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Catalog Number:
48168
CAS Number:
288149-55-3
Fmoc-Glu-NH2
Purity:
≥ 95% (HPLC)
Synonym(s):
Na-Fmoc-L-glutamylamide
Documents
$35.00 /100MG
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Product Information

Fmoc-Glu-NH2 is a versatile amino acid derivative widely utilized in peptide synthesis and research applications. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, facilitates the efficient assembly of peptides by providing a stable and easily removable protecting group for the amino functionality. Its unique structure allows for the selective introduction of the glutamic acid residue into peptides, making it invaluable in the development of bioactive compounds, pharmaceuticals, and research reagents.

Researchers and industry professionals appreciate Fmoc-Glu-NH2 for its role in enhancing the solubility and stability of peptides, which is crucial for various applications, including drug development and therapeutic protein engineering. The compound's ability to streamline the synthesis process while maintaining high purity levels makes it a preferred choice in laboratories focused on peptide chemistry. With its proven track record in facilitating complex peptide synthesis, Fmoc-Glu-NH2 stands out as an essential tool for advancing research in biochemistry and molecular biology.

Synonyms
Na-Fmoc-L-glutamylamide
CAS Number
288149-55-3
Purity
≥ 95% (HPLC)
Molecular Formula
C20H20N2O5
Molecular Weight
368.38
MDL Number
MFCD01861342
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
Na-Fmoc-L-glutamylamide
CAS Number
288149-55-3
Purity
≥ 95% (HPLC)
Molecular Formula
C20H20N2O5
Molecular Weight
368.38
MDL Number
MFCD01861342
Appearance
White to off-white powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Glu-NH2 is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various applications in drug development.
  • Drug Discovery: Its role in modifying amino acids makes it essential in the design of novel therapeutics, particularly in targeting specific biological pathways.
  • Bioconjugation: Fmoc-Glu-NH2 is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and diagnostic tools.
  • Research in Neuroscience: This compound is valuable in studying neurotransmitter systems, as it can be incorporated into peptides that mimic or inhibit natural signaling pathways.
  • Protein Engineering: It aids in the modification of proteins, enhancing their stability and functionality, which is vital for applications in biotechnology and pharmaceuticals.

Citations