1H,1H,2H,2H-Tridecafluoro-1-n-octanol

CAS: 647-42-7

Ref. 3D-FT60466

Product Information

• Name: 1H,1H,2H,2H-Tridecafluoro-1-n-octanol
• Synonyms: 2-(Perfluorohexyl)ethanol, 1,1,2,2-Tetrahydroperfluorooctan-1-ol, 1,1,2,2-Tetrahydroperfluorooctanol, 1,1,2,2-Tetrahydrotridecafluorooctanol, 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, 1H,1H,2H,2H-Perfluoro-1-octanol, 1H,1H,2H,2H-Perfluorooctan-1-ol, 1H,1H,2H,2H-Perfluorooctanol, 1H,1H,2H,2H-Tetrahydroperfluoro-1-octanol, 1H,1H,2H,2H-Tridecafluoro-1-octanol, 1H,1H,2H,2H-Tridecafluoro-n-octanol, 1H,1H,2H,2H-Tridecafluorooctanol, 2-(Perfluorohexyl)Ethyl Alcohol, 2-(Tridecafluorohexyl)ethanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluoro-1-octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctanol, 6:2 Fluorotelomer alcohol, 6:2 Ftoh, A 1620, Capstone 62AL, Capstone AL 62, Cheminox FA 6, Fluowet EA 600, Foralkyl EOH 6, H 829808, Perfluorohexylethanol, S 104, S 104 (fluorocompound), Teoh 6

Description

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.

• Brand: Biosynth

Chemical properties

• Molecular weight: 364.1 g/mol
• Formula: C₈H₅F₁₃O
• Purity: Min. 95%
• InChI: InChI=1S/C8H5F13O/c9-3(10,1-2-22)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21/h22H,1-2H2
• InChI key: InChIKey=GRJRKPMIRMSBNK-UHFFFAOYSA-N
• SMILES: OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F