Synthetic Tannins by Georg Grasser
page 10 of 193 (05%)
page 10 of 193 (05%)
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as HO.C_6H_4.SO_2.O.C_6H_4HSO_3. It is, however, probable that this
substance is not homogeneous, but consists of a mixture of higher condensation products. Klepl [Footnote: _Jour. pr. Chem._, 1883, 28, 208.] obtained--by simply heating _p_-hydroxybenzoic acid--a so-called di- and tridepside, but this simple method is not applicable to many other hydroxybenzoic acids, since these are decomposed by the high temperature required to induce reaction. Amongst other attempts to produce condensation products with characteristics similar to those possessed by the tannins, those by Gerhardt [Footnote: Liebig's _Ann_, 1853, 87, 159.] and Loewe [Footnote: _Jahresh. f. Chem._, 1868, 559.] must be especially noted; they treated gallic acid with phosphorus oxychloride or arsenic acid, and thereby obtained amorphous compounds, exhibiting the reactions characteristic of tanning substances. E. Fischer and Freudenberg, [Footnote: Liebig's _Ann._, 372, 45.] by treating _p_-hydroxybenzoic acid in the same way, succeeded in obtaining a didepside, and during the last years practically only these two investigators have demonstrated the syntheses of these depsides and produced high-molecular polydepsides. At the same time researches were instituted with the object of determining the constitution of tannin, and E. Fischer succeeded in demonstrating its probable composition as being that of a glucoside containing 5 molecules of digallic acid per 1 molecule of glucose. This last-named class of synthetic tannins--which may be properly termed "tanning matters" in contradistinction to the true tannins--exhibit very distinct tanning character when brought in contact with animal hide, but |
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