Home Disinfecting activity of some diphenyltin(IV) benzoate derivative compounds
Article
Licensed
Unlicensed Requires Authentication

Disinfecting activity of some diphenyltin(IV) benzoate derivative compounds

  • Sutopo Hadi EMAIL logo , Tati Suhartati , Noviany Noviany , Kamisah D. Pandiangan , Yandri Yandri , Wasinton Simanjuntak and Junaidi Junaidi
Published/Copyright: March 17, 2022
Pure and Applied Chemistry
From the journal Pure and Applied Chemistry Volume 94 Issue 7

Abstract

Disinfecting activity test of four diphenyltin(IV) benzoate derivative compounds has been carried out. The four compounds investigated were diphenyltin (IV) di 4 aminobenzoate (DPDA) (2), diphenyltin (IV) di 4 chlorobenzoate (DPDC) (3), diphenyltin(IV) di-4-hydroxybenzoate (DPDH) (4), and diphenyltin(IV) di-4-nitrobenzoate (DPDN) (5), and they were prepared by reacting diphenyltin(IV) oxide (DPO) (1) with benzoic acid derivatives of 4-aminobenzoic acid (4-HABz), 4-chlorobenzoic acid (4-HCBz), 4-hydroxybenzoic acid (4-HHBz) and 4-nitrobenzoic acid (4-HNBz), respectively. The compounds were well characterized by 1H, 13C NMR, IR, UV spectroscopies, and their pieces were defined using microanalytical data. The disinfectant test was carried out on two bacteria, Gram-negative Salmonella sp., and Gram-positive Staphylococus aureus. The result showed that all of the compounds were active as a disinfectant (disinfecting agent) with a minimum inhibitory concentration of 5 × 10−4 M. Compound 5 was found to be most active compared to others which exhibited the ability to reduce the concentration of the S. aureus bacteria within 5 min.

Keywords: Chemistry and its applications; diphenyltin(IV) dibenzoate derivative; disinfecting activity; S. aureus ; Salmonella sp.; VCCA-2021

Article note:

A collection of invited papers based on presentations at the Virtual Conference on Chemistry and its Applications (VCCA-2021) held on-line, 9–13 August 2021.

Corresponding author: Sutopo Hadi, Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Lampung, Bandar Lampung 35145, Indonesia, E-mail:

Acknowledgments

We would like to thank some people who have to help us in the experimental part, including our students Anggit A. Putri, Dini Aulia, Ahmad Farisi, Olivia Margareta, and also Liza Aprilia and Tri Kiswantari for their help and for allowing us to use some spaces in the laboratory.

  1. Research funding: The authors’ gratitude to the Institute of Research and Community Services, Universitas Lampung as well as Directorate of Research and Community Services, The Ministry of Education, Cultural. Research and Technology, Indonesia that gave access to funding the assignment carried out through Penelitian Dasar (Basic Research Grant Scheme) 2021 with Agreement Numbers of 120/E4.1/AK.04.PT/2021 and 3972/UN26.21/PN/2021.

References

[1] M. Tariq, S. Ali, N. Muhammad, N. A. Shah, M. Sirajuddin, M. N. Thahir, N. Khalid, M. R. Khan. J. Coord. Chem. 67, 323 (2014).10.1080/00958972.2014.884217Search in Google Scholar

[2] M. Sirajuddin, S. Ali, V. McKee, M. Sohail, H. Pasha. Eur. J. Med. Chem. 84, 343 (2014).10.1016/j.ejmech.2014.07.028Search in Google Scholar PubMed

[3] M. Sirajuddin, S. Ali, M. N. Thahir. Inorg. Chim. Acta. 439, 145 (2016).10.1016/j.ica.2015.10.017Search in Google Scholar

[4] M. Tariq, N. Muhammad, M. Sirajuddin, S. Ali, N. A. Shah, N. Khalid, M. N. Thahir, M. R. Khan. J. Organomet. Chem. 723, 79 (2013).10.1016/j.jorganchem.2012.09.011Search in Google Scholar

[5] M. Sirajuddin, S. Ali, V. McKee, S. Zaib, J. Iqbal. RSC Adv. 4, 57505 (2014).10.1039/C4RA10487KSearch in Google Scholar

[6] M. Sirajuddin, V. McKee, M. Tariq, S. Ali. Eur. J. Med. Chem. 143, 1903 (2018).10.1016/j.ejmech.2017.11.001Search in Google Scholar PubMed

[7] A. C. T. Kuate, M. M. Naseer, M. Lutter, K. Jurckschat. Chem. Commun. 54, 739 (2018).10.1039/C7CC09263FSearch in Google Scholar

