5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphine

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Reagent Code: #242949
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CAS Number 145362-97-6

science Other reagents with same CAS 145362-97-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 999.55 g/mol
Formula C₆₄H₆₂N₄Si₄
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a photosensitizer in photodynamic therapy due to its strong absorption in the visible light range and ability to generate singlet oxygen. Its extended conjugation and silicon-containing side groups enhance photostability and solubility in organic solvents, making it suitable for thin-film applications in organic photovoltaics and light-emitting diodes. Also employed in sensing platforms for metal ion detection, where fluorescence quenching or enhancement occurs upon binding to specific cations. The trimethylsilyl-ethynyl groups allow further functionalization via desilylation, enabling covalent attachment to surfaces or polymers for use in molecular electronics and catalytic systems.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿18,140.00
inventory 100mg
10-20 days ฿30,810.00
inventory 250mg
10-20 days ฿52,360.00

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5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphine
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Used as a photosensitizer in photodynamic therapy due to its strong absorption in the visible light range and ability to generate singlet oxygen. Its extended conjugation and silicon-containing side groups enhance photostability and solubility in organic solvents, making it suitable for thin-film applications in organic photovoltaics and light-emitting diodes. Also employed in sensing platforms for metal ion detection, where fluorescence quenching or enhancement occurs upon binding to specific cations. T

Used as a photosensitizer in photodynamic therapy due to its strong absorption in the visible light range and ability to generate singlet oxygen. Its extended conjugation and silicon-containing side groups enhance photostability and solubility in organic solvents, making it suitable for thin-film applications in organic photovoltaics and light-emitting diodes. Also employed in sensing platforms for metal ion detection, where fluorescence quenching or enhancement occurs upon binding to specific cations. The trimethylsilyl-ethynyl groups allow further functionalization via desilylation, enabling covalent attachment to surfaces or polymers for use in molecular electronics and catalytic systems.

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