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Perfluoro-2-methyl-2-pentene

Perfluoro-2-methyl-2-pentene Structure
CAS No.
1584-03-8
Chemical Name:
Perfluoro-2-methyl-2-pentene
Synonyms
-2-pentene), 97%;Hexafluoropropene dimer;Perfluoro-2-methyl-2-penten;Perfluoro-2-methyl-2-pentene;-Methylpent-2-ene, perfluoro-;2-Methylpent-2-ene, perfluoro-;Dodecafluoro-2-methyl-2-pentene;PERFLUORO-2-METHYL-2-PENTENE 98;Perfluoro(2-methylpent-2-ene)90%;2-(Trifluoromethyl)perfluoro-2-pentene
CBNumber:
CB9499175
Molecular Formula:
C6F12
Molecular Weight:
300.05
MOL File:
1584-03-8.mol
Modify Date:
2024/3/28 16:55:20

Perfluoro-2-methyl-2-pentene Properties

Melting point 48-50 °C
Boiling point 53-61 °C(lit.)
Density 1.622 g/mL at 25 °C(lit.)
vapor pressure 4.31 psi ( 20 °C)
Flash point 10 °F
refractive index ca. 1.3
storage temp. Flammables area
form Liquid
Specific Gravity 1.62
color Clear colorless to light yellow
Water Solubility insoluble
InChI InChI=1S/C6F12/c7-2(3(8,9)6(16,17)18)1(4(10,11)12)5(13,14)15
InChIKey FAEGGADNHFKDQX-UHFFFAOYSA-N
SMILES C(F)(F)(F)/C(/C(F)(F)F)=C(\F)/C(F)(F)C(F)(F)F
CAS DataBase Reference 1584-03-8(CAS DataBase Reference)
NIST Chemistry Reference Perfluoro-2-methyl-2-pentene(1584-03-8)
EPA Substance Registry System Perfluoro(2-methylpent-2-ene) (1584-03-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02
Signal word  Warning
Hazard statements  H225
Precautionary statements  P210-P240-P241-P280a-P303+P361+P353-P501a
Hazard Codes  F,Xi
Risk Statements  11
Safety Statements  16-29-33
RIDADR  UN 1993 3/PG 2
WGK Germany  3
Hazard Note  Irritant
HazardClass  3
PackingGroup  II
HS Code  29033990
NFPA 704
3
2 0

Perfluoro-2-methyl-2-pentene Chemical Properties,Uses,Production

Chemical Properties

clear colourless to light yellow liquid

Reactions

Perfluoro-2-methyl-2-pentene reacts withα-oxides in the presence of CsF, like perfluoro isobutylene. Olefins containing a perfluoro(dimethylpropyl)methyl group and cesium perfluoro-2-methyl-penten-3-olate are formed.
The reaction of this compound with epichlorohydrin in the presence of CSP results in the formation of trans-1,1,1,7,7,8,8,9,9,9-decafluoro-2,6,6-tris(trifluoromethyl)-4-nonene, 2-fluoro-2-pentafluoroethyl-3,3-bis(trifluoromethyl)-5-[α,α-(hydro-β,β-bis(trifluoromethyl)perfluoroamyl] tetrahydrofuran, and 2-H-perfluoro-2-methylpentane.
The hexafluoropropylene dimer perfluoro-2-methyl-2-pentene is partially converted under the action of CsF into the thermodynamically most stable hexafluoropropylene trimer perfluoro-2,4-dimiethyl-3-heptene[1].
It reacts with alcohols to give either fluorine substitution products or addition products, depending on the amount of essential catalyst used. Alcohols containing branched substituents give another product in addition to those derived from the substitution of a vinyl fluorine atom in perfluoro-2-methyl-2-pentene, namely isomeric vinyl ethers, which are derivatives of perfluoro-2-methyl-1-pentene[2].

References

[1] L. L. Gervits, I. L. Knunyants, K. N. Makarov. “Reaction of perfluoro-2-methyl-2-pentene and perfluoroisobutylene with α-oxides in the presence of cesium fluoride.” Russian Chemical Bulletin 30 5 (1981): 846–852.
[2] V. F. Snegirev, K. N. Makarov. “Reaction of perfluoro-2-methylpent-2-ene with oxygen nucleophiles.” Russian Chemical Bulletin 35 1 (1986): 91–103.

Perfluoro-2-methyl-2-pentene Preparation Products And Raw materials

Raw materials

Preparation Products

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PERFLUORO-2-METHYL-2-PENTENE 98 2-Methylpent-2-ene, perfluoro- 2-Pentene, 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)- -Methylpent-2-ene, perfluoro- 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-4-ene PERFLUORO(2-METHYL-2-PENTENE) TECH 90% Nonafluoro-2-(trifluoromethyl)pent-2-ene Perfluoro(2-methylpent-2-ene)90% 2-(Trifluoromethyl)perfluoro-2-pentene Dodecafluoro-2-methyl-2-pentene Hexafluoropropene dimer Perfluoro-2-methyl-2-pentene 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-2-ene -2-pentene), 97% Perfluoro-2-methyl-2-pentene ISO 9001:2015 REACH TIANFUCHEM-- 1584-03-8--High purity Perfluoro-2-methyl-2-pentene in stock Perfluoro-2-methyl-2-penten 1584-03-8 C2F5CFCCF32 CF32CCFCF2CF3