethoxy)Methyl]Piperidinehydrochloride
CAS No. 1220021-43-1
Molecular Formula C15H23NO2·HCl
Molecular Weight 285.81 g/mol
Synonyms 3-[(2-Phenoxyethoxy)methyl]piperidine hydrochloride; 3-(2-Phenoxyethoxymethyl)piperidine HCl; Piperidine, 3-[(2-phenoxyethoxy)methyl]-, hydrochloride (1:1); 1220021-43-1
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Quality Control

Our 3-[(2-Phenoxyethoxy)Methyl]Piperidinehydrochloride 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 stringent specifications for pharmaceutical intermediates. A Certificate of Analysis (COA) detailing identity, purity, and related substances is provided with every shipment, supporting compliance with cGMP and ICH guidelines where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); the container must be kept tightly sealed to prevent absorption of atmospheric moisture. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

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