N-Succinimidyl Maleimidoacetate丨CAS 55750-61-3

N-Succinimidyl Maleimidoacetate丨CAS 55750-61-3
Product Introduction:
Catalog No.: SS131988
CAS No.: 55750-61-3
Purity(HPLC): 98% min
Product Name: N-Succinimidyl maleimidoacetate
Molecular Formula: C10H8N2O6
Molecular Weight: 252.18
Synonym(s): Maleimidoacetic acid N-hydroxysuccinimide ester
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Technical Parameters
Description

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Specifications

 

Appearance Yellowish to white crystalline powder
Purity (HPLC) 98% min
Melting point 188°C to 193°C

 

 

 

Applications

 

N-Succinimidyl maleimidoacetate is widely used as a bifunctional crosslinking reagent in bioconjugation, protein modification, and biomolecular research. It contains both an N-hydroxysuccinimide (NHS) ester and a maleimide group, allowing selective conjugation to primary amines and thiol groups, respectively. This makes it ideal for linking peptides, proteins, antibodies, or other biomolecules in a controlled manner. The compound is also employed in the preparation of targeted drug delivery systems, fluorescent probes, and diagnostic reagents, where stable and site-specific attachment of functional molecules is critical. Additionally, it serves as a tool in chemical biology and proteomics for studying protein interactions and labeling specific biomolecular sites.

 

Benefits

 

The benefits of N-Succinimidyl maleimidoacetate include its high reactivity, selectivity, and ability to form stable covalent linkages under mild conditions. The NHS ester reacts efficiently with amino groups, while the maleimide selectively targets thiols, enabling precise dual-functional modification. Its chemical stability in dry form and predictable reactivity in aqueous or organic media support reproducible conjugation reactions. This dual functionality reduces unwanted side reactions, improves labeling efficiency, and allows controlled orientation of conjugated biomolecules, making it a practical reagent for research and therapeutic applications.

 

Conclusion

 

N-Succinimidyl maleimidoacetate is a versatile crosslinking reagent used in protein modification, bioconjugation, and biomolecular research. Its dual reactive groups, selectivity, and stability enable site-specific and efficient conjugation of biomolecules, supporting applications in drug delivery, diagnostics, and chemical biology. These properties make it a reliable and valuable tool in both laboratory and applied research contexts.

 

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