Catalytic conversion of citronellal to citronellol over skeletal Ni catalyst was written by Sudiyarmanto, S.;Adilina, I. B.;Aditya, R. R.;Sukandar, D.;Tursiloadi, S.. And the article was included in Journal of Physics: Conference Series in 2020.Recommanded Product: 106-21-8 The following contents are mentioned in the article:
Catalytic conversion of citronellal to citronellol was performed via hydrogenation over skeletal Ni catalyst. The reaction parameters applied include variation of reactant-catalyst ratio, reaction temperature, pressure, and time. Citronellal 78% obtained from the fractionation of citronella oil was used as the reactant. The reaction was carried out using reactant-catalyst ratio of 1:5% and 1:10% at temperatures of 100°C, 150°C and 200°C and pressure of 10 bar, 15 bar and 20 bar for 1 and 3 h. Results show that the optimum reaction condition was at 100°C with reactant-catalyst ratio of 1:10% under pressure of 20 bar for 1 h giving 100% conversion of citronellal, 51.78% yield of citronellol and 40.39% selectivity. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Recommanded Product: 106-21-8).
3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 106-21-8
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts