129526-35-8Relevant academic research and scientific papers
Totally hindered phenols. 2,6-Di-t-butyl-4-(1,1-dialkyl-1-acetamide)-phenols and their persistent phenoxy radicals
Lai, John T.
, p. 557 - 560 (2001)
2,6-Di-t-butyl-4-(1,1-dialkyl-1-acetamide)-phenols were prepared from 2,6-di-t-butylphenol, chloroform, ketone and amine with sodium hydroxide. Their phenoxy radicals were found to be more persistent than the well-known 2,4,6-tri-t-butylphenoxy blue aroxyl radical.
N,N-disubstituted, α-(3,5-dialkyl-4-hydroxyphenyl)-α,α-disubstituted acetamides and composition stabilized therewith
-
, (2008/06/13)
N-substituted, N-(polysubstituted-4-piperidinyl)-α-(3,5-dialkyl-4-hydroxyphenyl)-α,α-disubstituted acetamide ("3,5-DHPIPA") generates an exceptionally stable hindered acetamide aroxyl radical which is far more stable than the "blue aroxyl radical" derived
