Boc-aminooxy-ethyl-SS-propanol

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Reagent Code: #141509
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CAS Number 2128735-21-5

science Other reagents with same CAS 2128735-21-5

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Weight 269.38 g/mol
Formula C₉H₁₉NO₄S₂
badge Registry Numbers
MDL Number MFCD31536770
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in bioconjugation and protein modification due to its ability to form stable oxime linkages with carbonyl groups (aldehydes or ketones) under mild conditions. The Boc-protected aminooxy group allows for selective and controlled coupling, while the SS (disulfide) linker provides a cleavable bond in reducing environments, making it ideal for drug delivery systems and reversible immobilization of biomolecules. Commonly applied in the development of antibody-drug conjugates (ADCs), peptide modifications, and functionalization of surfaces in biosensors. The propanol end can be further modified for attachment to solid supports or fluorescent tags.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿47,980.00

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Boc-aminooxy-ethyl-SS-propanol
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Used in bioconjugation and protein modification due to its ability to form stable oxime linkages with carbonyl groups (aldehydes or ketones) under mild conditions. The Boc-protected aminooxy group allows for selective and controlled coupling, while the SS (disulfide) linker provides a cleavable bond in reducing environments, making it ideal for drug delivery systems and reversible immobilization of biomolecules. Commonly applied in the development of antibody-drug conjugates (ADCs), peptide modifications

Used in bioconjugation and protein modification due to its ability to form stable oxime linkages with carbonyl groups (aldehydes or ketones) under mild conditions. The Boc-protected aminooxy group allows for selective and controlled coupling, while the SS (disulfide) linker provides a cleavable bond in reducing environments, making it ideal for drug delivery systems and reversible immobilization of biomolecules. Commonly applied in the development of antibody-drug conjugates (ADCs), peptide modifications, and functionalization of surfaces in biosensors. The propanol end can be further modified for attachment to solid supports or fluorescent tags.

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