Fmoc-NH-PEG-amine compounds (Fmoc-NH-PEG-NH2) combine an Fmoc-protected amine and a free amine linked by a PEG spacer. They work well in peptide synthesis, bioconjugation, and surface modification, providing flexibility and precise control in reactions.
Fmoc-NH-PEG-amine
| Cat# | Name | Structure | Pricing |
|---|---|---|---|
| AP10716 | FmocNH-PEG2-amine | Pricing | |
| AP10715 | FmocNH-PEG3-amine | Pricing | |
| AP10714 | FmocNH-PEG4-amine | Pricing | |
| AP10713 | FmocNH-PEG5-amine | Pricing |
Fmoc-NH-PEG-amine compounds (Fmoc-NH-PEG-NH2) are a versatile class of molecules used in peptide synthesis and bioconjugation. They have an Fmoc-protected amine on one end and a free amine group (NH2) on the other. A PEG spacer connects these groups, adding flexibility and improving solubility in both water and organic solvents.
Key Features:
- Fmoc Protection: Temporarily shields the amine, allowing controlled reactions.
- PEG Spacer: Enhances solubility and flexibility for various applications.
- Dual Amine Groups: One protected, one free, enabling functionalization.
Key Applications:
- Peptide Synthesis: Allows controlled, stepwise synthesis by protecting the amine.
- Bioconjugation: Easily links proteins, peptides, and drugs through the free amine.
- Surface Modification: Functionalizes nanoparticles or biomaterials with reactive amines.
- Drug Delivery: PEGylates molecules to boost solubility and improve bioavailability.
These compounds excel in peptide synthesis and bioconjugation, thanks to their flexibility and controlled reactivity.