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Catalog Number:
06314
CAS Number:
198544-42-2
Nα-Fmoc-Nβ-Boc-D-2,3-diaminopropionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Dap(Boc)-OH, (R)-3-(Boc-amino)-2-(Fmoc-amino)propionic acid
Documents
$85.00 /250MG
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Product Information

Na-Fmoc-Nb-Boc-D-2,3-diaminopropionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features protective groups that enhance its stability and reactivity, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure allows for the selective incorporation of D-amino acids into peptides, which can significantly influence the biological activity and stability of the resulting compounds.

In practical applications, Na-Fmoc-Nb-Boc-D-2,3-diaminopropionic acid is particularly valuable in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to facilitate the synthesis of complex peptides with improved pharmacological properties positions it as a key reagent for researchers aiming to explore new drug candidates or optimize existing ones. Additionally, its compatibility with various coupling reagents and solid-phase synthesis techniques enhances its utility in laboratory settings, making it a preferred choice for peptide chemists.

Synonyms
Fmoc-D-Dap(Boc)-OH, (R)-3-(Boc-amino)-2-(Fmoc-amino)propionic acid
CAS Number
198544-42-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O6
Molecular Weight
426.5
MDL Number
MFCD00798648
PubChem ID
3605438
Melting Point
133 - 143 °C (Lit.)
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = 21.2 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Dap(Boc)-OH, (R)-3-(Boc-amino)-2-(Fmoc-amino)propionic acid
CAS Number
198544-42-2
Purity
≥ 98% (HPLC)
Molecular Formula
C23H26N2O6
Molecular Weight
426.5
MDL Number
MFCD00798648
PubChem ID
3605438
Melting Point
133 - 143 °C (Lit.)
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = 21.2 ± 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-Boc-D-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as an important 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 novel therapeutics, particularly in targeting specific biological pathways.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Protein Engineering: The compound aids in the design of modified proteins with improved stability and activity, which is crucial for various biotechnological applications.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for potential applications in neuroprotective agents and treatments for neurodegenerative diseases.

Citations