N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl)

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Reagent Code: #106366
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CAS Number 2112737-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 604.73 g/mol
Formula C₂₉H₅₂N₂O₁₁
badge Registry Numbers
MDL Number MFCD30730360
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, dry, sealed

description Product Description

This chemical is primarily used in bioconjugation and click chemistry applications. Its structure, featuring PEG (polyethylene glycol) chains and a propargyl group, makes it highly suitable for attaching biomolecules, such as proteins or peptides, to other compounds or surfaces. The t-Boc (tert-butyloxycarbonyl) protecting group allows for controlled deprotection, enabling selective reactions. It is often employed in drug delivery systems to create PEGylated conjugates, enhancing the solubility, stability, and bioavailability of therapeutic agents. Additionally, the propargyl groups facilitate copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, a key process in labeling and modifying biomolecules for research or diagnostic purposes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,100.00
inventory 250mg
10-20 days ฿48,600.00
N-(t-Boc-Aminooxy-PEG2)-N-bis(PEG3-propargyl)
This chemical is primarily used in bioconjugation and click chemistry applications. Its structure, featuring PEG (polyethylene glycol) chains and a propargyl group, makes it highly suitable for attaching biomolecules, such as proteins or peptides, to other compounds or surfaces. The t-Boc (tert-butyloxycarbonyl) protecting group allows for controlled deprotection, enabling selective reactions. It is often employed in drug delivery systems to create PEGylated conjugates, enhancing the solubility, stability, and bioavailability of therapeutic agents. Additionally, the propargyl groups facilitate copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, a key process in labeling and modifying biomolecules for research or diagnostic purposes.
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