Unlock Peptide Synthesis Efficiency with High-Purity Fmoc-Val-OH
Your essential building block for advanced peptide synthesis, ensuring purity and performance.
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Fmoc-Val-OH
Fmoc-Val-OH is a highly purified N-Fmoc protected amino acid derivative, crucial for the efficient and precise synthesis of peptides. Its chemical structure, C20H21NO4, and its CAS number 126727-02-4 make it a reliably identifiable compound in chemical research and pharmaceutical development.
- Discover the optimal Fmoc-Val-OH price and understand its wholesale availability from trusted manufacturers.
- Explore the production processes that guarantee the high purity required for sensitive peptide synthesis applications.
- Learn why choosing a reliable Fmoc-amino acid supplier is critical for the success of your research.
- Investigate the synthesis pathways that lead to the superior quality of Fmoc-Val-OH for your peptide projects.
Advantages Offered by the Product
Uncompromised Purity
Ensuring the highest purity of Fmoc-Val-OH is paramount for achieving successful peptide synthesis outcomes, free from unwanted side reactions or contaminants.
Synthesis Versatility
This Fmoc-amino acid derivative serves as a versatile building block, enabling the construction of a wide array of complex peptides for various applications.
Reliable Sourcing
Partnering with reputable Fmoc-Val-OH manufacturers and suppliers guarantees a consistent and dependable supply chain for your ongoing research needs.
Key Applications
Peptide Synthesis
Fmoc-Val-OH is indispensable in solid-phase peptide synthesis, forming peptide bonds with high efficiency and stereochemical integrity.
Organic Synthesis
Beyond peptides, this compound can be utilized in broader organic synthesis pathways, leveraging its unique chemical properties.
Pharmaceutical Research
As a key intermediate, Fmoc-Val-OH plays a vital role in the development of novel peptide-based therapeutics and diagnostic agents.
Biochemical Studies
Researchers use Fmoc-Val-OH to create custom peptides for studying protein-protein interactions, enzyme mechanisms, and biological pathways.