Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
03721
CAS Number:
76265-69-5
N α -Fmoc- N ε -trifluoroacétyl-L-lysine
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Lys(Tfa)-OH
Documents
$22.43 /1G
Taille
Request Bulk Quote
Informations sur le produit

Na-Fmoc-Ne-trifluoroacetyl-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective coupling of amino acids during solid-phase peptide synthesis. The trifluoroacetyl group enhances the stability and solubility of the compound, making it an excellent choice for researchers focusing on the synthesis of complex peptides and proteins. Its unique structure allows for the introduction of lysine residues into peptides, which can be critical for enhancing biological activity or improving pharmacokinetic properties.

In addition to its role in peptide synthesis, Na-Fmoc-Ne-trifluoroacetyl-L-lysine is also valuable in the development of bioconjugates and targeted drug delivery systems. The trifluoroacetyl moiety can serve as a reactive site for further modifications, allowing for the creation of tailored compounds with specific functionalities. This compound is particularly beneficial for researchers in the fields of medicinal chemistry and biochemistry, providing a reliable building block for innovative therapeutic applications.

Numéro CAS 
76265-69-5
Formule moléculaire
C23H23F5N2O5
Poids moléculaire 
464.4
Point de fusion 
163 - 178 ºC
Rotation optique 
[a] D 20 = -12 ± 2 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
76265-69-5
Formule moléculaire
C23H23F5N2O5
Poids moléculaire 
464.4
Point de fusion 
163 - 178 ºC
Rotation optique 
[a] D 20 = -12 ± 2 º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Na-Fmoc-Ne-trifluoroacetyl-L-lysine 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: Its unique protective groups allow for selective reactions, making it valuable in the pharmaceutical industry for developing new therapeutic peptides with enhanced stability and bioactivity.
  • Bioconjugation: The trifluoroacetyl group can be used to facilitate bioconjugation processes, allowing for the attachment of various biomolecules, which is essential in creating targeted drug delivery systems.
  • Protein Engineering: Researchers utilize this compound in the modification of lysine residues in proteins, which can help in studying protein interactions and functions, ultimately aiding in the design of novel proteins.
  • Analytical Chemistry: It is also employed in analytical methods for characterizing peptides and proteins, providing insights into their structure and function, which is crucial for quality control in biopharmaceuticals.

Citations