(S)-2-((tert-Butoxycarbonyl)amino)-4-(tritylthio)butanoic acid

≥95%

Reagent Code: #38094
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CAS Number 201419-16-1

science Other reagents with same CAS 201419-16-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 477.62 g/mol
Formula C₂₈H₃₁NO₄S
badge Registry Numbers
MDL Number MFCD00672309
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The tert-butoxycarbonyl (Boc) group safeguards the amino functionality, while the trityl (Trt) group protects the thiol side chain of cysteine, preventing unwanted reactions during peptide bond formation. Its application is crucial in solid-phase peptide synthesis (SPPS), where selective deprotection of these groups allows for the controlled assembly of complex peptides. Additionally, it finds use in the development of peptide-based drugs and biochemical research, enabling the study of protein structure and function. Its stability under various reaction conditions makes it a valuable tool in organic and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,835.00
inventory 250mg
10-20 days ฿5,238.00
inventory 1g
10-20 days ฿12,888.00

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(S)-2-((tert-Butoxycarbonyl)amino)-4-(tritylthio)butanoic acid
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This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The tert-butoxycarbonyl (Boc) group safeguards the amino functionality, while the trityl (Trt) group protects the thiol side chain of cysteine, preventing unwanted reactions during peptide bond formation. Its application is crucial in solid-phase peptide synthesis (SPPS), where selective deprotection of these groups allows for the controlled assembly of complex peptides. Additionally, it finds use in the dev

This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The tert-butoxycarbonyl (Boc) group safeguards the amino functionality, while the trityl (Trt) group protects the thiol side chain of cysteine, preventing unwanted reactions during peptide bond formation. Its application is crucial in solid-phase peptide synthesis (SPPS), where selective deprotection of these groups allows for the controlled assembly of complex peptides. Additionally, it finds use in the development of peptide-based drugs and biochemical research, enabling the study of protein structure and function. Its stability under various reaction conditions makes it a valuable tool in organic and medicinal chemistry.

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