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Catalog Number:
23029
CAS Number:
79886-55-8
4-( p -maleimidofenil)butirato de succinimidilo
Purity:
≥ 99 % (HPLC)
Synonym(s):
SMPB, Éster N -hidroxisuccinimida del ácido 4-(4-maleimidofenil)butírico
Documents
$148.22 /100 mg
Tamaño
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Información del producto

Succinimidyl 4-(p-maleimidophenyl)butyrate is a versatile crosslinking reagent widely utilized in bioconjugation applications. This compound features a unique maleimide functionality that allows for selective conjugation to thiol groups, making it an ideal choice for the development of antibody-drug conjugates, protein labeling, and the creation of complex biomolecular structures. Its ability to form stable thioether bonds enhances the stability and efficacy of the resulting conjugates, which is crucial in therapeutic and diagnostic applications. Researchers appreciate its ease of use and the efficiency it brings to the conjugation process, enabling the creation of highly specific and potent biomolecules.

In addition to its applications in drug development, Succinimidyl 4-(p-maleimidophenyl)butyrate is also employed in the fabrication of biosensors and in the study of protein interactions. Its unique properties facilitate the exploration of cellular mechanisms and the development of innovative therapeutic strategies. With its reliable performance and broad applicability, this compound stands out as a valuable tool for researchers and industry professionals seeking to advance their work in biochemistry and molecular biology.

Número CAS
79886-55-8
Fórmula molecular
C18H16N2O6
Peso molecular
356.32
Número MDL
MFCD00054961
Punto de fusión
130 - 132 °C
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
79886-55-8
Fórmula molecular
C18H16N2O6
Peso molecular
356.32
Número MDL
MFCD00054961
Punto de fusión
130 - 132 °C
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Succinimidyl 4-(p-maleimidophenyl)butyrate is widely utilized in research focused on:

  • Bioconjugation: This compound is commonly used to link proteins, peptides, or antibodies to other molecules, enhancing their functionality in various applications, such as drug delivery systems.
  • Diagnostic Applications: It plays a crucial role in the development of diagnostic tools, allowing for the creation of targeted imaging agents that can improve the accuracy of disease detection.
  • Vaccine Development: Researchers use it to create conjugate vaccines, which can stimulate a stronger immune response by linking antigens to carrier proteins.
  • Cellular Studies: This chemical is employed in cell biology to study protein interactions and cellular signaling pathways, providing insights into disease mechanisms.
  • Therapeutic Applications: Its ability to form stable conjugates makes it valuable in developing targeted therapies, particularly in cancer treatment, where precision is critical.

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