Pentaerythritol Triallyl Ether

75%

Reagent Code: #225525
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CAS Number 1471-17-6

science Other reagents with same CAS 1471-17-6

blur_circular Chemical Specifications

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Weight 256.34 g/mol
Formula C₁₄H₂₄O₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a crosslinking agent in polymer chemistry, particularly in the production of thermosetting resins and coatings. Enhances heat resistance, chemical stability, and mechanical strength of polymers. Commonly applied in UV-curable systems such as inks, adhesives, and protective coatings due to its ability to participate in free radical polymerization. Also serves as a modifier in synthetic rubbers and elastomers to improve cure efficiency and network formation. Its trifunctional allyl groups enable efficient network building in silicone elastomers and radiation-cured materials.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿250.00
inventory 25g
10-20 days ฿520.00
inventory 100g
10-20 days ฿1,510.00
inventory 500g
10-20 days ฿4,590.00
inventory 2.5kg
10-20 days ฿19,980.00

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Pentaerythritol Triallyl Ether
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Used as a crosslinking agent in polymer chemistry, particularly in the production of thermosetting resins and coatings. Enhances heat resistance, chemical stability, and mechanical strength of polymers. Commonly applied in UV-curable systems such as inks, adhesives, and protective coatings due to its ability to participate in free radical polymerization. Also serves as a modifier in synthetic rubbers and elastomers to improve cure efficiency and network formation. Its trifunctional allyl groups enable ef

Used as a crosslinking agent in polymer chemistry, particularly in the production of thermosetting resins and coatings. Enhances heat resistance, chemical stability, and mechanical strength of polymers. Commonly applied in UV-curable systems such as inks, adhesives, and protective coatings due to its ability to participate in free radical polymerization. Also serves as a modifier in synthetic rubbers and elastomers to improve cure efficiency and network formation. Its trifunctional allyl groups enable efficient network building in silicone elastomers and radiation-cured materials.

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