CAS:77387-57-6 | 3,5-DI-TERT-BUTYLBENZYL ALCOHOL

Introduction of CAS:77387-57-6 | 3,5-DI-TERT-BUTYLBENZYL ALCOHOL

3,5-Di-tert-butylbenzyl alcohol (DTBA) is a synthetic organic compound with a wide range of applications in the pharmaceutical, food, and cosmetic industries. It is a colorless, odorless, and slightly viscous liquid, and is used as a preservative and flavoring agent. DTBA has been studied extensively in the laboratory and has been found to have both biochemical and physiological effects on the body.

Specification of CAS:77387-57-6 | 3,5-DI-TERT-BUTYLBENZYL ALCOHOL

Research Application of CAS:77387-57-6 | 3,5-DI-TERT-BUTYLBENZYL ALCOHOL

Antioxidant and Stabilizer Applications:

3,5-Di-tert-butylbenzyl Alcohol derivatives, specifically 1,3,5-tris(4-hydroxy-3,5-di-tert-butylbenzyl)cyanuric acid, have been designed as antioxidants for polyolefins. Their transformation during reactions with tert-butylperoxyls and the impact on the oxidation of tetralin and isotactic polypropylene have been studied (Lerchová & Pospíšil, 1974).

Catalytic Applications:

The compound has been used in solid-phase catalytic oxidation systems, such as the transformation of 2-hydroxy-3,5-di-tert-butylbenzyl alcohol to 2-hydroxy-3,5-di-tert-butylbenzaldehyde using MnO2-NaOH, demonstrating its potential in catalytic processes (Dokukina et al., 1994).

Chromatographic Applications:

4-hydroxy-3,5-di-tert-butylbenzyl alcohol (HBBA) has been evaluated as a combined antioxidant tail-reducer for packed-column gas-liquid chromatography. Its efficiency in surface deactivation of chromatographic supports has been studied, offering insights into its potential use in analytical chemistry (Evans & Pearmain, 1991).

Complex Formation and Molecular Interaction Studies:

Research on the structure of the 4-tert-butylbenzyl alcohol–β-cyclodextrin complex has shed light on the geometric features of β-cyclodextrin dimeric complexes, which is significant for understanding molecular interactions in various chemical and biological processes (Mentzafos et al., 1991).

Polymer Science:

The compound has been studied in the context of polymer science, particularly in the polymerization behavior of monomeric antioxidants like 3,5-di-tert-butyl-4-hydroxy-benzylmethacrylate. Such studies are crucial for the development of new polymer materials with enhanced properties (Munteanu et al., 1985).

Synthetic Chemistry:

In synthetic chemistry, the electrochemical oxidation of 3,5-di-tert-butylcatechol in the presence of 2-methoxybenzylamine has been explored to synthesize benzoxazole derivatives, demonstrating the compound's utility in organic synthesis and chemical transformations (Salehzadeh & Nematollahi, 2014).

Material Science:

In material science, research on the melt-grafting of maleimides with 3,5-di-tert-butyl-4-hydroxybenzyl alcohol onto polypropylene highlights its application in modifying material properties, particularly in enhancing the antioxidant properties of polymers (Kim & Lee, 2003).

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