1-(4-tert-butylphenyl)piperidin-4-one CAS 1019341-74-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1019341-74-2
Molecular FormulaC15H21NO
Molecular Weight231.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-tert-butylphenyl)piperidin-4-one CAS 1019341-74-2 chemical structure

Description

The occurrence of 1-(4-tert-butylphenyl)piperidin-4-one 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.

1-(4-tert-butylphenyl)piperidin-4-one (CAS 1019341-74-2) is a high-purity analytical reference standard with the molecular formula C15H21NO and a molecular weight of 231.33 g/mol.

The molecular framework of 1-(4-tert-butylphenyl)piperidin-4-one (C15H21NO) 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).

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 1-(4-tert-butylphenyl)piperidin-4-one 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 FormulaC15H21NO
Molecular Weight231.33 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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