cis-3,7-Dimethyl-2,6-octadien-1-ol (CAS 106-25-2)
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cis-3,7-Dimethyl-2,6-octadien-1-ol, also known as Nerol, a natural monoterpene alcohol, can be found in various essential oils and boasts a colorless, sweet-smelling liquid with a potent aroma. Although the precise mechanism of action of cis-3,7-Dimethyl-2,6-octadien-1-ol remains somewhat elusive, it is believed to engage with both cell membranes and the cytoplasm. Its interaction with cell membranes is thought to modify permeability, facilitating the passage of molecules. Concurrently, within the cytoplasm, cis-3,7-Dimethyl-2,6-octadien-1-ol is believed to affect biochemical properties. These intriguing characteristics make cis-3,7-Dimethyl-2,6-octadien-1-ol a compound of great interest for numerous applications in diverse fields.
cis-3,7-Dimethyl-2,6-octadien-1-ol (CAS 106-25-2) References
- Mechanism of inhibition of aldehyde dehydrogenase by citral, a retinoid antagonist. | Kikonyogo, A., et al. 1999. Eur J Biochem. 262: 704-12. PMID: 10411631
- Structural and kinetic studies of a novel nerol dehydrogenase from Persicaria minor, a nerol-specific enzyme for citral biosynthesis. | Tan, CS., et al. 2018. Plant Physiol Biochem. 123: 359-368. PMID: 29304481
- Genotoxicity induced by nerol, an essential oil present in citric plants using human peripheral blood mononuclear cells (PBMC) and HepG2/C3A cells as a model. | Silva, BO., et al. 2021. J Toxicol Environ Health A. 84: 518-528. PMID: 33761836
- Parameters affecting the synthesis of geranyl butyrate by esterase 30,000 from Mucor miehei | Maha Karra-Chaabouni, Sylviane Pulvin, Didier Touraud, Daniel Thomas. 1998. Journal of the American Oil Chemists' Society. 75: 1201-1206.
- Selective hydrogenation of citral over gold nanoparticles on alumina | C. Caballero a b, J. Valencia a, M. Barrera b, A. Gil c. 2010. Powder Technology. 203: 412-414.
- NMR Analysis of Hydroxyl-Terminated Polybutadiene End Groups and Reactivity Differences with Monoisocyanates | Timothy S. Haddad, Levi M. J. Moore, Josiah T. Reams, Michael D. Ford, Jacob C. Marcischak, Andrew J. Guenthner, Joseph M. Mabry, Kamran B. Ghiassi. 2018. 56: 2665-2671.
- Novel starch-g-copolymers obtained using acrylate monomers prepared from two geometric isomers of terpene alcohol | Marta Worzakowska. 2019. European Polymer Journal. 110: 265-275.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
cis-3,7-Dimethyl-2,6-octadien-1-ol, 5 ml | sc-234382 | 5 ml | $51.00 |