NHPI-PEG4-C2-Pfpester

97%

Reagent Code: #220462
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CAS Number 2101206-46-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 577.45 g/mol
Formula C₂₅H₂₄F₅NO₉
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in bioconjugation and surface functionalization due to its ability to form stable amide bonds with primary amines under mild conditions. The perfluorinated chain enhances solubility in fluorinated solvents and enables phase separation techniques, useful in purification processes. The PEG spacer improves water solubility and reduces non-specific binding, making it suitable for applications in bioassays and diagnostic probes. Commonly employed in the development of protein labeling reagents, targeted drug delivery systems, and immobilization of biomolecules on fluorinated surfaces. Its unique structure supports click-like reaction efficiency without requiring metal catalysts.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿30,810.00
NHPI-PEG4-C2-Pfpester
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Used in bioconjugation and surface functionalization due to its ability to form stable amide bonds with primary amines under mild conditions. The perfluorinated chain enhances solubility in fluorinated solvents and enables phase separation techniques, useful in purification processes. The PEG spacer improves water solubility and reduces non-specific binding, making it suitable for applications in bioassays and diagnostic probes. Commonly employed in the development of protein labeling reagents, targeted

Used in bioconjugation and surface functionalization due to its ability to form stable amide bonds with primary amines under mild conditions. The perfluorinated chain enhances solubility in fluorinated solvents and enables phase separation techniques, useful in purification processes. The PEG spacer improves water solubility and reduces non-specific binding, making it suitable for applications in bioassays and diagnostic probes. Commonly employed in the development of protein labeling reagents, targeted drug delivery systems, and immobilization of biomolecules on fluorinated surfaces. Its unique structure supports click-like reaction efficiency without requiring metal catalysts.

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