Fmoc-Tyr(tBu)-OH

98%

Reagent Code: #105137
label
Alias Fluorenylmethoxycarbonyl-O-tert-butyl-L-tyrosine
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CAS Number 71989-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 459.53 g/mol
Formula C₂₈H₂₉NO₅
badge Registry Numbers
EC Number 276-262-7
MDL Number MFCD00037129
thermostat Physical Properties
Melting Point ~150 °C (dec.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for creating peptides, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of the tyrosine residue, preventing unwanted reactions. It is especially valuable in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of deprotection make it a preferred choice in automated peptide synthesizers. Additionally, it is utilized in the synthesis of peptide-based vaccines, hormones, and other therapeutic agents.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Crystal
Purity (HPLC) 98-100
Specific Rotation [a]20/D (C=1, DMF) -32 to -28
Infrared Spectrum Conforms To Structure
Melting Point (°C) 150-154

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿700.00
inventory 25g
10-20 days ฿2,990.00
inventory 100g
10-20 days ฿8,960.00
Fmoc-Tyr(tBu)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for creating peptides, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of the tyrosine residue, preventing unwanted reactions. It is especially valuable in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of deprotection make it a preferred choice in automated peptide synthesizers. Additionally, it is utilized in the synthesis of peptide-based vaccines, hormones, and other therapeutic agents.
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