8-Bromomethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene

≥98%

Reagent Code: #141498
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CAS Number 216434-81-0

science Other reagents with same CAS 216434-81-0

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scatter_plot Molecular Information
Weight 341 g/mol
Formula C₁₄H₁₆BBrF₂N₂
badge Registry Numbers
MDL Number MFCD00467595
inventory_2 Storage & Handling
Storage -20°C, avoiding light

description Product Description

Used as a fluorescent labeling reagent in bioimaging and molecular probes due to its strong photostability and bright emission. Its bromomethyl functional group allows for easy conjugation to biomolecules such as proteins, nucleic acids, and small molecule tracers. Commonly employed in fluorescence microscopy, flow cytometry, and cellular tracking applications. The difluoro and methyl substitutions enhance fluorescence quantum yield and improve lipophilicity for better cell membrane permeability. Ideal for developing sensors and dyes in life science research and diagnostic assays.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,250.00
inventory 25mg
10-20 days ฿26,580.00

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8-Bromomethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
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Used as a fluorescent labeling reagent in bioimaging and molecular probes due to its strong photostability and bright emission. Its bromomethyl functional group allows for easy conjugation to biomolecules such as proteins, nucleic acids, and small molecule tracers. Commonly employed in fluorescence microscopy, flow cytometry, and cellular tracking applications. The difluoro and methyl substitutions enhance fluorescence quantum yield and improve lipophilicity for better cell membrane permeability. Ideal f

Used as a fluorescent labeling reagent in bioimaging and molecular probes due to its strong photostability and bright emission. Its bromomethyl functional group allows for easy conjugation to biomolecules such as proteins, nucleic acids, and small molecule tracers. Commonly employed in fluorescence microscopy, flow cytometry, and cellular tracking applications. The difluoro and methyl substitutions enhance fluorescence quantum yield and improve lipophilicity for better cell membrane permeability. Ideal for developing sensors and dyes in life science research and diagnostic assays.

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