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Catalog Number:
47701
CAS Number:
439864-51-4
Acide N a -Fmoc- N b -Boc- N b -Boc-aminoéthyl-L-2,3-diaminopropionique
Purity:
≥ 99,9 % (pureté chirale)
Synonym(s):
Fmoc-Dap(Boc,2-Boc-aminoéthyl)-OH, Acide (2 S )-3-[( tert -butoxycarbonyl)({2-[( tert -butoxycarbonyl)amino]éthyl})amino]-2-{[(9H-fluoren-9-ylméthoxy)carbonyl]amino}propanoïque
Documents
$195.00 /25 mg
Taille
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Product Information

Na-Fmoc-Nb-Boc-Nb-Boc-aminoethyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features multiple protective groups, making it an ideal choice for researchers looking to enhance the stability and solubility of peptides during synthesis. Its unique structure allows for selective deprotection, facilitating the stepwise assembly of complex peptide sequences. This capability is particularly beneficial in the pharmaceutical industry, where precision and efficiency in peptide synthesis are paramount for developing therapeutic agents.

In addition to its applications in peptide synthesis, this compound is also valuable in the field of bioconjugation, where it can be used to attach peptides to various biomolecules, enhancing their functionality and targeting capabilities. Researchers appreciate its ability to improve the pharmacokinetic properties of peptides, making them more effective as drug candidates. With its robust profile and practical applications, Na-Fmoc-Nb-Boc-Nb-Boc-aminoethyl-L-2,3-diaminopropionic acid stands out as a critical tool for advancing research and development in medicinal chemistry and biotechnology.

Synonyms
Fmoc-Dap(Boc,2-Boc-aminoéthyl)-OH, Acide (2 S )-3-[( tert -butoxycarbonyl)({2-[( tert -butoxycarbonyl)amino]éthyl})amino]-2-{[(9H-fluoren-9-ylméthoxy)carbonyl]amino}propanoïque
CAS Number
439864-51-4
Purity
≥ 99,9 % (pureté chirale)
Molecular Formula
C30H39N3O8
Molecular Weight
569.7
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a]D20 = -13.5 - 16.5 °(C=1 in MeOH)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Fmoc-Dap(Boc,2-Boc-aminoéthyl)-OH, Acide (2 S )-3-[( tert -butoxycarbonyl)({2-[( tert -butoxycarbonyl)amino]éthyl})amino]-2-{[(9H-fluoren-9-ylméthoxy)carbonyl]amino}propanoïque
CAS Number
439864-51-4
Purity
≥ 99,9 % (pureté chirale)
Molecular Formula
C30H39N3O8
Molecular Weight
569.7
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a]D20 = -13.5 - 16.5 °(C=1 in MeOH)
Conditions
Conserver entre 2 et 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-Nb-Boc-Nb-Boc-aminoethyl-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, particularly in solid-phase peptide synthesis, allowing for the creation of complex and functional peptides.
  • Drug Development: It is used in the design of peptide-based therapeutics, providing a scaffold for developing new drugs with enhanced efficacy and specificity.
  • Bioconjugation: The chemical facilitates the conjugation of peptides to various biomolecules, which is essential in creating targeted drug delivery systems and improving the pharmacokinetics of therapeutic agents.
  • Research in Neuroscience: Its derivatives are explored in studies related to neuropeptides, aiding in the understanding of neurological pathways and potential treatments for neurodegenerative diseases.
  • Custom Synthesis: Researchers can utilize this compound for custom synthesis projects, allowing for tailored modifications that meet specific research needs, thus enhancing experimental outcomes.

Citations