2,6-Di-tert-butylpyrylium trifluoromethanesulfonate CAS 125455-66-5

Purity 97%+In StockPharmaceutical Standards
CAS No.125455-66-5
Molecular FormulaC13H21O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-Di-tert-butylpyrylium trifluoromethanesulfonate CAS 125455-66-5 chemical structure

Description

CATO supplies 2,6-Di-tert-butylpyrylium trifluoromethanesulfonate (CAS 125455-66-5), a certified reference material (molecular formula C13H21OCF3O3S, MW 342.37 g/mol) for analytical method development and quality control.

Structurally, 2,6-Di-tert-butylpyrylium trifluoromethanesulfonate (C13H21OCF3O3S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 3.0, corresponding to approximately 3 ring(s) or double-bond equivalent(s). With a molecular weight of 342.37 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

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 FormulaC13H21O CF3O3S
Molecular Weight342.37 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1992
Halogen ContentF-containing
Sulfur Atoms1

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