Description

Ethyl-[2-(Piperidin-3-Yloxy)-Pyrimidin-4-Yl]-Amine Hydrochloride is a high-purity organic salt compound of significant interest in advanced chemical synthesis. This molecule serves as a critical pharmaceutical intermediate and building block for the development of novel active ingredients. It is primarily utilized by research institutions and industrial manufacturers in the life sciences sector requiring precise and reliable chemical components for their development pipelines.

Application

This specialized intermediate is designed for high-value synthetic applications, particularly in regulated industries.

• Pharmaceutical Intermediate: A key precursor in the synthesis of potential drug candidates, especially for central nervous system (CNS) or other therapeutic targets.
• Active Pharmaceutical Ingredient (API) Development: Used in research and process chemistry for constructing complex molecular architectures during API development.
• Biochemical Research: Serves as a building block for creating novel compounds in medicinal chemistry and pharmacology research programs.
• Contract Manufacturing (CMO/CDMO): Supplied to contract research and manufacturing organizations for use in client-specific synthesis projects.
• Chemical Reference Standard: Can be utilized as a high-purity standard for analytical method development and validation.

Basic Information

Product Name	Ethyl-[2-(Piperidin-3-Yloxy)-Pyrimidin-4-Yl]-Amine Hydrochloride
CAS No.	1417793-55-5
Molecular Formula	C11H18N4O • HCl
Molecular Weight	258.75 g/mol
Synonyms	4-Pyrimidinamine, N-ethyl-2-(3-piperidinyloxy)-, hydrochloride; N-Ethyl-2-(3-piperidinyloxy)-4-pyrimidinamine hydrochloride; 2-(Piperidin-3-yloxy)pyrimidin-4-amine, N-ethyl-, hydrochloride; Ethyl 2-(piperidin-3-yloxy)pyrimidin-4-amine hydrochloride; 1417793-55-5
EINECS	Contact for details

Quality Control

Our Ethyl-[2-(Piperidin-3-Yloxy)-Pyrimidin-4-Yl]-Amine Hydrochloride is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting key parameters such as assay, impurity profile, and residual solvents. We support compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive); keep the container tightly sealed in a dry environment to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
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.