|
| PERFLUOROHEXANE Basic information |
Product Name: | PERFLUOROHEXANE | Synonyms: | Perfluorohexane Mixed isomers;Perfluorohexanes, 98+%;3M FC-72 Fluorinet, PF-5060 3M;Perfluoro-compound FC-72(TM);Perfluorohexane ,99%;Perfluoro-compound FC-72§3;Tetradecafluorohexane A Mixture of perfluorinated hexanes, 95%;Perfluoro-coMpound FC-72100GR | CAS: | 355-42-0 | MF: | C6F14 | MW: | 338.04 | EINECS: | 206-585-0 | Product Categories: | organofluorine compounds;refrigerants | Mol File: | 355-42-0.mol | |
| PERFLUOROHEXANE Chemical Properties |
Melting point | −4 °C(lit.) | Boiling point | 58-60 °C(lit.) | density | 1.669 g/mL at 25 °C(lit.) | vapor pressure | 26.5kPa at 25℃ | refractive index | n20/D 1.252(lit.) | Fp | 56-60°C | form | Liquid | Specific Gravity | 1.699 | color | Clear colorless | Water Solubility | Immiscible with water. | Merck | 14,7157 | BRN | 1802113 | Stability: | Stable. Incompatible with strong oxidizing agents. | InChIKey | ZJIJAJXFLBMLCK-UHFFFAOYSA-N | LogP | 4.5 at 20℃ and pH7 | CAS DataBase Reference | 355-42-0(CAS DataBase Reference) | EPA Substance Registry System | Perfluorohexane (355-42-0) |
| PERFLUOROHEXANE Usage And Synthesis |
Chemical Properties | colourless liquid | Uses | Tetradecafluorohexane has been used:
- as a fluorocarbon organic solvent in the preparation of temperature-induced phase-separation solution
- to investigate boiling heat transfer mechanisms
- as a photosensitizer in fluorous biphasic singlet oxygenation
- as a novel reaction medium for photooxidation reactions
| Uses | In the electronics industry as a coolant and test bath medium. Non-toxic, non-ozone-depleting, inert reaction medium. | Uses | Perfluorohexanes is used as a coolant, photosensitizer in fluorous biphasic singlet oxygenation and an inert reaction medium. It is used in the electronic cooling liquid and insulator. It plays a vital role as a reaction medium, especially for photooxidation reactions. Further, it finds application as an ultrasound contrast agent. | Definition | ChEBI: Perfluorohexane is a fluoroalkane that is hexane in which all of the hydrogens have been replaced by fluorines. It has a role as a radioopaque medium and a non-polar solvent. It is a fluorocarbon, a fluoroalkane and a volatile organic compound. It derives from a hydride of a hexane. | Application | Perfluorohexane uses and applications include: dispersant for lubricants, mold release agents, protective coatings; reaction media for polymerizations, purification, separation processes; solvent for removal of halogenated lubricants, oils, greases; carrier for halogenated material; for quick-cooling or freezing foods; heat-transfer fluid.
Because it is biologically inert and chemically stable, perfluorohexane has attracted attention in medicine. Like other fluorocarbons, perfluorohexane dissolves gases, including oxygen from the air, to a higher concentration than ordinary organic solvents. This effect is attributed to the weak intermolecular forces between perfluorohexane molecules, which allows "space" for gas molecules to partition into the liquid. Animals can be submerged in a bath of perfluorohexane without drowning, as there is sufficient oxygen available in the solvent to allow respiration to continue. This effect has led to the experimental use of perfluorohexane in treating burn victims, as their lungs can be filled with either perfluorohexane vapor or in extreme cases liquid perfluorohexane, allowing breathing to continue without the problems normally seen with pulmonary edema that sometimes occur when the inside of the lungs have been burnt e.g. by inhalation of hot smoke.
| General Description | Tetradecafluorohexane in the gas phase reacts spontaneously with lithium amalgam, to give a solid and intimate mixture of lithium fluoride and elemental polymeric carbon with a small amount of superstoichiometric lithium. | Purification Methods | Purify the fluorohexane by fractional freezing. The methods described for perfluoroheptane should be applicable here. [Beilstein 1 IV 348.] |
| PERFLUOROHEXANE Preparation Products And Raw materials |
Raw materials | 1,1,1,2,2,3,4,4,5,5,5-undecafluoro-3-(trifluoromethyl)pentane-->PERFLUORO-2-METHYLPENTANE-->PERFLUORO(METHYLCYCLOPENTANE)-->3-METHYLPENTANE-->Methylcyclopentane-->Hexane |
|