10-methyl-9-(phenoxycarbonyl)acridi-nium fluorosulfonat

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Reagent Code: #59786
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CAS Number 149300-54-9

science Other reagents with same CAS 149300-54-9

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scatter_plot Molecular Information
Weight 413.4188 g/mol
Formula C₂₁H₁₆FNO₅S
badge Registry Numbers
MDL Number MFCD01320487
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as a chemiluminescent reagent in analytical chemistry, this specialty chemical enables highly sensitive detection and quantification of specific biomolecules (e.g., in immunoassays, ATP assays, and nucleic acid hybridization) through intense light emission upon reaction with alkaline hydrogen peroxide. It also exhibits strong fluorescence properties suitable for fluorescent labeling and markers. In organic synthesis, it serves as a key intermediate for acridine derivatives used in dyes and advanced materials. Its structure supports exploration in photodynamic therapy for light-activated reactive oxygen species generation and in material science for organic electronics, including efficient LEDs and sensors.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿11,952.00
inventory 100mg
10-20 days ฿39,114.00

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10-methyl-9-(phenoxycarbonyl)acridi-nium fluorosulfonat
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Used primarily as a chemiluminescent reagent in analytical chemistry, this specialty chemical enables highly sensitive detection and quantification of specific biomolecules (e.g., in immunoassays, ATP assays, and nucleic acid hybridization) through intense light emission upon reaction with alkaline hydrogen peroxide. It also exhibits strong fluorescence properties suitable for fluorescent labeling and markers. In organic synthesis, it serves as a key intermediate for acridine derivatives used in dyes and

Used primarily as a chemiluminescent reagent in analytical chemistry, this specialty chemical enables highly sensitive detection and quantification of specific biomolecules (e.g., in immunoassays, ATP assays, and nucleic acid hybridization) through intense light emission upon reaction with alkaline hydrogen peroxide. It also exhibits strong fluorescence properties suitable for fluorescent labeling and markers. In organic synthesis, it serves as a key intermediate for acridine derivatives used in dyes and advanced materials. Its structure supports exploration in photodynamic therapy for light-activated reactive oxygen species generation and in material science for organic electronics, including efficient LEDs and sensors.

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