Description

N~2~-(2-Methoxyethyl)-6-(3-Methyl-1-Piperidinyl)-5-Nitro-2,4-Pyrimidinediamine is a high-purity, advanced pharmaceutical intermediate with a defined molecular structure. This compound matters for its role as a critical building block in the synthesis of complex active pharmaceutical ingredients (APIs), where consistent quality and reliable supply are paramount. It is primarily needed by research institutions and pharmaceutical manufacturers engaged in the development and production of novel therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key precursor in the multi-step synthesis of target drug molecules, particularly in research and development pipelines.
• API Synthesis: Used in the controlled construction of complex heterocyclic cores essential for specific biological activity in final Active Pharmaceutical Ingredients.
• Medicinal Chemistry Research: A valuable scaffold for structure-activity relationship (SAR) studies and the exploration of new chemical entities in drug discovery.
• Process Chemistry Development: Employed in scaling up synthetic routes from laboratory to pilot plant and commercial manufacturing scales.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development, validation, and quality control testing.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	N~2~-(2-Methoxyethyl)-6-(3-Methyl-1-Piperidinyl)-5-Nitro-2,4-Pyrimidinediamine
CAS No.	714935-48-5
Molecular Formula	C13H22N6O3
Molecular Weight	310.35 g/mol
Synonyms	6-(3-Methylpiperidin-1-yl)-N2-(2-methoxyethyl)-5-nitropyrimidine-2,4-diamine; 5-Nitro-6-(3-methyl-1-piperidinyl)-N2-(2-methoxyethyl)-2,4-pyrimidinediamine; 714935-48-5; UNII-4V4F66P65S; 4V4F66P65S; CHEMBL3185142; BDBM50121257; AKOS015915889
EINECS	Contact for details

Quality Control

Our products undergo rigorous quality testing to ensure compliance with industry standards. Each batch is characterized and controlled using advanced analytical techniques to guarantee identity, purity, and consistency. Certificates of Analysis (COA) detailing specific batch results are available upon request. Our quality system is designed to support cGMP (Current Good Manufacturing Practice) requirements for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials. For long-term storage, consider under an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	Yellow to brown powder or crystalline solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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