Fatty Acid Composition and Spectroscopic Analysis of Oil from Citrus Sinensis Seed

Authors

  • Ayotunde O. Babatolu

    Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria Department of Chemistry, University of Ilorin, Ilorin, Kwara State, Nigeria
    Author
  • Hammed O. Oloyede

    Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria
    Author
  • Ibrahim O. Oloruntele

    Department of Physical and Chemical Sciences, Federal University of Health Sciences, Ila-Orangun, Osun State, Nigeria
    Author
  • Justinah S. Amoko

    Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria
    Author
  • Tunde S. Ogungbemi

    Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria
    Author
  • Abidemi I. Demehin

    Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria
    Author

Keywords:

Citrus sinensis; Fatty acid composition; Physicochemical properties; Spectroscopic analysis.

Abstract

Oil from Citrus sinensis seeds was extracted via cold maceration using n-hexane after air-drying and pulverization, yielding 36.21% oil. The physicochemical properties of the oil were determined, giving an acid value of 7.55 mg KOH/g, saponification value of 193.58 mg KOH/g, and iodine value of 83.48 g I₂/100 g, indicating moderate unsaturation and suitability for industrial applications such as soap and cosmetic production. Gas Chromatography–Mass Spectrometry (GC–MS) analysis revealed that the oil is rich in unsaturated fatty acids (71.01%), with linoleic acid (35.43%) as the predominant component, followed by oleic acid (26.44%), while palmitic acid (20.90%) and stearic acid (5.10%) were the major saturated fatty acids. Fourier Transform Infrared (FT-IR) spectroscopy identified characteristic functional groups, including carbonyl (C=O), hydroxyl (O–H), and unsaturated (C=C) bonds, while UV–Visible spectroscopy showed absorption peaks at 290 nm and 370 nm corresponding to π–π* and n–π* transitions, respectively.

 

Author Biographies

  • Ibrahim O. Oloruntele, Department of Physical and Chemical Sciences, Federal University of Health Sciences, Ila-Orangun, Osun State, Nigeria

     

  • Tunde S. Ogungbemi, Department of Chemistry, Adeyemi Federal University of Education, Ondo, Ondo State, Nigeria

     

     

     

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Published

2026-04-20

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