Decyl β-D-glukopiranozyd, niejonowy środek powierzchniowo czynny, jest stosowany w opracowywaniu roztworów środków powierzchniowo czynnych na bazie cukru. Może być stosowany jako referencyjny glukozyd alkilowy w procedurach separacji i analizy oraz do badania jego właściwości fizykochemicznych i zachowania jako środka powierzchniowo czynnego.
Langmuir : the ACS journal of surfaces and colloids, 20(24), 10534-10541 (2004-11-17)
Surface tension isotherms were recorded for n-decyl-beta-d-glucopyranoside (Glu) and n-decyl-beta-D-maltopyranoside (Mal) solutions at temperatures of 8, 22, and 29 degrees C. Comparison was made with isotherms of n-decyl-beta-D-thiomaltopyranoside (S-Mal) at 22 degrees C. In addition to the transition from the
The journal of physical chemistry. B, 109(13), 6239-6246 (2006-07-21)
The adsorption of the surfactant n-nonyl-beta-D-glucopyranoside at the air-water interface after injection of the surfactant into the subphase was studied by infrared reflection absorption spectroscopy. In the first part, we investigated the equilibrium adsorption of n-nonyl-beta-D-glucopyranoside and the Gibbs adsorption
Langmuir : the ACS journal of surfaces and colloids, 20(25), 10935-10942 (2004-12-01)
Measurements of surface tension isotherms were conducted for water solutions of pure and mixed n-decyl-beta-d-glucopyranoside (C(10)-Glu) and n-decyl-beta-d-maltopyranoside (C(10)-Mal) surfactants. By applying the Gibbs surface tension equation, the surface densities of Glu and Mal were derived for different compositions and
Biotechnology and bioengineering, 89(4), 381-392 (2005-01-12)
Liquid-liquid extraction in two-phase aqueous complex-fluid systems has been proposed as a scalable, versatile, and cost-effective purification method for the downstream processing of biotechnological products. In the case of two-phase aqueous micellar systems, careful choices of the phase-forming surfactants or
There are many of pathogen parasite species with different susceptibility profile to antiparasitic drugs. Unfortunately, almost QSAR models predict the biological activity of drugs against only one parasite species. Consequently, predicting the probability with which a drug is active against
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