3-(1-Naphthyl)-D-alanine Hydrochloride

≥98%

Reagent Code: #104515
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CAS Number 122745-09-9

science Other reagents with same CAS 122745-09-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.71 g/mol
Formula C₁₃H₁₃NO₂HCl
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in peptide synthesis and biochemical research. It serves as a building block for creating modified peptides, particularly in studies involving fluorescence labeling and structural analysis. Its naphthyl group enhances fluorescence properties, making it valuable in tracking and imaging applications. Additionally, it is used in the development of enzyme inhibitors and receptor ligands due to its ability to mimic natural amino acids while introducing unique steric and electronic effects. Its application extends to exploring protein-protein interactions and designing peptide-based therapeutics.

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Test Parameter Specification
Appearance White to almost white crystal or powder
Purity (%) 98-100
Specific Rotation ([α]20/D) +6.0 to +10.0

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,130.00
inventory 5g
10-20 days ฿9,420.00
inventory 1g
10-20 days ฿3,270.00

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3-(1-Naphthyl)-D-alanine Hydrochloride
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This compound is primarily utilized in peptide synthesis and biochemical research. It serves as a building block for creating modified peptides, particularly in studies involving fluorescence labeling and structural analysis. Its naphthyl group enhances fluorescence properties, making it valuable in tracking and imaging applications. Additionally, it is used in the development of enzyme inhibitors and receptor ligands due to its ability to mimic natural amino acids while introducing unique steric and ele

This compound is primarily utilized in peptide synthesis and biochemical research. It serves as a building block for creating modified peptides, particularly in studies involving fluorescence labeling and structural analysis. Its naphthyl group enhances fluorescence properties, making it valuable in tracking and imaging applications. Additionally, it is used in the development of enzyme inhibitors and receptor ligands due to its ability to mimic natural amino acids while introducing unique steric and electronic effects. Its application extends to exploring protein-protein interactions and designing peptide-based therapeutics.

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