3-(2-Naphthyl)-D-alanine

98%

Reagent Code: #104905
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Alias D-3-(2-naphthyl)-alanine
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CAS Number 76985-09-6

science Other reagents with same CAS 76985-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₃H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00038546
inventory_2 Storage & Handling
Storage 2~8°C

description 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.

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Test Parameter Specification
Purity (HPLC) 98-100
Specific Rotation [A]20/D (C=1, 1 Mol/L HCl) 11-14
HCL

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿5,180.00

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3-(2-Naphthyl)-D-alanine
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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 pr

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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