500797-52-4

Upstream product

• 112-16-3 n-dodecanoyl chloride 
• 333-20-0 potassium thioacyanate 
• 62-53-3 aniline 
• 112-52-7 1-chlorododecane 

Relevant academic research and scientific papers

Synthesis, spectroscopic characterization and pH dependent electrochemical fate of two non-ionic surfactants

Two new nonionic surfactants; 1-sec-butyl-3-dodecanoylthiourea (DTU) and 1-dodecanoyl-3-phenylthiourea (DPTU) were synthesized and characterized by 1H NMR, 13C NMR and FTIR and UV-Vis spectroscopy. The detailed electrochemical fate of DTU and DPTU was investigated in a wide pH range of 2-12 by employing three electroanalytical techniques. The voltammetric signatures of the analytes showed a single irreversible anodic peak followed by two reversible peaks of the oxidation product. The irreversible behavior of the oxidation process was witnessed by the unequal components of total current in square wave voltammetry and scan rate based deviation of peak potential. The involvement of protons accompanying the electron transfer processes was ascertained from peak potential versus pH plots. Critical micelle concentration and hydrophilic-lipophilic balance of the synthesized surfactants were determined for the assessment of their cleaning, wetting and emulsifying properties.

High yield synthesis, detailed spectroscopic characterization and electrochemical fate of novel cationic surfactants

Two new cationic surfactants, N-(dodecanoyl(ethylammonio)carbonothioyl)-N- ethylbenzenaminium bromide and N-(dodecanoyl(ethylammonio)carbonothioyl)-N- ethyl-N-phenylbenzenaminium bromide were synthesized with a high yield by the reaction of appropriate amounts of lauryl chlorides, potassium thiocyanate, amine and alkyl halides. The structures were characterized by 1H-NMR, 13C-NMR, FTIR and UV-Vis spectroscopy. Cyclic, square wave and differential pulse voltammetry were used to investigate the electrochemical fate of both surfactants over a wide pH range.