O-(2-Aminoethyl)-O′-(2-azidoethyl)heptaethylene glycol

95%

Reagent Code: #77700
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CAS Number 857891-82-8

science Other reagents with same CAS 857891-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.52 g/mol
Formula C₁₈H₃₈N₄O₈
badge Registry Numbers
MDL Number MFCD03453241
inventory_2 Storage & Handling
Storage -20°C, stored with argon

description Product Description

This chemical is widely used in bioconjugation and labeling applications due to its bifunctional nature, which allows it to link biomolecules such as proteins, peptides, or antibodies with other entities like dyes, drugs, or solid supports. The aminoethyl group enables covalent attachment to carboxyl groups via coupling reactions, while the azidoethyl group facilitates click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This makes it valuable in the development of targeted drug delivery systems, diagnostic assays, and biophysical studies. Its polyethylene glycol (PEG) spacer enhances solubility and reduces steric hindrance, improving the efficiency of conjugation processes. Additionally, it is employed in surface modification and the creation of biofunctionalized materials for research and therapeutic purposes.

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Test Parameter Specification
Appearance Colorless to very light yellow and colorless to very light green-yellow liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,900.00
inventory 500mg
10-20 days ฿26,580.00

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O-(2-Aminoethyl)-O′-(2-azidoethyl)heptaethylene glycol
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This chemical is widely used in bioconjugation and labeling applications due to its bifunctional nature, which allows it to link biomolecules such as proteins, peptides, or antibodies with other entities like dyes, drugs, or solid supports. The aminoethyl group enables covalent attachment to carboxyl groups via coupling reactions, while the azidoethyl group facilitates click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This makes it valuable in the development of targeted

This chemical is widely used in bioconjugation and labeling applications due to its bifunctional nature, which allows it to link biomolecules such as proteins, peptides, or antibodies with other entities like dyes, drugs, or solid supports. The aminoethyl group enables covalent attachment to carboxyl groups via coupling reactions, while the azidoethyl group facilitates click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This makes it valuable in the development of targeted drug delivery systems, diagnostic assays, and biophysical studies. Its polyethylene glycol (PEG) spacer enhances solubility and reduces steric hindrance, improving the efficiency of conjugation processes. Additionally, it is employed in surface modification and the creation of biofunctionalized materials for research and therapeutic purposes.

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