Log in

Physicochemical and Toxicological Studies of the Polymorphic Modifications of the Rodenticidal Substance “Chlorophacinone”

  • BIOPHYSICAL CHEMISTRY AND PHYSICAL AND CHEMICAL BIOLOGY
  • Published:
Russian Journal of Physical Chemistry A Aims and scope Submit manuscript

Abstract

The results of studies of the polymorphism of the rodenticidal substance 2-[(4-chlorophenyl)phenylacetyl]-1H-indene-1,3(2H)-dione “chlorophacinone”, which has an anticoagulant mechanism of action, are presented. Methods for the synthesis of two new polymorphic forms (III and IV) have been established, for which data from physicochemical studies (IR, XRD) and information on the biological activity (toxicity) of polymorphs are given. Both forms crystallize in the monoclinic crystal system with space group P21/с and the following unit cell parameters: a = 16.698(1) Å, b = 5.632(1) Å, c = 20.253(2) Å, β = 109.65(1)° for III; and a = 9.853(1) Å, b = 9.041(1) Å, c = 20.474(1) Å, β = 97.322(3)° for IV. Polymorphic form IV with a toxicity parameter DL50 (gray rats) of 0.47 mg/kg has the highest biological activity versus 2.74 mg/kg for the less active form III. A method of identification of the most active form (IV) by IR spectroscopy was proposed.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.

REFERENCES

  1. The Market of Rodenticides in Russia, Vol. 1: Collection of Information, Normative and Methodological Materials, Ed. by V. K. Melkov, L. N. Rumyantseva, V. F. Kolkov, and V. L. Vorontsova (Proekt, Moscow, 2003) [in Russian].

    Google Scholar 

  2. V. A. Ryl’nikov, Dezinf. Delo, No. 2, 57 (2008).

  3. L. A. Nosikova and A. N. Kochetov, Pest-Menedzhm., No. 4, 42 (2015).

  4. V. Yu. Nazarov, A. M. Datskevich, and L. I. Kabai, Dezinf. Delo, No. 3, 26 (2011).

  5. A. N. Kochetov, L. G. Kuz’mina, and K. A. Shestakov, Dezinf. Delo, No. 2, 68 (2009).

  6. J. P. Saundrs, S. R. Heisey, A. D. Goldstone, and E. C. Bay, J. Agric. Food Chem. 3, 762 (1955).

    Article  Google Scholar 

  7. S. L. Shapiro, R. Geiger, and L. Freedman, Org. Chem. 25, 1860 (1960).

    Article  CAS  Google Scholar 

  8. M. Lund, J. Hygiene 69, 69 (1971).

    Article  CAS  Google Scholar 

  9. S. D. Karakotov, V. V. Shapilova, A. L. Chimishkyan, and L. Ya. Kozenasheva, Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol. 47 (8), 3 (2004).

