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HS Code |
539125 |
| Chemical Name | 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) |
| Molecular Formula | C44H40Cl2P2 |
| Molecular Weight | 715.64 g/mol |
| Appearance | White to off-white powder |
| Solubility | Soluble in water and polar solvents |
| Melting Point | Dec. >220°C (decomposes) |
| Cas Number | 13947-71-8 |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Purity | Typically >98% |
| Synonyms | trans-1,4-Bis(Triphenylphosphonium)-2-butene Dichloride |
| Chemical Structure | [(C6H5)3P+–CH2CH=CH–CH2–P+(C6H5)3]·2Cl– |
| Category | Organophosphorus compound |
| Uses | Precursor for Wittig reagents |
| Hazard Classification | Irritant |
As an accredited 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams, sealed with a tamper-evident cap, labeled with product name, purity, hazards, and CAS number. |
| Shipping | 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) should be shipped in tightly sealed containers, protected from moisture and light. Handle as per chemical shipping regulations—typically as a non-hazardous solid, but consult the SDS for exact classification. Avoid temperature extremes. Ensure appropriate labeling and include all relevant transport documentation per regional requirements. |
| Storage | 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature or as recommended by the manufacturer. Ensure proper labeling and secure from unauthorized access or accidental use. |
Applications of 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) in Industrial ManufacturingOur production of 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) supports critical advancements in chemical manufacturing, especially in sectors utilizing advanced organophosphorus compounds. By maintaining direct control over synthesis, batch traceability, and QHSE systems, we provide consistent quality and supply for targeted industrial applications. The following real-world usage scenarios outline evidence-based integration of this specialty reagent into downstream processes. 1. Homogeneous Catalysis Development for Olefin MetathesisChemical manufacturers specializing in homogeneous catalysis deploy this material as a phase transfer or ligand precursor during the development of advanced transition metal complex catalysts, notably for olefin metathesis in fine chemical and pharmaceutical active ingredient synthesis. Our consistent lot-to-lot reactivity profile helps catalyst manufacturers benchmark ligand performance during controlled pilot batch reactions, supporting scalable research and high-yield production. Industry compliance standards
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2. Synthesis of Quaternary Phosphonium Salts for Ionic Liquid ProductionThis compound acts as a tailored intermediate for downstream production of functionalized quaternary phosphonium salts, which subsequently serve as building blocks for custom ionic liquids. These specialty solvents find application in green separation, energy storage electrolytes, and specialty chemical processes. Our process capability for reliable impurity control ensures high compatibility with demanding ionic liquid end uses. Industry compliance standards
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3. Intermediate in Preparation of Polymerizable Phosphonium MonomersProducers of advanced polymer materials utilize this salt as a critical intermediate to introduce cationic phosphonium functionality into polymerizable monomers. Post-functionalization enables the preparation of specialty polymers with improved ion exchange capacity, antifouling properties, or high thermal stability, targeting performance films and membranes. Direct sourcing from our plant allows precise supply scheduling for just-in-time downstream campaigns. Industry compliance standards
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4. Starting Material for Supramolecular Host-Guest ChemistryResearch and specialty chemical companies in the coordination and supramolecular chemistry segment require high-purity phosphonium salts as starting materials for crafting host molecules with selective guest binding, which underpins probe development, molecular sensing, and advanced material self-assembly. Relying on our controlled batch outputs, formulators tune molecular recognition features for next-generation chemical sensing devices. Industry compliance standards
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We have worked with enough phosphonium salts over years in the shop to spot a molecule with genuine value. Among specialty organophosphorus compounds, 2-Butene-1,4-Bis(Triphenylphosphonium Chloride) stands out for its structural integrity and reactivity profile. Not every reagent manages to carve such a distinct position. Our manufacturing starts with scrutinizing incoming raw materials. The aromatic triphenylphosphine component cannot carry off-spec residues, and the butene backbone needs uniform geometry. After dozens of batches, our technical staff developed reliable synthesis pathways and solid handling methods that have raised our confidence in every package we ship.
This product has the chemical formula C44H40Cl2P2 and a molar mass that puts it among the heavier phosphonium salts. A close look shows two phosphonium centers linked by the flexible butene spacer. This structure, with its dual reactivity sites, brought us challenges during scale-up—especially when it came to controlling isomer content and batch crystallization. It’s the attention to those details that separates high-value material from inconsistent lots found elsewhere.
