Endo-BCN-PEG3-Boc-amine

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Reagent Code: #181099
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CAS Number 1807501-84-3

science Other reagents with same CAS 1807501-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 468.58 g/mol
Formula C₂₄H₄₀N₂O₇
thermostat Physical Properties
Boiling Point 602.2±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used in bioconjugation for site-specific labeling of biomolecules due to its strain-promoted alkyne functionality, enabling copper-free click chemistry with azides. The PEG3 spacer enhances solubility and reduces aggregation, making it ideal for modifying peptides, proteins, and antibodies in live-cell imaging and drug delivery systems. The Boc-amine group allows for controlled deprotection and further coupling reactions, facilitating stepwise synthesis in complex molecular architectures. Commonly applied in developing biotherapeutics, diagnostics, and functionalized surfaces where minimal nonspecific binding and high stability are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,220.00
inventory 50mg
10-20 days ฿12,840.00

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Endo-BCN-PEG3-Boc-amine
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Used in bioconjugation for site-specific labeling of biomolecules due to its strain-promoted alkyne functionality, enabling copper-free click chemistry with azides. The PEG3 spacer enhances solubility and reduces aggregation, making it ideal for modifying peptides, proteins, and antibodies in live-cell imaging and drug delivery systems. The Boc-amine group allows for controlled deprotection and further coupling reactions, facilitating stepwise synthesis in complex molecular architectures. Commonly applie

Used in bioconjugation for site-specific labeling of biomolecules due to its strain-promoted alkyne functionality, enabling copper-free click chemistry with azides. The PEG3 spacer enhances solubility and reduces aggregation, making it ideal for modifying peptides, proteins, and antibodies in live-cell imaging and drug delivery systems. The Boc-amine group allows for controlled deprotection and further coupling reactions, facilitating stepwise synthesis in complex molecular architectures. Commonly applied in developing biotherapeutics, diagnostics, and functionalized surfaces where minimal nonspecific binding and high stability are required.

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