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Catalog Number:
07050
CAS Number:
213383-02-9
Fmoc-4- tert -butyl-L-phénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Phe(4-tBu)-OH, Fmoc- p -tBu-L-Phe-OH, ( Acide S -Fmoc-2-amino-3-(4- tert -butyl-phényl)propionique
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$79.22 /1G
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Product Information

Fmoc-4-tert-butyl-L-phenylalanine 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 solid-phase peptide synthesis. Its unique structure, characterized by the tert-butyl group, enhances solubility and stability, making it an ideal choice for researchers looking to optimize peptide sequences.

In practical applications, Fmoc-4-tert-butyl-L-phenylalanine is particularly valuable in the pharmaceutical industry for the development of peptide-based therapeutics. Its ability to facilitate the synthesis of complex peptides allows for the exploration of novel drug candidates, especially in the fields of oncology and immunology. Additionally, its favorable properties contribute to improved yields and purity in peptide synthesis, making it a preferred choice among professionals in the field.

Synonyms
Fmoc-L-Phe(4-tBu)-OH, Fmoc- p -tBu-L-Phe-OH, ( Acide S -Fmoc-2-amino-3-(4- tert -butyl-phényl)propionique
CAS Number
213383-02-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 294
Molecular Weight
443.56
MDL Number
MFCD02094466
PubChem ID
50853302
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-L-Phe(4-tBu)-OH, Fmoc- p -tBu-L-Phe-OH, ( Acide S -Fmoc-2-amino-3-(4- tert -butyl-phényl)propionique
CAS Number
213383-02-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 28 H 294
Molecular Weight
443.56
MDL Number
MFCD02094466
PubChem ID
50853302
Appearance
Blanc cassé uni
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-4-tert-butyl-L-phenylalanine 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 sequences efficiently.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, which can be tailored for specific therapeutic targets, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach peptides to other biomolecules, facilitating the development of targeted drug delivery systems.
  • Research in Protein Engineering: It plays a significant role in the study of protein interactions and modifications, helping researchers understand protein folding and stability.
  • Cosmetic Formulations: Its properties are leveraged in the cosmetic industry for formulating anti-aging products, where peptides can promote skin health and rejuvenation.

Citations