Early inquiries came from academic labs pushing the limits of supramolecular chemistry. Soon after, we noticed the material getting traction in coordination chemistry, metathesis studies, and as a precursor for cationic frameworks. Custom synthesis requests became the norm, especially for research where standard tetraalkylphosphonium salts couldn’t deliver the right spatial orientation or redox properties. There are numerous ways to attach triphenylphosphonium to a molecule, but the placement across a 1,4-butene bridge grants this salt the right backbone for chelation studies and specialty ligand design.
Most competing materials in this space come as monophosphonium derivatives or use saturated linkers. Single site salts present a more rigid profile and lack the duality that helps our compound anchor into polymeric or supramolecular architectures. The flexibility of the butene linker means customers working on functional materials can achieve structures simply out of reach with longer or more sterically hindered alternatives. We’ve heard from synthetic chemists who already tried benzyl or tetramethylene bridges, only to report unpredictable solubility, poor reactivity, and issues during workup.
One point that deserves mention is the product’s crystalline nature. If you had asked us ten years ago about isolating this bis-phosphonium salt on larger scales without troublesome hygroscopicity, we would have been skeptical. Modern purification equipment and thoughtful desiccation protocols allow us to stabilize it not just for immediate use, but for long-term storage without degradation. There are no frustrating drying cycles at the bench or last-minute solubility issues that torment users of less-refined grades. We know the pain when a critical project stalls—so we’ve had to make stability a non-negotiable feature here.
We talk to customers running projects from gram-scale research to multi-kilogram custom synthesis. In our own laboratory, and out in the field, the compound functions well in the preparation of bis-phosphonium ylides, which are vital in Wittig-type reactions. The symmetrical structure allows generation of two ylide centers on a single backbone. People synthesizing cyclic or macrocyclic structures lean towards this design because the connectivity of the linker enables products impossible with monophosphonium precursors.
Other users exploit its potential in template-directed assemblies. They use the butene linkage to enforce pre-organization in molecular frameworks or to plug functional units into extended networks. Materials scientists have employed it in polymer modifications, where maintaining precise distances between charge-bearing sites drives conductivity or ion transport properties. Technical feedback told us that similar products using ethylene bridges result in local crowding and poor control over spacing, while those with saturated alkyl linkers fall short when flexibility is needed for layered or grid-like structures.
If a team wants to build coordination polymers, the salt’s structure allows metals to chelate at both ends with minimal distortion. Its presence in crystal engineering marks a sharp difference from random blends or impure technical grades. The reliability in geometry, charge density, and chemical stability makes it a sought-after starting point for creating new functional materials. These aren't vague talking points; customers routinely share their project data and attribute the break in bottlenecks to switching to our grade of phosphonium dication.
The journey from concept to steady production involved plenty of trial and error. Phosphonium chemistry can get messy. Early attempts produced unwanted by-products or color contamination, especially during alkylation steps. Staying hands-on, we revised temperature holds and added tighter controls to prevent side-chain oxidation and over-alkylation. Today’s lot consistency comes from those struggles—each batch cleared for isomer content and confirmed by NMR and elemental analysis. No short-cuts, no secret blending, just deliberate chemistry.
Handling of the final product required new solutions. As a dichloride, it showed decent moisture resistance but too long in ambient air and it could start clumping. We invested in better drying chambers and stored final material under controlled humidity, so it lands on the user’s bench in a predictable, pourable form, every time. Frequent feedback loops between R&D and plant staff keep refining these steps, and no shipment departs without comprehensive quality checks. Often, clients come back not only for the product but for application support. We know every production variable because we’ve sweated over each detail ourselves.
Some monophosphonium salts hit the market as convenient alternatives, but end up limiting the chemistry downstream. Once, a catalyst developer shared their comparison data—using triphenylphosphonium-based mono-salts generated lower conversions and left deals of unresolved side-products. In contrast, bis-phosphonium ions delivered precisely controlled assemblies and sharper reactivity for their intended applications. The spacing of the phosphonium sites plays a bigger role in three-dimensional structure than most appreciate until they test both forms side by side.
We hear similar stories from peptide chemists and supramolecular researchers. The twin cation arrangement simplified the creation of bis-ylide intermediates without the need for sequential functionalizations or protection steps. Attempts to mimic properties using two separated mono-salts led to uneven incorporation or required extra purification. Our manufacturing records show fewer returns and less customer troubleshooting when projects use the genuine bis-phosphonium chloride in a single, well-characterized entity. In scale-ups, the reduced number of side products directly cuts down on waste disposal costs and rework.
Supplying to both research and industrial clients means facing strict scrutiny. We support every shipment with real analytical data from each batch, not just the first or largest run. Typical specifications cover melting point, active content by titration, and water content. For projects targeting medical or advanced materials, we provide a detailed impurity profile. We have refused to blend or reformulate off-grade material into production lots. Customers say this transparency lets them plan their own experiments and regulatory approaches with more confidence.
