2006
DOI: 10.1007/s10953-005-9009-6
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Second Dissociation Constant of Bis-[(2-hydroxyethyl)amino]acetic Acid (BICINE) and pH of Its Buffer Solutions from 5 to 55 °C

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Cited by 18 publications
(36 citation statements)
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“…The hydrolysis corrections of m 1 /m 2 are negligible because of the pH of buffer solutions of NaADA and Na 2 ADA is very close to neutrality. In the present study this observation is consistent with other investigations of structurally related buffer compounds [3] [4]. The ionic strength of the solution for cell (B) is indicated by:…”
Section: Resultssupporting
confidence: 93%
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“…The hydrolysis corrections of m 1 /m 2 are negligible because of the pH of buffer solutions of NaADA and Na 2 ADA is very close to neutrality. In the present study this observation is consistent with other investigations of structurally related buffer compounds [3] [4]. The ionic strength of the solution for cell (B) is indicated by:…”
Section: Resultssupporting
confidence: 93%
“…The parent compound (GLYCINE) [1] has a pK 2 of 9.780 and whereas for (TRICINE) [ increase of the acidic strength for the protonated nitrogen group. It is worthwhile to mention that as the number of -CH 2 OH group becomes greater, the enhancement of the acidity decreases as in the case of (GLYCINE) [1], (BICINE) [3] and (TRICINE) [2]. This trend is consistent for ADA (present study in Table 4).…”
Section: Discussionsupporting
confidence: 86%
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“…Good et al [1,2] have recommended a set of zwitterionic amino acid buffers for the investigation of physiological solutions across a broad pH range.The second dissociation constant (pK 2 ) of the zwitterionic buffer BICINE has recently been published [3]. Standard pH values of six buffer solutions of BICINE and NaBICINE without NaCl in the ionic strength range I = 0.02 to 0.08 mol·kg -1 and four buffer solutions in isotonic saline media of I = 0.16 mol·kg -1 with NaCl from (278.15 to 328.15) K have been reported earlier from this laboratory [3].…”
Section: Introductionmentioning
confidence: 92%