According to Tim Patterson
Seed tannin can be extra-astringent when its terminal unit is a gallic acid ester, which doesn’t happen with skin tannins. But Harbertson observed that gallic acid is easily hydrolyzed and removed in winemaking, making that temporary astringency moot.
Characterizations such as the above make me wonder whether the author is inadvertently imprecise? I suspect he means that gallic acid ESTERS are easily hydrolyzed; not gallic acid itself?
See, for example:
[> http://tripatlas.com/Tannin> ] At the center of a hydrolyzable tannin molecule, there is a polyol carbohydrate (usually D-glucose). The hydroxyl groups of the carbohydrate are partially or totally esterified with phenolic groups such as gallic acid (in gallotannins) or ellagic acid (in ellagitannins). Hydrolyzable tannins are hydrolyzed by weak acids or weak bases to produce carbohydrate and phenolic acids.
Examples of gallotannins are the gallic acid esters of glucose in tannic acid ('C’76’H’52’O’46), found in the leaves and bark of many plant species.
According to Tim Patterson
Size matters for astringency
While much remains mysterious, we do at least know that the notion of a linear progression toward longer polymers isn’t the defining story. And it’s a good thing, too, because if that were the story, wine would get more and more “tannic” as it aged.
The feeling of astringency is produced when tannins grab the proteins from saliva, lessening the lubrication in the mouth and making tissue scratch against tissue. Research in France in 2003, conducted by Stéphane Vidal, Véronique Cheynier, Ann Noble and others, using model wines in which the tannin composition could be controlled, demonstrated through tasting panels that longer tannin chains register as more astringent than shorter ones.
See for example: http://www.ajcn.org/cgi/content/full/81/1/330S" onclick="window.open(this.href);return false;
Whereas ETS Labs explain: ETS Labs" onclick="window.open(this.href);return false;
The concentration of tannin in wine is the result of a balance between the amount of extractable tannin in grapes, extraction of grape tannin during fermentation/maceration, tannin additions, and tannin precipitation.
Tannin precursors form (relatively reactive?) tannins, many of which in turn become less reactive and/or eventually precipitate out of solution. I’m not so sure yet that previous (dogmatic?) interpretations have been decisively overturned as much as our language and concepts about complex polyphenol chemistry are rife with semantic ambiguities and apt to remain so for quite some time. Studying heterogeneous polymer chemistry can be a fast track to frustration.