3,8-Dinitro-6-phenyl-phenanthridine

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Reagent Code: #176676
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CAS Number 82921-86-6

science Other reagents with same CAS 82921-86-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 345.31 g/mol
Formula C₁₉H₁₁N₃O₄
badge Registry Numbers
MDL Number MFCD00075060
thermostat Physical Properties
Melting Point 273-274 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily in research as a fluorescent probe for DNA detection due to its strong intercalating properties with nucleic acids. Exhibits enhanced fluorescence upon binding to double-stranded DNA, making it valuable in biochemical assays for monitoring DNA interactions and structural changes. Also investigated for potential applications in photodynamic therapy and as a sensor in molecular biology for detecting specific DNA sequences. Its nitro groups contribute to electron-accepting characteristics, useful in studies involving electron transfer in biological systems.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿14,400.00

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3,8-Dinitro-6-phenyl-phenanthridine
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Used primarily in research as a fluorescent probe for DNA detection due to its strong intercalating properties with nucleic acids. Exhibits enhanced fluorescence upon binding to double-stranded DNA, making it valuable in biochemical assays for monitoring DNA interactions and structural changes. Also investigated for potential applications in photodynamic therapy and as a sensor in molecular biology for detecting specific DNA sequences. Its nitro groups contribute to electron-accepting characteristics, us

Used primarily in research as a fluorescent probe for DNA detection due to its strong intercalating properties with nucleic acids. Exhibits enhanced fluorescence upon binding to double-stranded DNA, making it valuable in biochemical assays for monitoring DNA interactions and structural changes. Also investigated for potential applications in photodynamic therapy and as a sensor in molecular biology for detecting specific DNA sequences. Its nitro groups contribute to electron-accepting characteristics, useful in studies involving electron transfer in biological systems.

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