Name | 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-4-ene |
Synonyms | 2-Methylpent-2-ene, perfluoro- -Methylpent-2-ene, perfluoro- PERFLUORO-2-METHYL-2-PENTENE 98 Nonafluoro-2-(trifluoromethyl)pent-2-ene 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-4-ene 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-2-ene 2-Pentene, 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)- |
CAS | 1584-03-8 |
EINECS | 216-436-1 |
InChI | InChI=1/C6F12/c7-2(3(8,9)6(16,17)18)1(4(10,11)12)5(13,14)15 |
Molecular Formula | C6F12 |
Molar Mass | 300.05 |
Density | 1.622g/mLat 25°C(lit.) |
Melting Point | 48-50 °C |
Boling Point | 53-61°C(lit.) |
Flash Point | 10°F |
Water Solubility | insoluble |
Vapor Presure | 4.31 psi ( 20 °C) |
Appearance | Liquid |
Specific Gravity | 1.62 |
Color | Clear colorless to light yellow |
Storage Condition | Flammables area |
Refractive Index | ca. 1.3 |
MDL | MFCD00015724 |
Risk Codes | 11 - Highly Flammable |
Safety Description | S16 - Keep away from sources of ignition. S29 - Do not empty into drains. S33 - Take precautionary measures against static discharges. |
UN IDs | UN 1993 3/PG 2 |
WGK Germany | 3 |
HS Code | 29033990 |
Hazard Note | Irritant |
Hazard Class | 3 |
Packing Group | II |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Physical properties | Perfluoro-2-methyl-2-pentene is a perfluoroolefin compound with a boiling point of 50.5 ℃ and a colorless liquid at room temperature and pressure. |
Use | Perfluoro-2-methyl-2-pentene has two reactive active sites, fluorine atoms directly connected by carbon-carbon double bonds and carbon-carbon double bonds This feature makes perfluoro-2-methyl-2-pentene easy to be used as an intermediate to synthesize surfactants, fabric treatment agents or paper treatment agents, etc.; because it does not contain chlorine, it will not destroy the atmospheric ozone layer, and has a certain activity of the double bond to make its life in the atmosphere shorter than saturated perfluoroalkanes, in many ways can replace the fluorochloroalkanes (CFCs), so it can also be used in electronic components of refrigerants, fire extinguishing agents, foam foaming agents and heat transfer agents. |