1-Phenylcycloheptane-1-carboxylic acid CAS 7086-29-5

Purity 97%+In StockPharmaceutical Standards
CAS No.7086-29-5
Molecular FormulaC14H18O2
Molecular Weight218.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Phenylcycloheptane-1-carboxylic acid CAS 7086-29-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 218.29 g/mol gives 1-Phenylcycloheptane-1-carboxylic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-Phenylcycloheptane-1-carboxylic acid (CAS 7086-29-5), molecular formula C14H18O2 and molecular weight 218.29 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-Phenylcycloheptane-1-carboxylic acid (C14H18O2) 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 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H18O2
Molecular Weight218.29 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1959

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