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Catalog Number:
04945
CAS Number:
126631-93-4
Ácido fmoc-8-aminocaprílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido fmoc-8-aminooctanoico, Ácido 8-(Fmoc-amino)-caprílico
Documents
$61.29 /1G
Tamaño
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Información del producto

Fmoc-8-aminocaprylic acid is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This amino acid derivative features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure not only enhances stability but also facilitates the efficient coupling of amino acids, making it an invaluable tool for researchers in the fields of medicinal chemistry and biotechnology.

The compound is particularly beneficial in the development of peptide-based therapeutics and drug delivery systems, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of cyclic peptides and the creation of complex biomolecules, allowing for innovative approaches in drug design and development. With its favorable properties, Fmoc-8-aminocaprylic acid stands out as a reliable choice for professionals seeking to enhance their peptide synthesis workflows and explore new avenues in pharmaceutical research.

Número CAS
126631-93-4
Fórmula molecular
C23H27Nº4
Peso molecular
381.5
Número MDL
MFCD00235890
Punto de fusión
117 - 129 °C
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
126631-93-4
Fórmula molecular
C23H27Nº4
Peso molecular
381.5
Número MDL
MFCD00235890
Punto de fusión
117 - 129 °C
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-8-aminocaprylic 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 interfering with other functional groups.
  • Drug Development: It plays a role in the design of peptide-based drugs, particularly in enhancing the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: Researchers use it for conjugating peptides to various biomolecules, facilitating the development of targeted drug delivery systems.
  • Protein Engineering: The compound aids in the modification of proteins, improving their properties for industrial applications, such as enzyme stability in biocatalysis.
  • Research in Neuroscience: It is applied in studies involving neuropeptides, helping to understand their role in signaling pathways and potential therapeutic targets for neurological disorders.

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