Abstract The reaction of ω-(4-hydroxyaryl) haloalkanes with various nitrogen-containing agents afforded primary, secondary, and tertiary amino derivatives of 2, 6-dialkylphenols. For the compounds synthesized, the reaction rate constants with peroxide radicals were measured for cumene and methyl oleate oxidation. The total inhibitory activity in the model reactions of thermal autooxidation of lard and hexadecane was studied. The rate ...
![4-[3-(dimethylamino)propyl]-2,6-dimethylphenol Structure](https://image.chemsrc.com/caspic/436/922724-53-6.png)