5-(octadecyloxy)isophthalic acid

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Reagent Code: #48348
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CAS Number 143294-86-4

science Other reagents with same CAS 143294-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.61 g/mol
Formula C₂₆H₄₂O₅
thermostat Physical Properties
Melting Point 157-161℃(lit.)
Boiling Point 587.3±35.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.036±0.06g/ml(Predicted)
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in the development of advanced materials, particularly in the field of liquid crystals and self-assembled monolayers. Its amphiphilic nature, due to the long alkyl chain and carboxylic acid groups, makes it suitable for creating ordered structures at the nanoscale. It is often employed in the synthesis of supramolecular assemblies, which are critical in designing materials with specific optical, electronic, or mechanical properties. Additionally, it finds application in surface modification processes, where it helps in altering surface properties to achieve desired wettability, adhesion, or corrosion resistance. Its role in organic electronics is also noteworthy, as it can be used to fabricate organic semiconductors or as a building block for organic frameworks.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,640.00
inventory 250mg
10-20 days ฿18,180.00

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5-(octadecyloxy)isophthalic acid
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This chemical is primarily utilized in the development of advanced materials, particularly in the field of liquid crystals and self-assembled monolayers. Its amphiphilic nature, due to the long alkyl chain and carboxylic acid groups, makes it suitable for creating ordered structures at the nanoscale. It is often employed in the synthesis of supramolecular assemblies, which are critical in designing materials with specific optical, electronic, or mechanical properties. Additionally, it finds application i

This chemical is primarily utilized in the development of advanced materials, particularly in the field of liquid crystals and self-assembled monolayers. Its amphiphilic nature, due to the long alkyl chain and carboxylic acid groups, makes it suitable for creating ordered structures at the nanoscale. It is often employed in the synthesis of supramolecular assemblies, which are critical in designing materials with specific optical, electronic, or mechanical properties. Additionally, it finds application in surface modification processes, where it helps in altering surface properties to achieve desired wettability, adhesion, or corrosion resistance. Its role in organic electronics is also noteworthy, as it can be used to fabricate organic semiconductors or as a building block for organic frameworks.

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