Our approach to compliance stems from years dealing with auditors and certification bodies. Every kilogram passes through documented, validated processes designed according to accepted chemical manufacturing regulations. Operators at our facility track inventory using barcoded systems and regular reconciliation, so no ambiguity creeps into chain-of-custody or batch history. Feedback from regulatory consultants has helped us refine our lot release protocols. In a market where some operators repack or relabel intermediates with little oversight, we maintain clear records and accountability at every step.
No chemical process can ignore sustainability. Waste reduction and solvent accountability sit at the front of every process evaluation. We have retrofitted solvent recovery units to reduce chlorinated waste generation, and batch filtration employs closed-loop systems that minimize air emissions. Users manufacturing similar salts from scratch often share their own environmental frustrations—solvent-intensive workups, persistent odors, frequent self-imposed downtime for maintenance. Our evolved procedures provide a pathway for scale without spikes in environmental compliance spending.
Sourcing triphenylphosphine with higher purity at acceptable prices continues to challenge the supply chain. Instead of turning to low-cost but impurity-laden material, we qualify new suppliers regularly and carry out secondary purifications ourselves. Users gain assurance that byproducts of origin do not build up in their process streams. This policy may slow our output compared to high-volume traders, but our customers prefer guaranteed performance over short-lived cost savings.
Long-term users have pressed for more environmentally benign variants. We are partnering with researchers trying to replace chloride anions with less persistent counterions. While the chloride offers ideal solubility and stability for many, some new projects in green chemistry demand increased biodegradability or new dispersibility thresholds, especially in water-based systems. The future likely holds a range of analogs serving broader needs, but our commitment to core quality and traceable production will not change.
Our technical staff rarely gets a quiet week. Chemists from across industries send requests for input—optimizing reaction protocols, troubleshooting solubility problems, and assisting with scale-up parameters. Experience tells us that real support comes from people who know the quirks of the molecule in both lab and plant settings. The stories that circulate in our support logs range from last-minute salvage missions in university labs to the pressure of hundred-liter reactors moving toward commercial production.
We do not treat these inquiries as interruptions. Each one feeds back into our improvement cycle, helping us advise newcomers and provide more relevant, up-to-date methods on real bottlenecks. Sometimes, this leads to creating custom forms of the product—different counterions, special particle sizes, or matched solvation levels. Those requests light the path to the future, as our product evolves along with our customers’ ambitions.
Feedback from users shapes much of the innovation behind our 2-Butene-1,4-Bis(Triphenylphosphonium Chloride). One research team managed a breakthrough with a new material for ion-selective membranes, observing that only the bis-phosphonium spatial arrangement delivered durable, high-conductivity films. Another group, seeking new methods in dynamic covalent chemistry, credited the robust but flexible linker as the reason they could create multi-component macrocycles previously thought unachievable. These successes trace back to a reliable supply chain and trusted technical partnership, not to marketing slogans or me-too products.
Working directly with diagnostics developers brought about a batch of new questions—how will modifications to the linker or the phenyl rings affect biocompatibility? Can we adapt drying and packaging for air-sensitive workflows? Each answer demanded fine-tuned process control at the factory and close communication with users exploring new scientific territory. We see a pattern: as our customers advance, so do the demands placed on the product. Meeting those demands requires focus, flexibility, and a refusal to cut corners at the point of production.
Direct customer feedback reminds us that packaging and storage matter as much as product quality. Our drums and bottles come with real-world sealing and protection against moisture. Reinforcing the routine—store tightly closed, away from damp conditions—prevents the unnecessary headaches of clumping or slow uptake in solution. Experience tells us that small lapses in moisture control at the user’s end can trigger cascading delays or create impurity issues, so we share detailed handling advice based on what our staff practice daily.
Transfer protocols and entry into gloveboxes, as performed in our facility, prove their worth every time a graduate student calls with a sudden solubility problem or crystallization failure. By sharing not just the product, but the behind-the-scenes know-how, we raise the odds of successful research and commercial manufacturing alike.
2-Butene-1,4-Bis(Triphenylphosphonium Chloride) grew from a challenging idea into an industrial reality thanks to repeated testing, frequent user input, and investment in reliable plant-scale chemistry. Our experience as the manufacturer—not a reseller, not a distributor—lets us keep direct control over every variable. We offer more than just material; we share insights gained from hands-on synthesis, batch refinement, and decades of fielding application challenges. Whether research teams are forging new classes of compounds or industry engineers are scaling new functional materials, our focus remains the same: deliver quality that stands up to scrutiny and performance that powers innovation.