2001Journal of Surfactants and DetergentsOpen access

Synthesis and surface properties of N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine‐N‐oxides

Andrzej Piasecki, Sławomir Karczewski, Ludwik Syper

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Abstract

Abstract A new group of saccharide surfactants, N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine‐N‐oxides (derivatives of d‐gluconic, d‐glucoheptonic, and lactobionic acids), were synthesized with high yields by one‐step oxidation reaction of an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)‐propyl]amine with an excess of 30 wt% of an aqueous solution of hydrogen peroxide. Their structures and purity were confirmed by means of elemental analysis, electrospray ionization mass spectrometry, and 1H and 13C nuclear magnetic resonance spectroscopy. In comparison to an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine, the investigated N‐oxides are more soluble in water with similar critical micelle concentration values and show higher surface effectiveness. They are low‐foamable but in mixtures with sodium dodecyl sulfate form high‐volume and stable foams in a wide range of mixture compositions.

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Abstract A new group of saccharide surfactants, N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine‐N‐oxides (derivatives of d‐gluconic, d‐glucoheptonic, and lactobionic acids), were synthesized with high yields by one‐step oxidation reaction of an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)‐propyl]amine with an excess of 30 wt% of an aqueous solution of hydrogen peroxide. Their structures and purity were confirmed by means of elemental analysis, electrospray ionization mass spectrometry, and 1H and 13C nuclear magnetic resonance spectroscopy. In comparison to an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine, the investigated N‐oxides are more soluble in water with similar critical micelle concentration values and show higher surface effectiveness. They are low‐foamable but in mixtures with sodium dodecyl sulfate form high‐volume and stable foams in a wide range of mixture compositions.

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Available abstract

Abstract A new group of saccharide surfactants, N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine‐N‐oxides (derivatives of d‐gluconic, d‐glucoheptonic, and lactobionic acids), were synthesized with high yields by one‐step oxidation reaction of an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)‐propyl]amine with an excess of 30 wt% of an aqueous solution of hydrogen peroxide. Their structures and purity were confirmed by means of elemental analysis, electrospray ionization mass spectrometry, and 1H and 13C nuclear magnetic resonance spectroscopy. In comparison to an appropriate N‐dodecyl‐N,N‐bis[3‐(aldonamido)propyl]amine, the investigated N‐oxides are more soluble in water with similar critical micelle concentration values and show higher surface effectiveness. They are low‐foamable but in mixtures with sodium dodecyl sulfate form high‐volume and stable foams in a wide range of mixture compositions.

Key concepts: Chemistry, Amine gas treating, Sodium dodecyl sulfate, Aqueous solution, Hydrogen peroxide, Micelle, Electrospray ionization, Critical micelle concentration

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