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Catalog Number:
02490
CAS Number:
88574-06-5
Ácido fmoc-6-aminohexanoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido fmoc-6-aminocaproico, Fmoc-ε-Ahx-OH
Documents
$20.20 /1G
Tamaño
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Información del producto

Fmoc-6-aminohexanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential tool for researchers in the field of medicinal chemistry. Its unique structure enhances solubility and stability, facilitating the formation of complex peptide sequences.

In practical applications, Fmoc-6-aminohexanoic acid is particularly valuable in the development of peptide-based therapeutics and biomaterials. Its ability to serve as a linker in solid-phase peptide synthesis enables the efficient assembly of peptides with specific biological activities. Additionally, this compound is recognized for its role in the design of drug delivery systems and targeted therapies, providing researchers with innovative solutions for enhancing drug efficacy. With its favorable properties and wide-ranging applications, Fmoc-6-aminohexanoic acid is an indispensable asset for professionals in pharmaceutical and biochemical research.

Número CAS
88574-06-5
Fórmula molecular
C21H23NO4
Peso molecular
353.3
Número MDL
MFCD00077045
Punto de fusión
110 - 123 °C
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
88574-06-5
Fórmula molecular
C21H23NO4
Peso molecular
353.3
Número MDL
MFCD00077045
Punto de fusión
110 - 123 °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
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Aplicaciones

Fmoc-6-aminohexanoic 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 is used in the design of peptide-based drugs, enhancing the stability and bioavailability of therapeutic peptides, which is crucial in pharmaceutical applications.
  • Bioconjugation: The compound facilitates the attachment of biomolecules to surfaces or other molecules, improving the efficacy of diagnostics and targeted drug delivery systems.
  • Research in Biochemistry: Researchers employ it in the study of protein interactions and functions, aiding in the understanding of biological processes and disease mechanisms.
  • Material Science: It finds applications in creating functionalized polymers and materials, which can be tailored for specific uses in coatings, adhesives, and drug delivery systems.

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