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2,2-Bis(3,4-dimethylphenyl)hexafluoropropane

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2,2-Bis(3,4-dimethylphenyl)hexafluoropropane Basic information

Product Name:
2,2-Bis(3,4-dimethylphenyl)hexafluoropropane
Synonyms:
  • 4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one
  • 1,1’-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[3,4-dimethyl-benzen
  • 4-[1-(3,4-Dimethylphenyl)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]-1,2-dimethylbenzene
  • Benzene, 1,1'-[2,2,2-trifluoro-1-(trifluoromethyl)ethylidene]bis[3,4-dimethyl-
  • Hexafluoro-2,2-bis-(3,4-dimethylphenyl)-propane
  • BIS-X-AF
  • 2,2-BIS(3,4-DIMETHYLPHENYL)HEXAFLUOROPROPANE
  • 4,4'-(HEXAFLUOROISOPROPYLIDENE)DI-O-XYLENE
CAS:
65294-20-4
MF:
C19H18F6
MW:
360.34
EINECS:
265-687-3
Product Categories:
  • PI
Mol File:
65294-20-4.mol
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2,2-Bis(3,4-dimethylphenyl)hexafluoropropane Chemical Properties

Melting point:
76-78°C
Boiling point:
110-120°C 2mm
Density 
1.198±0.06 g/cm3(Predicted)
Flash point:
>110°C
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Almost white
InChI
InChI=1S/C19H18F6/c1-11-5-7-15(9-13(11)3)17(18(20,21)22,19(23,24)25)16-8-6-12(2)14(4)10-16/h5-10H,1-4H3
InChIKey
GLFKFHJEFMLTOB-UHFFFAOYSA-N
SMILES
C(C1=CC=C(C)C(C)=C1)(C1=CC=C(C)C(C)=C1)(C(F)(F)F)C(F)(F)F
CAS DataBase Reference
65294-20-4(CAS DataBase Reference)
NIST Chemistry Reference
2,2-Bis-(3,4-dimethylphenyl)-hexafluoropropane(65294-20-4)
EPA Substance Registry System
2,2-Bis(3,4-dixylyl)hexafluoro propane (65294-20-4)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
22-24/25
HazardClass 
IRRITANT
HS Code 
2903998090
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2,2-Bis(3,4-dimethylphenyl)hexafluoropropane Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

2,2-Bis(3,4-dimethylphenyl)hexafluoropropane can be used as a gas separation membrane due to its good separation performance and high plasticization resistance to carbon dioxide

Synthesis

95-47-6

684-16-2

65294-20-4

In a 2000 mL three-necked flask, 1000 g of tetrahydrofuran (THF), 424 g of o-xylene, and 60 g of p-toluenesulfonic acid (p-TsOH) were added, and the reaction temperature was controlled to be below 40°C. The reaction was carried out by a slow pass of 400 g of hexafluoroacetone gas. 400 g of hexafluoroacetone gas was slowly passed. After heating and refluxing the reaction for 12 hours, it was cooled to room temperature. The reaction mixture was washed with saturated sodium bicarbonate (NaHCO3) aqueous solution to pH 7-8. 500 g of toluene was added, partitioned and the organic phase was washed with deionized water. The washed organic phase was concentrated to give a solid crude product. The crude product was recrystallized by dissolving in 1200 g of ethanol. The wet product was dried under vacuum at 40 ℃ for 12 hours to obtain 670 g of white crystal product with 93.1% yield. The product was analyzed by gas chromatography (GC), and the purity was 99.6%, the content of single impurity was less than 0.1%, and the content of all metal ions was less than 1 ppm.

References

[1] Patent: CN108395363, 2018, A. Location in patent: Paragraph 0052-0054
[2] Journal of Fluorine Chemistry, 2003, vol. 123, # 2, p. 221 - 225

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