Shen, Yichao team published research in Journal of Molecular Liquids in 2019 | 647-42-7

Computed Properties 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.

Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 647-42-7, formula is C8H5F13O, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Computed Properties of 647-42-7

Shen, Yichao;Jin, Yong;Lai, Shuangquan;Shi, Liangjie;Du, Weining;Zhou, Rong research published 《 Synthesis, surface properties and cytotoxicity evaluation of nonionic urethane fluorinated surfactants with double short fluoroalkyl chains》, the research content is summarized as follows. Developing suitable alternatives to long fluoroalkyl chain surfactants has drawn considerable attention on account of the concerns over the environmental safety and human health. However, low surface activity, poor water solubility and complex preparation process of most currently reported alternatives restrict their widespread applications. Herein, a series of nonionic urethane fluorinated surfactants (FmEGnFm) were synthesized by one-pot method using poly (ethylene glycol) (PEG), isophorone diisocyanate (IPDI) and short chain fluorinated alc. as raw materials. The surfactant mol. is composed of two short fluoroalkyl chains connected to a PEG mol. via two IPDI spacers. Benefit from the special mol. structure design, these fluorinated surfactants displayed high surface activities, which could reduce the surface tensions of 17.8-28.7 mN/m and had low critical micelle concentrations of 0.17-0.98 mmol/L. These fluorinated surfactants showed good salt and pH resistance. Furthermore, contact angle and emulsifying experiments demonstrated that these fluorinated surfactants possessed excellent wetting and emulsifying properties at an extremely low concentration of 0.1 wt%. More importantly, the cytotoxicity experiment verified that these fluorinated surfactants had no obvious cytotoxicity. The ideal properties coupled with a simple and green preparation process make this strategy a new avenue to fabricate sustainable alternatives to long fluoroalkyl chain surfactants.

Computed Properties 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