4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile CAS 89549-71-3

Purity 97%+In StockPharmaceutical Standards
CAS No.89549-71-3
Molecular FormulaC12H10N4
Molecular Weight210.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile CAS 89549-71-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 210.23 g/mol gives 4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile (CAS 89549-71-3) is a high-purity analytical reference standard with the molecular formula C12H10N4 and a molecular weight of 210.23 g/mol.

Structurally, 4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile (C12H10N4) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 210.23 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 4-Methyl-6-(phenylamino)pyrimidine-5-carbonitrile under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H10N4
Molecular Weight210.23 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1982
Nitrogen Atoms4

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