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Catalog Number:
14075
CAS Number:
135944-05-7
Fmoc-α-metil-L-fenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-α-Me-L-Phe-OH, Ácido Fmoc-( S )-2-amino-2-metil-3-fenilpropanoico
Documents
$48.67 /100 mg
Tamaño
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Product Information

Fmoc-a-methyl-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and research applications. 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, characterized by the presence of a methyl group and a phenyl side chain, enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis (SPPS). Researchers appreciate its ability to facilitate the formation of complex peptides while minimizing side reactions, thus improving yield and purity.

In the pharmaceutical and biotechnology industries, Fmoc-a-methyl-L-phenylalanine is employed in the development of peptide-based therapeutics and drug candidates. Its application extends to the synthesis of bioactive peptides, which are crucial in various biological processes and therapeutic interventions. The compound's favorable properties, such as its compatibility with various coupling reagents and its ease of deprotection, make it a preferred choice for chemists and researchers seeking efficient and reliable methods for peptide assembly.

Synonyms
Fmoc-α-Me-L-Phe-OH, Ácido Fmoc-( S )-2-amino-2-metil-3-fenilpropanoico
CAS Number
135944-05-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD02682285
PubChem ID
17750303
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-α-Me-L-Phe-OH, Ácido Fmoc-( S )-2-amino-2-metil-3-fenilpropanoico
CAS Number
135944-05-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD02682285
PubChem ID
17750303
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 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-a-methyl-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective addition of amino acids while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based drugs, particularly in enhancing the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: Researchers use it for attaching peptides to various biomolecules, facilitating the development of targeted drug delivery systems.
  • Protein Engineering: It aids in the modification of proteins to study structure-function relationships, helping scientists understand protein interactions and functions better.
  • Research in Neuroscience: The compound is utilized in studies related to neuropeptides, which can lead to advancements in understanding neurological disorders and developing new treatments.

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