Boc-Gln(Trt)-OH

98%

Reagent Code: #126628
label
Alias N-Boc-N'-trityl-L-glutamine; N-tert-butoxycarbonyl-N'-trityl-L-glutamine
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CAS Number 132388-69-3

science Other reagents with same CAS 132388-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 488.57 g/mol
Formula C₂₉H₃₂N₂O₅
badge Registry Numbers
MDL Number MFCD00153305
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in peptide synthesis as a protected form of glutamine. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group protects the side chain amide during the peptide assembly process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct sequence of amino acids. After the peptide chain is constructed, the protecting groups can be removed under specific conditions to yield the desired peptide. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology.

format_list_bulleted Product Specification

Test Parameter Specification
Melting Point 117-124.7
Purity (HPLC) 98-100
Specific Rotation [α]20/D (C=2, CH3OH) -4 to -2
Appearance White To Off-White Powder
TLC Analysis One Spot

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿990.00
inventory 25g
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿420.00
inventory 100g
10-20 days ฿12,220.00

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Boc-Gln(Trt)-OH
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This chemical is primarily used in peptide synthesis as a protected form of glutamine. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group protects the side chain amide during the peptide assembly process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct sequence of amino acids. After the peptide chain is constructed, the protecting groups can be removed under specific conditions to yield t

This chemical is primarily used in peptide synthesis as a protected form of glutamine. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group protects the side chain amide during the peptide assembly process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct sequence of amino acids. After the peptide chain is constructed, the protecting groups can be removed under specific conditions to yield the desired peptide. Its application is crucial in the production of peptides for research, pharmaceuticals, and biotechnology.

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