1,2-Bis(maleimido)ethane

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Reagent Code: #147525
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CAS Number 5132-30-9

science Other reagents with same CAS 5132-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.18 g/mol
Formula C₁₀H₈N₂O₄
badge Registry Numbers
MDL Number MFCD00458699
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a crosslinking agent in bioconjugation, particularly for linking proteins and peptides. Its two maleimide groups react selectively with thiol groups (-SH) under mild conditions, forming stable thioether bonds. Commonly applied in the preparation of antibody-drug conjugates, protein labeling, and immobilization of biomolecules on surfaces. Also utilized in polymer chemistry to modify and crosslink thiol-containing polymers, enhancing mechanical and thermal properties. Preferred in applications requiring controlled, site-specific coupling due to its homobifunctional structure and relatively short spacer arm.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿300.00
inventory 50mg
10-20 days ฿450.00
inventory 100mg
10-20 days ฿590.00
inventory 1g
10-20 days ฿2,800.00

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1,2-Bis(maleimido)ethane
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Used as a crosslinking agent in bioconjugation, particularly for linking proteins and peptides. Its two maleimide groups react selectively with thiol groups (-SH) under mild conditions, forming stable thioether bonds. Commonly applied in the preparation of antibody-drug conjugates, protein labeling, and immobilization of biomolecules on surfaces. Also utilized in polymer chemistry to modify and crosslink thiol-containing polymers, enhancing mechanical and thermal properties. Preferred in applications req

Used as a crosslinking agent in bioconjugation, particularly for linking proteins and peptides. Its two maleimide groups react selectively with thiol groups (-SH) under mild conditions, forming stable thioether bonds. Commonly applied in the preparation of antibody-drug conjugates, protein labeling, and immobilization of biomolecules on surfaces. Also utilized in polymer chemistry to modify and crosslink thiol-containing polymers, enhancing mechanical and thermal properties. Preferred in applications requiring controlled, site-specific coupling due to its homobifunctional structure and relatively short spacer arm.

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