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Product Line: Pharmaceutical Chemicals

N-Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate

CAS 64987-85-5

Molecular structure of N-Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate

CAS · 64987-85-5

01

Product Overview

N-Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance White to pale yellow solid
Purity (HPLC) 98% min
Water 1.0% max
Clarity of Solution 0.3 g in 2 ml DMF clear solution
Mass Spectrum In accordance with the standard
NMR Spectrum In accordance with the standard
03

Applications

N-Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate (commonly known as SMCC) is a widely used bifunctional crosslinking reagent in bioconjugation, pharmaceutical research, and protein engineering. It is primarily employed to link proteins, peptides, antibodies, or other biomolecules via amine and thiol functional groups, enabling the synthesis of antibody-drug conjugates (ADCs), protein-drug conjugates, and targeted therapeutics. SMCC is also used in immobilization of enzymes or ligands onto solid supports for diagnostics, biosensors, and affinity chromatography. Its selective reactivity towards primary amines (via the NHS ester) and sulfhydryl groups (via the maleimide moiety) allows precise, site-specific conjugation, which is crucial in maintaining biological activity and functionality of the conjugated molecules.

04

Benefits

The benefits of SMCC arise from its bifunctional reactivity, chemical stability, and specificity. The NHS ester allows efficient conjugation with primary amines under mild aqueous conditions, while the maleimide group reacts selectively with thiols, enabling targeted and stable crosslinking. This dual functionality minimizes side reactions and ensures reproducibility in bioconjugation processes. SMCC provides robust and stable linkages, maintaining the structural integrity and activity of proteins and other biomolecules. Its versatility in forming antibody-drug conjugates, enzyme immobilization, and targeted delivery systems makes it an indispensable tool in pharmaceutical development, diagnostics, and biochemical research.

05

Conclusion

In summary, N-Succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC) is a key bifunctional crosslinker with applications in antibody-drug conjugates, protein modification, enzyme immobilization, and bioconjugation research. Its benefits include selective reactivity, stable linkage formation, chemical stability, and preservation of biomolecular function. By combining precision, versatility, and reliability, SMCC continues to be a critical reagent in pharmaceutical development, targeted therapeutics, and advanced biochemical applications.

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