N-(4-Butylphenyl)-5-chloro-2-(methylthio)pyrimidine-4-carboxamide CAS 898646-60-1

Purity 97%+In StockPharmaceutical Standards
CAS No.898646-60-1
Molecular FormulaC16H18ClN3OS
Molecular Weight335.85 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Butylphenyl)-5-chloro-2-(methylthio)pyrimidine-4-carboxamide CAS 898646-60-1 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

N-(4-Butylphenyl)-5-chloro-2-(methylthio)pyrimidine-4-carboxamide (CAS 898646-60-1) is a high-purity analytical reference standard with the molecular formula C16H18ClN3OS and a molecular weight of 335.85 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution, N-(4-Butylphenyl)-5-chloro-2-(methylthio)pyrimidine-4-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 335.85 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

As a certified reference material (CRM), N-(4-Butylphenyl)-5-chloro-2-(methylthio)pyrimidine-4-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC16H18ClN3OS
Molecular Weight335.85 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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