Fmoc-Serinol(tBu)

98%

Reagent Code: #113427
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CAS Number 198561-87-4

science Other reagents with same CAS 198561-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.45 g/mol
Formula C₂₂H₂₇NO₄
badge Registry Numbers
MDL Number MFCD00235946
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Fmoc-Serinol(tBu) is widely used in peptide synthesis as a building block. It serves as a protected form of serinol, allowing for the controlled assembly of peptide chains. The Fmoc group provides temporary protection for the amine functionality, while the tBu group safeguards the hydroxyl group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides with high precision. Its application ensures the selective deprotection and coupling of amino acids, facilitating the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology.

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Test Parameter Specification
Appearance White to off-white powder
Purity (%) 97.5-100%
Water Content (KF) 0-2.0%
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿460.00
inventory 1g
10-20 days ฿1,750.00
inventory 5g
10-20 days ฿8,690.00

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Fmoc-Serinol(tBu)
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Fmoc-Serinol(tBu) is widely used in peptide synthesis as a building block. It serves as a protected form of serinol, allowing for the controlled assembly of peptide chains. The Fmoc group provides temporary protection for the amine functionality, while the tBu group safeguards the hydroxyl group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides with high precision. Its application ensures t

Fmoc-Serinol(tBu) is widely used in peptide synthesis as a building block. It serves as a protected form of serinol, allowing for the controlled assembly of peptide chains. The Fmoc group provides temporary protection for the amine functionality, while the tBu group safeguards the hydroxyl group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise construction of peptides with high precision. Its application ensures the selective deprotection and coupling of amino acids, facilitating the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology.

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