    CAS  Google Scholar 

  10. S. D. Karakotov, Agro XXI, Nos. 1–3, 32 (2006).

  11. S. T. Konyukhov, Vopr. Med. Khim. 10, 192 (1964).

    CAS  Google Scholar 

  12. A. Dolmella, S. Gatto, E. Girardi, and G. Bandoli, J. Mol. Struct. 513, 177 (1999).

    Article  CAS  Google Scholar 

  13. Inventor’s Certificate No. 180177 S07 S49/665 (1966).

  14. Inventor’s Certificate No. 180178 S07 S49/665 (1966).

  15. US Patent No. 3153612 C1 514-681 (1964).

  16. RF Patent No. 2218322 C07 (2003).

  17. RF Patent No. 2224739 C07 (2004).

  18. RF Patent No. 2748131 C07 (2021).

  19. RF Patent No. 2748259 C07 (2021).

  20. G. M. Sheldrick, Acta Crystallogr., A 64, 112 (2008).

    Article  CAS  PubMed  Google Scholar 

  21. K. Brandenburg, DIAMOND, Release 2.1d (Crystal Impact GbR, Bonn, Germany, 2000).

    Google Scholar 

  22. V. B. Prozorovskii, Farmakol. Toksikol., No. 1, 115 (1962).

  23. K. K. Palkina and A. N. Kochetov, Russ. J. Inorg. Chem. 55, 889 (2010).

    Article  CAS  Google Scholar 

  24. A. N. Kochetov, L. Yu. Alikberova, E. V. Savinkina, and V. V. Kravchenko, Tonk. Khim. Tekhnol. 1 (1), 60 (2006).

    Google Scholar 

  25. B. K. Paul and N. Guchhait, Comput. Theor. Chem. 1012, 20 (2013).

    Article  CAS  Google Scholar 

  26. A. Ahmedova, G. Pavlović, D. Zhiryakova, et al., J. Mol. Struct. 981, 10 (2010).

    Article  CAS  Google Scholar 

  27. A. Ahmedova, P. Marinova, S. Ciattini, et al., Struct. Chem. 20, 101 (2009).

    Article  CAS  Google Scholar 

  28. S. Angelova, V. Enchev, K. Kostova, et al., J. Phys. Chem. A 111, 9901 (2007).

    Article  CAS  PubMed  Google Scholar 

  29. Y.-S. Chen, P.-Y. Kuo, T.-L. Shie, and D.-Y. Yang, Tetrahedron 62, 9410 (2006).

    Article  CAS  Google Scholar 

  30. V. V. Gromak, V. G. Avakyan, F. S. Pashkovskii, et al., J. Appl. Spectrosc. 70, 14 (2003).

    Article  CAS  Google Scholar 

  31. V. Enchev, S. Bakalova, G. Ivanova, and N. Stoyanov, Chem. Phys. Lett. 314, 234 (1999).

    Article  CAS  Google Scholar 

  32. M. J. Kurth, P. Bruins, and M. E. Mount, Tetrahedron Lett. 26, 4883 (1985).

    Article  CAS  Google Scholar 

  33. J. Song, M. Mishima, and Z. Rappoport, Org. Lett. 9, 4307 (2007).

    Article  CAS  PubMed  Google Scholar 

  34. M. Sigalov, N. G. Lemcoff, B. Shainyan, et al., Eur. J. Org. Chem. 14, 2800 (2010).

    Article  Google Scholar 

  35. K. Müller-Dethlefs and P. Hobza, Chem. Rev. 100, 143 (2000).

    Article  PubMed  Google Scholar 

  36. K. K. Palkina, A. N. Kochetov, E. V. Savinkina, and L. Yu. Alikberova, Russ. J. Inorg. Chem. 51, 1743 (2006).

    Article  Google Scholar 

  37. G. N. Zaeva, M. M. Mal’tseva, R. P. Rodionova, et al., RET-Info, No. 4, 8 (1998).

  38. G. N. Zaeva, M. M. Mal’tseva, O. I. Berezovskii, et al., Dezinf. Delo, No. 3, 58 (2004).

  39. G. H. Rady, Am.-Eur. J. Toxicol. Sci. 5, 7 (2013).

    CAS  Google Scholar 

  40. Handbuch gerichtliche Medizin, Band 2, Ed. by B. Madea and B. Brinkmann (Springer, Berlin, 2019).

    Google Scholar 

  41. T. M. Primus, D. A. Goldade, E. E. Petty, and J. J. Johnston, J. Chromatogr. Sci. 34, 389 (1996).

    Article  CAS  Google Scholar 

  42. L. A. Nosikova and A. N. Kochetov, Tonk. Khim. Tekhnol. 10 (6), 88 (2015).

    CAS  Google Scholar 

  43. L. A. Nosikova and A. N. Kochetov, Pest-Menedzhm., No. 4, 22 (2018).

  44. L. A. Nosikova and A. N. Kochetov, Pest-Menedzhm., No. 1, 36 (2019).

  45. L. A. Nosikova, A. N. Kochetov, and L. G. Kuz’mina, Agrokhimiya, No. 10, 89 (2020).

Download references

Funding

The X-ray diffraction studies were performed using the equipment purchased due to the grant of the Moscow University Development Program.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. N. Kochetov.

Ethics declarations

The authors declare that they have no conflicts of interest.

Additional information

Translated by L. Smolina

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kochetov, A.N., Nosikova, L.A., Kudryashova, Z.A. et al. Physicochemical and Toxicological Studies of the Polymorphic Modifications of the Rodenticidal Substance “Chlorophacinone”. Russ. J. Phys. Chem. 97, 1335–1343 (2023). https://doi.org/10.1134/S0036024423060109

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0036024423060109

Keywords:

Navigation