Oxyalkylation of N‐(2‐hydroxyethyl) amides and N,N‐bis‐(2‐hydroxyethyl) amides gave products which were valuable as detergent additives and detergent intermediates. Oxyalkylation of simple amides was difficult to carry out, and the product contained large quantities of unreacted amide which had an adverse effect on surfactant properties. Amides with short oxyalkyl chains and long fatty chains were not soluble by themselves but were solubilized by aqueous detergent solutions and had characteristic “Krafft Points.” This temperature, at which the mixed solution became clear, was independent of detergent used, amide to detergent ratio up to 1.4, total concentration, and water hardness. Krafft point of poorly soluble detergents such as sodium octadecyl sulfate and disodium α‐sulfostearate was lowered by mixing with alkanolamides. N,N‐Bis‐(hydroxyethyl)‐hexadecanamide and the oxyalkylated products of N,N‐bis‐(hydroxyethyl) hexadecanamide and N,N‐bis‐(hydroxyethyl) octadecanamide increased the viscosity of solutions of linear alkylbenzene sulfonate and sodium dodecyl sulfate in the same was as the N,N‐bis‐(hydroxyethyl) amide prepared from coconut oil. Foam stabilizing properties ere observed for some of oxyethylated amides. One per cent N,N‐bis‐(2‐hydroxyethyl) oleamide and 2‐(2‐hydroxyethoxy)‐ethyloleamide formed petrolatum‐water emulsions which were stable for more than a month.