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Catalog Number:
30478
CAS Number:
1217471-94-7
(S)-4-(Fmoc-amino)-3-(Z-amino)butyric acid
Purity:
≥ 99% (Assay by titration, HPLC)
Synonym(s):
Z-D-Dbu(Fmoc)-OH
Documents
$198.80 /100MG
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Product Information

(S)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for the introduction of various functional groups, making it an ideal candidate for creating complex peptide sequences. Researchers appreciate its stability and ease of use, which significantly enhances the efficiency of synthetic pathways in pharmaceutical applications.

In addition to its role in peptide synthesis, (S)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is also employed in the development of novel therapeutics and biologically active compounds. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists and researchers. This compound not only streamlines the synthesis process but also opens avenues for the exploration of new drug candidates, ultimately contributing to advancements in medicinal chemistry.

Synonyms
Z-D-Dbu(Fmoc)-OH
CAS Number
1217471-94-7
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C27H26N2O6
Molecular Weight
474.5
MDL Number
MFCD03788645
PubChem ID
3337413
Melting Point
169 - 178 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -6.5 to -8.0 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Z-D-Dbu(Fmoc)-OH
CAS Number
1217471-94-7
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C27H26N2O6
Molecular Weight
474.5
MDL Number
MFCD03788645
PubChem ID
3337413
Melting Point
169 - 178 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -6.5 to -8.0 º (C=1 in DMF)
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

(S)-4-(Fmoc-amino)-3-(Z-amino)butyric acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development and therapeutic applications.
  • Drug Discovery: Its unique structure allows for the modification of peptide sequences, making it valuable in the discovery of new pharmaceuticals that target specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking peptides to other biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter systems, helping researchers understand the role of peptides in neurological functions and disorders.
  • Custom Synthesis: Laboratories often utilize this compound for custom synthesis projects, providing flexibility in developing tailored peptides for various applications in biotechnology and pharmaceuticals.

Citations