2-Butyl-6-(methylsulfonyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione

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Reagent Code: #140837
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CAS Number 135980-66-4

science Other reagents with same CAS 135980-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.39 g/mol
Formula C₁₇H₁₇NO₄S
thermostat Physical Properties
Boiling Point 559.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.330±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as a fluorescent probe in biochemical and analytical applications, this compound exhibits strong fluorescence properties that make it suitable for labeling biomolecules such as proteins and nucleic acids. Its high photostability and quantum yield allow for sensitive detection in imaging techniques, including fluorescence microscopy and flow cytometry. It is also employed in the development of sensors for monitoring environmental pollutants due to its selective response to specific ions or organic molecules. Additionally, its structural characteristics support use in studying molecular interactions and binding dynamics in solution.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿3,660.00
inventory 5mg
10-20 days ฿12,750.00

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2-Butyl-6-(methylsulfonyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione
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Used primarily as a fluorescent probe in biochemical and analytical applications, this compound exhibits strong fluorescence properties that make it suitable for labeling biomolecules such as proteins and nucleic acids. Its high photostability and quantum yield allow for sensitive detection in imaging techniques, including fluorescence microscopy and flow cytometry. It is also employed in the development of sensors for monitoring environmental pollutants due to its selective response to specific ions or

Used primarily as a fluorescent probe in biochemical and analytical applications, this compound exhibits strong fluorescence properties that make it suitable for labeling biomolecules such as proteins and nucleic acids. Its high photostability and quantum yield allow for sensitive detection in imaging techniques, including fluorescence microscopy and flow cytometry. It is also employed in the development of sensors for monitoring environmental pollutants due to its selective response to specific ions or organic molecules. Additionally, its structural characteristics support use in studying molecular interactions and binding dynamics in solution.

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