endo-BCN-PEG2-alcohol

≥95%

Reagent Code: #65316
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CAS Number 1807501-85-4

science Other reagents with same CAS 1807501-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.4 g/mol
Formula C₁₇H₂₇NO
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in bioconjugation and click chemistry applications. Its endo-BCN (bicyclo[6.1.0]nonyne) group enables efficient and selective reactions with azide-containing molecules, making it valuable for labeling, imaging, and drug delivery systems. The PEG2 (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, improving the efficiency of conjugation. The alcohol functional group allows for further chemical modifications or attachment to other molecules. It is commonly used in the development of targeted therapies, diagnostic probes, and biomaterials, where precise and stable conjugation is essential. Its versatility makes it a key tool in chemical biology and pharmaceutical research.

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

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endo-BCN-PEG2-alcohol
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This compound is primarily utilized in bioconjugation and click chemistry applications. Its endo-BCN (bicyclo[6.1.0]nonyne) group enables efficient and selective reactions with azide-containing molecules, making it valuable for labeling, imaging, and drug delivery systems. The PEG2 (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, improving the efficiency of conjugation. The alcohol functional group allows for further chemical modifications or attachment to other molecules. I

This compound is primarily utilized in bioconjugation and click chemistry applications. Its endo-BCN (bicyclo[6.1.0]nonyne) group enables efficient and selective reactions with azide-containing molecules, making it valuable for labeling, imaging, and drug delivery systems. The PEG2 (polyethylene glycol) spacer enhances solubility and reduces steric hindrance, improving the efficiency of conjugation. The alcohol functional group allows for further chemical modifications or attachment to other molecules. It is commonly used in the development of targeted therapies, diagnostic probes, and biomaterials, where precise and stable conjugation is essential. Its versatility makes it a key tool in chemical biology and pharmaceutical research.

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