955-01-1

Upstream product

• 98-88-4 benzoyl chloride 
• 88-27-7 N,N-dimethyl-(3,5-di-tert-butyl-4-hydroxybenzyl)amine 
• 75-36-5 acetyl chloride 
• 88-26-6 3,5-di-tert-butyl-4-hydroxybenzyl alcohol 
• 16373-02-7 2,4-di-tert-butyl-6-hydroxymethylphenol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 78536-43-3 <3,5-di(tert-butyl)>-4-hydroxybenzylthiocyanate 
• 39266-77-8 2,2-bis-(3,5-di-tert-butyl-4-hydroxybenzyl)-malonic acid di-[4-(1,1,3,3-tetramethylbutyl)-phenyl]-ester 
• 67739-12-2 (3,5-di-t-Butyl-4-hydroxybenzyl)-formamidomalonsaeure-diaethylester 
• 1611-03-6 3,5-di-tert-butyl-4-hydroxyphenyl acetic acid 
• 1516-94-5 1,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)ethane 
• 21920-68-3 diethyl 2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate 
• 67739-21-3 diethyl N-acetylamino-(3,5-di-tert-butyl-4-hydroxybenzyl)malonate 
• 1066-06-4 2,4,6-tris(4-hydroxy-3,5-di-tert-butylbenzylthio)-symm-triazine 
• 67739-15-5 2-amino-3-(4-hydroxy-3,5-di-t-butylphenyl)propanoic acid 
• 67739-19-9 3-Amino-3-(3,5-di-t-butyl-4-hydroxyphenyl)-propionsaeuremethylester 
• 67739-14-4 3-(3,5-Di-t-butyl-4-hydroxybenzyl)-2-formamidopropionsaeure 
• 67739-18-8 2-(acetylamino)-3-[3',5'-di(tert-butyl)-4'-hydroxyphenyl]propanoic acid 
• 67739-13-3 (3,5-Di-t-butyl-4-hydroxybenzyl)-formamidomalonsaeure 
• 67739-22-4 N-acetylamino(3,5-di-tert-butyl-4-hydroxybenzyl)malonic acid 

Relevant academic research and scientific papers

Synthesis of derivatives of alkylamino alkyloxy propanol structures by N-alkylation, acylation, and nitration. Application as fuel additives

Polyfunctional compounds were prepared by alkylation, acylation, and nitration of hydroxyl and amine functions of the following alkanolamine ether structures: (di)alkylamino alkyloxy propanol, hydroxy alkyloxy (di)alkylamino propanol, and their dimer comp

New analogues of butylated hydroxytoluene as anti-inflammatory and antioxidant agents

Amine or amide derivatives bearing the 2,6-di-tert-butyl phenol moiety are synthesised. Almost all are antioxidants, reduce acute inflammation and inhibit COX-1 and lipoxygenase activity. The most potent anti-inflammatory, COX-1 inhibitor and antioxidant agent, with low toxicity, is 2,6-di-tert-butyl-4-thiomorpholin-4-ylmethyl-phenol.

Salts of acyl halides and 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine in benzylation reactions

The interaction of 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine with various acyl halides has been studied.The N-acyl quaternary salts obtained can be used to introdice a sterically hindered phenol fragment into organic compounds containing an active methylene group.

Multifunctional thiocyanate amine salt additive for fuels and lubricating oils and compositions containing said additive

This invention relates to a hydrocarbon-soluble sulfur-nitrogen compound resulting from the reaction of a dialkyl-4-hydroxy benzyl thiocyanate and a C12 --C24 alkyl primary amine which compounds have utility as multifunctional, i.e.

Antioxidant ester substituted phenols and process for their preparation

This invention comprises an alkylation, reduction and transesterification process for the preparation of ester substituted phenols. The products are useful as antioxidants and may be prepared in high yields and with a high degree of purity.