(3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-one CAS 125010-17-5

Purity 97%+In StockPharmaceutical Standards
CAS No.125010-17-5
Molecular FormulaC15H16O
Molecular Weight212.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-one CAS 125010-17-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including (3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-one.

CATO supplies (3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-one (CAS 125010-17-5), a certified reference material (molecular formula C15H16O, MW 212.29 g/mol) for analytical method development and quality control.

The molecular framework of (3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-one (C15H16O) is characterized by a hydroxyl group, an ether linkage, a polycyclic aromatic system. 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.

CATO manufactures (3E,5E,7E)-3-Methyl-8-phenylocta-3,5,7-trien-2-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 FormulaC15H16O
Molecular Weight212.29 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992

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