|
HS Code |
866609 |
| Product Name | 1-Allyl-3-Vinylimidazolium Hexafluorophosphate |
| Cas Number | 881041-27-6 |
| Molecular Formula | C8H11N2.PF6 |
| Molecular Weight | 278.16 g/mol |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and polar organic solvents |
| Boiling Point | Decomposes before boiling |
| Purity | Typically ≥98% (depending on supplier) |
| Storage Conditions | Store at room temperature, in a tightly closed container, protected from moisture |
| Iupac Name | 1-allyl-3-ethenyl-1H-imidazol-3-ium hexafluorophosphate |
As an accredited 1-Allyl-3-Vinylimidazolium Hexafluorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with tamper-evident seal; labeled with chemical name, formula, hazard symbols, and manufacturer details. |
| Shipping | **Shipping Description:** 1-Allyl-3-Vinylimidazolium Hexafluorophosphate should be shipped in a tightly sealed, chemical-resistant container, protected from moisture and light. Transport under cool, dry conditions, and in accordance with local, national, and international regulations for hazardous materials, particularly those applicable to hexafluorophosphate salts. Safety documentation (SDS) must accompany the shipment. |
| Storage | 1-Allyl-3-Vinylimidazolium Hexafluorophosphate should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. The container must be tightly closed and clearly labeled. Protect from direct sunlight and sources of heat or ignition. Use only in areas equipped with appropriate chemical-resistant containment and ensure all handling follows standard laboratory safety protocols. |
Applications of 1-Allyl-3-Vinylimidazolium Hexafluorophosphate in Industrial Manufacturing1-Allyl-3-Vinylimidazolium Hexafluorophosphate is a high-purity ionic liquid produced under strict QC control at our factory, supporting a range of precise and regulated industrial applications. The following sections highlight key downstream manufacturing sectors, each detailing industrial compliance, formulation practices, integration into processing, and the final goods produced using this advanced ionic compound. 1. Electrolytes for High-Performance Lithium-Ion BatteriesBattery manufacturers rely on our ionic liquid as a nonflammable component in advanced electrolyte systems, improving electrochemical stability and cycle life for high-energy lithium-ion cells. Production facilities introduce this conductor after the initial solvent blending stage, achieving targeted conductivity and thermal management benchmarks required for automotive and grid-scale battery packs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Antistatic Additives for Polymer Film and Fiber ProductionPolymer processors incorporate our ionic liquid as a functional antistatic agent for specialty polymer films and synthetic fiber extrusion lines, targeting reduced surface resistivity and static charge build-up in packaging and electronics substrates. The compound disperses directly into the polymer melt phase, supporting continuous and consistent anti-static characteristics throughout roll-to-roll production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electrochemical Plating for MicroelectronicsSemiconductor and PCB fabricators use our ionic liquid to formulate low-volatility electroplating baths, achieving precise deposits of metals such as gold, palladium, and copper on micro-scale features. The raw material enters after bath conditioning and maintains bath conductivity and surface finish requirements, critical for reliable interconnects and conductor paths in advanced electronics assembly. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Green Solvent Systems for Organometallic CatalysisChemical process plants utilize this ionic liquid as a non-volatile, recyclable reaction medium for organometallic cross-coupling and alkylation steps, supporting GMP-compliant synthesis of APIs and specialty fine chemicals. Operators blend it with metal catalysts before substrate introduction, benefiting from enhanced selectivity and easy product separation compared to traditional solvents. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Ionic Conductive Layers in Advanced SupercapacitorsProducers of large-format supercapacitors integrate our ionic liquid as the core ionic conductor for electrode systems, targeting operational safety and broad temperature range. Blending with activated carbon slurries enables optimization of charge/discharge rates, with the material added before electrode casting or coating, ensuring reliable device performance in hybrid vehicle and industrial backup power applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1-Allyl-3-Vinylimidazolium Hexafluorophosphate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Every product coming out of our reactors reflects choices we’ve made on raw materials, process controls, and quality assurance. It’s easy to talk about innovation, but our group relies on technical depth and direct hands-on experience to inform every batch of 1-Allyl-3-vinylimidazolium hexafluorophosphate we manufacture. This ionic liquid remains a standout for its capability in advanced materials synthesis and electrochemical applications, and our approach is one of careful, iterative refinement informed by years standing over glassware and pilot vessels.
Over the past decade, the family of imidazolium-based ionic liquids has drawn considerable attention for its exceptional physical and electrochemical properties. Among them, 1-allyl-3-vinylimidazolium hexafluorophosphate stands apart due to the unsaturated groups on the imidazole ring. These vinyl and allyl substituents are not mere side-chains; they provide unique handles for subsequent chemical modification and polymerization, making the compound much more than just another ionic liquid salt.
