Date published: 2025-12-8

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Silver carbonate (CAS 534-16-7)

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Alternate Names:
Disilver carbonate; Fetizon′s reagent
CAS Number:
534-16-7
Purity:
≥99% (metals basis)
Molecular Weight:
275.75
Molecular Formula:
CAg2O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Silver carbonate is a chemical compound that functions as a source of silver ions in various experimental applications. It is known for its ability to participate in reactions involving the transfer of electrons, particularly in organic synthesis and catalysis. At the molecular level, silver carbonate interacts with other compounds to facilitate the formation of new chemical bonds, enabling the creation of complex organic molecules. Its mechanism of action involves the coordination of silver ions with specific functional groups in organic substrates, leading to the activation of certain chemical reactions. Silver carbonate may contribute to the advancement of chemical synthesis and the exploration of new molecular structures.


Silver carbonate (CAS 534-16-7) References

  1. Silver carbonate staining reveals mitochondrial heterogeneity.  |  López-Cepero, JM. 2004. J Histochem Cytochem. 52: 211-6. PMID: 14729873
  2. Silver carbonate nanoparticles stabilised over alumina nanoneedles exhibiting potent antibacterial properties.  |  Buckley, JJ., et al. 2008. Chem Commun (Camb). 4013-5. PMID: 18758610
  3. Determination of silver carbonate in silver oxide(Ag2O) by infrared spectroscopy.  |  Keats, NG. and Scaife, PH. 1966. Talanta. 13: 156-8. PMID: 18959860
  4. A silver carbonate staining method for oligodendrocytes and microglia for routine use.  |  McCarter, JC. 1940. Am J Pathol. 16: 233-235.2. PMID: 19970498
  5. Use of silver carbonate in the Wittig reaction.  |  Jedinak, L., et al. 2013. J Org Chem. 78: 12224-8. PMID: 24251875
  6. Preparation of Silver Carbonate and its Application as Visible Light-driven Photocatalyst Without Sacrificial Reagent.  |  Jiang, W., et al. 2015. Photochem Photobiol. 91: 1315-23. PMID: 26174413
  7. Regioselective Radical Reaction of Monometallofullerene Y@C2v(9)-C82 With N-arylbenzamidine Mediated by Silver Carbonate.  |  Li, J., et al. 2020. Front Chem. 8: 593602. PMID: 33195099
  8. Silver-containing polysaccharide-based tricomponent antibacterial fibres for wound care applications.  |  Masood, R., et al. 2021. J Wound Care. 30: 81-88. PMID: 33439087
  9. Effects of Silver Carbonate and p-Nitrobenzoic Acid for Accelerating Palladium-Catalyzed Allylic C-H Acyloxylation.  |  Skhiri, A., et al. 2021. Org Lett. 23: 7044-7048. PMID: 34432479
  10. Crystal structure of silver carbonate iodide Ag10(CO3)3I4.  |  Suzuki, R., et al. 2021. Acta Crystallogr E Crystallogr Commun. 77: 734-738. PMID: 34513021
  11. Correction to 'Effects of Silver Carbonate and p-Nitrobenzoic Acid for Accelerating Palladium-Catalyzed Allylic C-H Acyloxylation'.  |  Skhiri, A., et al. 2021. Org Lett. 23: 9012. PMID: 34752119
  12. Access to Conjugated Enynes via Allenyl Silver Formation/Cyclization/Decarboxylation Reaction Catalyzed by Silver Carbonate(I).  |  Yu, B., et al. 2022. Org Lett. 24: 5721-5725. PMID: 35920719
  13. Microwaves applied to silver impregnations with ammoniacal silver carbonate.  |  Rugerio-Vargas, C., et al. 1994. Biotech Histochem. 69: 273-8. PMID: 7819422

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Silver carbonate, 5 g

sc-250979
5 g
$46.00

Silver carbonate, 25 g

sc-250979A
25 g
$133.00