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Catalog Number:
33494
CAS Number:
757960-24-0
N α -Fmoc- N β -(N-Boc-amino-oxyacétyl)-L-lysine
Purity:
≥ 98 % (HPLC)
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
Documents
$75.00 /250 mg
Taille
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Informations sur le produit

Na -Fmoc- Nb -(N-Boc-amino-oxyacetyl)-L-lysine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its unique structure, including the Boc (tert-butyloxycarbonyl) protecting group, enhances stability and solubility, making it an ideal choice for researchers focusing on complex peptide sequences.

In the pharmaceutical industry, Na -Fmoc- Nb -(N-Boc-amino-oxyacetyl)-L-lysine is particularly valuable for the development of peptide-based therapeutics, where precise control over amino acid functionality is crucial. Its application extends to the creation of targeted drug delivery systems and the synthesis of bioactive peptides, which can lead to innovative treatments for various diseases. The compound's ability to improve the yield and purity of synthesized peptides sets it apart from similar products, making it a preferred choice for professionals in biochemistry and medicinal chemistry.

Numéro CAS 
757960-24-0
Formule moléculaire
C28H35N3O8
Poids moléculaire 
541.6
Point de fusion 
108 - 113 °C
Rotation optique 
[a] D 20 = -11 ± 2 ° (C = 1 dans DMF)
Informations générales
Numéro CAS 
757960-24-0
Formule moléculaire
C28H35N3O8
Poids moléculaire 
541.6
Point de fusion 
108 - 113 °C
Rotation optique 
[a] D 20 = -11 ± 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

Na -Fmoc- Nb -(N-Boc-amino-oxyacetyl)-L-lysine 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 structures for various biological studies.
  • Drug Development: Its unique functional groups facilitate the development of novel therapeutics, particularly in targeting specific biological pathways, enhancing drug efficacy.
  • Bioconjugation: The compound is ideal for bioconjugation applications, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic delivery systems.
  • Protein Modification: It is used to modify proteins for better stability and activity, making it valuable in enzyme engineering and protein therapeutics.
  • Research in Cancer Biology: The compound's ability to selectively target cancer cells is being explored, providing potential pathways for more effective cancer treatments.

Citations