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Catalog Number:
04161
CAS Number:
181954-34-7
Acide N α - Fmoc-L-2,3-diaminopropionique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Dap-OH
Documents
$45.30 /1G
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Product Information

Na-Fmoc-L-2,3-diaminopropionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an essential tool for researchers in medicinal chemistry and biochemistry. Its unique structure enhances the stability and solubility of peptides, facilitating the development of complex biomolecules.

In practical applications, Na-Fmoc-L-2,3-diaminopropionic acid is particularly valuable in the synthesis of peptide-based therapeutics, where precise amino acid sequences are crucial for biological activity. Its ability to form stable linkages and maintain structural integrity under various conditions makes it a preferred choice for researchers aiming to create novel peptides with enhanced efficacy. Additionally, this compound can be employed in the development of targeted drug delivery systems, contributing to advancements in personalized medicine.

Synonyms
Fmoc-L-Dap-OH
CAS Number
181954-34-7
Purity
≥ 97 % (HPLC)
Molecular Formula
C18H18N2O4
Molecular Weight
326.34
MDL Number
MFCD00237019
PubChem ID
5165519
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-L-Dap-OH
CAS Number
181954-34-7
Purity
≥ 97 % (HPLC)
Molecular Formula
C18H18N2O4
Molecular Weight
326.34
MDL Number
MFCD00237019
PubChem ID
5165519
Appearance
Poudre cristalline blanche
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

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

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various applications in biochemistry and pharmaceuticals.
  • Drug Development: Its unique properties facilitate the design of novel drug candidates, particularly in targeting specific biological pathways, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, which is crucial in developing targeted therapies and diagnostics.
  • Protein Engineering: It plays a significant role in protein engineering, helping scientists modify protein structures to improve their stability and functionality, which is essential in various industrial applications.
  • Research in Neuroscience: The compound is also applied in neuroscience research, particularly in studying neuropeptides and their roles in signaling pathways, contributing to advancements in understanding brain functions.

Citations