Perfluorophenyl 3-(2-(2-(4-formylbenzamido)ethoxy)ethoxy)propanoate

98%

Reagent Code: #223192
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CAS Number 2101206-60-2

science Other reagents with same CAS 2101206-60-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 475.36 g/mol
Formula C₂₁H₁₈F₅NO₆
badge Registry Numbers
MDL Number MFCD28556930
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a functional crosslinking agent in bioconjugation and surface modification, particularly in the development of biosensors and diagnostic assays. The aldehyde group enables covalent attachment to amine-containing biomolecules such as antibodies, peptides, or proteins under mild conditions. The perfluorophenyl ester moiety reacts efficiently with nucleophiles like amines to form stable amide bonds, allowing stepwise construction of complex molecular architectures. Its hydrophilic polyether spacer enhances solubility in aqueous and organic media, reduces non-specific binding, and improves accessibility of the reactive aldehyde group. Commonly employed in immobilizing biomolecules on solid supports, including microarrays, nanoparticles, and polymer surfaces, for applications in targeted drug delivery, immunoassays, and molecular imaging.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿41,550.00
Perfluorophenyl 3-(2-(2-(4-formylbenzamido)ethoxy)ethoxy)propanoate
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Used as a functional crosslinking agent in bioconjugation and surface modification, particularly in the development of biosensors and diagnostic assays. The aldehyde group enables covalent attachment to amine-containing biomolecules such as antibodies, peptides, or proteins under mild conditions. The perfluorophenyl ester moiety reacts efficiently with nucleophiles like amines to form stable amide bonds, allowing stepwise construction of complex molecular architectures. Its hydrophilic polyether spacer e

Used as a functional crosslinking agent in bioconjugation and surface modification, particularly in the development of biosensors and diagnostic assays. The aldehyde group enables covalent attachment to amine-containing biomolecules such as antibodies, peptides, or proteins under mild conditions. The perfluorophenyl ester moiety reacts efficiently with nucleophiles like amines to form stable amide bonds, allowing stepwise construction of complex molecular architectures. Its hydrophilic polyether spacer enhances solubility in aqueous and organic media, reduces non-specific binding, and improves accessibility of the reactive aldehyde group. Commonly employed in immobilizing biomolecules on solid supports, including microarrays, nanoparticles, and polymer surfaces, for applications in targeted drug delivery, immunoassays, and molecular imaging.

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