ChemicalBook--->CAS DataBase List--->144317-44-2

144317-44-2

144317-44-2 Structure

144317-44-2 Structure
IdentificationBack Directory
[Name]

Triphenylsulfonium nonaflate
[CAS]

144317-44-2
[Synonyms]

TPS-PFBS
Triphenylsulfonium nonaflate
TRIPHENYLSULFONIUM PERFLUORO-1-
TRIPHENYLSULFONIUM PERFLUORO-1-BUTANESUL
Triphenylsulfonium perfluoro-1-butanesufonate
TriphenylsulfoniuM perfluoro-1-butanesufonate electronic grade, >=99%
Triphenyl sulfonium salt with 1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfonic acid(1:1)
[Molecular Formula]

C22H15F9O3S2
[MDL Number]

MFCD02683476
[MOL File]

144317-44-2.mol
[Molecular Weight]

562.47
Chemical PropertiesBack Directory
[Melting point ]

84-88 °C (lit.)
[solubility ]

PGMEA: ~50%
[InChI]

InChI=1S/C18H15S.C4HF9O3S/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;5-1(6,3(9,10)11)2(7,8)4(12,13)17(14,15)16/h1-15H;(H,14,15,16)/q+1;/p-1
[InChIKey]

VLLPVDKADBYKLM-UHFFFAOYSA-M
[SMILES]

[S+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(F)(F)(C(F)(F)S([O-])(=O)=O)C(F)(F)C(F)(F)F
[EPA Substance Registry System]

Sulfonium, triphenyl-, salt with 1,1,2,2,3,3,4,4,4-nonafluoro-1-butanesulfonic acid (1:1) (144317-44-2)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[REACH Registrations]

Active
[HS Code ]

2930909899
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

Cationic photoinitiator. Photoacid generator.
[Application]

Triphenylsulfonium nonaflate is used as a light stabilizer in polymers and films, due to its ability to absorb ultraviolet radiation.
[Synthesis]

Add a mixed compound solvent ethyl acetate and water solution into a 1L four-neck flask equipped with a stirring blade, condenser tube, and thermometer, and turn on the stirring. Add triphenylthiobromide to the system, slowly add sodium perfluorobutane sulfonate to the reaction system, and raise the temperature to 60°C. Incubate the reaction for 9 hours, monitor its progress, take samples to detect completion, and cool it to 0-5°C—centrifugation to obtain wet crude triphenyl sulfur perfluorobutane sulfonium salt. The crude product was recrystallized with a mixed solution of n-butanol and water under stirring at 85°C for 40min, and after cooling to 0-5°C, the obtained solid was dried below 80°C to obtain 150.32g of solid product. The product yield was 81.17%.Triphenylsulfonium nonaflate
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