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Dimethylamino -benzaldehyde-Acid Reagents

Many known color reactions involve electrophilic substitution at an electron-rich aromatic or heteroaromatic (cf. 4-(dimethylamino)-benzaldehyde - acid reagents and vanillin reagents ). Here aliphatic or aromatic aldehydes react in acid medium to yield polymethyne cations which are intensely colored di- or triarylcarbenium ions [4, 10]. [Pg.39]

A whole series of derivatization reagents contain 4-(dimethylamino)-benzaldehyde as a fundamental component. They differ in the type and concentration of the mineral acid components used in their preparation. Other components of the reagent generally play a minor role. [Pg.126]

Ehrlich s reagent as 4-(dimethylamino)-benzaldehyde — hydrochloric acid and... [Pg.126]

Van Urk s reagent as 4-(dimethylamino)-benzaldehyde - sulfuric acid, but the experimental section incorrectly refers to a solution of 4-(dimethylamino)-benzaldehyde in hydrochloric acid/ethanol as Van Urk s reagent [1]. [Pg.126]

It can be concluded from the publications of Rohde [2] and Freund and Lebach [3, 4] that it was Ehrlich who first suggested the use of 4-(dimethylamino)-benzalde-hyde in the presence of hydrochloric acid for color reactions with methylketols that was found also to apply to indole derivatives [S]. Auterhoff [6] designated a reagent for urobilinogen, consisting of a solution of 2 g 4-(dimethylamino)-benzaldehyde in 20 percent hydrochloric acid, correctly as Ehrlich s solution. Hence, it is essentially correct to refer to all reagents which contmn these components as Ehrlich s reagent. [Pg.126]

Auterhoff described a reagent made up of 4-(dimethylamino)-benzaldehyde, sulfuric acid with additional iron(lll) ions as Van Urk s reagent solution . A more correct name would have been Van Urk-Salkowski reagent, since the Salkowski reagent (iron(lll) chloride/sulfuric acid) has been used alongside the Van Urk s reagent [8]. [Pg.126]

Dimethylamino)-benzaldehyde-Acetic Acid-Phosphoric Acid Reagent... [Pg.127]

Note The individual components of the reagent can also be applied separately one after the other [12, IS], e.g. the chromatogram is first immersed in an 8% methanolic 4-(dimethylamino)-benzaldehyde solution and then, after intermediate drying, sprayed v th 25% sulfuric acid [12]. 4-(Dimethylamino)-benzaldehyde can be replaced in the reagent with 4-(dimethylamino)-ciimamaldehyde [1]. [Pg.135]

Tin(II) Chloride-Hydrochloric Acid-4-(Dimethylamino)-benzaldehyde Reagent... [Pg.220]


See other pages where Dimethylamino -benzaldehyde-Acid Reagents is mentioned: [Pg.126]    [Pg.126]    [Pg.127]    [Pg.368]    [Pg.742]    [Pg.861]    [Pg.126]    [Pg.126]    [Pg.126]    [Pg.127]    [Pg.368]    [Pg.742]    [Pg.861]    [Pg.126]    [Pg.195]    [Pg.130]    [Pg.131]    [Pg.131]    [Pg.131]    [Pg.132]    [Pg.132]    [Pg.133]    [Pg.134]    [Pg.135]    [Pg.135]    [Pg.136]    [Pg.136]    [Pg.371]    [Pg.372]    [Pg.373]    [Pg.375]    [Pg.864]    [Pg.866]    [Pg.866]    [Pg.867]   


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