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Product Information

Product Name
Fmoc-L-lysine
Brand Name
Chem Impex
Product Number
01641
CAS
105047-45-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7010557
IUPAC Name
(2S)-6-amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
InChI Key
YRKFMPDOFHQWPI-IBGZPJMESA-N
SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC@@H(CCCCN)C(=O)O

Application

Fmoc-L-lysine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of lysine residues. Its protective Fmoc group simplifies the process of sequential addition of amino acids.

Drug Development: In pharmaceutical research, Fmoc-L-lysine is used to create peptide-based drugs, enhancing the stability and bioavailability of therapeutic agents.

Bioconjugation: The compound is valuable in bioconjugation techniques, where it can be linked to various biomolecules, facilitating the development of targeted drug delivery systems.

Protein Engineering: Researchers utilize Fmoc-L-lysine in the design of modified proteins, which can improve their functionality and stability for various applications in biotechnology.

Diagnostics: In the field of diagnostics, Fmoc-L-lysine is employed in the creation of peptide-based assays, which can enhance the sensitivity and specificity of disease detection methods.

References Data Source From Pubchem

Exploring tunable characteristics of anthranilic acid in peptide-based nanostructures

Publication Name: Journal of Materials Research
Publication Date: 2025-09-02
DOI: 10.1557/s43578-025-01683-8

Synthesis of Bicyclic Peptides Using Cyanopyridine-Aminothiol Click Chemistry

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2025
DOI: 10.1007/978-1-0716-4562-8_2

Multiple reaction monitoring assays for large-scale quantitation of proteins from 20 mouse organs and tissues

Publication Name: Communications Biology
Publication Date: 2024-01-02
DOI: 10.1038/s42003-023-05687-0

Improving the Antibacterial Activity of Tryptophan-Containing Peptide Nanostructures Through Self-Assembly

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2023-11-06
DOI: 10.1007/s10989-023-10575-6

Novel cyclic undecapeptides immobilized on reduced graphene oxide surface for enhanced antibacterial properties

Publication Name: International Journal of Environmental Science and Technology
Publication Date: 2023-06-17
DOI: 10.1007/s13762-023-05035-z