meso-tetra(3,5-dibromo-4-hydroxyphenyl)porphyrin

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Reagent Code: #207603
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CAS Number 125299-79-8

science Other reagents with same CAS 125299-79-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1309.9 g/mol
Formula C₄₄H₂₂Br₈N₄O₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a highly selective chromogenic chemosensor for detecting metal ions, particularly mercury (Hg²⁺) and copper (Cu²⁺), in environmental and biological samples. The compound undergoes a distinct color change upon binding with these metals, enabling visual or spectrophotometric detection without the need for complex instrumentation. Its brominated phenolic structure enhances sensitivity and selectivity due to strong electron-withdrawing effects and favorable coordination geometry. Also employed in studies related to oxidative stress and catalysis, where it mimics peroxidase-like activity in aqueous systems. Due to its stability and sharp optical response, it is integrated into sensor platforms for monitoring heavy metal contamination in water and industrial effluents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,190.00
inventory 250mg
10-20 days ฿4,860.00
inventory 1g
10-20 days ฿15,980.00
inventory 5g
10-20 days ฿47,950.00

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meso-tetra(3,5-dibromo-4-hydroxyphenyl)porphyrin
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Used as a highly selective chromogenic chemosensor for detecting metal ions, particularly mercury (Hg²⁺) and copper (Cu²⁺), in environmental and biological samples. The compound undergoes a distinct color change upon binding with these metals, enabling visual or spectrophotometric detection without the need for complex instrumentation. Its brominated phenolic structure enhances sensitivity and selectivity due to strong electron-withdrawing effects and favorable coordination geometry. Also employed in stu

Used as a highly selective chromogenic chemosensor for detecting metal ions, particularly mercury (Hg²⁺) and copper (Cu²⁺), in environmental and biological samples. The compound undergoes a distinct color change upon binding with these metals, enabling visual or spectrophotometric detection without the need for complex instrumentation. Its brominated phenolic structure enhances sensitivity and selectivity due to strong electron-withdrawing effects and favorable coordination geometry. Also employed in studies related to oxidative stress and catalysis, where it mimics peroxidase-like activity in aqueous systems. Due to its stability and sharp optical response, it is integrated into sensor platforms for monitoring heavy metal contamination in water and industrial effluents.

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