Aroma stability and sensory aspects of commercially produced orange juice: gas chromatography-olfactometry study was written by Kopuncova, Maria;Sadecka, Jana;Kolek, Emil;Dimitrov, Filip;Tobolkova, Blanka;Durec, Jan;Blasko, Jaroslav. And the article was included in Chemical Papers in 2022.Synthetic Route of C10H20O2 The following contents are mentioned in the article:
The effects of pasteurization and 4-mo storage on the aroma profile of orange juices with pulp that were fully processed and packed in inert nitrogen atm. were investigated within the span of 2 years (2018 and 2019). Headspace solid-phase microextraction, gas chromatog.-mass spectrometry, as well as gas chromatog. coupled to flame ionization detection and olfactometry, were used for extraction, and subsequent anal. of the odor-active volatiles. Observed changes in their odor intensity, including the formation of some off-flavors such as methional, furaneol, 4-vinylguaiacol and guaiacol, were not significant to that extent to lead to an evident worsening in the overall flavor of juices. Thus, the use of nitrogen atm. proved its ability to protect the organoleptic quality of juice from undesirable changes caused by oxidative load or acid-catalyzed reactions. Aroma profiles of fresh juices were considerably influenced by diverse climatic conditions, and different seasons of orange harvest in monitored years. Pasteurization and storage had lesser impact on the volatiles in 2018 as in 2019, probably due to the inter-annual variability in such parameters of juices as content of pulp and pH. This study involved multiple reactions and reactants, such as Octyl acetate (cas: 112-14-1Synthetic Route of C10H20O2).
Octyl acetate (cas: 112-14-1) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Synthetic Route of C10H20O2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics