Sodium 1-((3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoyl)oxy)-2,5-dioxopyrrolidine-3-sulfonate

Reagent Code: #232737
fingerprint
CAS Number 92921-25-0

science Other reagents with same CAS 92921-25-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 416.29 g/mol
Formula C₁₅H₉N₂NaO₉S
badge Registry Numbers
MDL Number MFCD00054983
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a bifunctional crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to surfaces or other biomolecules. The compound contains a succinimide ester and a maleimide group, enabling selective reactions with primary amines and thiol groups, respectively. Commonly applied in the development of immunoassays, antibody-drug conjugates, and functionalized nanoparticles. Its sulfonate group enhances water solubility, making it suitable for use in aqueous reaction environments without organic solvents. Also employed in immobilizing biomolecules on biosensor surfaces due to its stable linkage and controlled orientation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,990.00
Sodium 1-((3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoyl)oxy)-2,5-dioxopyrrolidine-3-sulfonate
No image available

Used as a bifunctional crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to surfaces or other biomolecules. The compound contains a succinimide ester and a maleimide group, enabling selective reactions with primary amines and thiol groups, respectively. Commonly applied in the development of immunoassays, antibody-drug conjugates, and functionalized nanoparticles. Its sulfonate group enhances water solubility, making it suitable for use in aqueous reaction environments

Used as a bifunctional crosslinking agent in bioconjugation, particularly for coupling peptides or proteins to surfaces or other biomolecules. The compound contains a succinimide ester and a maleimide group, enabling selective reactions with primary amines and thiol groups, respectively. Commonly applied in the development of immunoassays, antibody-drug conjugates, and functionalized nanoparticles. Its sulfonate group enhances water solubility, making it suitable for use in aqueous reaction environments without organic solvents. Also employed in immobilizing biomolecules on biosensor surfaces due to its stable linkage and controlled orientation.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...