Chremos, George N.; Zimmerman, Howard K. published an article in 1962, the title of the article was Protolysis equilibrium of N-substituted diethanolamines.Formula: C8H19NO2 And the article contains the following content:
Limiting pK values for the acidic dissociation of 6 N-substituted diethanolammonium ions in sq. solution are given, each at a series of temperatures in the range 15-55掳. The effect of the 3rd substituent on the N atom on the equilibrium appears to be chiefly an influence on the mutual interaction between the 2 hydroxyethyl groups present in each mol., although the ex- pected basicity-depressing effects are also found for the N-phenyl and N-benzyl compounds The experimental process involved the reaction of 2,2′-(tert-Butylazanediyl)diethanol(cas: 2160-93-2).Formula: C8H19NO2
2,2′-(tert-Butylazanediyl)diethanol(cas:2160-93-2) belongs to alcohols. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Formula: C8H19NO2
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts