1-(6-(aminooxy)hexyl)-1H-pyrrole-2,5-dione

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Reagent Code: #63848
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CAS Number 937025-28-0

science Other reagents with same CAS 937025-28-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.245 g/mol
Formula C₁₀H₁₇ClN₂O₃
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This chemical is primarily utilized in bioconjugation and protein modification applications. It serves as a crosslinking agent, enabling the attachment of biomolecules such as proteins, peptides, or antibodies to various surfaces or other molecules. The aminooxy group allows for efficient conjugation with carbonyl-containing compounds, while the pyrrole-2,5-dione moiety facilitates reactions with thiol groups. This dual functionality makes it valuable in creating stable, site-specific linkages in bioconjugation processes. It is often employed in the development of biosensors, drug delivery systems, and diagnostic assays, where precise and stable molecular interactions are critical. Additionally, it is used in research to study protein interactions and to immobilize biomolecules on solid supports for analytical purposes.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿23,355.00
inventory 1g
10-20 days ฿42,030.00

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1-(6-(aminooxy)hexyl)-1H-pyrrole-2,5-dione
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This chemical is primarily utilized in bioconjugation and protein modification applications. It serves as a crosslinking agent, enabling the attachment of biomolecules such as proteins, peptides, or antibodies to various surfaces or other molecules. The aminooxy group allows for efficient conjugation with carbonyl-containing compounds, while the pyrrole-2,5-dione moiety facilitates reactions with thiol groups. This dual functionality makes it valuable in creating stable, site-specific linkages in bioconjuga
This chemical is primarily utilized in bioconjugation and protein modification applications. It serves as a crosslinking agent, enabling the attachment of biomolecules such as proteins, peptides, or antibodies to various surfaces or other molecules. The aminooxy group allows for efficient conjugation with carbonyl-containing compounds, while the pyrrole-2,5-dione moiety facilitates reactions with thiol groups. This dual functionality makes it valuable in creating stable, site-specific linkages in bioconjugation processes. It is often employed in the development of biosensors, drug delivery systems, and diagnostic assays, where precise and stable molecular interactions are critical. Additionally, it is used in research to study protein interactions and to immobilize biomolecules on solid supports for analytical purposes.
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