Boc-Glu(OtBu)-OSu

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Reagent Code: #105723
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CAS Number 32886-55-8

science Other reagents with same CAS 32886-55-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 400.42 g/mol
Formula C₁₈H₂₈N₂O₈
badge Registry Numbers
MDL Number MFCD00153303
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is widely used in peptide synthesis as a protecting group for glutamic acid. It helps in preventing unwanted side reactions during the assembly of peptide chains. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group of glutamic acid. The OSu (N-hydroxysuccinimide ester) moiety makes it highly reactive towards amino groups, facilitating efficient coupling with other amino acids or peptides. This reagent is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, ensuring high yield and purity of the final peptide product. Its stability and ease of removal under mild acidic conditions make it a preferred choice in peptide chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿891.00
inventory 5g
10-20 days ฿3,276.00

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Boc-Glu(OtBu)-OSu
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This compound is widely used in peptide synthesis as a protecting group for glutamic acid. It helps in preventing unwanted side reactions during the assembly of peptide chains. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group of glutamic acid. The OSu (N-hydroxysuccinimide ester) moiety makes it highly reactive towards amino groups, facilitating efficient coupling with other amino acids or peptides. This reagent is particu

This compound is widely used in peptide synthesis as a protecting group for glutamic acid. It helps in preventing unwanted side reactions during the assembly of peptide chains. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the OtBu (tert-butyl ester) group protects the carboxyl group of glutamic acid. The OSu (N-hydroxysuccinimide ester) moiety makes it highly reactive towards amino groups, facilitating efficient coupling with other amino acids or peptides. This reagent is particularly useful in solid-phase peptide synthesis (SPPS) and solution-phase synthesis, ensuring high yield and purity of the final peptide product. Its stability and ease of removal under mild acidic conditions make it a preferred choice in peptide chemistry.

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