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Malvidin 3-glucoside

Gomez-Miguez, M. et al., Influence of different phenolic copigments on the color of malvidin 3-glucoside, J. Agric. Food Chem., 54, 5422, 2006. [Pg.83]

The degradation kinetics of malvidin 3-glucoside in ethanolic solutions under conditions simulating wine accelerated with the increase of ethanol concentration, probably because the extent of anthocyanin self-association decreased with elevated ethanol concentration. ... [Pg.264]

The color of malvidin 3-glucoside in aqueous solution can be stabilized by selfassociation or copigmentation with the di-chalcone form, according to the pH of the solution. ... [Pg.265]

The effects of catechin, epicatechin, procyanidin B2, caffeic acid, / -coumaric acid, myricetrin, and quercetrin on the color intensity and stability of malvidin 3-glucoside at a molar ratio of 1 1 under conditions similar to red wine were evaluated. " Flavan 3-ols appeared to have the lowest protective effects and flavonols the highest strong color changes were visually perceptible. " In the complexation of malvin chloride and natural polyphenols, flavonol glycosides by far exerted the best protector effect. ... [Pg.265]

In the intermolecular reactions between anthocyaifins and flavonoids mediated by acetaldehyde, new compounds linked by an ethyl bridge are formed. Three new compounds were detected by the reaction of malvidin 3-glucoside and proanthocy-... [Pg.266]

Houbiers, C. et al.. Color stabilization of malvidin 3-glucoside self-aggregation on the of flavylium cation and copigmentation with the Z-chalcone form, J. Phys. Chem. B, 102, 3578, 1998. [Pg.269]

Pissarra, J. et al.. Reaction between malvidin 3-glucoside and (-t-)-catechin in model solutions containing different aldehydes, J. Food Sci., 68, 476, 2003. [Pg.276]

Degenhardt, A., Knapp, H., and Winterhalter, P., Rapid isolation of malvidin 3-glucoside from red wine by high speed counter-current chromatography (HSCCC), Vitis, 39, 43, 2000. [Pg.502]

Direct condensation product between catechin and malvidin-3-glucoside... [Pg.256]

The synthesis of two new red wine pigments by nucleophilic addition of vinylphenols to malvidin 3-glucoside has been described. The structures of the two new pigments and their formation are shown in Fig. 2.105. HPLC-DAD and HPLCMS confirmed the occurrence of these two anthocyanin derivatives in red wine [239],... [Pg.259]

As nowadays wine making has factory dimensions, the need for a rapid method is important, so a flow injection techniqne for liqnid-solid extraction coupled to an HPLC was developed [368]. The target analytes were extracted from wine in a continuous way by means of a minicolumn packed with C18, the elntion was carried ont by means of acid water (pH 2) and acetonirile, then the solvent was evaporated by nitrogen stream on-line to a HPLC injector. Malvidin-3-glucoside, cyaniding-3-glncosyde, and peonidin-3-glncoside antocyanins were determined in a more rapid, accurate, and sensitive way than with the traditional methods. [Pg.602]

Catechin(-furfurylmethine)-malvidin 3-glucoside Model solution 859 ([M+ - 2H+] ) 280, 450, 545 HPLC-DAD-ESI-MS 214... [Pg.284]


See other pages where Malvidin 3-glucoside is mentioned: [Pg.256]    [Pg.263]    [Pg.263]    [Pg.266]    [Pg.266]    [Pg.267]    [Pg.267]    [Pg.267]    [Pg.341]    [Pg.258]    [Pg.241]    [Pg.248]    [Pg.251]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.255]    [Pg.256]    [Pg.256]    [Pg.256]    [Pg.256]    [Pg.256]    [Pg.256]    [Pg.256]    [Pg.259]    [Pg.266]    [Pg.272]    [Pg.285]   
See also in sourсe #XX -- [ Pg.256 ]




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Anthocyanins malvidin-3-glucoside

Catechins reaction with malvidin 3-glucoside

Malvidin

Malvidin-3- glucoside pyruvic

Malvidin-3- glucoside pyruvic derivative

Malvidin-3-O- glucosid

Malvidin-3-O- glucoside

Malvidin-3-glucoside and catechin

Malvidin-3-glucoside cinnamic acid

Malvidin-3-glucoside derivatives

Malvidin-3-glucoside-8-ethyl-catechin

Malvidin-3-glucoside-8-ethyl-epicatechin

Pyruvate reaction with malvidin-3-glucoside

Reaction of malvidin-3-glucoside

Reaction of malvidin-3-glucoside and

Stability of malvidin-3-glucoside

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