7-Ethoxyacridine-3,9-diamine

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Reagent Code: #133765
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CAS Number 442-16-0

science Other reagents with same CAS 442-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.29 g/mol
Formula C₁₅H₁₅N₃O
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry, inert gas

description Product Description

Used as a fluorescent probe in biological imaging due to its strong emission properties in aqueous environments. It binds selectively to nucleic acids, making it valuable in DNA and RNA detection assays. Its ethoxy group enhances cell membrane permeability, allowing for live-cell staining without transfection agents. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species under light exposure. Additionally, it serves as an intermediate in synthesizing antimalarial and antitumor agents due to its acridine core's affinity for intercalating into DNA.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿3,560.00
inventory 25mg
10-20 days ฿10,660.00
inventory 100mg
10-20 days ฿31,990.00
inventory 250mg
10-20 days ฿63,980.00
inventory 1g
10-20 days ฿159,900.00

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7-Ethoxyacridine-3,9-diamine
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Used as a fluorescent probe in biological imaging due to its strong emission properties in aqueous environments. It binds selectively to nucleic acids, making it valuable in DNA and RNA detection assays. Its ethoxy group enhances cell membrane permeability, allowing for live-cell staining without transfection agents. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species under light exposure. Additionally, it serves as an intermediate in synthesizing antim

Used as a fluorescent probe in biological imaging due to its strong emission properties in aqueous environments. It binds selectively to nucleic acids, making it valuable in DNA and RNA detection assays. Its ethoxy group enhances cell membrane permeability, allowing for live-cell staining without transfection agents. Also employed in photodynamic therapy research owing to its ability to generate reactive oxygen species under light exposure. Additionally, it serves as an intermediate in synthesizing antimalarial and antitumor agents due to its acridine core's affinity for intercalating into DNA.

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