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Catalog Number:
15036
CAS Number:
1014018-41-7
Acide Fmoc-( S )-4-aminopentanoïque
Purity:
≥ 99 % (HPLC)
Documents
$93.14 /100 mg
Taille
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Product Information

Fmoc-(S)-4-aminopentanoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its chirality, denoted by the (S) configuration, enhances its relevance in the development of enantiomerically pure compounds, making it particularly valuable in pharmaceutical applications. Researchers appreciate its stability under various conditions, which facilitates its use in solid-phase peptide synthesis (SPPS) and other synthetic methodologies.

In addition to its role in peptide synthesis, Fmoc-(S)-4-aminopentanoic acid is also employed in the design of bioactive compounds and drug candidates. Its unique structure allows for the incorporation of this amino acid into larger peptide sequences, thereby influencing the biological activity of the resulting molecules. This compound is ideal for researchers focused on developing therapeutics that require precise control over molecular structure and function. With its proven track record in the synthesis of complex peptides, Fmoc-(S)-4-aminopentanoic acid stands out as a critical reagent for advancing research in medicinal chemistry and biochemistry.

CAS Number
1014018-41-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 20 H 214
Molecular Weight
339.39
MDL Number
MFCD05663762
PubChem ID
58165143
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = +7 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
General Information
CAS Number
1014018-41-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 20 H 214
Molecular Weight
339.39
MDL Number
MFCD05663762
PubChem ID
58165143
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = +7 ± 2º (C=1 dans DMF)
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(S)-4-aminopentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its role in modifying amino acids makes it valuable in the pharmaceutical industry for developing new therapeutic agents, particularly in designing peptide-based drugs.
  • Bioconjugation: The Fmoc protecting group enables selective reactions in bioconjugation processes, facilitating the attachment of biomolecules for targeted drug delivery systems.
  • Research in Neuroscience: This compound is used in studies related to neuropeptides, helping scientists understand their functions and potential therapeutic applications in neurological disorders.
  • Custom Peptide Libraries: It is instrumental in generating diverse peptide libraries for screening and identifying novel bioactive compounds, which is crucial in drug discovery.

Citations