Fmoc-Cys(Trt)-OH

98%

Reagent Code: #105160
label
Alias Fmoc-S-trityl-L-cysteine ​​; Fmoc-S-trityl-L-cysteine
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CAS Number 103213-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 585.71 g/mol
Formula C₃₇H₃₁NO₄S
badge Registry Numbers
MDL Number MFCD00038538
thermostat Physical Properties
Melting Point 170-173 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of cysteine, where the Fmoc (9-fluorenylmethoxycarbonyl) group protects the amino group, and the Trt (trityl) group protects the thiol side chain of cysteine. This protection is crucial to prevent unwanted reactions during the synthesis process. The compound is especially valuable in the production of peptides that require the incorporation of cysteine residues, which are essential for forming disulfide bonds that stabilize the peptide structure. Its use ensures high efficiency and purity in peptide assembly, making it a key reagent in the development of therapeutic peptides, research peptides, and other biologically active compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98-100
Water (Karl Fischer) 0.1
Melting Point 171-176
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days $16.38
inventory 25g
10-20 days $58.63
inventory 100g
10-20 days $191.41
Fmoc-Cys(Trt)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of cysteine, where the Fmoc (9-fluorenylmethoxycarbonyl) group protects the amino group, and the Trt (trityl) group protects the thiol side chain of cysteine. This protection is crucial to prevent unwanted reactions during the synthesis process. The compound is especially valuable in the production of peptides that require the incorporation of cysteine residues, which are essential for forming disulfide bonds that stabilize the peptide structure. Its use ensures high efficiency and purity in peptide assembly, making it a key reagent in the development of therapeutic peptides, research peptides, and other biologically active compounds.
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