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Catalog Number:
15044
CAS Number:
183071-07-0
Fmoc-3-pyrényl-L-alanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Ala(pyrényl)-OH
Documents
$331.60 /100 mg
Taille
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Product Information

Fmoc-3-pyrenyl-L-alanine is a versatile amino acid derivative that combines the well-known Fmoc (9-fluorenylmethyloxycarbonyl) protecting group with a pyrene moiety, making it an invaluable tool in peptide synthesis and bioconjugation applications. This compound is particularly favored in the development of fluorescent probes and sensors due to its unique photophysical properties, which allow for effective monitoring in biological systems. Researchers utilize Fmoc-3-pyrenyl-L-alanine for its ability to enhance the stability and solubility of peptides, facilitating the study of protein interactions and dynamics.

In addition to its role in peptide synthesis, this compound is also employed in materials science, particularly in the creation of functionalized surfaces and nanomaterials. Its pyrene group contributes to strong π-π stacking interactions, which can be harnessed in the design of advanced materials with tailored optical properties. With its dual functionality in both biological and material applications, Fmoc-3-pyrenyl-L-alanine stands out as a crucial compound for researchers aiming to innovate in the fields of biochemistry and nanotechnology.

Synonyms
Fmoc-L-Ala(pyrényl)-OH
CAS Number
183071-07-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 34 H 254
Molecular Weight
511.58
MDL Number
MFCD01861376
PubChem ID
4712555
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-L-Ala(pyrényl)-OH
CAS Number
183071-07-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 34 H 254
Molecular Weight
511.58
MDL Number
MFCD01861376
PubChem ID
4712555
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-3-pyrenyl-L-alanine is widely utilized in research focused on:

  • Fluorescent Probes: This compound is used as a fluorescent label in biochemical assays, allowing researchers to track protein interactions and cellular processes with high sensitivity.
  • Peptide Synthesis: It serves as a key building block in solid-phase peptide synthesis, enabling the creation of complex peptides for drug development and therapeutic applications.
  • Biomolecular Studies: Researchers employ this compound to study protein folding and dynamics, providing insights into the behavior of proteins in various environments.
  • Nanotechnology: Its unique pyrene structure makes it suitable for developing nanomaterials, which can be used in sensors and drug delivery systems, enhancing their effectiveness.
  • Fluorescence Resonance Energy Transfer (FRET): This chemical is utilized in FRET experiments to study molecular interactions, offering a powerful tool for understanding biological mechanisms at the molecular level.

Citations