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Catalog Number:
04069
CAS Number:
218457-73-9
Acide Fmoc-D-α-aminoadipique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Aad-OH, Acide Fmoc-D-2-aminohexanedioïque
Documents
$93.14 /250 mg
Taille
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Informations sur le produit

Fmoc-D-a-aminoadipic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it invaluable for researchers in the field of medicinal chemistry. Its unique structure, characterized by a hexanedioic acid backbone, enhances its solubility and reactivity, facilitating the formation of complex peptides with improved biological activity.

In practical applications, Fmoc-D-a-aminoadipic acid is employed in the synthesis of bioactive peptides and pharmaceuticals, particularly in the development of therapeutics targeting various diseases. Its ability to serve as a chiral building block also makes it a preferred choice for researchers aiming to create enantiomerically pure compounds. With its robust performance in peptide coupling reactions, this compound stands out for its efficiency and reliability, making it an essential tool for both academic and industrial laboratories focused on peptide research and development.

Numéro CAS 
218457-73-9
Formule moléculaire
C 21 H 216
Poids moléculaire 
383.4
Point de fusion 
139-147º C
Rotation optique 
=+11,50º ± 1º (c=1,021 en DMF)
Informations générales
Numéro CAS 
218457-73-9
Formule moléculaire
C 21 H 216
Poids moléculaire 
383.4
Point de fusion 
139-147º C
Rotation optique 
=+11,50º ± 1º (c=1,021 en 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-D-a-aminoadipic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting the overall structure.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, enhancing the stability and bioavailability of drug candidates.
  • Biotechnology: Researchers use it in the development of novel biomaterials, leveraging its properties to create hydrogels and scaffolds for tissue engineering applications.
  • Analytical Chemistry: The compound is utilized in various analytical techniques, including chromatography, to help separate and identify complex mixtures of peptides and proteins.
  • Academic Research: It is frequently employed in laboratories for educational purposes, allowing students and researchers to explore peptide chemistry and its applications in a hands-on manner.

Citations