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Catalog Number:
02394
CAS Number:
78553-23-8
Ester β- tert -butylique d'acide Fmoc-L-aspartique et ester α- N- hydroxysuccinimide
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Asp(OtBu)-OSu
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$50.00 /1G
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Informations sur le produit

Fmoc-L-aspartic acid b-tert-butyl ester a-N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc group that facilitates the selective coupling of amino acids, making it an essential building block in the synthesis of peptides and proteins. Its unique structure allows for efficient conjugation reactions, particularly in the formation of peptide-based therapeutics and bioconjugates. Researchers appreciate its stability under various conditions, which enhances its applicability in both academic and industrial settings.

In addition to its role in peptide synthesis, this compound is also valuable in the development of targeted drug delivery systems. The N-hydroxysuccinimide ester functionality enables the formation of stable amide bonds with primary amines, allowing for the creation of complex biomolecules. This characteristic is particularly beneficial in the design of drug carriers and diagnostic agents, where precise targeting and controlled release are crucial. Overall, Fmoc-L-aspartic acid b-tert-butyl ester a-N-hydroxysuccinimide ester stands out for its efficiency and versatility in various biochemical applications.

Numéro CAS 
78553-23-8
Formule moléculaire
C27H28N2O8
Poids moléculaire 
508.5
Point de fusion 
126 - 133 °C
Rotation optique 
[a] D 20 = -30 ± 2 ° (C = 1 dans DMF)
Informations générales
Numéro CAS 
78553-23-8
Formule moléculaire
C27H28N2O8
Poids moléculaire 
508.5
Point de fusion 
126 - 133 °C
Rotation optique 
[a] D 20 = -30 ± 2 ° (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

Fmoc-L-aspartic acid b-tert-butyl ester a-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, particularly in solid-phase peptide synthesis, enabling researchers to create complex peptide sequences efficiently.
  • Drug Development: It is used in the development of peptide-based drugs, allowing for the modification of peptide structures to enhance stability and bioactivity, which is crucial in pharmaceutical research.
  • Bioconjugation: The compound facilitates the conjugation of peptides to various biomolecules, such as antibodies or drugs, improving targeted delivery systems in therapeutic applications.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter signaling, particularly in the synthesis of aspartic acid derivatives, which are important in understanding synaptic transmission.
  • Protein Engineering: This chemical is utilized in modifying proteins to study their function and interactions, providing insights into protein behavior and potential applications in biotechnology.

Citations