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 |
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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 |
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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 |
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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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