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Catalog Number:
26443
CAS Number:
1423018-04-5
Nα-Fmoc-Nβ-Octanoyl-2,3-diaminopropionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Dap(Octanoyl)-OH
Documents
$58.39 /100MG
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Product Information

Na-Fmoc-Nb-Octanoyl-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amine functionalities during solid-phase peptide synthesis. Its octanoyl side chain enhances lipophilicity, making it particularly valuable in the design of bioactive peptides and pharmaceuticals that require improved membrane permeability. Researchers appreciate its ability to facilitate the synthesis of complex peptides with enhanced stability and bioavailability, which is crucial in therapeutic applications.

In addition to its role in peptide synthesis, Na-Fmoc-Nb-Octanoyl-2,3-diaminopropionic acid is also explored in the development of novel drug delivery systems and biomaterials. Its unique structural features allow for the incorporation of specific functionalities that can target particular biological pathways, making it an attractive candidate for further research in medicinal chemistry and biotechnology. This compound not only streamlines the synthesis process but also opens avenues for innovative applications in drug formulation and delivery.

Synonyms
Fmoc-L-Dap(Octanoyl)-OH
CAS Number
1423018-04-5
Purity
≥ 99% (HPLC)
Molecular Formula
C26H32N2O5
Molecular Weight
452.55
MDL Number
MFCD18427298
PubChem ID
23072550
Melting Point
140-145 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -14 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Dap(Octanoyl)-OH
CAS Number
1423018-04-5
Purity
≥ 99% (HPLC)
Molecular Formula
C26H32N2O5
Molecular Weight
452.55
MDL Number
MFCD18427298
PubChem ID
23072550
Melting Point
140-145 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -14 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nb-Octanoyl-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others, which is crucial for creating complex biomolecules.
  • Drug Development: Its unique structure enables researchers to design and optimize drug candidates, particularly in the development of peptide-based therapeutics that target specific biological pathways.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and drug delivery systems in the pharmaceutical industry.
  • Research in Neuroscience: It can be utilized to create modified peptides that interact with neuronal receptors, aiding in the study of neurological diseases and the development of potential treatments.
  • Cosmetic Formulations: The compound's properties allow it to be incorporated into skincare products, providing benefits such as improved skin penetration and targeted delivery of active ingredients.

Citations