BOC-Met-Leu-Phe

≥98%

Reagent Code: #99843
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CAS Number 67247-12-5

science Other reagents with same CAS 67247-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 509.66 g/mol
Formula C₂₅H₃₉N₃O₆S
inventory_2 Storage & Handling
Storage -20℃

description Product Description

BOC-Met-Leu-Phe is primarily used in peptide synthesis and research applications. It serves as a protected tripeptide, where the BOC (tert-butyloxycarbonyl) group safeguards the amino terminus during the synthesis process. This compound is particularly valuable in studying peptide interactions, enzyme-substrate relationships, and protein folding mechanisms. It is also employed in the development of peptide-based drugs and therapeutic agents, especially in areas targeting immune responses and inflammation. Additionally, it is utilized in biochemical assays to investigate the role of specific peptide sequences in cellular signaling pathways. Its stability and ease of deprotection make it a practical choice for solid-phase peptide synthesis.

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Test Parameter Specification
Appearance White to Off-white Powder
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿16,470.00
inventory 5mg
10-20 days ฿4,110.00
inventory 1mg
10-20 days ฿1,020.00

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BOC-Met-Leu-Phe
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BOC-Met-Leu-Phe is primarily used in peptide synthesis and research applications. It serves as a protected tripeptide, where the BOC (tert-butyloxycarbonyl) group safeguards the amino terminus during the synthesis process. This compound is particularly valuable in studying peptide interactions, enzyme-substrate relationships, and protein folding mechanisms. It is also employed in the development of peptide-based drugs and therapeutic agents, especially in areas targeting immune responses and inflammation

BOC-Met-Leu-Phe is primarily used in peptide synthesis and research applications. It serves as a protected tripeptide, where the BOC (tert-butyloxycarbonyl) group safeguards the amino terminus during the synthesis process. This compound is particularly valuable in studying peptide interactions, enzyme-substrate relationships, and protein folding mechanisms. It is also employed in the development of peptide-based drugs and therapeutic agents, especially in areas targeting immune responses and inflammation. Additionally, it is utilized in biochemical assays to investigate the role of specific peptide sequences in cellular signaling pathways. Its stability and ease of deprotection make it a practical choice for solid-phase peptide synthesis.

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