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Catalog Number:
30459
CAS Number:
105661-40-3
Nb-Azido-L-2,3-diaminopropionic acid hydrochloride
Purity:
≥ 99% (HPLC)
Synonym(s):
2-(S-amino-3-azidopropionic acid·HCl, H-L-Dap(N3)-OH·HCl, L-Ala(N3)·HCl
Documents
$93.14 /100MG
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Product Information

Nb-Azido-L-2,3-diaminopropionic acid hydrochloride is a versatile compound that has garnered attention in the fields of biochemistry and medicinal chemistry. This azido derivative of L-2,3-diaminopropionic acid serves as a valuable building block for the synthesis of various bioactive molecules, particularly in the development of peptide-based therapeutics. Its unique azido functional group enables efficient click chemistry reactions, facilitating the conjugation of biomolecules, which is essential for drug development and targeted delivery systems.

Researchers appreciate this compound for its ability to enhance the stability and bioavailability of therapeutic agents. Its applications extend to the creation of novel drug candidates and the exploration of new pathways in metabolic engineering. With its potential to streamline the synthesis of complex molecules, Nb-Azido-L-2,3-diaminopropionic acid hydrochloride stands out as a crucial tool for scientists aiming to innovate in drug discovery and development.

Synonyms
2-(S-amino-3-azidopropionic acid·HCl, H-L-Dap(N3)-OH·HCl, L-Ala(N3)·HCl
CAS Number
105661-40-3
Purity
≥ 99% (HPLC)
Molecular Formula
C3H7ClN4O2
Molecular Weight
166.6
MDL Number
MFCD18382048
PubChem ID
55785
Melting Point
131-138 °C (dec.)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = +30 ± 2º (C=1 in H2O)
Conditions
Store at 0-8 °C
General Information
Synonyms
2-(S-amino-3-azidopropionic acid·HCl, H-L-Dap(N3)-OH·HCl, L-Ala(N3)·HCl
CAS Number
105661-40-3
Purity
≥ 99% (HPLC)
Molecular Formula
C3H7ClN4O2
Molecular Weight
166.6
MDL Number
MFCD18382048
PubChem ID
55785
Melting Point
131-138 °C (dec.)
Appearance
White crystalline powder
Optical Rotation
[a]D20 = +30 ± 2º (C=1 in H2O)
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

Nb-Azido-L-2,3-diaminopropionic acid hydrochloride is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules, such as proteins and antibodies, to surfaces or other molecules, enhancing the development of targeted therapies.
  • Drug Development: Its unique azide functional group enables click chemistry applications, facilitating the rapid synthesis of drug candidates and improving the efficiency of pharmaceutical research.
  • Protein Labeling: The compound is used for labeling proteins with fluorescent tags, which is crucial in studying protein interactions and dynamics in cellular environments.
  • Material Science: In the field of materials science, it is applied in the creation of functionalized polymers, which can be used in biosensors and drug delivery systems, offering tailored properties for specific applications.
  • Diagnostic Tools: Researchers utilize this compound in the development of diagnostic assays, where its ability to selectively bind to target molecules enhances the sensitivity and specificity of tests.

Citations