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Structure of 87345-22-0
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This porphyrin features three phenyl rings at the 10,15,20-positions and a para-hydroxyphenyl group at the 5-position, enhancing solubility and enabling site-specific functionalization. The extended π-conjugation supports strong visible absorption and efficient singlet oxygen generation, making it effective in photodynamic therapy applications and organic optoelectronics.
5-(4-Hydroxyphenyl)-10,15,20-triphenylporphyrin serves as a versatile porphyrin scaffold for photodynamic therapy research and catalytic applications. The phenolic functionality enables straightforward derivatization via etherification or esterification, while the triphenyl-substituted core provides enhanced solubility and stability. This compound functions as a robust building block in the synthesis of functionalized metalloporphyrins and conjugated materials.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: