Nalpha-Boc-Nomega-(4-methoxy-2,3,6-trimethylphenylsulfonyl)-L-arginine

≥95%

Reagent Code: #59188
label
Alias Boc-Arg(Mtr)-OH; N-BOC-N(4-methoxy-2,3,6 trimethylbenzenesulfonyl) cyanamide; N-A-tert-butoxycarbonyl N-Ω-(4 -Methoxy-2,3,6-trimethylbenzenesulfonyl)arginine
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CAS Number 102185-38-6

science Other reagents with same CAS 102185-38-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.53 g/mol
Formula C₂₁H₃₄N₄O₇S
badge Registry Numbers
MDL Number MFCD00043097
inventory_2 Storage & Handling
Density 1.3±0.1 g/cm3
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily used in peptide synthesis as a protected arginine derivative. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the Mtr (4-methoxy-2,3,6-trimethylphenylsulfonyl) group protects the guanidine moiety of arginine. This dual protection is crucial in preventing unwanted side reactions during the stepwise assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are essential. The Mtr group can be removed under mild acidic conditions, making it suitable for synthesizing complex peptides without disrupting other sensitive functional groups. Its application is significant in producing peptides for research, pharmaceuticals, and biotechnology, especially when arginine residues are involved.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,557.00
inventory 1g
10-20 days ฿522.00

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Nalpha-Boc-Nomega-(4-methoxy-2,3,6-trimethylphenylsulfonyl)-L-arginine
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This chemical is primarily used in peptide synthesis as a protected arginine derivative. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the Mtr (4-methoxy-2,3,6-trimethylphenylsulfonyl) group protects the guanidine moiety of arginine. This dual protection is crucial in preventing unwanted side reactions during the stepwise assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are essential. The M

This chemical is primarily used in peptide synthesis as a protected arginine derivative. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the Mtr (4-methoxy-2,3,6-trimethylphenylsulfonyl) group protects the guanidine moiety of arginine. This dual protection is crucial in preventing unwanted side reactions during the stepwise assembly of peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are essential. The Mtr group can be removed under mild acidic conditions, making it suitable for synthesizing complex peptides without disrupting other sensitive functional groups. Its application is significant in producing peptides for research, pharmaceuticals, and biotechnology, especially when arginine residues are involved.

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