Ac-lys(ac)-OH

98%

Reagent Code: #105587
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CAS Number 499-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD00236760
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily utilized in peptide synthesis, where it serves as a protected form of lysine. The acetyl groups protect the amino and hydroxyl functionalities, preventing unwanted reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides with high precision. Additionally, it finds applications in biochemical research, where modified amino acids are required to study protein interactions, enzyme mechanisms, and post-translational modifications. Its use ensures the stability and specificity of lysine residues in synthetic peptides, making it a critical component in the development of peptide-based drugs and research tools.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,980.00
inventory 500mg
10-20 days ฿12,560.00
Ac-lys(ac)-OH
This chemical is primarily utilized in peptide synthesis, where it serves as a protected form of lysine. The acetyl groups protect the amino and hydroxyl functionalities, preventing unwanted reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides with high precision. Additionally, it finds applications in biochemical research, where modified amino acids are required to study protein interactions, enzyme mechanisms, and post-translational modifications. Its use ensures the stability and specificity of lysine residues in synthetic peptides, making it a critical component in the development of peptide-based drugs and research tools.
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