3,3’,5,5’-TETRA-T-BUTYLBIPHENYL-2,2’,6,6’-TETRAOL CAS 21243-76-5

Purity 97%+In StockPharmaceutical Standards
CAS No.21243-76-5
Molecular FormulaC28H42O4
Molecular Weight442.63 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,3’,5,5’-TETRA-T-BUTYLBIPHENYL-2,2’,6,6’-TETRAOL CAS 21243-76-5 chemical structure

Description

The occurrence of 3,3’,5,5’-TETRA-T-BUTYLBIPHENYL-2,2’,6,6’-TETRAOL is closely related to a steroid core, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3,3’,5,5’-TETRA-T-BUTYLBIPHENYL-2,2’,6,6’-TETRAOL (CAS 21243-76-5), a certified reference material (molecular formula C28H42O4, MW 442.63 g/mol) for analytical method development and quality control.

Owing to a steroid core, a hydroxyl group, an ether linkage, 3,3’,5,5’-TETRA-T-BUTYLBIPHENYL-2,2’,6,6’-TETRAOL is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 442.63 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC28H42O4
Molecular Weight442.63 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963

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