55719-54-5

Upstream product

• 46170-85-8 2,3-dimethyl-6-tert-butyl phenol 

Downstream Products

• 56823-72-4 5-tert.-butyl-2,3-dimethyl-4-hydroxyphenylacetonitrile 
• 56808-21-0 dimethyl (5-tert.-butyl-2,3-dimethyl-4-hydroxybenzyl)malonate 
• 56823-88-2 (5-tert-Butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetic acid 3-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxy]-2,2-bis-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxymethyl]-propyl ester 
• 56823-89-3 (5-tert-Butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetic acid 2,2-bis-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxymethyl]-pentyl ester 
• 56823-85-9 (5-tert-Butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetic acid 3-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxy]-2-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxymethyl]-2-methyl-propyl ester 
• 56823-86-0 thiodiethylene bis-(5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate) 
• 56823-80-4 (5-tert-Butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetic acid 6-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxy]-hexyl ester 
• 56823-79-1 (5-tert-Butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetic acid 3-[2-(5-tert-butyl-4-hydroxy-2,3-dimethyl-phenyl)-acetoxy]-2,2-dimethyl-propyl ester 
• 56823-93-9 N-Methyl-N-n-octadecyl-(5-tert.-butyl-2,3-dimethyl-4-hydroxyphenyl)acetamid 
• 56823-75-7 n-octadecyl 5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate 
• 56823-78-0 n-dodecyl 5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate 
• 56823-77-9 n-octyl 5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate 
• 56823-76-8 n-butyl 5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate 
• 56823-74-6 methyl 5-t-butyl-2,3-dimethyl-4-hydroxyphenylacetate 

Relevant academic research and scientific papers

Trialkylsubstituted hydroxybenzyl malonates and stabilized compositions

Compounds having the formula STR1 wherein R1, R2 and R3 are alkyl or cycloalkyl; R4 and R5 are alkyl or phenyl; and R is hydrogen, alkyl or a trialkylhydroxybenzyl, Are good antioxidants and thermal s

2,3,5-Trialkylsubstituted hydroxybenzyl isocyanurates

The compounds are 2,3,5-trialkylsubstituted hydroxy benzyl isocyanurates having the formula STR1 where Ra is a 2,3,5-trialkylsubstituted hydroxybenzyl group of the formula II or hydrogen, and Rb is a 2,3,5-trialkylsubstituted hydroxy

Esters of trisubstituted hydroxyphenylalkanoic acids

The compounds are esters and amides of trialkylhydroxyphenylalkanoic acid having the formula SPC1 Wherein R, R1 and R2 are independently lower alkyl or cycloalkyl groups, R3 is hydrogen, alkyl, cycloalkyl, alkylene, phenyl

2,3,5-Trialkyl-4-hydroxybenzylphosphonates and phosphinates

The compounds are trialkylsubstituted hydroxybenzylphosphonates and phosphinates having the formula SPC1 Wherein R, R1 and R2 are independently lower alkyl or cycloalkyl groups, R3 is alkyl, alkyl substituted with one halogen atom, phenyl, phenyl substituted with alkyl groups, alkoxy, alkoxy substituted with one halogen group, phenoxy, phenoxy substituted with alkyl groups, alkylthioethoxy, alkylpolyoxyalkylenoxy, R4 is alkyl, alkylsubstituted with one halogen atom, cycloalkyl, phenyl, phenyl substituted with alkyl groups alkylthioethyl, thiobis-alkylene, alkyleneoxyalkylene, polyoxyalkylene, alkylpolyoxyalkylene, alkylene, polyvalent cyclic or acyclic hydrocarbon radical, R 5 and R 6 are independently hydrogen, alkyl of 1 to 12 carbon atoms, R6 may also be the group Ic SPC2 Or together R5 and R6 represent the group Id SPC3 R7 is hydrogen, alkyl or phenyl, A is lower alkylene and n is 1 to 4. These compounds are usually prepared by reacting the trialkylsubstituted hydroxybenzyl or hydroxyphenylalkyl halide with the appropriate trialkyl or triaryl phosphite or appropriate substituted phosphonite. The compounds are useful as stabilizers of organic materials subject to oxidative, thermal and photochemical degradation.