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HS Code |
353654 |
| Cas Number | 83846-86-0 |
| Molecular Formula | C8H14O2 |
| Molecular Weight | 142.20 g/mol |
| Iupac Name | 1,4-bis(ethenoxy)butane |
| Synonyms | 1,4-Divinyl oxybutane |
| Appearance | Colorless liquid |
| Boiling Point | 72-74°C at 8 mmHg |
| Density | 0.917 g/cm³ at 25°C |
| Refractive Index | n20/D 1.438 |
| Flash Point | 25°C |
As an accredited 1,4-Bis(Vinyloxy)-Butane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,4-Bis(Vinyloxy)-Butane is packaged in a 100 mL amber glass bottle, sealed with a Teflon-lined screw cap. |
| Shipping | 1,4-Bis(Vinyloxy)-Butane should be shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions, protected from light and moisture. Label appropriately as a chemical substance. Ensure compliance with local, national, and international regulations for handling and transportation, and include relevant safety documentation such as Safety Data Sheets (SDS). |
| Storage | 1,4-Bis(Vinyloxy)-Butane should be stored in a cool, dry, and well-ventilated area, away from sources of heat, sparks, open flames, and direct sunlight. Keep the container tightly closed and properly labeled. Store separately from strong oxidizers and acids. Use compatible materials for containers, such as glass or certain plastics, to prevent unwanted reactions or leaks. |
Applications of 1,4-Bis(Vinyloxy)-Butane in Industrial Manufacturing1,4-Bis(Vinyloxy)-Butane is a specialty ether compound widely adopted in several high-value chemical production chains. As a direct manufacturer, we focus on consistent purity and process-grade supply to support rigorous demands in polymers, coatings, electronics, and specialty adhesives industries. Below are core industrial applications with process, regulatory, and end-use details for downstream partners. 1. Specialty Crosslinking Agent for UV-Curable CoatingsIn the coatings sector, formulators incorporate 1,4-Bis(Vinyloxy)-Butane as a reactive crosslinking agent in UV-curable systems. The material reacts through cationic polymerization during the curing stage. This process enables enhanced film hardness, solvent resistance, and improved adhesion on difficult substrates, such as plastics and metals. Consistent monomer quality ensures predictable crosslink density and minimizes batch-to-batch deviation in final coatings. Industry compliance standards
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2. Intermediate for Polyvinyl Ether Synthesis in Electrical InsulationProducers of high-performance dielectrics utilize 1,4-Bis(Vinyloxy)-Butane as a key polyvinyl ether monomer. This compound provides multiple vinyl ether groups, which participate in polyaddition reactions, forming polymers with excellent insulating properties, resistance to electrical breakdown, and long-term stability under thermal and ambient stress. The controlled reactivity of each vinyl group allows tight process control, meeting strict reproducibility targets in cable and capacitor segments. Industry compliance standards
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3. Functional Monomer in High-Performance Adhesive FormulationsIn specialty adhesives, formulators add 1,4-Bis(Vinyloxy)-Butane as a reactive monomer to enhance flexibility, hydrolytic stability, and crosslink density. Its dual vinyloxy groups facilitate network formation via cationic or radical mechanisms in multi-component adhesive systems. Controlled compatibility with other functional monomers allows manufacturers to design rapid-curing, durable adhesives for challenging substrates, supporting reliable industrial assembly applications. Industry compliance standards
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4. Crosslinking Component in Specialty Polymer ElectrolytesBattery and supercapacitor manufacturers employ 1,4-Bis(Vinyloxy)-Butane as a crosslinkable agent in advanced polymer electrolyte formulations. It promotes network integrity and mechanical strength in thin-film electrolytes, supporting high ionic conductivity and dimensional stability for next-generation lithium-ion cells and solid-state batteries. The compound’s structure assists retention of electrolyte properties after extended charge/discharge cycles. Industry compliance standards
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