Date published: 2025-9-18

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Tricarballylic acid (CAS 99-14-9)

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Alternate Names:
1,2,3-Propanetricarboxylic acid
CAS Number:
99-14-9
Purity:
≥97%
Molecular Weight:
176.12
Molecular Formula:
C6H8O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tricarballylic acid is frequently used in research related to biochemistry and environmental science, focusing on its chelating properties and biodegradability. This compound is of significant interest for its ability to bind metal ions, which is useful in studies of metal transport and removal from environments, as well as in the synthesis of biodegradable polymers. Researchers employ Tricarballylic acid to investigate its efficacy in sequestering harmful metals in contaminated soils and water systems. Additionally, it is explored for its role in the degradation pathways of citric acid cycle intermediates, providing insights into metabolic processes.


Tricarballylic acid (CAS 99-14-9) References

  1. Oligoacetic acid characterization by isocratic and linear salt gradient anion-exchange chromatography.  |  Li, H. and Patrickios, CS. 2001. J Chromatogr Sci. 39: 87-92. PMID: 11277257
  2. Combined synthetic/CD strategy for the stereochemical assignment of the tricarballylic acid side chains of fumonisin B(1).  |  Hartl, M. and Humpf, HU. 2001. J Org Chem. 66: 3678-81. PMID: 11374984
  3. Insertion of 2-carboxysuccinate and tricarballylic acid fragments into cyclic-pseudopeptides: new antagonists for the human tachykinin NK-2 receptor.  |  Harmat, NJ., et al. 2002. Bioorg Med Chem Lett. 12: 693-6. PMID: 11844703
  4. Functional characterization of CitM, the Mg2+-citrate transporter.  |  Li, H. and Pajor, AM. 2002. J Membr Biol. 185: 9-16. PMID: 11891560
  5. Synthesis, chemical speciation and SOD mimic assays of tricarballylic acid-copper(II) and imidazole-tricarballylic acid-copper(II) complexes.  |  Naso, L., et al. 2009. J Inorg Biochem. 103: 219-26. PMID: 19026447
  6. Citrate modulates lipopolysaccharide-induced monocyte inflammatory responses.  |  Ashbrook, MJ., et al. 2015. Clin Exp Immunol. 180: 520-30. PMID: 25619261
  7. Kinetics, Mechanism, and Secondary Organic Aerosol Yield of Aqueous Phase Photo-oxidation of α-Pinene Oxidation Products.  |  Aljawhary, D., et al. 2016. J Phys Chem A. 120: 1395-407. PMID: 26299576
  8. Metabolic fingerprints of human primary endothelial and fibroblast cells.  |  Žigon, P., et al. 2016. Metabolomics. 12: 92. PMID: 27330522
  9. Quantification of sugars and organic acids in tomato fruits.  |  Agius, C., et al. 2018. MethodsX. 5: 537-550. PMID: 30023316
  10. Conformation-Dependent Coordination of Carboxylic Acids with Fe3O4 Nanoparticles Studied by ATR-FTIR Spectral Deconvolution.  |  Zhang, X., et al. 2019. Langmuir. 35: 5770-5778. PMID: 30458104
  11. Nanostructured Chitosan-Based Biomaterials for Sustained and Colon-Specific Resveratrol Release.  |  Iglesias, N., et al. 2019. Int J Mol Sci. 20: PMID: 30669264
  12. Organic Surfactants Protect Dissolved Aerosol Components against Heterogeneous Oxidation.  |  Faust, JA. and Abbatt, JPD. 2019. J Phys Chem A. 123: 2114-2124. PMID: 30821460
  13. Artificial siderophores. 1. Synthesis and microbial iron transport capabilities.  |  Lee, BH., et al. 1985. J Med Chem. 28: 317-23. PMID: 3156248
  14. Uranyl Tricarballylate Triperiodic and Nanotubular Species. Counterion Control of Nanotube Diameter.  |  Thuéry, P., et al. 2020. Inorg Chem. 59: 6953-6962. PMID: 32352289
  15. Effect of tricarballylic acid, a nonmetabolizable rumen fermentation product of trans-aconitic acid, on Mg, Ca and Zn utilization of rats.  |  Schwartz, R., et al. 1988. J Nutr. 118: 183-8. PMID: 3339476

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tricarballylic acid, 25 g

sc-251302
25 g
$158.00

Tricarballylic acid, 100 g

sc-251302A
100 g
$465.00