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Catalog Number:
03763
CAS Number:
162558-25-0
Nα-Fmoc-Nβ-Boc-L-2,3-diaminopropionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Dap(Boc)-OH, Fmoc-Dap(Boc)-OH
Documents
$51.18 /1G
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Product Information

Na-Fmoc-Nb-Boc-L-2,3-diaminopropionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its protective groups, Fmoc and Boc, facilitate the selective modification of amino acids, allowing for the efficient assembly of complex peptide chains. This property is particularly beneficial in the design of peptide-based therapeutics, where precision and control over the synthesis process are paramount.

In addition to its applications in peptide synthesis, Na-Fmoc-Nb-Boc-L-2,3-diaminopropionic acid is also valuable in the development of novel biomaterials and drug delivery systems. Its ability to form stable conjugates with various biomolecules opens up possibilities for targeted therapy and improved bioavailability of therapeutic agents. Researchers and industry professionals can leverage this compound to innovate in drug formulation and enhance the efficacy of their products, making it a crucial addition to any laboratory focused on cutting-edge pharmaceutical research.

Synonyms
Fmoc-L-Dap(Boc)-OH, Fmoc-Dap(Boc)-OH
CAS Number
162558-25-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O6
Molecular Weight
426.46
MDL Number
MFCD00235896
PubChem ID
3605438
Appearance
White powder
Optical Rotation
[a]D20 = -21 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Dap(Boc)-OH, Fmoc-Dap(Boc)-OH
CAS Number
162558-25-0
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O6
Molecular Weight
426.46
MDL Number
MFCD00235896
PubChem ID
3605438
Appearance
White powder
Optical Rotation
[a]D20 = -21 ± 2º (C=1 in DMF)
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-Boc-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 with specific functionalities.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutics.
  • Research in Neuroscience: It plays a role in the study of neuropeptides, helping scientists understand their functions and potential therapeutic applications in neurological disorders.
  • Customizable Research Tools: The versatility of this compound allows researchers to modify it for various applications, making it a preferred choice for tailored research solutions.

Citations