LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Formation of 5α-sitostan-3-one, 5α-campestan-3-one and steroidal hydrocarbons in edible oils during catalytic hydrogenation.

Photo by taylorheeryphoto from unsplash

Targeted analysis confirmed the presence of new phytosterol degradation products in fully hydrogenated commercial samples. EI-MS, APCI-MS and 1D-NMR experiments let to the identification of 10 novel markers of catalytic… Click to show full abstract

Targeted analysis confirmed the presence of new phytosterol degradation products in fully hydrogenated commercial samples. EI-MS, APCI-MS and 1D-NMR experiments let to the identification of 10 novel markers of catalytic hydrogenation, among which 5α-sitostan-3-one, 5α-campestan-3-one, isomers of saturated and monounsaturated steroidal hydrocarbons were reported in edible oils for the first time. Examination of phytosterol degradation mechanism was done by catalytic transfer deuteration technique. Mitigation strategy of potentially detrimental compounds included optimization of processing parameters. The effect of catalyst dosage (≤ 0.1 % based on Ni basis) and temperature region (˂ 180 °C) were the most crucial factors in phytosterol degradation control.

Keywords: steroidal hydrocarbons; edible oils; campestan one; one campestan; sitostan one; catalytic hydrogenation

Journal Title: Journal of agricultural and food chemistry
Year Published: 2019

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.