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Catalog Number:
04964
CAS Number:
204316-32-5
Nα-Fmoc-Nγ-allyloxycarbonyl-L-2,4-diaminobutyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Dab(Aloc)-OH
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Product Information

Na-Fmoc-Ng-allyloxycarbonyl-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of amine functionalities during the synthesis of complex peptides. Its unique allyloxycarbonyl group enhances its reactivity, making it an excellent choice for researchers focused on developing novel therapeutic agents.

This compound is particularly valuable in the field of medicinal chemistry, where it serves as a building block for the synthesis of bioactive peptides and pharmaceuticals. Its ability to facilitate the introduction of various functional groups allows for the customization of peptides tailored to specific biological activities. Researchers appreciate its stability and ease of use, which streamline the synthesis process and improve yields. With its broad applicability in drug discovery and development, Na-Fmoc-Ng-allyloxycarbonyl-L-2,4-diaminobutyric acid stands out as a critical tool for advancing peptide-based therapeutics.

Synonyms
Fmoc-L-Dab(Aloc)-OH
CAS Number
204316-32-5
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.45
MDL Number
MFCD00798634
PubChem ID
4183956
Melting Point
132 - 145 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dab(Aloc)-OH
CAS Number
204316-32-5
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.45
MDL Number
MFCD00798634
PubChem ID
4183956
Melting Point
132 - 145 °C (Lit.)
Appearance
White to off-white crystalline powder
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-Ng-allyloxycarbonyl-L-2,4-diaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it is used to design and modify bioactive compounds, enhancing their efficacy and selectivity, which is critical in developing new medications.
  • Bioconjugation: The compound is effective in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Protein Engineering: Researchers employ this chemical in modifying proteins to study their functions and interactions, which is essential in fields such as biotechnology and molecular biology.
  • Diagnostics: It plays a role in the development of diagnostic tools, where its ability to form stable conjugates aids in the detection of specific biomolecules, improving the accuracy of tests.

Citations