Bis(2,5-dioxopyrrolidin-1-yl) (disulfanediylbis(ethane-2,1-diyl)) dicarbonate

97%

Reagent Code: #64764
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CAS Number 1688598-83-5

science Other reagents with same CAS 1688598-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 436.41 g/mol
Formula C₁₄H₁₆N₂O₁₀S₂
badge Registry Numbers
MDL Number MFCD32644554
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in bioconjugation and protein modification processes. It serves as a crosslinking agent, enabling the formation of stable bonds between biomolecules such as proteins, peptides, or antibodies. Its reactive groups, including N-hydroxysuccinimide (NHS) esters and disulfide bonds, facilitate efficient conjugation under mild conditions. This makes it particularly useful in the development of antibody-drug conjugates (ADCs) for targeted cancer therapies. Additionally, it is employed in the creation of bioconjugates for diagnostic assays, where precise and stable molecular linkages are essential. The disulfide bond within its structure allows for controlled release or cleavage in reducing environments, enhancing its versatility in drug delivery systems.

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Test Parameter Specification
Appearance solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,360.00
inventory 250mg
10-20 days ฿9,600.00

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Bis(2,5-dioxopyrrolidin-1-yl) (disulfanediylbis(ethane-2,1-diyl)) dicarbonate
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This chemical is primarily utilized in bioconjugation and protein modification processes. It serves as a crosslinking agent, enabling the formation of stable bonds between biomolecules such as proteins, peptides, or antibodies. Its reactive groups, including N-hydroxysuccinimide (NHS) esters and disulfide bonds, facilitate efficient conjugation under mild conditions. This makes it particularly useful in the development of antibody-drug conjugates (ADCs) for targeted cancer therapies. Additionally, it is employed in the creation of bioconjugates for diagnostic assays, where precise and stable molecular linkages are essential. The disulfide bond within its structure allows for controlled release or cleavage in reducing environments, enhancing its versatility in drug delivery systems.
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