Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
30514
CAS Number:
880637-82-1
Na-Azido-Nb-Fmoc-L-2,3-diaminopropionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
(S-2-azido-3-(Fmoc-amino)propionic acid, N3-L-Dap(Fmoc)-OH
Documents
$65.40 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Na-Azido-Nb-Fmoc-L-2,3-diaminopropionic acid is a versatile compound widely utilized in the fields of peptide synthesis and medicinal chemistry. This compound features an azido group, which enhances its reactivity, making it an excellent candidate for click chemistry applications. The Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides and bioactive molecules. Researchers appreciate its ability to streamline the synthesis process while maintaining high yields and purity.

In addition to its role in peptide synthesis, Na-Azido-Nb-Fmoc-L-2,3-diaminopropionic acid is also valuable in the development of novel therapeutics and drug delivery systems. Its unique structure allows for the incorporation of azide functionalities, which can be further modified for targeted drug delivery applications. This compound's stability and compatibility with various reaction conditions make it an essential tool for chemists and researchers aiming to innovate in drug design and development.

Synonyms
(S-2-azido-3-(Fmoc-amino)propionic acid, N3-L-Dap(Fmoc)-OH
CAS Number
880637-82-1
Purity
≥ 99% (HPLC)
Molecular Formula
C18H16N4O4
Molecular Weight
352.3
MDL Number
MFCD22989449
PubChem ID
72988743
Appearance
White crystalline powder
Optical Rotation
C18H16N4O4
Conditions
Store at 0-8 °C
General Information
Synonyms
(S-2-azido-3-(Fmoc-amino)propionic acid, N3-L-Dap(Fmoc)-OH
CAS Number
880637-82-1
Purity
≥ 99% (HPLC)
Molecular Formula
C18H16N4O4
Molecular Weight
352.3
MDL Number
MFCD22989449
PubChem ID
72988743
Appearance
White crystalline powder
Optical Rotation
C18H16N4O4
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Azido-Nb-Fmoc-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 the development of novel therapeutic agents.
  • Drug Development: Its unique azido group allows for click chemistry applications, facilitating the creation of complex drug molecules with improved efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and targeted therapies.
  • Research in Neuroscience: It is employed in studies involving neuropeptides, aiding in the understanding of neurological functions and potential treatments for neurodegenerative diseases.
  • Material Science: The azido functionality allows for the modification of polymers, enhancing their properties for applications in coatings and drug delivery systems.

Citations