Fmoc-Octyl-Gly-OH

≥95%

Reagent Code: #38625
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CAS Number 193885-59-5

science Other reagents with same CAS 193885-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.52 g/mol
Formula C₂₅H₃₁NO₄
badge Registry Numbers
MDL Number MFCD01311753
thermostat Physical Properties
Melting Point 142.6°C
Boiling Point 599.4±33.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Fmoc-Octyl-Gly-OH is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for introducing hydrophobic segments into peptide chains, which can influence the peptide's stability, solubility, and interaction with biological membranes. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during synthesis, ensuring precise control over the peptide assembly process. This compound is also valuable in creating peptide-based biomaterials, drug delivery systems, and surface modification agents, where the octyl chain enhances lipophilicity and membrane permeability. Additionally, it finds applications in research focused on studying peptide-lipid interactions and designing peptides with tailored biophysical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,719.00
inventory 5g
10-20 days ฿5,472.00
inventory 250mg
10-20 days ฿684.00
inventory 10g
10-20 days ฿9,297.00

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Fmoc-Octyl-Gly-OH
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Fmoc-Octyl-Gly-OH is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for introducing hydrophobic segments into peptide chains, which can influence the peptide's stability, solubility, and interaction with biological membranes. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during synthesis, ensuring precise control over the peptide assembly process. This compound is also valuable in creating

Fmoc-Octyl-Gly-OH is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for introducing hydrophobic segments into peptide chains, which can influence the peptide's stability, solubility, and interaction with biological membranes. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during synthesis, ensuring precise control over the peptide assembly process. This compound is also valuable in creating peptide-based biomaterials, drug delivery systems, and surface modification agents, where the octyl chain enhances lipophilicity and membrane permeability. Additionally, it finds applications in research focused on studying peptide-lipid interactions and designing peptides with tailored biophysical properties.

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