Exo-BCN-PEG2-Boc-amine

95%

Reagent Code: #185175
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CAS Number 1807501-87-6

science Other reagents with same CAS 1807501-87-6

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inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used in bioconjugation for site-specific labeling of biomolecules, particularly in click chemistry applications. Its strained alkyne group (BCN) reacts rapidly and selectively with azides via copper-free click reactions, making it ideal for labeling proteins, antibodies, or nucleic acids in live cells without cytotoxic effects. The PEG2 spacer improves solubility and reduces steric hindrance, enhancing reaction efficiency. The Boc-amine group allows for further chemical modifications under mild deprotection conditions, enabling stepwise synthesis in complex molecular constructs. Commonly employed in the development of antibody-drug conjugates (ADCs), imaging probes, and targeted therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,950.00
inventory 100mg
10-20 days ฿30,020.00
Exo-BCN-PEG2-Boc-amine
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Used in bioconjugation for site-specific labeling of biomolecules, particularly in click chemistry applications. Its strained alkyne group (BCN) reacts rapidly and selectively with azides via copper-free click reactions, making it ideal for labeling proteins, antibodies, or nucleic acids in live cells without cytotoxic effects. The PEG2 spacer improves solubility and reduces steric hindrance, enhancing reaction efficiency. The Boc-amine group allows for further chemical modifications under mild deprotect

Used in bioconjugation for site-specific labeling of biomolecules, particularly in click chemistry applications. Its strained alkyne group (BCN) reacts rapidly and selectively with azides via copper-free click reactions, making it ideal for labeling proteins, antibodies, or nucleic acids in live cells without cytotoxic effects. The PEG2 spacer improves solubility and reduces steric hindrance, enhancing reaction efficiency. The Boc-amine group allows for further chemical modifications under mild deprotection conditions, enabling stepwise synthesis in complex molecular constructs. Commonly employed in the development of antibody-drug conjugates (ADCs), imaging probes, and targeted therapeutics.

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