Propargyl-PEG1-SS-PEG1-PFP ester

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Reagent Code: #223199
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CAS Number 1817735-30-0

science Other reagents with same CAS 1817735-30-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.41 g/mol
Formula C₁₆H₁₅F₅O₄S₂
badge Registry Numbers
MDL Number MFCD29042354
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in bioconjugation for targeted drug delivery and surface modification. The PFP ester group reacts efficiently with primary amines on proteins or peptides, forming stable amide bonds. The disulfide (SS) linker provides a cleavable bond in reducing environments, such as inside cells, enabling controlled release of payloads. The propargyl group allows for click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating modular assembly in complex biological systems. Ideal for constructing antibody-drug conjugates (ADCs), functionalizing nanoparticles, and labeling biomolecules with fluorophores or other probes. PEG spacers enhance solubility and reduce non-specific binding, improving bioavailability and performance in biological applications.

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inventory 50mg
10-20 days ฿75,150.00

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Propargyl-PEG1-SS-PEG1-PFP ester
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Used in bioconjugation for targeted drug delivery and surface modification. The PFP ester group reacts efficiently with primary amines on proteins or peptides, forming stable amide bonds. The disulfide (SS) linker provides a cleavable bond in reducing environments, such as inside cells, enabling controlled release of payloads. The propargyl group allows for click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating modular assembly in complex biological systems. Ideal for const

Used in bioconjugation for targeted drug delivery and surface modification. The PFP ester group reacts efficiently with primary amines on proteins or peptides, forming stable amide bonds. The disulfide (SS) linker provides a cleavable bond in reducing environments, such as inside cells, enabling controlled release of payloads. The propargyl group allows for click chemistry via copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating modular assembly in complex biological systems. Ideal for constructing antibody-drug conjugates (ADCs), functionalizing nanoparticles, and labeling biomolecules with fluorophores or other probes. PEG spacers enhance solubility and reduce non-specific binding, improving bioavailability and performance in biological applications.

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