19263-36-6

Usage

Uses

Used in Polymer and Plastic Industry:
2,6-ditert-butyl-4-vinylphenol is used as a stabilizer for polymers and plastics to prevent degradation, ensuring the longevity and quality of these materials.
Used in Adhesive Industry:
In the adhesive industry, 2,6-ditert-butyl-4-vinylphenol serves as a stabilizer to enhance the durability and performance of adhesive products by protecting them from environmental factors.
Used in Rubber Production:
2,6-ditert-butyl-4-vinylphenol is used as an antioxidant in the production of rubber, contributing to the improvement of rubber's resistance to oxidation and wear.
Used in Lubricant Manufacturing:
2,6-ditert-butyl-4-vinylphenol is utilized as an antioxidant in the manufacturing of lubricants to enhance their stability and performance under various operating conditions.
Used in Food Packaging Materials:
2,6-ditert-butyl-4-vinylphenol is used in the production of food packaging materials to prevent spoilage and maintain the quality of the packaged products, ensuring their freshness and safety for consumption.
It is important to handle 2,6-ditert-butyl-4-vinylphenol with care due to its potential to cause skin and eye irritation, and its harmful effects if ingested or inhaled in large amounts. Proper safety measures should be adhered to in its use and application.

Upstream product

• 67-56-1 methanol 
• 7050-91-1 α-methyl-3,5-di-t-butyl-4-hydroxy-benzyl chloride 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 
• 95602-92-9 3,5-di-tert-butyl-4-hydroxycinnamic acid 
• 22014-01-3 3-(3,5-di-tert-butyl-4-hydroxyphenyl)prop-2-enoic acid 
• 24457-08-7 4-Hydroxy-1-oxo-2,6-di-tert.-butyl-4-ethinyl-cyclohexadien-(2,5) 

Downstream Products

• 865087-47-4 2,6-di-tert-butyl-4-{2-[4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl]-vinyl}phenol 

Relevant academic research and scientific papers

TWISTED PI-ELECTRON SYSTEM CHROMOPHORE COMPOUNDS WITH VERY LARGE MOLECULAR HYPERPOLARIZABILITIES AND RELATED COMPOSITIONS AND DEVICES

Unconventional twisted π-electron system electro-optic (EO) chromophores/compounds, compositions and related device structures. Crystallographic analysis of several non-limiting chromophores reveals, for instance, large ring-ring dihedral twist angles and

Ultralarge hyperpolarizability twisted π-electron system electro-optic chromophores: Synthesis, solid-state and solution-phase structural characteristics, electronic structures, linear and nonlinear optical properties, and computational studies

This contribution details the synthesis and chemical/physical characterization of a series of unconventional twisted π-electron system electro-optic (EO) chromophores. Crystallographic analysis of these chromophores reveals large ring-ring dihedral twist

Efficient synthesis and structural characteristics of zwitterionic twisted π-electron system biaryls

(Chemical Equation Presented) A series of unconventional twisted π-electron system molecules has been synthesized via Suzuki cross-coupling of two sterically hindered arenes. Crystallographic analysis of these molecules reveals a large ring-ring dihedral

Process for preparing hindered alkenyl phenols

Hindered alkenyl phenols, all of which can be used as antioxidants, and some of which can be used as monomers, can be prepared by the dehydrohalogenation of the α-haloalkyl phenol.