N-Fmoc-4-hydroxybenzeneethanamine

95%

Reagent Code: #218755
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CAS Number 114865-17-7

science Other reagents with same CAS 114865-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 359.4 g/mol
Formula C₂₃H₂₁NO₃
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used in peptide synthesis as a protected building block, enabling selective coupling reactions without interference from the amine group. The Fmoc group provides base-labile protection, allowing for orthogonal deprotection in solid-phase synthesis. The phenolic hydroxyl group can be further functionalized for conjugation or used to anchor the molecule to solid supports. Commonly employed in the preparation of bioconjugates, drug delivery systems, and labeled peptides where controlled release or site-specific modification is required. Its structure supports the development of enzyme substrates and probes in biochemical assays.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,400.00
inventory 1g
10-20 days ฿27,360.00

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N-Fmoc-4-hydroxybenzeneethanamine
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Used in peptide synthesis as a protected building block, enabling selective coupling reactions without interference from the amine group. The Fmoc group provides base-labile protection, allowing for orthogonal deprotection in solid-phase synthesis. The phenolic hydroxyl group can be further functionalized for conjugation or used to anchor the molecule to solid supports. Commonly employed in the preparation of bioconjugates, drug delivery systems, and labeled peptides where controlled release or site-spec

Used in peptide synthesis as a protected building block, enabling selective coupling reactions without interference from the amine group. The Fmoc group provides base-labile protection, allowing for orthogonal deprotection in solid-phase synthesis. The phenolic hydroxyl group can be further functionalized for conjugation or used to anchor the molecule to solid supports. Commonly employed in the preparation of bioconjugates, drug delivery systems, and labeled peptides where controlled release or site-specific modification is required. Its structure supports the development of enzyme substrates and probes in biochemical assays.

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