2-(Cyclopentylmethyl)-6-methoxyphenol CAS 148173-60-8

Purity 97%+In StockPharmaceutical Standards
CAS No.148173-60-8
Molecular FormulaC13H18O2
Molecular Weight206.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Cyclopentylmethyl)-6-methoxyphenol CAS 148173-60-8 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 2-(Cyclopentylmethyl)-6-methoxyphenol.

CATO supplies 2-(Cyclopentylmethyl)-6-methoxyphenol (CAS 148173-60-8), a certified reference material (molecular formula C13H18O2, MW 206.28 g/mol) for analytical method development and quality control.

The molecular framework of 2-(Cyclopentylmethyl)-6-methoxyphenol (C13H18O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 2-(Cyclopentylmethyl)-6-methoxyphenol 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 FormulaC13H18O2
Molecular Weight206.28 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999

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