In chemistry and biochemistry, the pH of weakly acidic chemical solutions can be estimated using the Henderson–Hasselbalch Equation:
pH = p K a + log 10 ( [ Base ] [ Acid ] ) {\displaystyle {\ce {pH}}={\ce {p}}K_{{\ce {a}}}+\log _{10}\left({\frac {[{\ce {Base}}]}{[{\ce {Acid}}]}}\right)} The equation relates the pH of the weak acid to the numerical value of the acid dissociation constant, Ka, of the acid, and the ratio of the concentrations of the acid and its conjugate base. Acid-base Equilibrium Reaction
H A ( a c i d ) ⇌ A − ( b a s e ) + H + {\displaystyle \mathrm {{\underset {(acid)}{HA}}\rightleftharpoons {\underset {(base)}{A^{-}}}+H^{+}} }
The Henderson–Hasselbalch equation is often used for estimating the pH of buffer solutions by approximating the actual concentration ratio as the ratio of the analytical concentrations of the acid and of a salt, MA. It is also useful for determining the volumes of the reagents needed before preparing buffer solutions, which prevents unnecessary waste of chemical reagents that may need to be further neutralized by even more reagents before they are safe to expose. For example, the acid may be carbonic acid
CO 2 + H 2 O ⇌ H 2 CO 3 ⇌ HCO 3 − + H + {\displaystyle {\ce {CO2}}+{\ce {H2O}}\rightleftharpoons {\ce {H2CO3}}\rightleftharpoons {\ce {HCO3-}}+\mathrm {H^{+}} }
The equation can also be applied to bases by specifying the protonated form of the base as the acid. For example, with an amine, R N H 2 {\displaystyle \mathrm {RNH_{2}} }
R N H 3 + ⇌ R N H 2 + H + {\displaystyle \mathrm {RNH_{3}^{+}\rightleftharpoons RNH_{2}+H^{+}} }
The Henderson–Hasselbalch buffer system also has many natural and biological applications, from physiological processes (e.g., metabolic acidosis) to geological phenomena.
History The Henderson–Hasselbalch equation was developed by Lawrence Joseph Henderson and Karl Albert Hasselbalch. Henderson was a biological chemist and Hasselbalch was a physiologist who studied pH. In 1908, Henderson derived an equation to calculate the hydrogen ion concentration of a bicarbonate buffer solution, which rearranged looks like this:
In 1909, Sørensen introduced the pH terminology, which allowed Hasselbalch to re-express Henderson's equation in logarithmic terms, resulting in the Henderson–Hasselbalch equation.
Assumptions, limitations, and derivation A simple buffer solution consists of a solution of an acid and a salt of the conjugate base of the acid. For example, the acid may be acetic acid and the salt may be sodium acetate. The Henderson–Hasselbalch equation relates the pH of a solution containing a mixture of the two components to the acid dissociation constant, Ka of the acid, and the concentrations of the species in solution.
To derive the equation a number of simplifying assumptions have to be made. Assumption 1: The acid, HA, is monobasic and dissociates according to the equations
HA ↽ − − ⇀ H + + A − {\displaystyle {\ce {HA <=> H^+ + A^-}}}
… excerpt ends here. Continue reading the full article.




