1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid CAS 1491056-57-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1491056-57-5
Molecular FormulaC11H11BrO2S
Molecular Weight287.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid CAS 1491056-57-5 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 1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid.

1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid (CAS 1491056-57-5) is a high-purity analytical reference standard with the molecular formula C11H11BrO2S and a molecular weight of 287.17 g/mol.

The molecular framework of 1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid (C11H11BrO2S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine 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.

As a certified reference material (CRM), 1-((3-Bromophenyl)thio)cyclobutane-1-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H11BrO2S
Molecular Weight287.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentBr-containing
Sulfur Atoms1

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