2-(tert-Butyl)-3-(trifluoromethyl)phenol CAS 1243474-76-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1243474-76-1
Molecular FormulaC11H13F3O
Molecular Weight218.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(tert-Butyl)-3-(trifluoromethyl)phenol CAS 1243474-76-1 chemical structure

Description

The occurrence of 2-(tert-Butyl)-3-(trifluoromethyl)phenol is closely related to a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2-(tert-Butyl)-3-(trifluoromethyl)phenol (CAS 1243474-76-1), a certified reference material (molecular formula C11H13F3O, MW 218.22 g/mol) for analytical method development and quality control.

Structurally, 2-(tert-Butyl)-3-(trifluoromethyl)phenol (C11H13F3O) contains a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 218.22 g/mol, it falls into the medium-molecular-weight range. 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.

As a certified reference material (CRM), 2-(tert-Butyl)-3-(trifluoromethyl)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 FormulaC11H13F3O
Molecular Weight218.22 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing

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