[8] V. Arens, M. M. Naseer, M. Lutter, L. Iovkova-Berends, K. Jurckschat. Eur. J. Inorg. Chem. 13, 1540 (2017).10.1002/ejic.201800054Search in Google Scholar

[9] A. Szorcsik, L. Nagy, K. Gadja-Schrantz, L. Pellerito, E. Nagy, E. T. Edelmann. J. Radioanal. Nucl. Chem. 252, 523 (2002).10.1023/A:1015802820423Search in Google Scholar

[10] S. Hadi, M. Rilyanti. Orient. J. Chem. 26, 775 (2010).10.1002/ejoc.201090009Search in Google Scholar

[11] S. Hadi, M. Rilyanti, Suharso. Indo. J. Chem. 12, 172 (2012).10.22146/ijc.21359Search in Google Scholar

[12] C. E. CarraherJr., M. R. Roner. J. Organomet. Chem. 751, 67 (2014).10.1016/j.jorganchem.2013.05.033Search in Google Scholar

[13] S. Hadi, E. Hermawati, Noviany, T. Suhartati, Yandri. Asian J. Microbiol. Biotech. Environ. Sci. 20, 113 (2018).Search in Google Scholar

[14] S. Samsuar, W. Simanjuntak, H. I. Qudus, Y. Yandri, H. Herasari, S. Hadi. J. Adv. Pharm. Edu. Res. 11(2), 17 (2021).10.51847/kaijZKAFCOSearch in Google Scholar

[15] S. Hadi, S. Samsuar, W. Simanjuntak, H. I. Qudus. ARPN J. Eng. Appl. Sci. 15, 1623 (2021).Search in Google Scholar

[16] S. Hadi, S. Lestari, T. Suhartati, H. I. Qudus, M. Rilyanti, D. Herasari, Y. Yandri. Pure Appl. Chem. 93(5), 623 (2021).10.1515/pac-2020-1103Search in Google Scholar

[17] C. Hansch, R. P. Verma. Eur. J. Med. Chem. 44, 260 (2009).10.1016/j.ejmech.2008.02.040Search in Google Scholar PubMed

[18] S. Hadi, Noviany, M. Rilyanti, Macedon. J. Chem. Chem. Eng. 37, 185 (2018).10.20450/mjcce.2018.1414Search in Google Scholar

[19] S. Hadi, M. D. Fenska, N. Noviany, H. Satria, W. Simanjuntak, M. M. Naseer. Main Group Met. Chem. 44, 256 (2021).10.1515/mgmc-2021-0028Search in Google Scholar

[20] R. Singh, P. Chaudary, N. K. Khausik. Rev. Inorg. Chem. 30, 275 (2010).10.1515/REVIC.2010.30.4.275Search in Google Scholar

[21] S. Hadi, H. Afriyani, W. D. Anggraini, H. I. Qudus, T. Suhartati. Asian J. Chem. 27, 1509 (2015).10.14233/ajchem.2015.18590Search in Google Scholar

[22] H. Kurniasih, M. Nurissalam, B. Iswantoro, H. Afriyani, H. I. Qudus, S. Hadi. Orient. J. Chem. 31, 2377 (2015).10.13005/ojc/310467Search in Google Scholar

[23] N. N. Hazani, Y. Mohd, S. A. I. S. M. Ghazali, Y. Farina, N. N. Dzulkifli. J. Electrochem. Sci. Technol. 10, 29 (2019).Search in Google Scholar

[24] P. Potter, A. G. Perry. Nursing Fundamental Textbook: Concepts, Processes and Practices, EGC, Jakarta, 4th ed. (2005) (in Indonesian).Search in Google Scholar

[25] C. Broker. Nursing Encyclopedia, EGC, Jakarta (2009) (in Indonesian).Search in Google Scholar

[26] V. D. Rosenthal, H. M. Al-Abdely, A. A. Elkholy, S. A. S. AlKhawaja, H. Leblebicioglu, Y. Mehta, V. Rai, N. V. Hung, S. S. Kanj, M. F. Salama, E. Salgado-Yepez, N. Elahi, R. M. Otero, A. Apisarnthanarak, B. M. De Carvalho, B. E. Ider, D. Fisher, M. C. S. G. Buenaflor, M. M. Petrov, A. M. Quesada-Mora, F. Zand, V. Gurskis, T. Anguseva, A. Ikram, D. A. de Moros, W. Duszynska, N. Mejia, F. G. Horhat, V. Belskiy, V. Mioljevic, G. Di Silvestre, K. Furova, G. Y. Ramos-Ortiz, M. O. G. Elanbya, H. I. Satari, U. Gupta, T. Dendane, L. Raka, H. Guanche-Garcell, B. Hu, D. Padgett, K. Jayatilleke, N. B. Jaballah, E. Apostolopoulou, W. E. P. Leon, A. Sepulveda-Chavez, H. M. Telechea, A. Trotte, C. Alvarez-Moreno, L. Kushner-Davalos. Am. J. Infect. Control 144, 1495 (2016).10.1016/j.ajic.2016.08.007Search in Google Scholar PubMed

