5-(Cyclohexylmethyl)-2-iodophenol CAS 1243312-69-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1243312-69-7
Molecular FormulaC13H17IO
Molecular Weight316.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(Cyclohexylmethyl)-2-iodophenol CAS 1243312-69-7 chemical structure

Description

5-(Cyclohexylmethyl)-2-iodophenol (CAS 1243312-69-7), molecular formula C13H17IO and molecular weight 316.18 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 5-(Cyclohexylmethyl)-2-iodophenol (C13H17IO) is characterized by a hydroxyl group, an ether linkage, iodine substitution, 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.

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 5-(Cyclohexylmethyl)-2-iodophenol 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 FormulaC13H17IO
Molecular Weight316.18 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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.)1990
Halogen ContentI-containing

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Why CATO?