3-(2-Naphthyl)-D-alanine

98%

  • Product Code: 104905
  Alias:    D-3-(2-naphthyl)-alanine
  CAS:    76985-09-6
Molecular Weight: 215.25 g./mol Molecular Formula: C₁₃H₁₃NO₂
EC Number: MDL Number: MFCD00038546
Melting Point: Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: 3-(2-Naphthyl)-D-alanine is primarily utilized in the field of peptide synthesis and biochemical research. It serves as a non-natural amino acid, often incorporated into peptide chains to study protein structure, function, and interactions. Its unique naphthyl group provides a hydrophobic and aromatic character, making it valuable for probing hydrophobic binding sites or enhancing peptide stability. Additionally, it is used in the development of peptide-based drugs and biomaterials, where its distinct properties can influence bioavailability, target specificity, and molecular recognition. In enzyme studies, it acts as a substrate or inhibitor to explore enzymatic mechanisms and kinetics. Its role in fluorescence-based assays is also noteworthy, as the naphthyl group can contribute to optical properties useful in detecting and tracking biological processes.
Product Specification:
Test Specification
Purity (HPLC) 98-100
Specific Rotation [A]20/D(C=1, 1Mol/L HCl) 11-14
HCL
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,280.00
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-
5.000 10-20 days ฿5,180.00
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-
3-(2-Naphthyl)-D-alanine
3-(2-Naphthyl)-D-alanine is primarily utilized in the field of peptide synthesis and biochemical research. It serves as a non-natural amino acid, often incorporated into peptide chains to study protein structure, function, and interactions. Its unique naphthyl group provides a hydrophobic and aromatic character, making it valuable for probing hydrophobic binding sites or enhancing peptide stability. Additionally, it is used in the development of peptide-based drugs and biomaterials, where its distinct properties can influence bioavailability, target specificity, and molecular recognition. In enzyme studies, it acts as a substrate or inhibitor to explore enzymatic mechanisms and kinetics. Its role in fluorescence-based assays is also noteworthy, as the naphthyl group can contribute to optical properties useful in detecting and tracking biological processes.
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