Back when we began synthesizing this compound, the primary demand came from researchers trying to embed ionic liquids directly into polymers or create solid-state electrolytes without simply blending in additives. Many commercial products lacked the reactivity or purity required for consistent, reproducible results. We recognized that careful control over both the nitrogen substituents and counterion opened the door to new performance levels, particularly for tailor-made ion-conductive materials or ionic liquid copolymer systems.
Structurally, this material features an imidazolium ring where one nitrogen bears an allyl group and the other a vinyl. The double bonds provide loci for further cross-linking, grafting, or polymerization—an option not present in more standard 1,3-dialkylimidazolium systems. The choice of hexafluorophosphate as a counterion is deliberate. Over multiple pilot batches, we compared PF6 salts with others like BF4 or NTf2, evaluating hydrolytic stability, compatibility in high-voltage electrochemical cells, and solubility in polar monomers. PF6 strikes a sweet spot: robust in damp conditions, high ionic conductivity, and no aggressive acidity or nucleophilicity that could decompose sensitive functional groups in adjacent materials.
On our line, specifications always come from function. 1-Allyl-3-vinylimidazolium hexafluorophosphate emerges as a pale yellow, viscous liquid at room temperature. We monitor water content, keeping it consistently below 0.1% by Karl Fischer titration. Even minor upticks lead to different drying protocols because moisture triggers hydrolysis of PF6 and alters both viscosity and conductivity in customer formulations. Each batch gets checked for halide contamination, since trace chloride from imidazole alkylation steps can poison downstream catalysts or interfere with polymerization.
Viscosity trends lower than most dialkylimidazolium PF6 salts, particularly due to the unsaturated substituents which disrupt molecular packing. Cooperative hydrogen bonding with minor water traces reveals itself quickly—customers often remark on batch-to-batch consistency after switching to our product due to how we monitor and control this attribute. Color, clarity, absence of particulates—those checks are easy, but our QC group puts electrochemical window and residual free vinyl/allyl monomer content high on the list, because the real issues only show after long polymerization runs or thermal cycling.
From the inquiries and feedback we receive, laboratories and production facilities reach for this ionic liquid in several key scenarios. In synthesizing polymer electrolytes for lithium batteries, direct copolymerization links the ionic liquid segment through those reactive vinyl and allyl groups, yielding stable matrices with high conductivity and negligible phase separation. We’ve watched university groups turn our batches into thin films and membranes that tolerate dozens of thermal cycles without fissuring—a direct result of tightly controlled side group chemistry.
Electrochemical deposition and catalysis groups push the PF6 version for its broad electrochemical window and negligible Lewis acidity. We know some teams have succeeded in immobilizing transition metal centers in polymerizable ionic liquid scaffolds, leading to stable, recyclable catalytic beds. In organic synthesis, the product’s function as a reaction medium with embedded polymerizable handle opens new methods for immobilized catalysis or permanent surface modifications. Our staff often gets looped into troubleshooting remote reactor startups where subtle variations in ionic liquid batches lead to big differences in polymer gel structure or electrode interface formation. Fine-tuning purity, side product control, and moisture content directly addresses these concerns, whether the material is heading into a university glovebox or industrial continuous reactor.
The big difference with 1-allyl-3-vinylimidazolium hexafluorophosphate comes from the dual functionality of its unsaturated side chains, something other ionic liquids lack. Many competitors only offer simple alkyl derivatives, which fall short when researchers want to build permanent, covalently linked structures. We’ve watched customer projects stall for weeks because a pilot-scale polymerization with non-reactive ionic liquids led to leach-out or phase instability; swapping in our dual-unsaturated material solved that issue. Electronic conductivity remains high, and the ionic conductivity in cross-linked matrices routinely beats what’s possible by dropping in non-functionalized analogs.
One area where importance really shows is during post-polymerization purification. Non-reactive ionic liquids tend to migrate or phase out, leading to unstable, color-changing copolymers or gels. Our version, once anchored via the double bonds, stays locked into the architecture, resisting mechanical aging and electrochemical cycling fatigue. Attempts to generate tough, stretchable films for sensors or flexible electronics typically require just what this molecule delivers: built-in performance rather than reliance on additives.
Comparisons with tetrafluoroborate or bis(trifluoromethanesulfonyl)imide ionic liquids highlight another clear edge: hydrolytic stability. PF6 maintains its structure under high humidity or moderate heat, where BF4 salts begin to break down and produce unwanted side products. Several customers initially tried BF4 versions in water-tolerant membranes, running into reproducibility roadblocks—our technical staff has fielded calls walking them through the switch to PF6 with instant gains in membrane lifetime and performance.
