1-Vinyl-1,2,4-triazole

≥97%

Reagent Code: #245556
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CAS Number 2764-83-2

science Other reagents with same CAS 2764-83-2

blur_circular Chemical Specifications

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Weight 95.1 g/mol
Formula C₄H₅N₃
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MDL Number MFCD00674553
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reactive monomer in polymer synthesis, particularly in the production of functional polymers and copolymers with enhanced thermal and chemical stability. Its vinyl group enables free-radical polymerization, making it suitable for creating specialty coatings, adhesives, and resins. Commonly employed in developing materials for electronics and optical devices due to its ability to improve dielectric properties and adhesion. Also investigated for use in pharmaceutical intermediates and agrochemicals owing to the bioactive nature of triazole rings. Shows promise in crosslinking agents for hydrogels and in stimuli-responsive polymers for controlled release systems.

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inventory 5ml
10-20 days ฿46,510.00

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1-Vinyl-1,2,4-triazole
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Used as a reactive monomer in polymer synthesis, particularly in the production of functional polymers and copolymers with enhanced thermal and chemical stability. Its vinyl group enables free-radical polymerization, making it suitable for creating specialty coatings, adhesives, and resins. Commonly employed in developing materials for electronics and optical devices due to its ability to improve dielectric properties and adhesion. Also investigated for use in pharmaceutical intermediates and agrochemica

Used as a reactive monomer in polymer synthesis, particularly in the production of functional polymers and copolymers with enhanced thermal and chemical stability. Its vinyl group enables free-radical polymerization, making it suitable for creating specialty coatings, adhesives, and resins. Commonly employed in developing materials for electronics and optical devices due to its ability to improve dielectric properties and adhesion. Also investigated for use in pharmaceutical intermediates and agrochemicals owing to the bioactive nature of triazole rings. Shows promise in crosslinking agents for hydrogels and in stimuli-responsive polymers for controlled release systems.

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