Ac-Tyr(tBu)-OH

97%

Reagent Code: #38193
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CAS Number 201292-99-1

science Other reagents with same CAS 201292-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.33 g/mol
Formula C₁₅H₂₁NO₄
badge Registry Numbers
MDL Number MFCD00236772
thermostat Physical Properties
Boiling Point 493.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is commonly used in peptide synthesis as a protected amino acid derivative. The tert-butyl group on the tyrosine side chain serves as a protective group, preventing unwanted reactions during the peptide chain assembly. It is particularly useful in solid-phase peptide synthesis (SPPS) to ensure the selective formation of peptide bonds. After the peptide chain is assembled, the tert-butyl group can be removed under mild acidic conditions, revealing the free tyrosine residue. This makes it a valuable building block in the production of peptides for research, pharmaceuticals, and biotechnology applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,289.00
inventory 250mg
10-20 days ฿1,161.00
inventory 1g
10-20 days ฿2,916.00
inventory 10g
10-20 days ฿13,473.00

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Ac-Tyr(tBu)-OH
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This compound is commonly used in peptide synthesis as a protected amino acid derivative. The tert-butyl group on the tyrosine side chain serves as a protective group, preventing unwanted reactions during the peptide chain assembly. It is particularly useful in solid-phase peptide synthesis (SPPS) to ensure the selective formation of peptide bonds. After the peptide chain is assembled, the tert-butyl group can be removed under mild acidic conditions, revealing the free tyrosine residue. This makes it a v

This compound is commonly used in peptide synthesis as a protected amino acid derivative. The tert-butyl group on the tyrosine side chain serves as a protective group, preventing unwanted reactions during the peptide chain assembly. It is particularly useful in solid-phase peptide synthesis (SPPS) to ensure the selective formation of peptide bonds. After the peptide chain is assembled, the tert-butyl group can be removed under mild acidic conditions, revealing the free tyrosine residue. This makes it a valuable building block in the production of peptides for research, pharmaceuticals, and biotechnology applications.

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