2-(tert-Butyl)-3-(methylthio)phenol CAS 1243456-50-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1243456-50-9
Molecular FormulaC11H16OS
Molecular Weight196.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)-3-(methylthio)phenol CAS 1243456-50-9 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-(tert-Butyl)-3-(methylthio)phenol.

CATO supplies 2-(tert-Butyl)-3-(methylthio)phenol (CAS 1243456-50-9), a certified reference material (molecular formula C11H16OS, MW 196.31 g/mol) for analytical method development and quality control.

2-(tert-Butyl)-3-(methylthio)phenol (C11H16OS) contains sulfur-containing functionality, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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), 2-(tert-Butyl)-3-(methylthio)phenol 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 FormulaC11H16OS
Molecular Weight196.31 g/mol
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Sulfur Atoms1

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