Description
Specifications Table
| Product Name | Fmoc-Tyr(tBu)-Ser(ψMe,MePro)-OH | 8.52189.0100 | Merck |
|---|---|
| Pack Size | 100 G |
| Form | Powder |
| Grade | Lab-grade |
| Application | Peptide synthesis, SPPS, research |
Product Description
Fmoc-Tyr(tBu)-Ser(ψMe,MePro)-OH is a specialized dipeptide building block designed for solid-phase peptide synthesis (SPPS). This high-purity reagent ensures efficient coupling and minimal side reactions, making it a reliable choice for researchers and laboratories working on peptide-based studies.
The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for orthogonal deprotection strategies, while the tert-butyl (tBu) protection on tyrosine and the pseudoproline (ψMe,MePro) modification on serine enhance solubility and reduce aggregation during synthesis. This combination is particularly useful for synthesizing difficult sequences or long peptides.
Whether you’re developing therapeutic peptides, studying protein interactions, or optimizing synthesis protocols, this reagent provides the consistency and performance needed for reproducible results. eqipped ensures you receive authentic Merck-quality products with proper documentation for your research needs.
Need high-purity peptide synthesis reagents? Buy Fmoc-Tyr(tBu)-Ser(ψMe,MePro)-OH online today for seamless delivery.
FAQs
What is the purity of Fmoc-Tyr(tBu)-Ser(ψMe,MePro)-OH?
This product meets lab-grade purity standards, typically >95% as confirmed by HPLC. Exact purity details are provided in the Certificate of Analysis (CoA).
Can this reagent be used for Fmoc-based SPPS?
Yes, it is specifically designed for Fmoc chemistry in solid-phase peptide synthesis, offering clean deprotection and coupling efficiency.
What is the shelf life of this product?
When stored properly at -20°C, the product remains stable for at least 24 months from the date of manufacture.
Is this product suitable for large-scale peptide synthesis?
While optimized for research-scale synthesis, it can be scaled up with proper protocol adjustments. Contact eqipped for bulk inquiries.
How does the pseudoproline modification help in peptide synthesis?
The ψMe,MePro modification improves serine solubility and reduces secondary structure formation, minimizing aggregation during synthesis.
