Boc-D-Gln(Trt)-OH

≥95%

Reagent Code: #104215
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CAS Number 210750-95-1

science Other reagents with same CAS 210750-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 488.57 g/mol
Formula C₂₉H₃₂N₂O₅
badge Registry Numbers
MDL Number MFCD00153306
thermostat Physical Properties
Boiling Point 728.9±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.188±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in peptide synthesis as a protected form of the D-enantiomer of glutamine. It serves as a building block in the creation of complex peptides, ensuring the glutamine residue remains stable during the synthesis process. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group shields the side chain of glutamine, preventing unwanted reactions. This protection is crucial in solid-phase peptide synthesis, where selective deprotection allows for the stepwise assembly of peptides. It is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide structure is essential.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿837.00
Boc-D-Gln(Trt)-OH
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This chemical is primarily used in peptide synthesis as a protected form of the D-enantiomer of glutamine. It serves as a building block in the creation of complex peptides, ensuring the glutamine residue remains stable during the synthesis process. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group shields the side chain of glutamine, preventing unwanted reactions. This protection is crucial in solid-phase peptide synthesis, where selective deprotection allows for
This chemical is primarily used in peptide synthesis as a protected form of the D-enantiomer of glutamine. It serves as a building block in the creation of complex peptides, ensuring the glutamine residue remains stable during the synthesis process. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Trt (trityl) group shields the side chain of glutamine, preventing unwanted reactions. This protection is crucial in solid-phase peptide synthesis, where selective deprotection allows for the stepwise assembly of peptides. It is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies, where precise control over peptide structure is essential.
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