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4-[2-(Cyclopropylmethoxy)Ethyl]Piperidinehydrochloride CAS NO 1219967-17-5


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CAS No.:1219967-17-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

4-[2-(Cyclopropylmethoxy)Ethyl]Piperidinehydrochloride is a high-purity, advanced pharmaceutical intermediate with a distinct molecular architecture. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in central nervous system (CNS) and antiviral research. It is primarily required by R&D chemists, process development scientists, and manufacturers in the pharmaceutical and biotechnology industries seeking to develop new therapeutic agents.

Application

  • Pharmaceutical Intermediate: A key synthetic precursor in the research and development of new drug candidates.
  • CNS Drug Discovery: Used in the synthesis of compounds targeting neurological disorders and psychiatric conditions.
  • Antiviral Agent Synthesis: Serves as a building block for potential antiviral medications.
  • Chemical Biology Research: Employed as a probe or ligand in studying biological pathways and protein interactions.
  • Process Chemistry & Scale-up: Utilized in optimizing synthetic routes from laboratory to pilot and commercial scale production.
  • Custom Synthesis: A starting material for the contract manufacturing of specialized fine chemicals and bespoke molecules.

Basic Information

Product Name 4-[2-(Cyclopropylmethoxy)Ethyl]Piperidinehydrochloride
CAS No. 1219967-17-5
Molecular Formula C11H22ClNO
Molecular Weight 219.75 g/mol
Synonyms 4-[2-(Cyclopropylmethoxy)ethyl]piperidine hydrochloride; 4-(2-(Cyclopropylmethoxy)ethyl)piperidine HCl; Piperidine, 4-[2-(cyclopropylmethoxy)ethyl]-, hydrochloride (1:1); UNII-9J3V6S6A1M; 9J3V6S6A1M; 4-(2-Cyclopropylmethoxy-ethyl)-piperidine hydrochloride; 4-(2-(Cyclopropylmethoxy)ethyl)piperidinium chloride
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Quality Control

Our 4-[2-(Cyclopropylmethoxy)Ethyl]Piperidinehydrochloride is manufactured under strict quality management systems. Each 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 cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical research and development processes.

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 an inert atmosphere or in a desiccator to prevent degradation. Keep away from incompatible materials.

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.

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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