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The Second Acidic Constant of Salicylic Acid

Annali di Chimica, 2005
AbstractThe second dissociation constant of salicylic acid (H2L) has been determined, at 25 °C, in NaCl ionic media by UV spectrophotometric measurements. The investigated ionic strength values were 0.16, 0.25, 0.50, 1.0, 2.0 and 3.0 M. The protolysis constants calculated at the different ionic strengths yielded, with the Specific Interaction Theory ...
PORTO R, DE TOMMASO G, FURIA, Emilia
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Acid Dissociation Constants of Phenylalkanolamines

Journal of Pharmaceutical Sciences, 1962
The acid dissociation constants of phenylephrine, synephrine, and tyramine were investigated by the new spectrophotometric method of Edsall. Epinephrine was studied by a titration and complexation method. It is concluded from analysis of the spectral data that the phenolic function is a stronger acid than the alkylammonium group.
S, RIEGELMAN, L A, STRAIT, E Z, FISCHER
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Dissociation constants of carboxymethyloxysuccinic acid

Talanta, 1974
The dissociation constants of carboxymethyloxysuccinic acid (CMOS) have been measured at 25 degrees and an ionic strength of 0.1M in sodium perchlorate. The values found were: pK(1) = 2.52, pK(2) = 3.77 and pK(3) = 5.00. CMOS is thus seen to be rather stronger than its isomer citric acid.
C E, Rodriguez, C D, Devine
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