Description
Specifications Table
| Product Name | FMOC-N-e-Z-L-Lysine | Fm0285 | CDH |
|---|---|
| Pack Size | 10 gm, 25 gm |
| Form | Powder |
| Grade | Reagent Grade |
| Application | Peptide Synthesis |
Product Description
FMOC-N-ε-Z-L-Lysine | FM0285 | CDH is a premium-grade Fmoc-protected amino acid with side-chain protection, specially developed for solid-phase peptide synthesis and advanced peptide chemistry. Manufactured under rigorous quality standards, it provides excellent purity, chemical stability, and reliable coupling performance for complex peptide synthesis applications.
This protected lysine derivative is widely used in pharmaceutical research, medicinal chemistry, biotechnology, and protein engineering for preparing peptides with controlled side-chain functionality. The combination of Fmoc and Z protecting groups enables selective deprotection strategies while minimizing unwanted side reactions during peptide assembly, resulting in high synthesis efficiency and reproducible performance.
CDH FMOC-N-ε-Z-L-Lysine | FM0285 is ideal for peptide synthesis laboratories, pharmaceutical manufacturers, biotechnology companies, universities, and research organizations performing advanced peptide development and analytical research.
FAQs
What is FMOC-N(e)-Z-L-Lysine used for?
It’s primarily used in solid-phase peptide synthesis to introduce lysine residues while protecting the side chain amino group.
How do I deprotect the Z group?
The Z group can be removed via hydrogenolysis using palladium catalyst or by strong acid treatment like HBr in acetic acid.
Is this compound soluble in water?
No, it’s insoluble in water but soluble in organic solvents like DMF, DCM, and methanol.
What’s the typical coupling time for this amino acid?
Standard coupling times range from 30-60 minutes, depending on the activator used (e.g., HATU, DIC/HOBt).
Can I use this for Fmoc/tert-butyl synthesis?
Yes, it’s fully compatible with Fmoc/tert-butyl protection strategies commonly used in SPPS.
