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. Synthetic Route of 647-42-7
Zhao, Nan;Zhao, Meirong;Liu, Weiping;Jin, Hangbiao research published 《 Atmospheric particulate represents a source of C8-C12 perfluoroalkyl carboxylates and 10:2 fluorotelomer alcohol in tree bark》, the research content is summarized as follows. In this study, we analyzed 30 legacy and emerging poly- and perfluoroalkyl substances (PFASs) in paired atm. particulate and bark samples collected around a Chinese fluorochem. manufacturing park (FMP), with the aim to explore the sources of PFASs in tree bark. The results showed that PFASs in atm. particulate and tree bark samples were consistently dominated by perfluorooctanoate (mean 73 ng/g; 44 pg/m3 ), perfluorohexanoate (47 ng/g; 36 pg/m3 ), perfluorononanoate (9.1 ng/g; 8.8 pg/m3 ), and 10:2 fluorotelomer alc. (10:2 FTOH; 5.6 ng/g; 12 pg/m3). Spatially, concentrations of C8-C12 perfluoroalkyl carboxylates (PFCAs) and 10:2 FTOH all showed a similar and exponentially decreased trend in both bark and atm. particulate samples with the increasing distance from the FMP. For the first time, we observed strongly significant (Spearmans correlation coefficient = 0.53-0.79, p < 0.01) correlations between bark and atm. particulate concentrations for C8-C12 PFCAs and 10:2 FTOH over 1-2 orders of magnitude, suggesting that the continues trapping of atm. particulates resulted in the accumulation of these compounds in bark. Overall, this study provides the first evidence that atm. particulate is an obvious source of C8-C12 PFCAs and 10:2 FTOH in tree bark. This result may further contribute to the application of tree bark as an indicator of certain PFASs in atm. particulate.
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., Synthetic Route of 647-42-7
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts