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Catalog Number:
37063
CAS Number:
460751-78-4
Nα -Allyloxycarbonyl- Nγ -Fmoc-L-2,4-diaminobutyric acid
Purity:
≥ 99% (Assay by titration, HPLC)
Synonym(s):
Aloc-L-Dab(Fmoc)-OH
Documents
$60.00 /100MG
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Product Information

Na-Allyloxycarbonyl-Ng-Fmoc-L-2,4-diaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique allyloxycarbonyl protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers focused on the synthesis of complex peptides and amino acids. Its Fmoc (9-fluorenylmethoxycarbonyl) group allows for easy deprotection under mild conditions, facilitating the efficient assembly of peptide chains.

In pharmaceutical research, this compound plays a crucial role in the development of therapeutic peptides, particularly in the design of targeted drug delivery systems. Its ability to form stable conjugates with various biomolecules opens avenues for innovative treatments in areas such as cancer therapy and regenerative medicine. Researchers appreciate its compatibility with a range of coupling reagents, which streamlines the synthesis process and enhances yield. Overall, Na-Allyloxycarbonyl-Ng-Fmoc-L-2,4-diaminobutyric acid is an essential tool for professionals aiming to advance peptide chemistry and drug formulation.

Synonyms
Aloc-L-Dab(Fmoc)-OH
CAS Number
460751-78-4
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.5
MDL Number
MFCD31560716
PubChem ID
91827835
Melting Point
143 - 145 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -12 ± 2 ° (C=1 in MeOH)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Aloc-L-Dab(Fmoc)-OH
CAS Number
460751-78-4
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C23H24N2O6
Molecular Weight
424.5
MDL Number
MFCD31560716
PubChem ID
91827835
Melting Point
143 - 145 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -12 ± 2 ° (C=1 in MeOH)
Conditions
Store at 2 - 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 -Allyloxycarbonyl- Ng -Fmoc-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 the selective modification of amino acids without affecting others. This is crucial for creating complex peptides used in drug development.
  • Drug Development: Its unique structure aids in the design of new pharmaceuticals, particularly in the development of targeted therapies that require precise molecular configurations.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostics and therapeutics in biotechnology.
  • Research in Cancer Therapy: It plays a role in the development of novel anticancer agents by modifying existing compounds to improve their efficacy and reduce side effects.
  • Material Science: This chemical is also explored in the creation of advanced materials, such as hydrogels, which can be used in drug delivery systems and tissue engineering.

Citations