endo-BCN-PEG3-NH2

≥95%

Reagent Code: #65330
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CAS Number 1883512-27-3

science Other reagents with same CAS 1883512-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.47 g/mol
Formula C₁₉H₃₂N₂O₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in bioconjugation and click chemistry, this compound is valuable for attaching biomolecules to surfaces or other molecules. Its endo-BCN group reacts efficiently with azides, enabling stable triazole linkages. The PEG3 spacer enhances solubility and reduces steric hindrance, making it ideal for modifying peptides, proteins, or nanoparticles. It is particularly useful in drug delivery systems, diagnostic probes, and targeted therapies, where precise molecular attachment is critical. The amine group allows further functionalization, expanding its utility in creating complex biomolecular constructs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,400.00

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endo-BCN-PEG3-NH2
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Used in bioconjugation and click chemistry, this compound is valuable for attaching biomolecules to surfaces or other molecules. Its endo-BCN group reacts efficiently with azides, enabling stable triazole linkages. The PEG3 spacer enhances solubility and reduces steric hindrance, making it ideal for modifying peptides, proteins, or nanoparticles. It is particularly useful in drug delivery systems, diagnostic probes, and targeted therapies, where precise molecular attachment is critical. The amine group a

Used in bioconjugation and click chemistry, this compound is valuable for attaching biomolecules to surfaces or other molecules. Its endo-BCN group reacts efficiently with azides, enabling stable triazole linkages. The PEG3 spacer enhances solubility and reduces steric hindrance, making it ideal for modifying peptides, proteins, or nanoparticles. It is particularly useful in drug delivery systems, diagnostic probes, and targeted therapies, where precise molecular attachment is critical. The amine group allows further functionalization, expanding its utility in creating complex biomolecular constructs.

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