Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 647-42-7, formula is C8H5F13O, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , HPLC of Formula: 647-42-7
Matsumoto, Takuya;Kannan, Eichi;Tomioka, Misato;Nishino, Takashi research published 《 Effects of the high side-chain densities of hydrophobic poly(substituted methylene)s on their surface free energies》, the research content is summarized as follows. All the carbon atoms in the main chains of poly(substituted methylene)s possess side chains. The densities and chem. structures of the side chains drastically change the polymers′ thermal, mech., and surface properties. Herein, we focused on the surface properties and structures of poly(substituted methylene)s with hydrophobic side chains of Et and perfluoroalkyl groups and evaluated the effects of their side-chain densities. The surface free energy of poly(substituted methylene) with Et groups, C1-PEA, was lower than that of poly(Et acrylate) because the high d. of the side chains in C1-PEA decreased its chain mobility, and the dispersion component of its surface free energy was also suppressed. The surface free energy of poly(substituted methylene) with perfluoroalkyl groups containing only six carbon atoms in each fluoroalkyl group, C1-PF, was less than 10 mJ/m2. In addition, the surface segregation of the perfluoroalkyl groups in the block-like copolymer and the greater hydrophobic properties of this polymer were observed compared to the corresponding random copolymer. The C1-PEA polymers showed dependence of their surface free energies and structures on their resp. preparation methods. Highly dense side chains facilitated the restriction of mol. chains and greater hydrophobic surface properties.
HPLC of Formula: 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