[27] K. Plata, E. R. Adriana, G. Wegrzyn. Acta. Biochim. Pol. 56, 597 (2009).10.18388/abp.2009_2491Search in Google Scholar

[28] M. J. Pelczar, E. C. S. Chan. in Element of Microbiology, p. 698, Mc Graw Hill Book Company, Auckland (1981).Search in Google Scholar

[29] V. Lorian. Antibiotics in Laboratory Medical. Wiliam and Wilkins Co., Baltimore, London, pp. 1–22, 170–178, 511–512 (1980).Search in Google Scholar

[30] D. Amsterdam. in Antibiotics in Laboratory Medicine, p. 807, LWW Publisher, Philadelphia, 6th ed. (2014).Search in Google Scholar
Published Online: 2022-03-17
Published in Print: 2022-07-26

© 2022 IUPAC & De Gruyter. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. For more information, please visit: http://creativecommons.org/licenses/by-nc-nd/4.0/

Articles in the same Issue

  1. Frontmatter
  2. In this issue
  3. Editorial
  4. The virtual conference on chemistry and its applications, VCCA-2021, 9–13 August 2021
  5. Conference papers
  6. Hexabenzocoronene functionalized with antiaromatic S- and Se-core-modified porphyrins (isophlorins): comparison with the dyad with regular porphyrin
  7. Bonding analysis of the C2 precursor Me3E–C2–I(Ph)FBF3 (E = C, Si, Ge)
  8. Supporting the fight against the proliferation of chemical weapons through cheminformatics
  9. Disinfecting activity of some diphenyltin(IV) benzoate derivative compounds
  10. HCV genotype-specific drug discovery through structure-based virtual screening
  11. ExcelAutomat 1.4: generation of supporting information
  12. Use of Circular Dichroism in the characterization of the fusion protein SARS-CoV-2 S protein (RBD)-hFc
  13. Experimental determination of activation rate constant and equilibrium constant for bromo substituted succinimide initiators for an atom transfer radical polymerization process
  14. Degradation of o-, m-, p-cresol isomers using ozone in the presence of V2O5-supported Mn, Fe, and Ni catalysts
  15. The beginnings of chemistry: from ancient times until 1661
  16. Chemical substitution in processes for inherently safer design: pros and cons
  17. Experimental and theoretical study of the dye-sensitized solar cells using Hibiscus sabdariffa plant pigment coupled with polyaniline/graphite counter electrode
https://doi.org/10.1515/pac-2021-1106
Keywords for this article
Chemistry and its applications; diphenyltin(IV) dibenzoate derivative; disinfecting activity; S. aureus; Salmonella sp.; VCCA-2021

Articles in the same Issue

  1. Frontmatter
  2. In this issue
  3. Editorial
  4. The virtual conference on chemistry and its applications, VCCA-2021, 9–13 August 2021
  5. Conference papers
  6. Hexabenzocoronene functionalized with antiaromatic S- and Se-core-modified porphyrins (isophlorins): comparison with the dyad with regular porphyrin
  7. Bonding analysis of the C2 precursor Me3E–C2–I(Ph)FBF3 (E = C, Si, Ge)
  8. Supporting the fight against the proliferation of chemical weapons through cheminformatics
  9. Disinfecting activity of some diphenyltin(IV) benzoate derivative compounds
  10. HCV genotype-specific drug discovery through structure-based virtual screening
  11. ExcelAutomat 1.4: generation of supporting information
  12. Use of Circular Dichroism in the characterization of the fusion protein SARS-CoV-2 S protein (RBD)-hFc
  13. Experimental determination of activation rate constant and equilibrium constant for bromo substituted succinimide initiators for an atom transfer radical polymerization process
  14. Degradation of o-, m-, p-cresol isomers using ozone in the presence of V2O5-supported Mn, Fe, and Ni catalysts
  15. The beginnings of chemistry: from ancient times until 1661
  16. Chemical substitution in processes for inherently safer design: pros and cons
  17. Experimental and theoretical study of the dye-sensitized solar cells using Hibiscus sabdariffa plant pigment coupled with polyaniline/graphite counter electrode
Sign up now to receive a 20% welcome discount
Institutional Access
How does access work?
Have an idea on how to improve our website?
Please write us.
© 2025 De Gruyter Brill
Downloaded on 22.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/pac-2021-1106/html?lang=en
Scroll to top button