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Catalog Number:
02692
CAS Number:
116821-47-7
Fmoc-γ-aminobutyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-γ-Abu-OH, Fmoc-4-aminobutyric acid
Documents
$22.03 /1G
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Product Information

Fmoc-g-aminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an essential building block in the production of bioactive peptides and pharmaceuticals. Researchers appreciate its stability and compatibility with various coupling reagents, which enhances the efficiency of peptide synthesis protocols.

In addition to its role in peptide synthesis, Fmoc-g-aminobutyric acid has potential applications in the development of neuroprotective agents and in studies related to neurotransmitter modulation. Its ability to mimic natural amino acids makes it a valuable tool for exploring the biochemical pathways involved in neurological functions. With its robust performance in laboratory settings, Fmoc-g-aminobutyric acid stands out as a reliable choice for researchers seeking to innovate in the fields of medicinal chemistry and biochemistry.

Synonyms
Fmoc-γ-Abu-OH, Fmoc-4-aminobutyric acid
CAS Number
116821-47-7
Purity
≥ 98% (HPLC)
Molecular Formula
C19H19NO4
Molecular Weight
325.4
MDL Number
MFCD00144889
PubChem ID
2756086
Melting Point
165-175 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-γ-Abu-OH, Fmoc-4-aminobutyric acid
CAS Number
116821-47-7
Purity
≥ 98% (HPLC)
Molecular Formula
C19H19NO4
Molecular Weight
325.4
MDL Number
MFCD00144889
PubChem ID
2756086
Melting Point
165-175 °C
Appearance
White 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

Fmoc-g-aminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice in organic chemistry labs.
  • Drug Development: Researchers use this compound to develop novel pharmaceuticals, particularly in the field of neuropharmacology, where it can help in designing compounds that target specific receptors in the brain.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostic agents.
  • Material Science: The compound is applied in creating functionalized polymers, which can be used in drug delivery systems, improving the efficacy and targeting of therapeutic agents.
  • Research in Neuroscience: Its role in modulating neurotransmitter systems makes it valuable for studies aimed at understanding neurological disorders and developing potential treatments.

Citations