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Effect of Boric Acid on a-Hydroxy Acids Compounds in Thin Layer Chromatography

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style="font-size:.9rem">Effect of Boric Acid on a-Hydroxy Acids Compounds in Thin Layer Chromatography</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/search?q=Elham%20Moniri">Elham Moniri</a>, <a href="https://publications.waset.org/search?q=Homayon%20Ahmad%20Panahi"> Homayon Ahmad Panahi</a>, <a href="https://publications.waset.org/search?q=Ahmad%20Izadi"> Ahmad Izadi</a>, <a href="https://publications.waset.org/search?q=Mohamad%20Mehdi%20Parvin"> Mohamad Mehdi Parvin</a>, <a href="https://publications.waset.org/search?q=Atyeh%20Rahimi"> Atyeh Rahimi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this investigation Salicylic acid, Sulfosalicylic acid and Acetyl salicylic acid were chosen as a sample for thin layer chromatography (TLC) on silica gel plates. Bicarbonate buffer at different pH containing different amounts of boric acid was applied as mobile phase. Specific interaction of these substances with boric acid has effect on Rf in thin layer chromatography. Regular and similar trend was observed in variations of Rf for mentioned compounds in TLC by altering of percentages of boric acid in mobile phase in pH range of 8-10. Also effect of organic solvent, mixture of water/ organic solvent and organic solvent containing boric acid as mobile phase was studied. <iframe src="https://publications.waset.org/524.pdf" style="width:100%; height:400px;" frameborder="0"></iframe> <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/search?q=Thin%20layer%20chromatography%20%28TLC%29" title="Thin layer chromatography (TLC)">Thin layer chromatography (TLC)</a>, <a href="https://publications.waset.org/search?q=Aspirin" title=" Aspirin"> Aspirin</a>, <a href="https://publications.waset.org/search?q=Salicylic%20acid" title="Salicylic acid">Salicylic acid</a>, <a href="https://publications.waset.org/search?q=Sulfosalycylic%20acid" title=" Sulfosalycylic acid"> Sulfosalycylic acid</a>, <a href="https://publications.waset.org/search?q=Boric%20acid." title=" Boric acid."> Boric acid.</a> </p> <p class="card-text"><strong>Digital Object Identifier (DOI):</strong> <a href="https://doi.org/10.5281/zenodo.1328586" target="_blank">doi.org/10.5281/zenodo.1328586</a> </p> <a href="https://publications.waset.org/524/effect-of-boric-acid-on-a-hydroxy-acids-compounds-in-thin-layer-chromatography" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/524/apa" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">APA</a> <a href="https://publications.waset.org/524/bibtex" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">BibTeX</a> <a href="https://publications.waset.org/524/chicago" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">Chicago</a> <a href="https://publications.waset.org/524/endnote" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">EndNote</a> <a href="https://publications.waset.org/524/harvard" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">Harvard</a> <a href="https://publications.waset.org/524/json" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">JSON</a> <a href="https://publications.waset.org/524/mla" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">MLA</a> <a href="https://publications.waset.org/524/ris" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">RIS</a> <a href="https://publications.waset.org/524/xml" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">XML</a> <a href="https://publications.waset.org/524/iso690" target="_blank" rel="nofollow" class="btn btn-primary btn-sm">ISO 690</a> <a href="https://publications.waset.org/524.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">2326</span> </span> <p class="card-text"><strong>References:</strong></p> <br>[1] The Salt Collaborative Group. 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Philips and G. Welssmann. Pro. Natl. Acad. Sci. USA., vol. 95, pp. 14540-14545, 1998. <br>[10] P. Ricchi, S. Pignata, A. Dipoplo, A.M. Memoli, A. Apicellu, R. Zarrilli, and A.M. Acquaviva, Int. J. cancer, vol. 73, pp. 880-884, 1997. <br>[11] P. Ricchi, T. Dimatola, A. Ruggieog , D. Zanzi, A. Apicellu, A. Dipalma, M. Pensabene, S. Pignata, R. Zarrilli, and A.M. Acquaviva, Brj. Cancer, vol. 86, pp. 1501-1509, 2002. <br>[12] B. K. Low, M. E. Waltner-Low, A. J. Entingh, A. Chytil, M.E. Akre, P. Norgaard, and H.L. Moses, J. Biol. Chem., vol. 275, pp. 38261-38267, 2000. <br>[13] P. Ricchi, A.D. Palma, T.D. Matola, A. Apicella,, R. Fortuato, R. Zarrilli and A. M. Acquaviva, Mol. Pharmacol. vol. 64, pp. 407-414, 2003. <br>[14] J. Kochana, A. Zakrzewska, A. Parczewski, and J. Wilamowski, J. of Liq. Chro. & Relat. Tech., vol. 28, pp. 2875-2886, 2005. <br>[15] J. Kochana, A. Parczewski and J. Wilamowski, J. of Liq. Chro. & Relat. 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