Phytochemical study and structural determination of the isolated product of Ricinus communis (Euphorbiaceae)

  • Andrianarijaona Mamy Doctoral School of Geosciences, Physics, Environmental Chemistry and High-Pathogen Systems (GPCEHP), University of Toliara, Toliara, Madagascar.
  • Ralaivaon-dratsitonta Jumaël Edith Fabrice Doctoral School of Geosciences, Physics, Environmental Chemistry and High-Pathogen Systems (GPCEHP), University of Toliara, Toliara, Madagascar. , Androy Regional University Center (CURA), University of Toliara, Toliara, Madagascar.
  • Fatiany Pierre Ruphin Doctoral School of Geosciences, Physics, Environmental Chemistry and High-Pathogen Systems (GPCEHP), University of Toliara, Toliara, Madagascar.
  • Robijaona Rahelivololoniaina Baholy Polytechnic High School of Antananarivo, University of Antananarivo, Antananarivo, Madagascar. ,Doctoral School of Industrial, Agricultural and Food Process and Systems Engineering, University of Antananarivo, Antananarivo, Madagascar.
Keywords: Phytochemical, Ricinus communis, Chromatography, NMR Spectroscopy, Brassicosterol.

Abstract

A phytochemical and structural study of the leaves of Ricinus communis (castor bean plant) was conducted to identify and characterize its active compounds. The plant material, sourced from Madagascar, was subjected to sequential maceration with solvents of increasing polarity, yielding hexane, dichloromethane (DCM), and methanolic extracts. Phytochemical screening revealed the presence of polysaccharides as the most abundant components, with moderate amounts of steroids and low concentrations of alkaloids and saponins. The DCM extract was further purified using thin-layer chromatography and column chromatography, leading to the isolation of a pure compound. Structural elucidation was performed using mass spectrometry (EI-MS) and one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy, including 1H, 13C, and DEPT-135 experiments. The spectroscopic data established a molecular formula of C28H46O and a tetracyclic steroid structure with two degrees of unsaturation. A comparison of the obtained chemical shifts with those reported in the literature confirmed the compound's identity as Brassicosterol, a key phytosterol.

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Published
2025-09-02