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Catalog Number:
12348
CAS Number:
52773-66-7
Ester de Z- O -benzyl-L-tyrosine N -hydroxysuccinimide
Purity:
≥ 98 % (HPLC)
Synonym(s):
ZL-Tyr(Bzl)-OSu
Documents
$60.39 /1G
Taille
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Informations sur le produit

Z-O-benzyl-L-tyrosine N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique structure that enhances its reactivity, making it an excellent choice for researchers looking to create stable linkages between biomolecules. Its N-hydroxysuccinimide ester functionality allows for efficient coupling reactions, which are essential in the development of peptide-based therapeutics and targeted drug delivery systems.

In addition to its role in peptide synthesis, Z-O-benzyl-L-tyrosine N-hydroxysuccinimide ester is also employed in the modification of proteins and antibodies, facilitating the creation of conjugates with improved pharmacokinetic properties. Researchers appreciate its ability to provide a high degree of specificity and stability in bioconjugation processes, which is crucial for the development of effective diagnostic tools and therapeutic agents. With its robust performance and reliability, this compound stands out as a valuable asset in both academic research and industrial applications.

Numéro CAS 
52773-66-7
Formule moléculaire
C28H26N2O7
Poids moléculaire 
502.52
Point de fusion 
136-144 °C
Rotation optique 
[α] D 20 = -56 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
52773-66-7
Formule moléculaire
C28H26N2O7
Poids moléculaire 
502.52
Point de fusion 
136-144 °C
Rotation optique 
[α] D 20 = -56 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Z-O-benzyl-L-tyrosine N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development and biological studies.
  • Drug Delivery Systems: Its ability to form stable conjugates makes it valuable in designing drug delivery systems, enhancing the bioavailability of therapeutic agents.
  • Bioconjugation: It is commonly used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostic applications.
  • Research in Neuroscience: The compound's structural properties make it useful in studying neurotransmitter pathways and developing potential treatments for neurological disorders.
  • Antibody Labeling: This ester is effective in labeling antibodies for immunological assays, improving the sensitivity and specificity of detection methods.

Citations