7089-36-3Relevant academic research and scientific papers
A structure-activity study of spermicidal and anti-HIV properties of hydroxylated cationic surfactants
Wong, Yue-Ling,Hubieki,Curfman, Christopher L,Doncel, Gustavo F,Dudding, Travis C,Savle, Prashant S,Gandour, Richard D
, p. 3599 - 3608 (2007/10/03)
The syntheses of 2-hydroxy-N-(2-hydroxyethyl)-N,N-dimethylhexadecan-1-aminium chloride [1(16)Cl] and iodide [1(16)I], 2-hydroxy-N,N,N-trimethylhexadecan-1-aminium chloride (6), N-(2-hydroxyethyl)-N,N-dimethylhexadecan-1-aminium chloride (8), N,N-bis(2-hydroxyethyl)-N-methylhexadecan-1-aminium chloride (11), and 2-hydroxy-N-(2-hydroxyethyl)-N,N-dimethyl-4-oxahexadecan-1-aminium chloride (14) are reported along with the critical micelle concentrations (cmcs), as measured by conductivity at 25°C, of 1(16)Cl, 1(16)I, 6, 8, 11, and N,N,N-trimethylhexadecan-1-aminium chloride (12). All compounds display spermicidal and virucidal activity. A plot of minimum effective concentration (MEC) in the Sander-Cramer spermicidal assay and cmc shows that 1(16)Cl and 6 have the best spermicidal activity and highest cmcs. Compounds 8, 11, and 1(16)Cl are the most active at 0.05 mg mL-1 against cell-free and cell-associated virus. In conclusion, 1(16)Cl shows the best combination of dual activity against sperm and HIV; it is a promising candidate for further preclinical studies as a topical, contraceptive microbicide.
Cleavage of Phosphate Esters by Hydroxyl-Functionalized Micellar and Vesicular Reagents
Moss, Robert A.,Ihara, Yasuji
, p. 588 - 592 (2007/10/02)
In order to compare the kinetic efficiencies of hydroxyl-functionalized surfactant vesicles with those of comparably functionalized micellar reagents, we studied the cleavages of p-nitrophenyl diphenyl phosphate (2) at pH 9.0 and lithium 2.4-dinitrophenyl
