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Catalog Number:
12606
CAS Number:
600153-12-6
Na-Fmoc-Nb-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Dap(Boc-Aoa)-OH
Documents
$115.00 /250MG
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Product Information

Na-Fmoc-Nb-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid is a versatile building block in peptide synthesis, particularly valued for its role in the development of peptide-based therapeutics and research applications. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely used in solid-phase peptide synthesis, allowing for the selective deprotection of amino acids. The Boc (tert-butyloxycarbonyl) group enhances stability and solubility, making it an excellent choice for complex peptide sequences.

Researchers and industry professionals can leverage this compound in the synthesis of modified peptides that exhibit enhanced biological activity or stability. Its unique structure allows for the incorporation of amino-oxyacetyl functionalities, which can facilitate the formation of peptide conjugates and drug delivery systems. This compound is particularly beneficial in the fields of medicinal chemistry and biochemistry, where the design of novel peptides is crucial for advancing therapeutic strategies. With its robust properties and functional versatility, Na-Fmoc-Nb-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid stands out as a key reagent for innovative peptide research and development.

Synonyms
Fmoc-L-Dap(Boc-Aoa)-OH
CAS Number
600153-12-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29N3O8
Molecular Weight
499.5
MDL Number
MFCD02682868
PubChem ID
4712560
Appearance
White crystalline powder or white power
Optical Rotation
[a]D20 = -20 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dap(Boc-Aoa)-OH
CAS Number
600153-12-6
Purity
≥ 98% (HPLC)
Molecular Formula
C25H29N3O8
Molecular Weight
499.5
MDL Number
MFCD02682868
PubChem ID
4712560
Appearance
White crystalline powder or white power
Optical Rotation
[a]D20 = -20 ± 2 º (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-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting other functional groups. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: It plays a significant role in the development of new drugs, particularly in designing peptide-based therapeutics that can target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps to attach biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems and diagnostic tools.
  • Research in Neuroscience: Its application in neuroscience research allows for the development of peptide inhibitors that can modulate neurotransmitter activity, providing insights into neurological disorders and potential treatments.
  • Custom Synthesis: Researchers benefit from its versatility in custom synthesis projects, enabling the creation of tailored compounds for specific applications in various fields, including materials science and molecular biology.

Citations