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. , Application In Synthesis of 647-42-7
Shen, Yichao;Jin, Yong;Lai, Shuangquan;Shi, Liangjie;Zhou, Yutang;Zhou, Rong research published 《 Nonionic short-chain fluorinated surfactants in the fatliquoring of chrome-tanned goat skin》, the research content is summarized as follows. Surfactants as essential auxiliaries are used in almost all chem. processes in leather production In this work, a series of nonionic short-chain fluorinated surfactants (Fn-Fn, where n = 2, 4, or 6) were successfully prepared and used as fatliquoring auxiliaries in the fatliquoring process of chrome-tanned goat skin. The chem. structure of these nonionic short-chain fluorinated surfactants was characterized by FTIR and the mol. weight was determined by GPC. The surface tension measurement results revealed that these three fluorinated surfactants showed excellent surface activities. The effect of type and dosage of Fn-Fn as well as fatliquoring temperature on fatliquoring properties of chrome-tanned goat skin were estimated by the softness and phys. mech. properties characteristic of resultant leather. The results revealed that the leather treated with 1 wt% F4-F4 at the fatliquoring temperature of 40°C showed the best overall performance, whose softness and phys. mech. properties were improved significantly. Moreover, the collagen fiber morphol. and waterproof performance of leather treated with Fn-Fn were also investigated which showed that the addition of Fn-Fn in the fatliquoring process could promote the loosening of collagen fibers while effectively enhancing the water repellency of the leather surface. Therefore, such types of nonionic short-chain fluorinated surfactants are promising to be as desired fatliquoring auxiliaries in the leather industry.
Application In Synthesis 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