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Malvidin-3-glucoside and catechin

Pissara, J. et al., Reaction between malvidin 3-glucoside and (+)-catechin in model solutions containing different aldehydes. J. Food Sci. 68, 476, 2003. [Pg.315]

Colored adducts in which the anthocyanin and the flavanol are linked by a carboxy-methine bridge, have also been identified, in addition to colorless carboxy-methine-linked catechin dimers (Chapter 9B), in model solutions containing (-i-)-catechin, malvidin-3-glucoside and glyoxylic acid (Es-Safi et al. 2003). [Pg.448]

Sousa, C., Mateus, N., SUva, A.M.S., Gonzalez-Paramas, A.M., Santos-Buelga, C., De Freitas, V. (2007). Stmctural and chromatic characterization of a new malvidin-3-glucoside-vanillyl-catechin pigment. Food Chem. 102, 1344—1351. [Pg.462]

The presence of the dimers malvidin-3-glucoside-ethyl-catechin (m/z 809, [M]" and malvidin-3-(6-p-coumaroyl)-glucoside-ethyl-catechin (m/z 955, [M] ) has been confirmed in wine and wine fractions with the help of ESI-MS. Other pigments (see below), in which the anthocyanin is joined to a flavanol via a vinyl fragment, can also be produced in the presence of acetaldehyde. [Pg.90]

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]

Duenas, M., et al., UV-visible spectroscopic investigation of the 8,8-methylmethine catechin-malvidin-3-glucoside pigments in aqueous solutions structural transformations and molecular complexations with chlorogenic acid, J. Agric. Food. Chem., 54, 189, 2006. [Pg.276]

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

Several aldehydes, namely furfural, 5-hydroxymethylfurfural, " isovaleraldehyde, benzal-dehyde, propionaldehyde, isobutyraldehyde, formaldehyde, and 2-methylbutyraledehyde, were shown to react with catechin and malvidin 3-glucoside in the same way as acetaldehyde or... [Pg.298]

Escribano-Bailon, T. et al., Color and stability of pigments derived from the acetaldehyde-mediated condensation between malvidin-3-O-glucoside and (+)-catechin. J. Agric. Food Chem. 49, 1213, 2001. [Pg.307]


See other pages where Malvidin-3-glucoside and catechin is mentioned: [Pg.267]    [Pg.292]    [Pg.548]    [Pg.267]    [Pg.292]    [Pg.548]    [Pg.292]    [Pg.294]    [Pg.297]    [Pg.445]    [Pg.446]    [Pg.447]    [Pg.448]    [Pg.451]    [Pg.112]    [Pg.112]    [Pg.113]    [Pg.266]    [Pg.267]    [Pg.285]    [Pg.286]    [Pg.286]    [Pg.272]    [Pg.289]    [Pg.291]    [Pg.293]    [Pg.293]    [Pg.296]    [Pg.302]    [Pg.156]    [Pg.445]   
See also in sourсe #XX -- [ Pg.132 , Pg.133 ]




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Catechine

Catechins

Malvidin

Malvidin catechin

Malvidin-3- glucoside

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