(4-Heptylphenyl)(3-methylpyridin-2-yl)methanone CAS 1187164-32-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1187164-32-4
Molecular FormulaC20H25NO
Molecular Weight295.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Heptylphenyl)(3-methylpyridin-2-yl)methanone CAS 1187164-32-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 295.42 g/mol gives (4-Heptylphenyl)(3-methylpyridin-2-yl)methanone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (4-Heptylphenyl)(3-methylpyridin-2-yl)methanone (CAS 1187164-32-4), a certified reference material (molecular formula C20H25NO, MW 295.42 g/mol) for analytical method development and quality control.

The molecular framework of (4-Heptylphenyl)(3-methylpyridin-2-yl)methanone (C20H25NO) is characterized by a steroid core, 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC20H25NO
Molecular Weight295.42 g/mol
AppearancePale yellow to yellow crystalline powder
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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