Chemical composition and biological potential of Thymus Willdenowii Boiss. & Reut. essential oil was written by Zeghib, Assia;Calliste, Claude-Alain;Simon, Alain;Charfeddine, Rim;Aouni, Mahjoub;Duroux, Jean-Luc;Kabouche, Ahmed;Kabouche, Zahia. And the article was included in Natural Product Research in 2021.COA of Formula: C10H20O2 The following contents are mentioned in the article:
The fresh aerial parts of Thymus willdenowii Boiss. & Reut. (syn. Thymus hirtus Willd.) were hydrodistd. in a Clevenger type apparatus and analyzed by GC and GC-MS. 44 Components were identified representing 97.3%, with 1,8-cineole (34.62%), camphor (18.55%), α-pinene (9.46%) and camphene (5.38%) as the main components. T. willdenowii essential oil was not cytotoxic (CC50 = 97.65μg/mL) towards Vero non-tumoral cells, exhibiting good antibacterial and antiproliferative (30.8 ± 3.1% inhibition) potentials against four tested pathogenic bacteria and Human colorectal cell line HT-29, resp. The essential oil did not show a DPPH radical scavenging activity, by ESR spectroscopy (ESR), and it lacks antiviral effect towards coxsackievirus B3. This study involved multiple reactions and reactants, such as Octyl acetate (cas: 112-14-1COA of Formula: C10H20O2).
Octyl acetate (cas: 112-14-1) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.COA of Formula: C10H20O2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics