FMOC-N-ME-HIS(TRT)-OH

95%

Reagent Code: #76418
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CAS Number 1217840-61-3

science Other reagents with same CAS 1217840-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 633.73 g/mol
Formula C₄₁H₃₅N₃O₄
badge Registry Numbers
MDL Number MFCD04974256
thermostat Physical Properties
Melting Point 183-188°C
Boiling Point 793.8±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the FMOC group acts as a temporary protecting group for the amino function, and the TRT group protects the imidazole side chain of histidine. This protection is crucial to prevent unwanted side reactions during the peptide chain assembly process. The N-methylation of histidine enhances the stability and bioavailability of the resulting peptides, making it valuable in the development of therapeutic peptides and peptidomimetics. Additionally, it is utilized in research to study peptide-protein interactions and enzyme mechanisms, contributing to advancements in drug discovery and biochemical studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿25,128.00

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FMOC-N-ME-HIS(TRT)-OH
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the FMOC group acts as a temporary protecting group for the amino function, and the TRT group protects the imidazole side chain of histidine. This protection is crucial to prevent unwanted side reactions during the peptide chain assembly process. The N-methylation of histidine enhances the stability and bioavailability of the resulting peptides,

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the FMOC group acts as a temporary protecting group for the amino function, and the TRT group protects the imidazole side chain of histidine. This protection is crucial to prevent unwanted side reactions during the peptide chain assembly process. The N-methylation of histidine enhances the stability and bioavailability of the resulting peptides, making it valuable in the development of therapeutic peptides and peptidomimetics. Additionally, it is utilized in research to study peptide-protein interactions and enzyme mechanisms, contributing to advancements in drug discovery and biochemical studies.

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