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HENDERSON HASSELBALCH
EQUATION
By
Mrs Sanchita Choubey
(M.Sc., PGDCR, Pursuing Ph. D)
Assistant Professor of Microbiology
Dr. D Y Patil Arts Commerce and Science College Pimpri, Pune
The Henderson–
Hasselbalch
Equation
Describes the derivation of pH as a
measure of acidity in biological and
chemical systems.
 The equation is also useful for
estimating the pH of a buffer
solution.
it is widely used to calculate the
isoelectric point of proteins( point at
which protein neither accept nor yield
proton) .
The Henderson hasselbalch equation for
acid is :-
pH = pKa + log [ Aˉ ]
[HA]
Here, pKa= -log(Ka)
where Ka is the acid dissociation constant,
that is pKa= -log [H3O+][A-]
[HA]
for the non-specific Brønsted acid-base
reaction:
A-
HA + H20 + H3O+
( Acid ) ( Conjugate
The Henderson Hasselbalch Equation for
base is :
pOH = pKb + log [ BH+ ]
[B]
where BH+ denotes the conjugate acid of
the corresponding base B.
B + H2O+ BH + OH-
(Base ) (Conjugate acid)
Histoy
- Lawrence Joseph Henderson wrote an
equation, in 1908, describing the use of
carbonic acid as a buffer solution.
- Karl Albert Hasselbalch later re-expressed
that formula in logarithmic terms, resulting in
the Henderson–Hasselbalch equation.
- Hasselbalch was using the
formula to study metabolic
acidosis.
Henderson-Hasselbalch
Equation Derivation:
-According to the Brønsted-Lowry theory of
acids and bases, an acid (HA) is capable of
donating a proton (H+) and a base (B) is
capable of accepting a proton.
-After the acid (HA) has lost its proton,
it is said to exist as the conjugate base
(A-).
-Similarly, a protonated base is said to
exist as the conjugate acid (BH+).
The dissociation of an acid can be
described by an equilibrium expression:
HA + H20 H3O+ + A-
Consider the case of acetic acid
(CH3COOH) and acetate anion
(CH3COO-):
CH3COOH + H2O CH3COO- + H3O+
Acetate is the conjugate base of acetic acid.
Acetic acid and acetate are a conjugate
acid/base pair. We can describe this
relationship with an equilibrium constant:
Ka = [H3O+][A-]
[HA]
Taking the negative log of both sides of the
equation gives
-logKa = -log [H3O+][A-]
[HA]
or, -logKa = -log [H3O+] + (-log [A-] )
[HA]
By definition,
pKa = -logKa and pH = -log[H3O+],
so
pka=pH – log [A-]
[HA]
This equation can then be rearranged to
give the Henderson-Hasselbalch
equation:
pH = pKa + log [A-]
[HA]
= pKa + log [conjugate
base]
[acid]
Estimating blood
pH
A modified version of the Henderson–
Hasselbalch equation can be used to relate
the pH of blood to constituents of the
bicarbonate buffering system.
pH = pKaH2CO3 + log [HCO3
-]
[H2CO3]
, where:
-pKa H2CO3 is the acid dissociation constant of
carbonic
acid. It is equal to 6.1.
[HCO3
-] is the concentration of bicarbonate in the
blood
Limitation :
-The most significant is the assumption that
the concentration of the acid and its
conjugate base at equilibrium will remain the
same.
-This neglects the dissociation of the acid
and the hydrolysis of the base.
-The dissociation of water itself is neglected as
well.
-These approximations will fail when dealing
with: relatively strong acids or bases
dilute or very concentrated solutions (less
than 1mM or greater than1M),

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HENDERSON-HASSELBALCH EQUATION EXPLAINED

  • 1. HENDERSON HASSELBALCH EQUATION By Mrs Sanchita Choubey (M.Sc., PGDCR, Pursuing Ph. D) Assistant Professor of Microbiology Dr. D Y Patil Arts Commerce and Science College Pimpri, Pune
  • 2. The Henderson– Hasselbalch Equation Describes the derivation of pH as a measure of acidity in biological and chemical systems.  The equation is also useful for estimating the pH of a buffer solution. it is widely used to calculate the isoelectric point of proteins( point at which protein neither accept nor yield proton) .
  • 3. The Henderson hasselbalch equation for acid is :- pH = pKa + log [ Aˉ ] [HA] Here, pKa= -log(Ka) where Ka is the acid dissociation constant, that is pKa= -log [H3O+][A-] [HA] for the non-specific Brønsted acid-base reaction: A- HA + H20 + H3O+ ( Acid ) ( Conjugate
  • 4. The Henderson Hasselbalch Equation for base is : pOH = pKb + log [ BH+ ] [B] where BH+ denotes the conjugate acid of the corresponding base B. B + H2O+ BH + OH- (Base ) (Conjugate acid)
  • 5. Histoy - Lawrence Joseph Henderson wrote an equation, in 1908, describing the use of carbonic acid as a buffer solution. - Karl Albert Hasselbalch later re-expressed that formula in logarithmic terms, resulting in the Henderson–Hasselbalch equation. - Hasselbalch was using the formula to study metabolic acidosis.
  • 6. Henderson-Hasselbalch Equation Derivation: -According to the Brønsted-Lowry theory of acids and bases, an acid (HA) is capable of donating a proton (H+) and a base (B) is capable of accepting a proton. -After the acid (HA) has lost its proton, it is said to exist as the conjugate base (A-). -Similarly, a protonated base is said to exist as the conjugate acid (BH+).
  • 7. The dissociation of an acid can be described by an equilibrium expression: HA + H20 H3O+ + A- Consider the case of acetic acid (CH3COOH) and acetate anion (CH3COO-): CH3COOH + H2O CH3COO- + H3O+
  • 8. Acetate is the conjugate base of acetic acid. Acetic acid and acetate are a conjugate acid/base pair. We can describe this relationship with an equilibrium constant: Ka = [H3O+][A-] [HA] Taking the negative log of both sides of the equation gives -logKa = -log [H3O+][A-] [HA] or, -logKa = -log [H3O+] + (-log [A-] ) [HA]
  • 9. By definition, pKa = -logKa and pH = -log[H3O+], so pka=pH – log [A-] [HA] This equation can then be rearranged to give the Henderson-Hasselbalch equation: pH = pKa + log [A-] [HA] = pKa + log [conjugate base] [acid]
  • 10. Estimating blood pH A modified version of the Henderson– Hasselbalch equation can be used to relate the pH of blood to constituents of the bicarbonate buffering system. pH = pKaH2CO3 + log [HCO3 -] [H2CO3] , where: -pKa H2CO3 is the acid dissociation constant of carbonic acid. It is equal to 6.1. [HCO3 -] is the concentration of bicarbonate in the blood
  • 11. Limitation : -The most significant is the assumption that the concentration of the acid and its conjugate base at equilibrium will remain the same. -This neglects the dissociation of the acid and the hydrolysis of the base. -The dissociation of water itself is neglected as well. -These approximations will fail when dealing with: relatively strong acids or bases dilute or very concentrated solutions (less than 1mM or greater than1M),