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Catalog Number:
05120
CAS Number:
1217631-22-5
Acide N α,β -Bis-Fmoc-D-2,3-diaminopropionique
Purity:
≥ 99,9 % (HPLC chirale)
Synonym(s):
Fmoc-D-Dap(Fmoc)-OH
Documents
$85.00 /100 mg
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Product Information

Na,b-Bis-Fmoc-D-2,3-diaminopropionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features two Fmoc (9-fluorenylmethoxycarbonyl) protecting groups, which provide excellent stability during the synthesis process, making it an ideal choice for researchers focused on complex peptide structures. Its unique properties allow for selective deprotection, facilitating the formation of intricate peptide sequences essential in pharmaceuticals and biochemistry.

In addition to its role in peptide synthesis, Na,b-Bis-Fmoc-D-2,3-diaminopropionic acid is also valuable in the development of novel therapeutic agents. Its ability to enhance solubility and bioavailability makes it a preferred choice for medicinal chemists aiming to optimize drug formulations. Researchers in the fields of biotechnology and pharmaceuticals can leverage this compound to create targeted therapies, improving efficacy and reducing side effects. With its robust applications and significant advantages over similar compounds, Na,b-Bis-Fmoc-D-2,3-diaminopropionic acid stands out as a crucial tool in modern chemical research.

Synonyms
Fmoc-D-Dap(Fmoc)-OH
CAS Number
1217631-22-5
Purity
≥ 99,9 % (HPLC chirale)
Molecular Formula
C33H28N2O6
Molecular Weight
548.58
MDL Number
MFCD01632030
PubChem ID
5193992
Appearance
Poudre cristalline blanc cassé
Optical Rotation
[a] D 20 = 14 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-D-Dap(Fmoc)-OH
CAS Number
1217631-22-5
Purity
≥ 99,9 % (HPLC chirale)
Molecular Formula
C33H28N2O6
Molecular Weight
548.58
MDL Number
MFCD01632030
PubChem ID
5193992
Appearance
Poudre cristalline blanc cassé
Optical Rotation
[a] D 20 = 14 ± 1 ° (C = 1 dans DMF)
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,b-Bis-Fmoc-D-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 for the introduction of specific amino acid sequences that are crucial for developing therapeutic proteins.
  • Drug Development: It plays a significant role in pharmaceutical research, particularly in the design of novel drug candidates that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents, improving their delivery and effectiveness in targeted therapies.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, aiding researchers in understanding the role of specific peptides in neurological functions and disorders.
  • Custom Synthesis: This compound is favored in custom synthesis projects, providing researchers with the flexibility to create tailored compounds for specific applications in various fields, including materials science and diagnostics.

Citations