38146-17-7

Usage

Uses

Used in Polymer Manufacturing:
Phenol, 4,4',4''-(1,3,5-triazine-2,4,6-triyltri-2,1-ethanediyl)tris[2,6-bis(1,1-dimethylethyl)is used as a key component in the production of polymers for its high stability and melting point, which contribute to the overall performance and durability of the final product.
Used in Plastics Production:
Phenol,4,4',4''-(1,3,5-triazine-2,4,6-triyltri-2,1-ethanediyl)tris[2,6-bis(1,1-dimethylethyl)is used as a stabilizer in the manufacturing of plastics, thanks to its antioxidant properties. It helps in preventing the degradation of plastics caused by exposure to heat, light, or oxygen, thereby enhancing their longevity and performance.
Used in Adhesive Formulations:
Phenol, 4,4',4''-(1,3,5-triazine-2,4,6-triyltri-2,1-ethanediyl)tris[2,6-bis(1,1-dimethylethyl)is used as an additive in adhesive formulations to improve their stability and performance in high-temperature environments. Its antioxidant properties also help in protecting the adhesive from degradation, ensuring a stronger bond and longer-lasting adhesion.
Used in High-Temperature Applications:
Due to its high melting point and stability, Phenol,4,4',4''-(1,3,5-triazine-2,4,6-triyltri-2,1-ethanediyl)tris[2,6-bis(1,1-dimethylethyl)- is used in various high-temperature applications, such as in the production of materials for automotive parts, aerospace components, and other industrial products that require resistance to extreme temperatures.
Used in Material Stabilization:
Phenol, 4,4',4''-(1,3,5-triazine-2,4,6-triyltri-2,1-ethanediyl)tris[2,6-bis(1,1-dimethylethyl)is used as a stabilizer in various materials to protect them from degradation caused by heat, light, or oxygen exposure, ensuring their durability and performance over time.

Upstream product

• 84654-57-9 β-[3,5-di(tert-butyl)-4-hydroxyphenyl]propionic acid ethyl imino ester hydrochloride 
• 57529-38-1 3-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-propionimidic acid ethyl ester 

Relevant academic research and scientific papers

2-(2′-hydroxyphenyl)benzotriazoles used as U.V. stabilizers

2-(2′-hydroxyphenyl)benzotriazoles having general formula (I). The above 2-(2′-hydroxyphenyl)benzotriazoles are useful as light stabilizers for organic polymers.

2-(2′-hydroxyphenyl) benzotriazoles containing a 2,4-imidazolidinedione group and process for their preparation

2-(2′-hydroxyphenyl)benzotriazoles having general formula (I). The above 2-(2′-hydroyzphenyl)benzotriazoles having general formula (I) are useful as heat, oxygen and light stabilizers for organic polymers. In particular they are useful as UV stabilizers for organic polymers.

2-(2'Hydroxyphenyl) benzotriazoles and process for their preparation

2-(2'-hydroxyphenyl)benzotriazoles having general formula (I): The above 2-(2'-hydroxyphenyl)benzotriazoles can be used as light stabilizers for organic polymers.

2-(2'Hydroxyphenyl) benzotriazoles and their use as light stabilizers for organic polymers

2-(2'-hydroxyphenyl)benzotriazoles having general formula (I): The above 2-(2'-hydroxyphenyl)benzotriazoles can be used as light stabilizers for organic polymers.

Piperidine compounds containing silane groups for use as stabilisers for organic materials

The present invention relates to novel piperidine compounds of the formula (I) STR1 in which A is e.g. a group of the formula STR2 where R4 is e.g. hydrogen or methyl, X3 is e.g. --O-- or --NH-- and R5 ' is e.g. ethylene, propylene or decamethylene, R1 is e.g. methyl, methoxy, ethoxy or OH, R2 and R3 are e.g. methyl, m+n is e.g. a number from 1 to 40, n varies e.g. from zero to 50% of the sum m+n, X1 is e.g. as defined for R1 or is a group (CH3)3 SiO-- and X2 is e.g. hydrogen, methyl, ethyl, a group (CH3)3 Si-- or a group STR3 and, when m+n is a number from 3 to 10, X1 and X2 together also form a direct bond. The compounds of the formula (I) are effective in stabilising an organic material against thermal, oxidative and light-induced degradation.

SYNTHESIS AND PROPERTIES OF symm-TRIAZINE DERIVATIVES. 4.* SYNTHESIS OF 2,4,6-TRISUBSTITUTED symm-TRIAZINES CONTAINING STERICALLY-HINDERED PHENOL FRAGMENTS

2,4,6-Trisubstituted symm-triazines containing sterically-hindered phenol fragments were synthesized by the cyclotrimerization of ethyl iminoesters. 2,4,6-Trimercapto-symm-triazine derivatives containing shielded phenol residues may be formed by the cyclo