H-Lys(Aloc)-OH

≥95%

Reagent Code: #38580
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CAS Number 6298-03-9

science Other reagents with same CAS 6298-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD00237142
thermostat Physical Properties
Boiling Point 414.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of lysine, where the Aloc (allyloxycarbonyl) group protects the amine functionality, preventing unwanted reactions during the synthesis process. This protection is crucial for achieving selective deprotection and coupling steps, ensuring the accurate assembly of peptide chains. It is especially valuable in synthesizing complex peptides and proteins, where precise control over amino acid reactivity is required. Additionally, the Aloc group can be selectively removed under mild conditions, making it suitable for sensitive peptide sequences. This compound is widely utilized in pharmaceutical research, drug development, and biochemical studies involving peptide-based molecules.

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Test Parameter Specification
Appearance White to off-white solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿480.00
inventory 1g
10-20 days ฿1,560.00
inventory 5g
10-20 days ฿5,960.00

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H-Lys(Aloc)-OH
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This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of lysine, where the Aloc (allyloxycarbonyl) group protects the amine functionality, preventing unwanted reactions during the synthesis process. This protection is crucial for achieving selective deprotection and coupling steps, ensuring the accurate assembly of peptide chains. It is especially valuable in synthesizing complex peptides and proteins, where preci

This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected form of lysine, where the Aloc (allyloxycarbonyl) group protects the amine functionality, preventing unwanted reactions during the synthesis process. This protection is crucial for achieving selective deprotection and coupling steps, ensuring the accurate assembly of peptide chains. It is especially valuable in synthesizing complex peptides and proteins, where precise control over amino acid reactivity is required. Additionally, the Aloc group can be selectively removed under mild conditions, making it suitable for sensitive peptide sequences. This compound is widely utilized in pharmaceutical research, drug development, and biochemical studies involving peptide-based molecules.

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