endo-BCN-PEG4-NHS ester

≥95%

Reagent Code: #65332
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CAS Number 1807501-86-5

science Other reagents with same CAS 1807501-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 538.59 g/mol
Formula C₂₆H₃₈N₂O₁₀
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is widely used in bioconjugation and click chemistry applications. It serves as a linker for attaching biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The endo-BCN group enables efficient and selective reactions with azide-containing compounds through strain-promoted azide-alkyne cycloaddition (SPAAC), a type of click chemistry. The PEG4 spacer enhances solubility and flexibility, reducing steric hindrance during conjugation. The NHS ester group allows for straightforward coupling with primary amines, making it ideal for labeling or modifying biomolecules. This compound is particularly valuable in drug delivery, diagnostics, and the development of bioconjugates for research and therapeutic purposes.

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Test Parameter Specification
Appearance Liquid
Purity(NMR)(%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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

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endo-BCN-PEG4-NHS ester
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This chemical is widely used in bioconjugation and click chemistry applications. It serves as a linker for attaching biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The endo-BCN group enables efficient and selective reactions with azide-containing compounds through strain-promoted azide-alkyne cycloaddition (SPAAC), a type of click chemistry. The PEG4 spacer enhances solubility and flexibility, reducing steric hindrance during conjugation. The NHS ester group allo

This chemical is widely used in bioconjugation and click chemistry applications. It serves as a linker for attaching biomolecules, such as proteins, peptides, or antibodies, to other molecules or surfaces. The endo-BCN group enables efficient and selective reactions with azide-containing compounds through strain-promoted azide-alkyne cycloaddition (SPAAC), a type of click chemistry. The PEG4 spacer enhances solubility and flexibility, reducing steric hindrance during conjugation. The NHS ester group allows for straightforward coupling with primary amines, making it ideal for labeling or modifying biomolecules. This compound is particularly valuable in drug delivery, diagnostics, and the development of bioconjugates for research and therapeutic purposes.

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