DBCO-SS-COOH

95%

Reagent Code: #78714
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CAS Number 2576471-49-1

science Other reagents with same CAS 2576471-49-1

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Weight 468.6 g/mol
Formula C₂₄H₂₄N₂O₄S₂
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is widely used in bioorthogonal chemistry due to its DBCO (dibenzocyclooctyne) group, which enables rapid and selective reactions with azide-containing molecules without the need for catalysts. The SS (disulfide) linker provides a cleavable bond, making it suitable for applications where controlled release of a payload is required, such as in drug delivery systems. The COOH (carboxyl) group allows for further conjugation with amines or other functional groups, facilitating its use in the development of targeted therapeutics, bioconjugation, and labeling of biomolecules. It is particularly valuable in click chemistry reactions for studying biological processes or designing advanced materials.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿44,460.00

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DBCO-SS-COOH
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This compound is widely used in bioorthogonal chemistry due to its DBCO (dibenzocyclooctyne) group, which enables rapid and selective reactions with azide-containing molecules without the need for catalysts. The SS (disulfide) linker provides a cleavable bond, making it suitable for applications where controlled release of a payload is required, such as in drug delivery systems. The COOH (carboxyl) group allows for further conjugation with amines or other functional groups, facilitating its use in the de

This compound is widely used in bioorthogonal chemistry due to its DBCO (dibenzocyclooctyne) group, which enables rapid and selective reactions with azide-containing molecules without the need for catalysts. The SS (disulfide) linker provides a cleavable bond, making it suitable for applications where controlled release of a payload is required, such as in drug delivery systems. The COOH (carboxyl) group allows for further conjugation with amines or other functional groups, facilitating its use in the development of targeted therapeutics, bioconjugation, and labeling of biomolecules. It is particularly valuable in click chemistry reactions for studying biological processes or designing advanced materials.

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