In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 647-42-7, formula is C8H5F13O, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Related Products of 647-42-7
Eid, Nadim;Ameduri, Bruno;Gimello, Olinda;Bonnet, Anthony;Devisme, Samuel research published 《 Vinylidene fluoride polymerization by metal-free selective activation of hydrogen peroxide: microstructure determination and mechanistic study》, the research content is summarized as follows. Hydrogen peroxide-initiated radical polymerization of vinylidene fluoride (VDF) at 130°C in di-Me carbonate is presented. Various reaction parameters such as the nature of the solvent, the nature and the amount of the additive, and the reaction temperature were optimized. Hydrogen peroxide was activated with azobisisobutyronitrile (AIBN), which was not able to initiate the radical polymerization of VDF but afforded hydroxyl radicals via selective homolytic cleavage of the O-O bond of H2O2. The reactivity of hydroxyl radicals with the different components of the medium was evaluated. The microstructure of the resulting PVDFs was determined by NMR spectroscopy and MALDI-TOF spectrometry. Seven different chain-ends were identified and could be well revealed from synthesized models: 60% were functional, e.g., carbonates, alcs., carboxylic acids and fluorinated olefins, whereas 40% were CF2H and CF2CH3 fluoroalkyls as the products of hydrogen transfer termination reactions. Finally, based on the collected exptl. data, a mechanistic pathway of the polymerization was proposed in order to explain the formation of such different functional and non-functional end-groups. In addition, the selectivity of the different radical additions onto VDF was studied and is discussed.
Related Products of 647-42-7, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-ol, also known as 1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol , is a useful research compound. Its molecular formula is C8H5F13O and its molecular weight is 364.1 g/mol. The purity is usually 95%.
1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol is a material used to improve nanotube composites. It is also used in the synthesis of a recyclable fluorous hydrazine carbothioate compound with NCS to catalyze the acetalization of aldehydes.
1H,1H,2H,2H-Tridecafluoro-1-n-octanol is a potent and selective halogenated hydrocarbon. It binds to DNA at the dinucleotide phosphate site, which is an important site for polymerase chain reaction (PCR) activation. 1HFN has been shown to be more effective than other halogenated hydrocarbons in vitro assays on rat liver microsomes. It has been used as an additive in wastewater treatment to remove organic contaminants and metal ions. In vivo studies have been carried out in CD-1 mice to determine the effects of 1HFN on the liver and kidneys; these studies showed no toxicological effects on these organs. 1HFN also has been shown to inhibit enzymes such as cytochrome P450 and monoamine oxidase B that are involved in drug metabolism and may lead to adverse reactions with drugs metabolized by these enzymes., 647-42-7.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts