Year-end Sale % OFF 
Abstract
The formation of fluorescent substances through the reaction of degradation products of four geometrical isomers of methyl linoleate hydroperoxides with amylamine was studied. The 9-and 13-positional monohydroperoxide isomers having the cis-trans and trans-trans configurations were separated from autoxidized methyl linoleate by high performance liquid chromatography (HPLC) and their abilities to form fluorescent substances with amylamine in the presence of heme were compared. These four isomers produced the same fluorescent substances exhibiting excitation and emission maxima at 350 and 420 nm, respectively, and also showed the same abilities for fluorescence formation and the same elution profiles of fluorescent substances (FS-1 and FS-II) on HPLC. This study proved that all four geometrical isomers were involved in the production of fluorescent substances upon reaction with amino compounds.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
