(4-Methylpyridin-3-yl)(4-propylphenyl)methanone CAS 1187167-52-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1187167-52-7
Molecular FormulaC16H17NO
Molecular Weight239.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Methylpyridin-3-yl)(4-propylphenyl)methanone CAS 1187167-52-7 chemical structure

Description

The occurrence of (4-Methylpyridin-3-yl)(4-propylphenyl)methanone 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.

(4-Methylpyridin-3-yl)(4-propylphenyl)methanone (CAS 1187167-52-7) is a high-purity analytical reference standard with the molecular formula C16H17NO and a molecular weight of 239.31 g/mol.

The molecular framework of (4-Methylpyridin-3-yl)(4-propylphenyl)methanone (C16H17NO) 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures (4-Methylpyridin-3-yl)(4-propylphenyl)methanone 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 FormulaC16H17NO
Molecular Weight239.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms1

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