trans-4-(3,5-Dimethylbenzoyl)cyclohexane-1-carboxylic acid CAS 736136-27-9

Purity 97%+In StockPharmaceutical Standards
CAS No.736136-27-9
Molecular FormulaC16H20O3
Molecular Weight260.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-4-(3,5-Dimethylbenzoyl)cyclohexane-1-carboxylic acid CAS 736136-27-9 chemical structure

Description

The molecular framework of trans-4-(3,5-Dimethylbenzoyl)cyclohexane-1-carboxylic acid (C16H20O3) is characterized by a carboxylic acid group, 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).

CATO supplies trans-4-(3,5-Dimethylbenzoyl)cyclohexane-1-carboxylic acid (CAS 736136-27-9), a certified reference material (molecular formula C16H20O3, MW 260.33 g/mol) for analytical method development and quality control.

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 trans-4-(3,5-Dimethylbenzoyl)cyclohexane-1-carboxylic acid 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 FormulaC16H20O3
Molecular Weight260.33 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986

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