Potassium 2-ethylhexanoate

Last updated
Potassium 2-ethylhexanoate
Potassium 2-ethylhexanoate Structure.svg
Names
IUPAC name
Potassium 2-ethylhexanoate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.019.660 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 221-625-7
PubChem CID
UNII
  • InChI=1S/C8H16O2.K/c1-3-5-6-7(4-2)8(9)10;/h7H,3-6H2,1-2H3,(H,9,10);/q;+1/p-1 Yes check.svgY
    Key: ZUFQCVZBBNZMKD-UHFFFAOYSA-M Yes check.svgY
  • InChI=1/C8H16O2.K/c1-3-5-6-7(4-2)8(9)10;/h7H,3-6H2,1-2H3,(H,9,10);/q;+1/p-1
    Key: ZUFQCVZBBNZMKD-REWHXWOFAE
  • [K+].[O-]C(=O)C(CC)CCCC
Properties
C8H15KO2
Molar mass 182.304 g·mol−1
Appearanceslightly yellow glassy solid
Hazards
GHS labelling:
GHS-pictogram-acid.svg GHS-pictogram-exclam.svg
Danger
H315, H318, H319
P264, P264+P265, P280, P302+P352, P305+P351+P338, P305+P354+P338, P317, P321, P332+P317, P337+P317, P362+P364
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Potassium 2-ethylhexanoate, also known as potassium iso-octanoate, is a chemical used to convert the tert-butylammmonium salt of clavulanic acid into potassium clavulanate (clavulanate potassium). [1] It is also used as a corrosion inhibitor in automotive antifreeze [ citation needed ] and as a catalyst for polyurethane systems. [2]

References

  1. "Potassium 2-ethylhexanoate, 99.9% (metals basis), 75% w/w soln., Thermo Scientific Chemicals". www.thermofisher.com. Retrieved 2025-05-23.
  2. "Potassium 2-ethylhexanoate". haz-map.com.