Synthetic Route of 24034-73-9, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 24034-73-9, name is (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.
Barman, Monica;Soren, Monika;Mishra, Chinmaya;Mitra, Adinpunya research published 《 Dehydrated jasmine flowers obtained through natural convective solar drying retain scent volatiles and phenolics – A prospective for added-value utility》, the research content is summarized as follows. Although season-specific, Jasminum spp. are cultivated com. for their sweet-scented flowers and their postharvest utility in various value-added products. However, to ensure year-round availability of quality floral biomass, jasmines are to be dehydrated and stored. In the present study, we attempted to dehydrate fresh jasmine flowers using a custom-made natural convective solar drying and compared the outcome with four widely used drying methods namely, sun drying, shade drying, oven drying and freeze drying. Subsequently, the retention capacities of scent volatiles and phenolics in dehydrated flowers of Jasminum auriculatum and J. sambac were compared. Total phenolic contents (TPC) were found to be high in both freeze dried and natural convective dried samples whereas the antioxidant capacity was high in natural convective dried samples. Phenolic acids viz. protocatechuic acid, vanillic acid, and caffeic acid were detected; these phenolic acids were shown to retain in higher amount in natural convective dried samples. Further, freeze and convective-dried flowers were also shown to retain maximum contents of scent volatiles. These observations suggest that custom-made low-cost natural convective solar dryer could be explored at large scale to obtain good quality dried flowers of Jasminum spp. for added-value utility.
24034-73-9, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.
Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, Synthetic Route of 24034-73-9
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts