ChemicalBook > Product Catalog > Catalyst and Auxiliary > Initiator > Bis(4-methylphenyl)iodonium hexafluorophosphate
Bis(4-methylphenyl)iodonium hexafluorophosphate
Bis(4-methylphenyl)iodonium hexafluorophosphate Basic information
- Product Name:
- Bis(4-methylphenyl)iodonium hexafluorophosphate
- Synonyms:
-
- iodonium bis(4-methylphenyl)hexafluorophosphate
- BIS(4-METHYLPHENYL)IODONIUM HEXAFLUOROPHOSPHATE
- bis(p-tolyl)iodonium hexafluorophosphate
- Bis (4-methylphenyl)-hexafluoro- phosphate-(1-)-iodonium
- IHT-PI 440
- Bis(4-methylphenyl)iodonium hexafluorophosphate 98%
- bis(4-methylphenyl)iodanium:hexafluorophosphate
- Iodonium,bis(4-methylphenyl)-, hexafluorophosphate(1-) (1:1)
- CAS:
- 60565-88-0
- MF:
- C14H14F6IP
- MW:
- 454.13
- EINECS:
- 262-301-5
- Mol File:
- 60565-88-0.mol
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Bis(4-methylphenyl)iodonium hexafluorophosphate Chemical Properties
- form
- solid
- BRN
- 3581445
- InChI
- InChI=1S/C14H14I.F6P/c1-11-3-7-13(8-4-11)15-14-9-5-12(2)6-10-14;1-7(2,3,4,5)6/h3-10H,1-2H3;/q+1;-1
- InChIKey
- LHLVGWWCRPPKBC-UHFFFAOYSA-N
- SMILES
- [P-](F)(F)(F)(F)(F)F.[I+](C1C=CC(=CC=1)C)C1=CC=C(C=C1)C
- CAS DataBase Reference
- 60565-88-0(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- C
- Risk Statements
- 34
- Safety Statements
- 26-36/37/39-45
- RIDADR
- UN 1759 8 / PGII
- WGK Germany
- 3
- Storage Class
- 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- Skin Corr. 1B
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Bis(4-methylphenyl)iodonium hexafluorophosphate Usage And Synthesis
Uses
- Covalent Functionalisation of Few-Layer Black Phosphorus using Aryl Iodonium Salts and Comparison to Diazonium Modified Black Phosphorus: Explores the functionalization of black phosphorus using bis(4-methylphenyl)iodonium hexafluorophosphate and compares it to diazonium modification (M Van Druenen, 2019).
- Iodonium sulfonates as high‐performance coinitiators and additives for CQ‐based systems: Toward aromatic amine‐free photoinitiating systems: Examines the effectiveness of iodonium sulfonates and bis(4-methylphenyl)iodonium hexafluorophosphate in CQ-based photoinitiating systems (J Kirschner et al., 2019).
- Thiophene-substituted phenothiazine-based photosensitisers for radical and cationic photopolymerization reactions under visible laser beams (405 and 455 nm): Studies the use of thiophene-substituted phenothiazine in combination with bis(4-methylphenyl)iodonium hexafluorophosphate for effective photopolymerization (P Chao et al., 2016).
General Description
Bis(4-methylphenyl)iodonium hexafluorophosphate is a white powder. It melts at 175-180 °C and shows an UV absorption peak at 267nm. 1
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