The product we are discussing here is n-6-trifluoroacetyl-l-lysine. It has a CAS number of 10009 - 20 - 8. This indicates its unique identity in the chemical world, allowing for easy identification and traceability in scientific research and industrial applications. The product is factory - supplied, which means it benefits from large - scale production processes that can ensure consistent quality and relatively lower costs. The best price offered further enhances its value proposition for potential buyers. Chemically, n-6-trifluoroacetyl-l-lysine is an amino acid derivative. Its structure contains a trifluoroacetyl group attached to the 6 - position of the lysine molecule. This modification can significantly alter its physical and chemical properties compared to unmodified lysine, such as solubility, reactivity, and stability.
In the field of biochemistry, n-6-trifluoroacetyl-l-lysine can serve as a valuable tool for studying protein structure and function. It can be incorporated into peptides or proteins during synthesis, acting as a probe to monitor conformational changes or interactions. For example, the trifluoroacetyl group can be detected using nuclear magnetic resonance (NMR) techniques, providing insights into the local environment of the amino acid within the protein. In the pharmaceutical industry, it may be used as an intermediate in the synthesis of novel drugs. Its unique chemical structure can be exploited to create compounds with improved pharmacological properties, such as better bioavailability or enhanced target specificity. In addition, it can also be used in the development of diagnostic reagents, where its reactivity or binding properties can be harnessed to detect specific biomarkers.
When using n-6-trifluoroacetyl-l-lysine, proper handling procedures should be followed. First, ensure that the product is stored in a cool, dry place, away from direct sunlight and sources of heat. This helps to maintain its stability and prevent degradation. Before use, the product should be carefully inspected for any signs of damage or contamination. When weighing the product, use accurate measuring equipment to ensure the correct dosage. In a laboratory setting, it is typically dissolved in an appropriate solvent, such as water or an organic solvent, depending on the specific application. The solution should be prepared under sterile conditions if necessary, especially for biological applications. When incorporating it into a reaction or a biological system, follow the recommended protocols and reaction conditions, including temperature, pH, and reaction time.
Case 1: Protein Structure Analysis
A research group was studying the structure of a membrane - associated protein. They incorporated n-6-trifluoroacetyl-l-lysine into specific sites of the protein during its synthesis. By using 19F - NMR spectroscopy, they were able to monitor the changes in the chemical environment of the trifluoroacetyl group as the protein interacted with its ligands. This provided detailed information about the conformational changes of the protein upon ligand binding, which was crucial for understanding its mechanism of action.
Case 2: Drug Synthesis
A pharmaceutical company was developing a new anti - cancer drug. They used n-6-trifluoroacetyl-l-lysine as an intermediate in the synthesis pathway. By modifying the trifluoroacetyl group and combining it with other chemical moieties, they were able to create a novel compound with high selectivity for cancer cells. In pre - clinical trials, this compound showed promising anti - cancer activity with fewer side effects compared to existing drugs.
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