The field of material science is constantly seeking novel building blocks that offer unique chemical properties and functionalities. Among these, modified amino acids, particularly those incorporating reactive groups like nitro substituents, are gaining significant attention. 4-Nitro-L-phenylalanine Methyl Ester Hydrochloride (CAS: 17193-40-7) is a prime example, offering a combination of a chiral amino acid structure and a reactive nitro-phenyl group, making it a versatile component for advanced material development.

The Role of Nitro-Amino Acids in Material Design

Nitro-amino acids, such as H-Phe(4-NO2)-OMe.HCl, are attractive to material scientists for several reasons:

  • Enhanced Reactivity: The electron-withdrawing nature of the nitro group makes the phenyl ring susceptible to various nucleophilic aromatic substitution reactions. This reactivity can be exploited to graft the amino acid onto polymer backbones or create cross-linked structures.
  • Functionalization Opportunities: The nitro group itself can be reduced to an amine group, providing a new reactive site for further functionalization, such as conjugation with dyes, biomolecules, or other active compounds.
  • Chiral Properties: As a derivative of L-phenylalanine, it introduces chirality, which is important for creating materials with specific optical or recognition properties.

Specific Applications in Material Science:

When considering the purchase of 4-Nitro-L-phenylalanine Methyl Ester Hydrochloride, its potential in material science research should not be overlooked. Here are some areas where this compound can be particularly impactful:

  1. Functionalized Polymers: Researchers can polymerize monomers derived from H-Phe(4-NO2)-OMe.HCl or graft it onto existing polymers. These functionalized polymers can exhibit altered mechanical, thermal, or chemical properties, suitable for coatings, membranes, or drug delivery systems.
  2. Self-Assembling Materials: The specific chemical interactions and potential for intermolecular hydrogen bonding or pi-pi stacking involving the nitro-phenyl moiety can contribute to the formation of organized supramolecular structures.
  3. Bio-integrated Materials: By leveraging the amino acid component, materials can be designed for biocompatibility or to interact with biological systems, perhaps for biosensing or tissue engineering applications. The ability to buy these specialty chemicals from reliable manufacturers is key to exploring these frontiers.
  4. Advanced Coatings: The nitro group can influence surface properties, and derivatives might be used in developing specialized coatings with enhanced adhesion, corrosion resistance, or specific optical characteristics.

Procurement Considerations for Material Scientists

For material scientists looking to procure 4-Nitro-L-phenylalanine Methyl Ester Hydrochloride, the emphasis remains on purity and consistent supply. When searching for a 'manufacturer price' or 'supplier' for this compound, ensure they provide detailed specifications and support for chemical synthesis. Companies offering bulk quantities are often more cost-effective for material development projects that require larger volumes. We, as a dedicated chemical supplier and manufacturer, are equipped to support your material science innovations with high-quality intermediates.

By incorporating innovative compounds like 4-Nitro-L-phenylalanine Methyl Ester Hydrochloride into your research, you can push the boundaries of what is possible in material science. We encourage you to explore the potential of this versatile amino acid derivative for your next project.