Boc-Aminooxy-PEG4-azide

≥95%

Reagent Code: #107874
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CAS Number 2100306-64-5

science Other reagents with same CAS 2100306-64-5

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Weight 378.42 g/mol
Formula C₁₅H₃₀N₄O₇
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is widely used in bioconjugation and click chemistry applications due to its unique functional groups. The Boc group serves as a protective group for the aminooxy functionality, allowing selective deprotection when needed. The aminooxy group enables efficient conjugation with aldehydes or ketones, forming stable oxime bonds. The PEG4 spacer enhances solubility and provides flexibility, reducing steric hindrance in reactions. The azide group facilitates click chemistry, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling the formation of triazole linkages with alkynes. This makes it valuable in drug delivery systems, protein labeling, and the development of biomaterials. Its multifunctional nature allows for the creation of complex molecular architectures in fields like biopharmaceuticals, diagnostics, and materials science.

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

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Boc-Aminooxy-PEG4-azide
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This compound is widely used in bioconjugation and click chemistry applications due to its unique functional groups. The Boc group serves as a protective group for the aminooxy functionality, allowing selective deprotection when needed. The aminooxy group enables efficient conjugation with aldehydes or ketones, forming stable oxime bonds. The PEG4 spacer enhances solubility and provides flexibility, reducing steric hindrance in reactions. The azide group facilitates click chemistry, particularly in coppe

This compound is widely used in bioconjugation and click chemistry applications due to its unique functional groups. The Boc group serves as a protective group for the aminooxy functionality, allowing selective deprotection when needed. The aminooxy group enables efficient conjugation with aldehydes or ketones, forming stable oxime bonds. The PEG4 spacer enhances solubility and provides flexibility, reducing steric hindrance in reactions. The azide group facilitates click chemistry, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling the formation of triazole linkages with alkynes. This makes it valuable in drug delivery systems, protein labeling, and the development of biomaterials. Its multifunctional nature allows for the creation of complex molecular architectures in fields like biopharmaceuticals, diagnostics, and materials science.

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