Date published: 2026-4-29

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Xanthene-9-carboxylic acid (CAS 82-07-5)

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CAS Number:
82-07-5
Molecular Weight:
226.23
Molecular Formula:
C14H10O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Xanthene-9-carboxylic acid is a compound that functions as a fluorescent dye in various experimental applications. It is used as a fluorescent label for biomolecules, allowing for the visualization and tracking of specific cellular or molecular components. Xanthene-9-Carboxylic Acid interacts with target molecules, emitting fluorescence upon excitation by a specific wavelength of light. Its mechanism of action involves binding to specific cellular or molecular targets, leading to the emission of light at a longer wavelength. This property may be a useful for studying biological processes, such as protein-protein interactions, cellular localization, and gene expression. Xanthene-9-carboxylic acid labels and visualizes various biomolecules.


Xanthene-9-carboxylic acid (CAS 82-07-5) References

  1. The effects of alkyl substitution in drugs. III. The spasmolytic activity of alkyl-substituted xanthene-9-carboxylic esters.  |  GOOTJES, J., et al. 1961. J Med Pharm Chem. 3: 157-65. PMID: 13900363
  2. Precision improvement for the analysis of flavonoids in selected Thai plants by capillary zone electrophoresis.  |  Suntornsuk, L. and Anurukvorakun, O. 2005. Electrophoresis. 26: 648-60. PMID: 15690438
  3. Reversal of chloroquine resistance in Plasmodium falciparum by 9H-xanthene derivatives.  |  Wu, CP., et al. 2005. Int J Antimicrob Agents. 26: 170-5. PMID: 16009536
  4. Synthesis, crystal structures, and photophysical properties of homodinuclear lanthanide xanthene-9-carboxylates.  |  Shyni, R., et al. 2007. Inorg Chem. 46: 11025-30. PMID: 18044953
  5. [Morphoregulatory effects of xanthene derivatives].  |  Buchenauer, H. and Grossmann, F. 1970. Planta. 93: 86-8. PMID: 24496665
  6. A highly sensitive HPLC method for the assay of propantheline used to measure its uptake by rat intestinal brush border membrane vesicles.  |  Saitoh, H., et al. 1987. J Pharm Pharmacol. 39: 9-12. PMID: 2880994
  7. Binding of organic cations to brush border membrane from rat small intestine.  |  Saitoh, H., et al. 1988. J Pharm Pharmacol. 40: 776-80. PMID: 2907557
  8. The identification of an ammonolysis product of pro-banthine.  |  Brown, C., et al. 1972. J Forensic Sci Soc. 12: 375-8. PMID: 5070858
  9. A new method for assaying propantheline and its degradation product, xanthene-9-carboxylic acid using high-performance liquid chromatography.  |  Charles, BG. and Ravenscroft, PJ. 1983. J Pharm Sci. 72: 96-8. PMID: 6827471
  10. Alkali Metal Cation Control of Oxidation Reactions of Radicals in Zeolites  |  Frances L. Cozens, Maria Luz Cano, Hermenegildo García, and Norman P. Schepp. 1998,. J. Am. Chem. Soc. 120, 23,: 5667–5673.
  11. Synthesis, Crystal Structure, and Magnetic Properties of One Copper(II) Complex Based on Mixed Xanthene-9-carboxylate and 2,2′-Bipyridine Ligands  |  Chun-Sen Liu, et al. 2010 -. Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry. Volume 40, Issue 8: Pages 503-509.
  12. One catalyst for both enantiomers: uncovering the inversion of enantioselectivity in cinchona-mediated desymmetrization of glutaric meso-anhydrides  |  T Ivšić, J Novak, N Došlić, Z Hameršak - Tetrahedron, 2012 - Elsevier. 30 September 2012,. Tetrahedron. Volume 68, Issue 39,: Pages 8311-8317.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Xanthene-9-carboxylic acid, 5 g

sc-224373
5 g
$31.00