2-Hydroxy-6-(4-methylphenyl)pyridine-3-carbonitrile CAS 37670-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.37670-85-2
Molecular FormulaC13H10N2O
Molecular Weight210.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Hydroxy-6-(4-methylphenyl)pyridine-3-carbonitrile CAS 37670-85-2 chemical structure

Description

The occurrence of 2-Hydroxy-6-(4-methylphenyl)pyridine-3-carbonitrile 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.

CATO supplies 2-Hydroxy-6-(4-methylphenyl)pyridine-3-carbonitrile (CAS 37670-85-2), a certified reference material (molecular formula C13H10N2O, MW 210.23 g/mol) for analytical method development and quality control.

2-Hydroxy-6-(4-methylphenyl)pyridine-3-carbonitrile (C13H10N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC13H10N2O
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.)1967
Nitrogen Atoms2

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