The Role of Fmoc-Dopa(acetonide)-OH (CAS 852288-18-7) in Modern Drug Development
The landscape of drug development is continually evolving, with a growing emphasis on sophisticated molecular entities like peptides and modified amino acids. For researchers and development teams, securing reliable access to high-quality specialty chemicals is crucial. One such compound, (S)-2-(FMOC-amino)-3-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)propanoic acid, commonly known as Fmoc-Dopa(acetonide)-OH, plays a significant role in this advancement. If your team is looking to buy this vital intermediate, understanding its function and sourcing it effectively is paramount.
Understanding the Chemical Profile: Fmoc-Dopa(acetonide)-OH
Fmoc-Dopa(acetonide)-OH, identified by its CAS number 852288-18-7, is a synthetically derived amino acid. The FMOC group attached to the alpha-amino group serves as a standard protecting group in peptide synthesis, removable under mild basic conditions. This allows for controlled coupling reactions, essential for building precise peptide sequences. The 'Dopa' component, a modified tyrosine with an additional hydroxyl group, coupled with the acetonide protection for the catechol moiety, provides unique chemical properties. These features make it valuable for introducing specific structural elements into peptides or small molecules being investigated as drug candidates. Typically supplied as a powder with a purity of ≥97%, its quality is critical for successful downstream applications.
Applications in Pharmaceutical R&D and Drug Development
The primary value proposition for buyers of Fmoc-Dopa(acetonide)-OH lies in its application in:
- Peptide Therapeutics: It's used as a building block for synthesizing peptide-based drugs, where specific modifications can enhance biological activity, stability, and targeted delivery.
- Small Molecule Drug Design: The unique functional groups present in this molecule can be incorporated into small molecule drug candidates to improve their binding to target proteins or modulate their pharmacokinetic profiles.
- Chemical Biology Research: Researchers use it in various studies to probe biological pathways or develop novel diagnostic agents.
For pharmaceutical companies, securing a consistent supply of high-purity intermediates like Fmoc-Dopa(acetonide)-OH is a strategic necessity. Identifying a reputable manufacturer, especially from China, can offer significant advantages.
Key Considerations for Buyers: Quality and Sourcing
When looking to purchase Fmoc-Dopa(acetonide)-OH, buyers should prioritize:
- Purity and Quality Control: Always verify the purity specifications (≥97%) and ensure the supplier provides a Certificate of Analysis (CoA) detailing purity, identity, and any impurities. This is crucial for ensuring the reproducibility and reliability of your research and development efforts.
- Supplier Reliability: Partner with manufacturers who have a proven history of producing and supplying fine chemicals consistently. A stable supply chain is essential for projects with tight timelines.
- Technical Support: Good manufacturers offer technical support, including detailed product information and assistance with application-specific queries.
- Cost-Effectiveness: While quality is non-negotiable, competitive pricing, particularly from Chinese manufacturers, can make advanced research more accessible and budget-friendly. Requesting quotes for bulk purchases is advisable.
By carefully selecting a trusted supplier, pharmaceutical developers can ensure they have access to the high-quality Fmoc-Dopa(acetonide)-OH necessary to drive innovation and bring new therapies to market.
Perspectives & Insights
Quantum Pioneer 24
“If your team is looking to buy this vital intermediate, understanding its function and sourcing it effectively is paramount.”
Bio Explorer X
“Understanding the Chemical Profile: Fmoc-Dopa(acetonide)-OHFmoc-Dopa(acetonide)-OH, identified by its CAS number 852288-18-7, is a synthetically derived amino acid.”
Nano Catalyst AI
“The FMOC group attached to the alpha-amino group serves as a standard protecting group in peptide synthesis, removable under mild basic conditions.”