Triphenylsulfonium Bromide

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Products Intro: Product Name:Triphenylsulfonium bromide
CAS:3353-89-7
Purity:99%
Company Name: Dayang Chem (Hangzhou) Co.,Ltd.
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Products Intro: Product Name:Triphenylsulfonium Bromide
CAS:3353-89-7
Purity:0.95&0.99 Package:0.1KG;1KG;1000KG Remarks:High quality
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Products Intro: Product Name:Triphenylsulfonium Bromide
CAS:3353-89-7
Purity:HPLC:>=99% Package:5KG;10KG;25KG Remarks:Photoelectric material
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Products Intro: Product Name:Triphenylsulfonium bromide
CAS:3353-89-7
Purity:NLT 98% Package:1G;1KG;100KG Remarks:AS109928
Company Name: Changzhou waston chemical technology Co.,Ltd
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Products Intro: Product Name:Triphenylsulfonium Bromide
CAS:3353-89-7
Purity:99% Package:1kg

Triphenylsulfonium Bromide manufacturers

  • Triphenylsulfonium Bromide
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  • $0.00 / 1kg
  • 2023-05-12
  • CAS:3353-89-7
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: according to customer's requirements
Triphenylsulfonium Bromide Basic information
Product Name:Triphenylsulfonium Bromide
Synonyms:TRIPHENYLSULFONIUM BROMIDE;Triphenyl sulphonium bromide;Triphenylsulfonium Bromid;riphenylsulfanium,bromide
CAS:3353-89-7
MF:C18H15BrS
MW:343.28
EINECS:
Product Categories:Iodonium Sulfonium & Oxonium Compounds;Sulfonium Compounds
Mol File:3353-89-7.mol
Triphenylsulfonium Bromide Structure
Triphenylsulfonium Bromide Chemical Properties
Melting point 293 °C
form powder to crystal
color White to Almost white
CAS DataBase Reference3353-89-7
Safety Information
HS Code 2930.90.2900
MSDS Information
Triphenylsulfonium Bromide Usage And Synthesis
UsesTriphenylsulfonium Bromide is used in the preparation of sulfonium salt photoacid generator for deep-UV microlithography.
PreparationTriphenylsulfonium bromide synthesis: A 3.0 M solution of phenylmagnesium bromide in diethyl ether (50 ml, 0.15 mole) was distilled under vacuum with slow heating from 20° to 80°C. Benzene (40 ml) was added, followed by n-heptane (300 ml). The resulting mixture was stirred and a solution of diphenylsulfoxide 10.1 g, (0.050 mol), in benzene (60 ml) was added during 1 hour at 80°C. The mixture was stirred for 3 hours and cooled to room temperature. An 25% aqueous hydrobromic acid solution (180 ml) was slowly added to the reaction mixture (exotherm-). The layers were separated and the organic layer was extracted twice with 5% aqueous hydrobromic acid (2 x 30 ml). The combined aqueous extracts were extracted three times with dichloromethane (3×250 ml). The dichloromethane extracts were dried over magnesium sulfate, filtered and the organic solvent evaporated to leave triphenylsulfonium bromide (10.2 g, 60%), which was crystallized from dichloromethane/diethyl ether. M.p. 285-7°C.
Triphenylsulfonium Bromide Preparation Products And Raw materials
Raw materialsPHENYLMAGNESIUM BROMIDE-->Diethyl ether-->Benzene-->Phenyl sulfoxide-->Heptane
Tag:Triphenylsulfonium Bromide(3353-89-7) Related Product Information
TRIPHENYLSILANETHIOL TRIPHENYLPHOSPHINEGOLD(I) TRIFLUOROMETHANESULFONATE Triphenylsulfonium nonaflate TRIPHENYLCARBENIUM TETRAFLUOROBORATE Triphenylsulfonium chloride Ethyltriphenylphosphonium bromide TRIMETHYLSULFONIUM HYDROXIDE Trimethylsulfonium bromide Triphenylsulfonium Bromide