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Catalog Number:
29685
CAS Number:
1310680-19-3
R,S-Fmoc-2-amino-3-methyl-3-phenyl-butyric acid
Purity:
≥ 98% (HPLC)
Synonym(s):
(R,S-Fmoc-β, β-dimethyl-phenylalanine
Documents
$93.14 /25MG
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Product Information

(R,S)-Fmoc-2-amino-3-methyl-3-phenyl-butyric acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. Known for its protective Fmoc (fluorenylmethyloxycarbonyl) group, this amino acid derivative facilitates the efficient assembly of peptides by providing a stable and easily removable protecting group. Its unique structure, featuring a branched chain and aromatic phenyl group, enhances solubility and stability, making it an ideal choice for researchers focused on developing complex peptide sequences.

This compound is particularly beneficial in the synthesis of bioactive peptides, which have applications in drug development, therapeutics, and diagnostics. Its ability to improve the yield and purity of synthesized peptides sets it apart from other amino acid derivatives, making it a preferred choice in both academic and industrial settings. Researchers can leverage (R,S)-Fmoc-2-amino-3-methyl-3-phenyl-butyric acid to streamline their workflows and achieve high-quality results in their peptide synthesis projects.

Synonyms
(R,S-Fmoc-β, β-dimethyl-phenylalanine
CAS Number
1310680-19-3
Purity
≥ 98% (HPLC)
Molecular Formula
C26H25NO4
Molecular Weight
415.49
MDL Number
MFCD18782839
PubChem ID
86810472
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(R,S-Fmoc-β, β-dimethyl-phenylalanine
CAS Number
1310680-19-3
Purity
≥ 98% (HPLC)
Molecular Formula
C26H25NO4
Molecular Weight
415.49
MDL Number
MFCD18782839
PubChem ID
86810472
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

(R,S)-Fmoc-2-amino-3-methyl-3-phenyl-butyric acid 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 modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of bioactive peptides, which are crucial in developing new therapeutic agents for various diseases.
  • Biotechnology: Used in the production of peptide-based vaccines, enhancing immune responses by providing a stable and effective delivery system for antigens.
  • Research in Neuroscience: The compound's derivatives are explored for their potential in modulating neuropeptide activity, offering insights into neurological disorders.
  • Analytical Chemistry: It is employed in chromatographic techniques for the separation and identification of complex mixtures, improving the accuracy of analytical results.

Citations