Nα-(9-Fluorenylmethoxycarbonyl)-L-ornithine Trifluoroacetate Salt

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Reagent Code: #216212
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CAS Number 172690-50-5

science Other reagents with same CAS 172690-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 468.43 g/mol
Formula C₂₂H₂₃O₆F₃N₂
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Widely used in solid-phase peptide synthesis, this compound serves as a protected amino acid building block. The Fmoc group enables reversible protection of the alpha-amino function, allowing stepwise assembly of peptides under mild basic conditions. Its ornithine side chain is useful for introducing positive charges or branching points in peptide structures, especially in the synthesis of bioactive peptides, antimicrobial agents, and peptide dendrimers. The trifluoroacetate salt form enhances solubility and stability during handling and storage. Commonly employed in automated synthesizers, it supports the production of custom peptides for research in drug development, molecular biology, and diagnostic applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,180.00
5g
10-20 days ฿7,710.00
25g
10-20 days ฿27,000.00
Nα-(9-Fluorenylmethoxycarbonyl)-L-ornithine Trifluoroacetate Salt
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Widely used in solid-phase peptide synthesis, this compound serves as a protected amino acid building block. The Fmoc group enables reversible protection of the alpha-amino function, allowing stepwise assembly of peptides under mild basic conditions. Its ornithine side chain is useful for introducing positive charges or branching points in peptide structures, especially in the synthesis of bioactive peptides, antimicrobial agents, and peptide dendrimers. The trifluoroacetate salt form enhances solubility

Widely used in solid-phase peptide synthesis, this compound serves as a protected amino acid building block. The Fmoc group enables reversible protection of the alpha-amino function, allowing stepwise assembly of peptides under mild basic conditions. Its ornithine side chain is useful for introducing positive charges or branching points in peptide structures, especially in the synthesis of bioactive peptides, antimicrobial agents, and peptide dendrimers. The trifluoroacetate salt form enhances solubility and stability during handling and storage. Commonly employed in automated synthesizers, it supports the production of custom peptides for research in drug development, molecular biology, and diagnostic applications.

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