3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol CAS 88-26-6

Purity >95%In StockPharmaceutical Standards
CAS No.88-26-6
Molecular FormulaC15H24O2
Molecular Weight236.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol CAS 88-26-6 chemical structure

Description

The occurrence of 3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol (CAS 88-26-6) is a high-purity analytical reference standard with the molecular formula C15H24O2 and a molecular weight of 236.35 g/mol.

3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol (C15H24O2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures 3,5-Di-Tert-Butyl-4-Hydroxybenzyl Alcohol under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC15H24O2
Molecular Weight236.35 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity>95%
StorageStore at room temperature
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.)1957

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