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Catalog Number:
03752
CAS Number:
101214-22-6
Ester γ- tert -butylique de l'acide Fmoc-L-glutamique Ester α- N -hydroxysuccinimide
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Glu(OtBu)-OSu
Documents
$29.34 /1G
Taille
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Informations sur le produit

Fmoc-L-glutamic acid g-tert-butyl ester a-N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is essential for the selective protection of amino acids during the synthesis of peptides. Its unique structure allows for the efficient coupling with various amines, making it an ideal choice for researchers looking to create complex peptide sequences or modify existing peptides for enhanced functionality.

The compound's N-hydroxysuccinimide ester functionality further enhances its reactivity, facilitating the formation of stable amide bonds with primary amines. This property is particularly beneficial in drug development and the creation of targeted therapeutics, where precise modifications are crucial. Additionally, the tert-butyl ester group provides stability under various conditions, ensuring that the compound remains effective throughout the synthesis process. Researchers and industry professionals can leverage this compound to streamline their workflows and achieve high yields in peptide synthesis and bioconjugation projects.

Numéro CAS 
101214-22-6
Formule moléculaire
C28H30N2O6
Poids moléculaire 
522.55
Point de fusion 
159 - 166 °C
Rotation optique 
[a] D 20 = -29 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
101214-22-6
Formule moléculaire
C28H30N2O6
Poids moléculaire 
522.55
Point de fusion 
159 - 166 °C
Rotation optique 
[a] D 20 = -29 ± 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

Fmoc-L-glutamic acid g-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, allowing researchers to create custom sequences for various applications in drug development and biotechnology.
  • Bioconjugation: Its reactive N-hydroxysuccinimide (NHS) group enables efficient conjugation to proteins or other biomolecules, facilitating the development of targeted therapies and diagnostics.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery vehicles, enhancing the stability and bioavailability of therapeutic agents, particularly in cancer treatments.
  • Research in Neuroscience: By modifying glutamic acid, it aids in studying neurotransmitter pathways, contributing to the understanding of neurological disorders and potential treatments.
  • Material Science: Its unique properties allow for the development of novel materials with specific functionalities, such as hydrogels for tissue engineering applications.

Citations