Acid dissociation constants (25 °C)

Stepwise pKa values of common weak acids and conjugate acids of weak bases — the table behind every acid–base calculation on this site.

41 rows
Nitric acidHNOX3\ce{HNO3}NOX3X−\ce{NO3-}1−1.40025.1
Sulfuric acidHX2SOX4\ce{H2SO4}HSOX4X−\ce{HSO4-}1——
Sulfuric acidHSOX4X−\ce{HSO4-}SOX4X2−\ce{SO4^2-}21.9900.0102
Acetic acidCHX3COOH\ce{CH3COOH}CHX3COOX−\ce{CH3COO-}14.7561.75 × 10⁻⁵
Formic acidHCOOH\ce{HCOOH}HCOOX−\ce{HCOO-}13.7451.80 × 10⁻⁴
Benzoic acidCX6HX5COOH\ce{C6H5COOH}CX6HX5COOX−\ce{C6H5COO-}14.2046.25 × 10⁻⁵
Chloroacetic acidClCHX2COOH\ce{ClCH2COOH}ClCHX2COOX−\ce{ClCH2COO-}12.8650.00136
Hydrofluoric acidHF\ce{HF}FX−\ce{F-}13.1706.76 × 10⁻⁴
Nitrous acidHNOX2\ce{HNO2}NOX2X−\ce{NO2-}13.1507.08 × 10⁻⁴
Hypochlorous acidHOCl\ce{HOCl}OClX−\ce{OCl-}17.5302.95 × 10⁻⁸
Hydrocyanic acidHCN\ce{HCN}CNX−\ce{CN-}19.2106.17 × 10⁻¹⁰
Boric acidB(OH)X3\ce{B(OH)3}B(OH)X4X−\ce{B(OH)4-}19.2375.79 × 10⁻¹⁰
PhenolCX6HX5OH\ce{C6H5OH}CX6HX5OX−\ce{C6H5O-}19.9971.01 × 10⁻¹⁰
Ammonium / ammoniaNHX4X+\ce{NH4+}NHX3\ce{NH3}19.2455.69 × 10⁻¹⁰
MethylamineCHX3NHX3X+\ce{CH3NH3+}CHX3NHX2\ce{CH3NH2}110.6452.26 × 10⁻¹¹
PyridineCX5HX5NHX+\ce{C5H5NH+}CX5HX5N\ce{C5H5N}15.2006.31 × 10⁻⁶
Tris bufferTrisHX+\ce{TrisH+}Tris\ce{Tris}18.0728.47 × 10⁻⁹
Phosphoric acidHX3POX4\ce{H3PO4}HX2POX4X−\ce{H2PO4-}12.1480.00711
Phosphoric acidHX2POX4X−\ce{H2PO4-}HPOX4X2−\ce{HPO4^2-}27.1986.34 × 10⁻⁸
Phosphoric acidHPOX4X2−\ce{HPO4^2-}POX4X3−\ce{PO4^3-}312.3754.22 × 10⁻¹³
Carbonic acidHX2COX3\ce{H2CO3}HCOX3X−\ce{HCO3-}16.3514.46 × 10⁻⁷
Carbonic acidHCOX3X−\ce{HCO3-}COX3X2−\ce{CO3^2-}210.3294.69 × 10⁻¹¹
Sulfurous acidHX2SOX3\ce{H2SO3}HSOX3X−\ce{HSO3-}11.8570.0139
Sulfurous acidHSOX3X−\ce{HSO3-}SOX3X2−\ce{SO3^2-}27.1726.73 × 10⁻⁸
Hydrogen sulfideHX2S\ce{H2S}HSX−\ce{HS-}17.0209.55 × 10⁻⁸
Hydrogen sulfideHSX−\ce{HS-}SX2−\ce{S^2-}214.0001.00 × 10⁻¹⁴
Oxalic acidHX2CX2OX4\ce{H2C2O4}HCX2OX4X−\ce{HC2O4-}11.2500.0562
Oxalic acidHCX2OX4X−\ce{HC2O4-}CX2OX4X2−\ce{C2O4^2-}24.2665.42 × 10⁻⁵
Phthalic acidHX2P\ce{H2P}HPX−\ce{HP-}12.9430.00114
Phthalic acidHPX−\ce{HP-}PX2−\ce{P^2-}25.4323.70 × 10⁻⁶
Citric acidHX3Cit\ce{H3Cit}HX2CitX−\ce{H2Cit-}13.1287.45 × 10⁻⁴
Citric acidHX2CitX−\ce{H2Cit-}HCitX2−\ce{HCit^2-}24.7611.73 × 10⁻⁵
Citric acidHCitX2−\ce{HCit^2-}CitX3−\ce{Cit^3-}36.3964.02 × 10⁻⁷
GlycineHX3NX+CHX2COOH\ce{H3N+CH2COOH}HX3NX+CHX2COOX−\ce{H3N+CH2COO-}12.3500.00447
GlycineHX3NX+CHX2COOX−\ce{H3N+CH2COO-}HX2NCHX2COOX−\ce{H2NCH2COO-}29.7781.67 × 10⁻¹⁰
EDTAHX6YX2+\ce{H6Y^2+}HX5YX+\ce{H5Y+}10.0001
EDTAHX5YX+\ce{H5Y+}HX4Y\ce{H4Y}21.5000.0316
EDTAHX4Y\ce{H4Y}HX3YX−\ce{H3Y-}32.0000.01
EDTAHX3YX−\ce{H3Y-}HX2YX2−\ce{H2Y^2-}42.6900.00204
EDTAHX2YX2−\ce{H2Y^2-}HYX3−\ce{HY^3-}56.1307.41 × 10⁻⁷
EDTAHYX3−\ce{HY^3-}YX4−\ce{Y^4-}610.3704.27 × 10⁻¹¹

Strong acids (HCl, HNO₃, the first step of H₂SO₄) ionize completely in water and are not listed. The pKa₂ of H₂S is poorly known; 14 is used here.

Sources

  1. D. C. Harris, Quantitative Chemical Analysis, 9th ed., W. H. Freeman (2016), Appendix G (thermodynamic constants, I → 0).
  2. W. M. Haynes (ed.), CRC Handbook of Chemistry and Physics, 97th ed. (2016), “Dissociation constants of inorganic and organic acids”.

Used in these lessons