125495-83-2Relevant academic research and scientific papers
Solid inclusion complexes of vanillin with cyclodextrins: Their formation, characterization, and high-temperature stability
Kayaci, Fatma,Uyar, Tamer
, p. 11772 - 11778 (2011)
This study reports the formation of solid vanillin/cyclodextrin inclusion complexes (vanillin/CD ICs) with the aim to enhance the thermal stability and sustained release of vanillin by inclusion complexation. The solid vanillin/CD ICs with three types of
Spectroscopic study on the inclusion complexes of β-cyclodextrin with selected metabolites of catecholamines
Korytkowska-Wa?ach, Anna,Dubrawska, Beata,?miga-Matuszowicz, Monika,Bieg, Tadeusz
, p. 532 - 538 (2017)
Inclusion complexes formed between β-cyclodextrin (β-CD) and metabolites of catecholamines, i.e. vanillylmandelic acid (VMA), homovanillic acid (HVA) as well as vanillin (VA) were studied using NMR spectroscopy. Due to the importance of these compounds fo
Spectral and molecular modeling studies on hydroxybenzaldehydes with native and modified cyclodextrins
Jenita, M. Jude,Mohandass,Rajendiran
, p. 695 - 707 (2014)
The inclusion complexation of 2-hydroxy-3-methoxybenzaldehyde (2HMB), 4-hydroxy-3-methoxybenzaldehyde (4HMB), 3,4-dimethoxybenzaldehyde (DMB) and 4-hydroxy-3,5-dimethoxybenzaldehyde (HDMB) with α-CD, β-CD, HP-α-CD and HP-β-CD were carried out by UV-Visibl
DOSY-NMR and raman investigations on the self-aggregation and cyclodextrin complexation of vanillin
Ferrazza, Ruggero,Rossi, Barbara,Guella, Graziano
, p. 7147 - 7155 (2014)
Vanillin (4-hydroxy-3-methoxybenzaldehyde) is a phenolic aldehyde with limited solubility in water; in this work, we investigate its self-aggregation, as well as its complexation equilibria with ?2-cyclodextrin by using nuclear magnetic resonance (NMR) an
