Ethanesulfonic acid

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Ethanesulfonic acid
Ethanesulfonic acid 2D Ethanesulfonic-acid-2D-flat.png
Ethanesulfonic acid 2D
Ethanesulfonic acid 3D Ethanesulfonic-acid-3D-balls.png
Ethanesulfonic acid 3D
Ethanesulfonic acid 3D bonds Ethanesulfonic-acid-3D-vdW.png
Ethanesulfonic acid 3D bonds
Names
Preferred IUPAC name
Ethanesulfonic acid
Other names
Esylic acid, ethylsulfonic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.008.950 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 209-843-0
PubChem CID
UNII
  • InChI=1S/C2H6O3S/c1-2-6(3,4)5/h2H2,1H3,(H,3,4,5)
  • InChI=1S/C2H6O3S/c1-2-6(3,4)5/h2H2,1H3,(H,3,4,5)
    Key: CCIVGXIOQKPBKL-UHFFFAOYSA-N
  • CCS(O)(=O)=O
Properties
C2H6O3S
Molar mass 110.13 g/mol
AppearanceColorless liquid
Density 1.35 g/mL
Melting point −17 °C (1 °F; 256 K)
Boiling point 122–123 °C (252–253 °F; 395–396 K) at 0.01 mmHg
Soluble
log P −0.37
Acidity (pKa)−1.68 [1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Ethanesulfonic acid (esylic acid) is a sulfonic acid with the chemical formula CH3CH2SO3H. The conjugate base is known as ethanesulfonate or, when used in pharmaceutical formulations, as esilate. It is a colorless liquid. [2]

References

  1. YK Ye & RW Stringham (2001-06-21). "Effect of mobile phase acidic additives on enantioselectivity for phenylalanine analogs". J Chromatogr A. 927 (1–2): 53–60. doi:10.1016/S0021-9673(01)01059-7. PMID   11572398.
  2. Kosswig K, ed. (2000). "Sulfonic Acids, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a25_503. ISBN   978-3-527-30673-2.