Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
05751
CAS Number:
95753-56-3
Fmoc-4-amino-L-phenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Phe(4-NH2)-OH, Fmoc-p-amino-L-Phe-OH, (S-Fmoc-2-amino-3-(4-aminophenyl)propionic acid
Documents
$86.23 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-4-amino-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 allows for selective deprotection during solid-phase peptide synthesis, making it an essential building block for researchers in the field of medicinal chemistry. Its unique structure not only enhances stability but also improves the solubility of peptides, facilitating easier handling and manipulation in laboratory settings.

This compound is particularly valuable in the synthesis of bioactive peptides and proteins, which are crucial in pharmaceutical research and development. Fmoc-4-amino-L-phenylalanine has been effectively employed in the creation of peptide-based therapeutics, including those targeting cancer and other diseases. Its ability to provide a stable and efficient pathway for peptide assembly positions it as a preferred choice among professionals seeking to innovate in drug design and development.

Synonyms
Fmoc-L-Phe(4-NH2)-OH, Fmoc-p-amino-L-Phe-OH, (S-Fmoc-2-amino-3-(4-aminophenyl)propionic acid
CAS Number
95753-56-3
Purity
≥ 98% (HPLC)
Molecular Formula
C24H22N2O4
Molecular Weight
402.5
MDL Number
MFCD00237664
PubChem ID
22660102
Melting Point
190-205 °C
Appearance
Off-white to light yellow powder
Optical Rotation
[a]D20 = -9 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Phe(4-NH2)-OH, Fmoc-p-amino-L-Phe-OH, (S-Fmoc-2-amino-3-(4-aminophenyl)propionic acid
CAS Number
95753-56-3
Purity
≥ 98% (HPLC)
Molecular Formula
C24H22N2O4
Molecular Weight
402.5
MDL Number
MFCD00237664
PubChem ID
22660102
Melting Point
190-205 °C
Appearance
Off-white to light yellow powder
Optical Rotation
[a]D20 = -9 ± 2º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-amino-L-phenylalanine is widely utilized in research focused on

  • Peptide Synthesis: This compound is a key building block in solid-phase peptide synthesis, allowing researchers to create custom peptides for various applications in biochemistry and pharmacology.
  • Drug Development: Its unique structure makes it valuable in the development of peptide-based drugs, particularly for targeting specific receptors in disease treatment.
  • Bioconjugation: Fmoc-4-amino-L-phenylalanine can be used to attach peptides to other molecules, enhancing the delivery and efficacy of therapeutic agents in targeted therapies.
  • Research in Neuroscience: This compound aids in the study of neurotransmitter systems, helping scientists understand the role of peptides in brain function and potential treatments for neurological disorders.
  • Protein Engineering: It serves as a versatile tool in the modification of proteins, allowing for the introduction of specific functionalities that can improve stability and activity in various applications.

Citations