Abstract
A series of cationic cleavable surfactants was prepared by condensation of 2-alkyl-1,3-propanediols with 3-bromopropanal, followed by reaction with triethylamine. Each surfactant is a mixture of two diastereomers, and their precursors’ stereochemical assignments were based on1H nuclear magnetic resonance spectra and melting points. The critical micelle concentrations, Krafft points and destructibility of these surfactants were determined.
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Wang, GW., Yuan, XY., Liu, YC. et al. Synthesis and characterization of cleavable cationic surfactants with a 1,3-dioxane ring. J Am Oil Chem Soc 72, 83–87 (1995). https://doi.org/10.1007/BF02635783
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DOI: https://doi.org/10.1007/BF02635783