Ammonium picolinate

Last updated
Ammonium picolinate
Ammonium picolinate.svg
Names
IUPAC name
azanium;pyridine-2-carboxylate
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C6H5NO2.H3N/c8-6(9)5-3-1-2-4-7-5;/h1-4H,(H,8,9);1H3
    Key: DYVKGOVCCLREIY-UHFFFAOYSA-N
  • C1=CC=NC(=C1)C(=O)[O-].[NH4+]
Properties
C6H8N2O2
Molar mass 140.142 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ammonium picolinate is an organic chemical compound. This is an organic ammonium salt of picolinic acid with the chemical formula C6H8N2O2. [1] [2] [3]

Contents

Physical properties

Organic ammonium salts are generally water-soluble, though specific solubility data for ammonium picolinate are not explicitly documented.

Uses

As a chelating agent, the compound may stabilize metal complexes in catalytic or industrial processes. [4]

References

  1. ↑ Reiersølmoen, Ann Christin; Fiksdahl, Anne (2020). "Pyridine- and Quinoline-Based Gold(III) Complexes: Synthesis, Characterization, and Application". European Journal of Organic Chemistry . 2020 (19): 2867–2877. doi: 10.1002/ejoc.202000139 . ISSN   1099-0690 . Retrieved 29 March 2025.
  2. ↑ "EUROPEAN PATENT APPLICATION" (PDF). data.epo.org. p. 46. Retrieved 29 March 2025.
  3. ↑ Sendor, Dorota; Hilder, Matthias; Juestel, Thomas; Junk, Peter C.; Kynast, Ulrich H. (30 June 2003). "One dimensional energy transfer in lanthanoid picolinates. Correlation of structure and spectroscopy" . New Journal of Chemistry . 27 (7): 1070–1077. doi:10.1039/B302499G. ISSN   1369-9261 . Retrieved 29 March 2025.
  4. ↑ Trusovs, Sergejs (30 December 2003). "Method for preparation of metal organic acid chelates" . Retrieved 29 March 2025.
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