Boc-Arg(Tos)-OH

98%

Reagent Code: #126682
label
Alias N-tert-butoxycarbonyl-N'-toluenesulfonyl-L-arginine ;N-tert-butoxycarbonyl-N'-toluenesulfonyl-L-arginine
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CAS Number 13836-37-8

science Other reagents with same CAS 13836-37-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 428.51 g/mol
Formula C₁₈H₂₈N₄O₆S
badge Registry Numbers
EC Number 237-549-2
MDL Number MFCD00065557
thermostat Physical Properties
Melting Point ~90 °C (dec.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Boc-Arg(Tos)-OH is widely used in peptide synthesis as a protected form of arginine. The tert-butyloxycarbonyl (Boc) group safeguards the amino group, while the tosyl (Tos) group protects the guanidine side chain, preventing unwanted reactions during the peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection allows for the stepwise construction of peptides. It ensures high purity and yield by minimizing side reactions. Additionally, it is employed in the synthesis of bioactive peptides, pharmaceuticals, and research compounds where arginine plays a critical role. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Almost White Powder To Crystal
Purity (%) 97.5-100%
Specific Rotation [α]20/D (C=4, DMF) -5.0 to -3.0
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,990.00
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿990.00
Boc-Arg(Tos)-OH
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Boc-Arg(Tos)-OH is widely used in peptide synthesis as a protected form of arginine. The tert-butyloxycarbonyl (Boc) group safeguards the amino group, while the tosyl (Tos) group protects the guanidine side chain, preventing unwanted reactions during the peptide chain assembly. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection allows for the stepwise construction of peptides. It ensures high purity and yield by minimizing side reactions. Additionally, it is employed in the synthesis of bioactive peptides, pharmaceuticals, and research compounds where arginine plays a critical role. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry.
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