Fmoc-N-Me-Ala-OH

97%

Reagent Code: #105126
label
Alias FMOC-N-methyl-L-alanine ; N-fluorenylmethoxycarbonyl-N-methyl-L-alanine
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CAS Number 84000-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.36 g/mol
Formula C₁₉H₁₉NO₄
badge Registry Numbers
MDL Number MFCD00153384
thermostat Physical Properties
Melting Point ~150 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Fmoc-N-Me-Ala-OH is primarily used in peptide synthesis as a building block. It is particularly valuable in solid-phase peptide synthesis (SPPS) for introducing N-methylated alanine residues into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protecting group for the amine, allowing selective deprotection during the synthesis process. This compound is essential in creating peptides with specific structural and functional properties, often employed in drug development and biochemical research. Its use enhances peptide stability and modulates biological activity, making it a critical tool in designing therapeutic peptides and studying protein interactions.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100%
Melting Point (°C) 156.0-160.0
Infrared Spectrum Conforms To Structure
Specific Rotation [a]20/D (C=1, DMF) -17.0 to -20.0

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days $931.10
inventory 5g
10-20 days $54.61
Fmoc-N-Me-Ala-OH
Fmoc-N-Me-Ala-OH is primarily used in peptide synthesis as a building block. It is particularly valuable in solid-phase peptide synthesis (SPPS) for introducing N-methylated alanine residues into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protecting group for the amine, allowing selective deprotection during the synthesis process. This compound is essential in creating peptides with specific structural and functional properties, often employed in drug development and biochemical research. Its use enhances peptide stability and modulates biological activity, making it a critical tool in designing therapeutic peptides and studying protein interactions.
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