Boc-Lys(N3)-OH

Overview

Boc-Lys(N3)-OH is an unusual amino acid specifically designed for use in Solid Phase Peptide Synthesis (SPPS). This compound plays a crucial role in synthesizing side-chain modified peptides and proteins, making it an essential addition for researchers focusing on peptide synthesis. The azido (N3) group attached to the lysine side chain is stable when exposed to common reagents used in SPPS, such as trifluoroacetic acid (TFA) and piperidine (Pip). This stability ensures that you can confidently utilize Boc-Lys(N3)-OH in your experiments without worrying about degradation of the compound.

Key Features

• Stability in TFA and piperidine, ideal for peptide synthesis
• Facilitates the synthesis of side-chain modified peptides
• Azido group can be converted to an amine through Staudinger reduction
• Perfect for research applications and protein labeling
• Available in various forms for different research needs

Specifications

FAQ

What is Boc-Lys(N3)-OH used for?

Boc-Lys(N3)-OH is primarily used in peptide synthesis, particularly for creating side-chain modified peptides that can be further analyzed or utilized in various applications.

How does the azido group benefit the synthesis process?

The azido group in Boc-Lys(N3)-OH is stable during peptide synthesis which means it can be used reliably under harsh conditions, and it allows for easy conversion to an amine, enhancing versatility in downstream applications.

Where can I learn more about similar products?

If you’re interested in other unusual amino acids similar to Boc-Lys(N3)-OH, you can check out our range of analogs of arginine and lysine or explore options like Fmoc-Lys(Me3)-OH chloride and Fmoc-Lys(Me, Boc)-OH.

Related Products

• Fmoc – Arg(Me)(Pbf)-OH