D-Lys(Z)-OtBu.HCl

95%

Reagent Code: #105491
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CAS Number 1426213-63-9

science Other reagents with same CAS 1426213-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.89 g/mol
Formula C₁₈H₂₉ClN₂O₄
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in peptide synthesis as a protected form of lysine. The Z (benzyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group, allowing selective reactions to occur at other sites of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS) where controlled deprotection and coupling steps are essential. The HCl form ensures stability and solubility in various solvents, facilitating its use in complex peptide chain assembly. Its application is crucial in producing peptides for pharmaceutical research, drug development, and biochemical studies.

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Test Parameter Specification
Appearance White Solid
Purity (%) 94.5-100%
Water 0-1%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,000.00
inventory 5g
10-20 days ฿13,000.00

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D-Lys(Z)-OtBu.HCl
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This compound is primarily used in peptide synthesis as a protected form of lysine. The Z (benzyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group, allowing selective reactions to occur at other sites of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS) where controlled deprotection and coupling steps are essential. The HCl form ensures stability and solubility in various solvents, facilitating its use in compl

This compound is primarily used in peptide synthesis as a protected form of lysine. The Z (benzyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group, allowing selective reactions to occur at other sites of the molecule. It is particularly valuable in solid-phase peptide synthesis (SPPS) where controlled deprotection and coupling steps are essential. The HCl form ensures stability and solubility in various solvents, facilitating its use in complex peptide chain assembly. Its application is crucial in producing peptides for pharmaceutical research, drug development, and biochemical studies.

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