Propargyl-O-C1-amido-PEG2-C2-NHS ester

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Reagent Code: #223191
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CAS Number 2101206-30-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 370.35 g/mol
Formula C₁₆H₂₂N₂O₈
badge Registry Numbers
MDL Number MFCD28898684
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in bioconjugation to link molecules via amine-reactive NHS ester and alkyne groups. The PEG2 spacer enhances solubility and flexibility, improving reaction efficiency in aqueous and mixed solvents. The propargyl group enables click chemistry, especially copper-catalyzed azide-alkyne cycloaddition (CuAAC), for labeling biomolecules like proteins, peptides, and nucleic acids. Commonly applied in developing antibody-drug conjugates (ADCs), fluorescent probes, and functionalized surfaces in diagnostic and therapeutic research. Stable under standard handling conditions but should be protected from moisture to preserve NHS ester activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿56,950.00
Propargyl-O-C1-amido-PEG2-C2-NHS ester
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Used in bioconjugation to link molecules via amine-reactive NHS ester and alkyne groups. The PEG2 spacer enhances solubility and flexibility, improving reaction efficiency in aqueous and mixed solvents. The propargyl group enables click chemistry, especially copper-catalyzed azide-alkyne cycloaddition (CuAAC), for labeling biomolecules like proteins, peptides, and nucleic acids. Commonly applied in developing antibody-drug conjugates (ADCs), fluorescent probes, and functionalized surfaces in diagnostic and
Used in bioconjugation to link molecules via amine-reactive NHS ester and alkyne groups. The PEG2 spacer enhances solubility and flexibility, improving reaction efficiency in aqueous and mixed solvents. The propargyl group enables click chemistry, especially copper-catalyzed azide-alkyne cycloaddition (CuAAC), for labeling biomolecules like proteins, peptides, and nucleic acids. Commonly applied in developing antibody-drug conjugates (ADCs), fluorescent probes, and functionalized surfaces in diagnostic and therapeutic research. Stable under standard handling conditions but should be protected from moisture to preserve NHS ester activity.
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