Tetradecyl methacrylate

98% (MEHQ as stabilizer)

Reagent Code: #242541
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CAS Number 2549-53-3

science Other reagents with same CAS 2549-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.46 g/mol
Formula C₁₈H₃₄O₂
badge Registry Numbers
MDL Number MFCD00085280
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a reactive diluent and comonomer in the formulation of specialty acrylate resins, enabling controlled hydrophobicity and flexibility in coatings and adhesives. Its long alkyl chain contributes to improved water resistance and low surface energy, making it valuable in protective coatings, release coatings, and low-friction surfaces. Also employed in polymer synthesis for biomedical materials and dental composites, where tailored hydrophobic interactions and mechanical properties are required. Additionally, it serves in the preparation of functional polymers for chromatography and controlled release systems due to its ability to modulate polymer crystallinity and permeability.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿480.00
inventory 100g
10-20 days ฿1,800.00
inventory 500g
10-20 days ฿6,680.00

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Tetradecyl methacrylate
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Used primarily as a reactive diluent and comonomer in the formulation of specialty acrylate resins, enabling controlled hydrophobicity and flexibility in coatings and adhesives. Its long alkyl chain contributes to improved water resistance and low surface energy, making it valuable in protective coatings, release coatings, and low-friction surfaces. Also employed in polymer synthesis for biomedical materials and dental composites, where tailored hydrophobic interactions and mechanical properties are require
Used primarily as a reactive diluent and comonomer in the formulation of specialty acrylate resins, enabling controlled hydrophobicity and flexibility in coatings and adhesives. Its long alkyl chain contributes to improved water resistance and low surface energy, making it valuable in protective coatings, release coatings, and low-friction surfaces. Also employed in polymer synthesis for biomedical materials and dental composites, where tailored hydrophobic interactions and mechanical properties are required. Additionally, it serves in the preparation of functional polymers for chromatography and controlled release systems due to its ability to modulate polymer crystallinity and permeability.
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