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Catalog Number:
47723
CAS Number:
894106-43-5
Na-Fmoc-Ne-Acryloyl-L-lysine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-Lys(Acryloyl)-OH
Documents
$60.00 /25MG
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Product Information

Na-Fmoc-Ne-Acryloyl-L-lysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential tool for researchers in the fields of medicinal chemistry and biochemistry. Its acryloyl group enhances its reactivity, enabling the formation of covalent bonds with various biomolecules, which is particularly valuable in drug delivery systems and the development of biomaterials.

Researchers and industry professionals can leverage Na-Fmoc-Ne-Acryloyl-L-lysine for the design of novel peptides and polymers, facilitating advancements in targeted therapies and regenerative medicine. Its unique properties, such as stability under physiological conditions and compatibility with various coupling reactions, make it a preferred choice for those looking to innovate in peptide-based therapeutics. This compound not only streamlines the synthesis process but also opens new avenues for functionalizing biomolecules, ultimately enhancing the efficacy of therapeutic agents.

Synonyms
Fmoc-Lys(Acryloyl)-OH
CAS Number
894106-43-5
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O5
Molecular Weight
422.5
Appearance
White powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Fmoc-Lys(Acryloyl)-OH
CAS Number
894106-43-5
Purity
≥ 98% (HPLC)
Molecular Formula
C24H26N2O5
Molecular Weight
422.5
Appearance
White powder
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-Fmoc-Ne-Acryloyl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, allowing for the introduction of acryloyl groups that can facilitate further modifications and functionalization.
  • Bioconjugation: It is used in bioconjugation processes, where it can help link biomolecules to surfaces or other compounds, enhancing the development of targeted drug delivery systems.
  • Polymer Chemistry: The acryloyl group enables its incorporation into polymer networks, making it useful in creating hydrogels for applications in tissue engineering and regenerative medicine.
  • Fluorescent Labeling: This chemical can be utilized for labeling proteins or other biomolecules, aiding in the visualization and tracking of biological processes in research settings.
  • Drug Development: Its unique structure allows for the design of novel therapeutic agents, particularly in the field of cancer research, where targeted delivery and controlled release are crucial.

Citations