Nα-Ac-Nδ-trityl-L-glutamine

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Reagent Code: #219710
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CAS Number 163277-79-0

science Other reagents with same CAS 163277-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 430.5 g/mol
Formula C₂₆H₂₆N₂O₄
badge Registry Numbers
MDL Number MFCD00236753
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling and preventing side reactions at the glutamine side chain. The trityl group protects the delta-amide, while the acetyl group blocks the alpha-amine, allowing for controlled stepwise assembly of complex peptides. Commonly applied in solid-phase peptide synthesis and pharmaceutical research where precise sequence control is critical. Its protecting groups are selectively removable under mild conditions, making it suitable for synthesizing sensitive bioactive peptides.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿9,770.00
Nα-Ac-Nδ-trityl-L-glutamine
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Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling and preventing side reactions at the glutamine side chain. The trityl group protects the delta-amide, while the acetyl group blocks the alpha-amine, allowing for controlled stepwise assembly of complex peptides. Commonly applied in solid-phase peptide synthesis and pharmaceutical research where precise sequence control is critical. Its protecting groups are selectively removable under mild conditions, making it su

Used in peptide synthesis as a protected amino acid derivative, enabling selective coupling and preventing side reactions at the glutamine side chain. The trityl group protects the delta-amide, while the acetyl group blocks the alpha-amine, allowing for controlled stepwise assembly of complex peptides. Commonly applied in solid-phase peptide synthesis and pharmaceutical research where precise sequence control is critical. Its protecting groups are selectively removable under mild conditions, making it suitable for synthesizing sensitive bioactive peptides.

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