2-((2-Ethylphenyl)amino)pyrimidin-4(1H)-one CAS 459196-57-7

Purity 97%+In StockPharmaceutical Standards
CAS No.459196-57-7
Molecular FormulaC12H13N3O
Molecular Weight215.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((2-Ethylphenyl)amino)pyrimidin-4(1H)-one CAS 459196-57-7 chemical structure

Description

The occurrence of 2-((2-Ethylphenyl)amino)pyrimidin-4(1H)-one is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

2-((2-Ethylphenyl)amino)pyrimidin-4(1H)-one (CAS 459196-57-7), molecular formula C12H13N3O and molecular weight 215.25 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-((2-Ethylphenyl)amino)pyrimidin-4(1H)-one (C12H13N3O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC12H13N3O
Molecular Weight215.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms3

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