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ChemicalBook--->CAS DataBase List--->15599-91-4

15599-91-4

15599-91-4 Structure

15599-91-4 Structure
IdentificationBack Directory
[Name]

HEXAFLUOROCYCLOTRIPHOSPHAZENE
[CAS]

15599-91-4
[Synonyms]

AURORA KA-1097
HEXAFLUOROCYCLOTRIPH
HEXAFLUOROCYCLOTRIPHO
Phosphonitrilefluoridetrimer
HEXAFLUOROCYCLOTRIPHOSPHAZENE
PHOSPHONITRILIC FLUORIDE TRIMER
Hexafluorocyclotriphosphazene>
tris(phosphorusnitridedifluoride)
1,3,5,2,4,6-Triazatriphosphorine, hexafluoro-
1,3,5-TRIAZA-2,4,6-TRIPHOSPHORIN-2,2,4,4,6,6-HEXAFLUORIDE
1,2,3,4,4,6-hexafluoro-1,2,3,6-tetrahydro-1,3,5,2,4,6-triazatriphosphinine
1,3,5,2,4,6-Triazatriphosphorine, 2,2,4,4,6,6-hexafluoro-2,2,4,4,6,6,-hexahydro-
1,3,5-Triaza-2,4,6-triphosphorin-2,2,4,4,6,6-hexafluoride, Hexafluorocyclotriphosphazene
[Molecular Formula]

F6N3P3
[MDL Number]

MFCD00192400
[MOL File]

15599-91-4.mol
[Molecular Weight]

248.93
Chemical PropertiesBack Directory
[Melting point ]

25-30 °C(lit.)
[Boiling point ]

50.9 °C(lit.)
[density ]

2.237 g/cm3 (20 ºC )
[refractive index ]

1.3183 (589.3 nm 32℃)
[storage temp. ]

2-8°C
[solubility ]

soluble in Toluene
[form ]

powder to lump
[pka]

-27.34±0.27(Predicted)
[color ]

White to Almost white
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

34
[Safety Statements ]

26-36/37/39-45
[RIDADR ]

UN 3260 8/PG 2
[WGK Germany ]

3
[F ]

10-21
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29319019
Hazard InformationBack Directory
[Uses]

Hexafluorocyclotriphosphazene is an intermediate for organic materials, which can be used as a raw material for the synthesis of other components or electronic materials, and can be used in the preparation of spiro ethers and flame retardant additives for lithium ion batteries.
[Synthesis]

Hexafluorocyclotriphosphazene is prepared by the reaction of potassium fluoride and 2,2,4,4,6,6-hexachloro-1,3,5-triaza-2,4,6-triphosphorine. The steps are as follows:
Put 104.3g of hexachlorocyclotriphosphazene, 113.3g of potassium fluoride, 0.011g of ionic liquid catalyst [Nbmm]OH, and 217.6g of anhydrous acetonitrile in an electric stirrer, thermometer, In the flask with reflux condenser, the reaction was carried out at 30°C, and the reaction was closed after 2h, filtered, The filtrate was rectified to obtain hexafluorocyclotriphosphazene with a yield of 98.7%.
Hexafluorocyclotriphosphazene synthesis
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