From batch charging to final filtration, we handle every step in-house, letting us monitor not only purity and yield, but also small contaminants that can spoil highly sensitive downstream chemistry. During alkylation, reaction temperature and time get mapped out across dozens of small-scale and pilot runs. Allyl and vinyl halides each carry different reactivities and byproducts; if you cut corners or scale too fast, you pick up non-functionalized imidazolium species, which can sabotage intended copolymerization or catalyst immobilization.
Hexafluorophosphoric acid quality matters. We've sourced from multiple global suppliers and have watched PF6-containing batches age differently over weeks depending on origin and transport conditions. Our QA team runs thermal gravimetric analysis and cyclic voltammetry on every synthesis lot, flagging shifts in window or any sign of impurity. This is not just procedure; every failed batch on our end translates to a lost week in the customer's R&D program.
Long before shipping, we test storage stability under variable humidity and temperature cycles. The ionic liquid’s hygroscopic tendency calls for tightly sealed containers and clear labeling. More than one third-party product arrived to customers with hydrolyzed PF6 and cloudy appearance—a problem we address by employing laminar flow packaging stations and argon sparging before capping every drum.
Having rooted relationships with both academic labs and industrial producers lets us get detailed feedback about real project bottlenecks. We value early feedback from process engineers who’ve tested our batches against the competition and reliably report improved polymer film toughness, ionic conductivity, and lower exudation in their applications. It’s not rare for formulation chemists to show us their membranes after 1,000 charge/discharge cycles with our material integrated; the performance speaks to the chemical bond strength introduced by those allyl and vinyl functional groups.
Research institutions working on next-generation energy storage devices demand not only purity, but a detailed profile of trace elements within each lot. Our analytics lab utilizes inductively coupled plasma (ICP) and NMR spectroscopy, tracking even the tiniest spills or trace halogen presence. This hands-on monitoring makes a key difference, especially in projects where ionic liquid residues could foul catalytic cycles or narrow electrochemical windows, as seen in advanced battery research.
Innovation doesn’t stop at initial synthesis. Several partners have approached us to tweak the ratio of vinyl to allyl substituents, aiming to steer rigidity or flexibility in custom polymers. We’ve collaborated to further purify the product, stripping trace stabilizer residues and optimizing reaction quenching to push residual chloro-derivatives below analytical detection. Each improvement passes back down our process line, tightening both in-process controls and end-point QC.
A major focus in our R&D lab centers on tuning the polymerizability of the ionic liquid. Managing inhibitor content, double bond conversion, and the possibility of post-synthetic functionalization all matter for polymer and membrane researchers—but they only translate to reliable process results due to tight factory control. The relationships we’ve built with teams in energy materials and conductive membranes help drive this hands-on iteration. Real-world product launches often hinge on being able to trace a film or coating property back to an honest-to-goodness batch record, and we treat that as an ongoing commitment.
Sustainability and safe handling remain nonnegotiable priorities. Imidazolium ionic liquids, especially with PF6 anions, demand respect. Our plant trains operators on the direct risks of hydrolysis, the proper containment of fluorinated byproducts, and careful management of waste streams, especially since PF6 can yield HF under harsh conditions. We maintain state-of-the-art capture and neutralization facilities, not just ticking a box, but preventing real product and environmental loss.
Tight control of water and exposure means drums leave our facility with clear recommendations for nitrogen or argon sparging during transfers. We provide direct technical documents and training for teams adopting the liquid for industrial-scale use. Our safety program stems from lessons learned the hard way—one spill or mismanagement can slow a project and compromise the well-being of people around the product.
What holds all these points together is our approach: production built on real technical feedback, not just textbook theory or spec sheet promises. Years of producing and continually improving 1-allyl-3-vinylimidazolium hexafluorophosphate have led us to make smart, informed decisions at every step—starting with the molecular design and carrying through to packaging and delivery. Laboratories and production teams worldwide have run side-by-side comparisons and found enduring value in chemical reliability, batch-traceable control, and customer support by practitioners who understand both the synthetic and application sides of the business.
Every decision around this ionic liquid reflects shared commitment to progress in advanced materials, energy, and catalysis technology. As new applications and technical challenges emerge, we continue investing in the expertise, equipment, and collaboration needed to drive both incremental and breakthrough gains. 1-Allyl-3-vinylimidazolium hexafluorophosphate represents decades of accumulated know-how and partnership—a product we keep building on, together with our customers, for the future of high-value chemistry.