Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
04069
CAS Number:
218457-73-9
Ácido fmoc-D-α-aminoadípico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Aad-OH, Ácido fmoc-D-2-aminohexanodioico
Documents
$93.14 /250 mg
Tamaño
Request Bulk Quote
Información del producto

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.

Número CAS
218457-73-9
Fórmula molecular
C21H21Nº6
Peso molecular
383.4
Número MDL
MFCD01317727
Punto de fusión
139-147º C
Rotación óptica
=+11,50º ± 1º (c=1,021 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
218457-73-9
Fórmula molecular
C21H21Nº6
Peso molecular
383.4
Número MDL
MFCD01317727
Punto de fusión
139-147º C
Rotación óptica
=+11,50º ± 1º (c=1,021 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

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.

Citas