25282-58-0

Usage

Uses

Used in Plastics Industry:
(2-tert-butylphenoxy)(trimethyl)silane is used as a silane coupling agent for improving the adhesion and compatibility between organic and inorganic materials in the production of plastics. This results in enhanced mechanical properties of the plastics, contributing to their durability and performance.
Used in Adhesives Industry:
In the adhesives industry, (2-tert-butylphenoxy)(trimethyl)silane is utilized as a silane coupling agent to boost the bonding strength between different materials. Its ability to improve adhesion ensures that the adhesives are more effective and long-lasting.
Used in Coatings Industry:
(2-tert-butylphenoxy)(trimethyl)silane is employed as a component in the production of coatings to enhance their mechanical properties, such as resistance to wear and tear. Its role as a silane coupling agent also promotes better adhesion between the coating and the substrate, ensuring a more durable and longer-lasting finish.
Used as a Surface Modifier:
(2-tert-butylphenoxy)(trimethyl)silane is used as a surface modifier to enhance the water repellency and anti-sticking properties of various materials. This application is particularly beneficial in industries where reducing friction, preventing contamination, and improving the longevity of products is crucial.

Upstream product

• 88-18-6 2-tert-Butylphenol 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 127354-49-8 trichloro (2-tert-butylphenoxo)titanium(IV) 
• 728924-22-9 dichloro bis(2-tert-butylphenoxo)titanium(IV) 
• 728924-24-1 chloro tris(2-tert-butylphenoxo)titanium(IV) 

Relevant academic research and scientific papers

Highly atom economical uncatalysed and I2-catalysed silylation of phenols, alcohols and carbohydrates, using HMDS under solvent-free reaction conditions (SFRC)

An uncatalysed silylation of phenols, regardless on the aggregate state and nature of the substituents with 0.55 equiv of HMDS under solvent-free reaction conditions (SFRC) at room temperature is reported. Sterically hindered phenols, carbohydrates and most of the alcohols additionally required a catalytic amount (up to 2 mol %) of iodine. The reaction protocol is very simple; obtaining a pure product, particularly of uncatalysed reactions, was frequently a completely solvent-free process.

Diaryl ether synthesis in supercritical carbon dioxide in batch and continuous flow modes

A high yielding, batch mode synthesis of diaryl ethers and sulfides by an SNAr fluoride-mediated process in scCO2 has been developed; the use of a polymer-supported imidazolium fluoride reagent in batch mode led to the development of

Synthesis and characterization of 2-tert.butyl phenoxotitanium(IV) complexes

Complexes of composition TiCl4-n(OC6H 4-Bu1-2)n (where n = 1 to 4 and OAr = OC 6H4-Bu1-2) have been prepared by the reaction of titanium(IV) chloride with Me3SiOAr in predetermined molar ratios in carbon tetrachloride/toluene as solvent These complexes have been characterized by elemental, IR, 1H NMR and TG analysis and molecular weight determinations. Lewis acid character of the complexes has also been established by isolating adducts with some monodentate aliphatic amines and bidentate aromatic amines.