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Catalog Number:
04945
CAS Number:
126631-93-4
Fmoc-8-aminocaprylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-8-aminooctanoic acid, 8-(Fmoc-amino)-caprylic acid
Documents
$61.29 /1G
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Product Information

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.

Synonyms
Fmoc-8-aminooctanoic acid, 8-(Fmoc-amino)-caprylic acid
CAS Number
126631-93-4
Purity
≥ 98% (HPLC)
Molecular Formula
C23H27NO4
Molecular Weight
381.5
MDL Number
MFCD00235890
PubChem ID
2756091
Melting Point
117 - 129 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-8-aminooctanoic acid, 8-(Fmoc-amino)-caprylic acid
CAS Number
126631-93-4
Purity
≥ 98% (HPLC)
Molecular Formula
C23H27NO4
Molecular Weight
381.5
MDL Number
MFCD00235890
PubChem ID
2756091
Melting Point
117 - 129 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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.

Citations