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Catalog Number:
12776
CAS Number:
193954-26-6
Fmoc-L-β-homoalanine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-L-β-HomoAla-OH, ( Acide S -3-(Fmoc-amino)-butyrique
Documents
$65.40 /100 mg
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Product Information

Fmoc-L-b-homoalanine is a versatile amino acid derivative 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 enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Fmoc-L-b-homoalanine is particularly valuable in the development of peptide-based therapeutics, where it can be employed to create novel compounds with improved bioactivity and specificity.

In addition to its applications in peptide synthesis, Fmoc-L-b-homoalanine can be used in the study of protein interactions and the design of enzyme inhibitors. Its ability to mimic natural amino acids while providing distinct chemical properties makes it a powerful tool for researchers looking to explore new biochemical pathways or develop innovative therapeutic strategies. With its robust profile and practical applications, Fmoc-L-b-homoalanine stands out as a key compound for advancing research in drug discovery and development.

Synonyms
Fmoc-L-β-HomoAla-OH, ( Acide S -3-(Fmoc-amino)-butyrique
CAS Number
193954-26-6
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 19 H 194
Molecular Weight
325.36
MDL Number
MFCD00270346
PubChem ID
5020712
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 11 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-β-HomoAla-OH, ( Acide S -3-(Fmoc-amino)-butyrique
CAS Number
193954-26-6
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 19 H 194
Molecular Weight
325.36
MDL Number
MFCD00270346
PubChem ID
5020712
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = 11 ± 2 º (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide structures efficiently.
  • Drug Development: It is employed in the development of novel therapeutic peptides, enhancing the design of drugs that can target specific biological pathways, which is crucial in pharmaceutical research.
  • Bioconjugation: Fmoc-L-b-homoalanine is used to modify biomolecules, facilitating the attachment of drugs or imaging agents to proteins, which is essential in creating targeted therapies and diagnostics.
  • Research in Neuroscience: This compound is valuable in studying neuropeptides and their functions, contributing to advancements in understanding neurological disorders and potential treatments.
  • Protein Engineering: It plays a role in the design of proteins with enhanced stability and functionality, which is important in biotechnology applications, including enzyme development and industrial processes.

Citations