N-(tert-Butoxycarbonyl)-5-aminovaleric Acid

≥98.0%(GC)

Reagent Code: #217064
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CAS Number 27219-07-4

science Other reagents with same CAS 27219-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
badge Registry Numbers
MDL Number MFCD00076903
thermostat Physical Properties
Melting Point 48-52°C (Lit.)
Boiling Point 160-168°C 0.8mm Hg (Lit.)
inventory_2 Storage & Handling
Storage 2~8℃, dry, sealed

description Product Description

Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling reactions without side-chain interference. Its Boc-protected amine group allows for controlled deprotection under mild acidic conditions, making it valuable in stepwise solid-phase and solution-phase peptide assembly. Also employed in the preparation of biologically active compounds, including pharmaceutical intermediates and enzyme inhibitors. Commonly used in research settings for labeling, conjugation, and the synthesis of complex organic molecules requiring orthogonal protection strategies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿300.00
5g
10-20 days ฿950.00
25g
10-20 days ฿4,690.00
100g
10-20 days ฿11,214.00
N-(tert-Butoxycarbonyl)-5-aminovaleric Acid
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Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling reactions without side-chain interference. Its Boc-protected amine group allows for controlled deprotection under mild acidic conditions, making it valuable in stepwise solid-phase and solution-phase peptide assembly. Also employed in the preparation of biologically active compounds, including pharmaceutical intermediates and enzyme inhibitors. Commonly used in research settings for labeling, conjugation, and the

Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling reactions without side-chain interference. Its Boc-protected amine group allows for controlled deprotection under mild acidic conditions, making it valuable in stepwise solid-phase and solution-phase peptide assembly. Also employed in the preparation of biologically active compounds, including pharmaceutical intermediates and enzyme inhibitors. Commonly used in research settings for labeling, conjugation, and the synthesis of complex organic molecules requiring orthogonal protection strategies.

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