Fmoc-D-His(Trt)-OH

98%

Reagent Code: #126684
label
Alias N-Fremoxycarbonyl-N'-trityl-D-histidine
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CAS Number 135610-90-1

science Other reagents with same CAS 135610-90-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 619.7 g/mol
Formula C₄₀H₃₃N₃O₄
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it serves as a protected form of D-histidine. The Fmoc group ensures selective deprotection during the synthesis process, while the Trt (trityl) group protects the imidazole side chain of D-histidine, preventing unwanted side reactions. This compound is essential for constructing peptides with D-histidine residues, which are crucial in many biologically active peptides and proteins. Its application is widespread in pharmaceutical research, drug development, and the study of protein-protein interactions.

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Test Parameter Specification
Purity (HPLC) 98-100
Specific Rotation [α]20/D (C=5, CHCl3) 94-100
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿540.00
inventory 5g
10-20 days ฿1,820.00
inventory 25g
10-20 days ฿7,370.00

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Fmoc-D-His(Trt)-OH
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Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it serves as a protected form of D-histidine. The Fmoc group ensures selective deprotection during the synthesis process, while the Trt (trityl) group protects the imidazole side chain of D-histidine, preventing unwanted side reactions. This compound is essential for constructing peptides with D-histidine residues, which are crucial in many biologically active peptides and proteins. Its application is widespread in pharma
Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), where it serves as a protected form of D-histidine. The Fmoc group ensures selective deprotection during the synthesis process, while the Trt (trityl) group protects the imidazole side chain of D-histidine, preventing unwanted side reactions. This compound is essential for constructing peptides with D-histidine residues, which are crucial in many biologically active peptides and proteins. Its application is widespread in pharmaceutical research, drug development, and the study of protein-protein interactions.
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