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HS Code |
613504 |
| Chemical Name | (2-Butyl)Triphenylphosphonium Bromide |
| Cas Number | 221701-79-9 |
| Molecular Formula | C22H24BrP |
| Molecular Weight | 399.31 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 141-145 °C |
| Solubility | Soluble in polar solvents like water and methanol |
| Storage Temperature | Store at room temperature, tightly closed |
| Purity | Typically ≥98% |
| Synonyms | Triphenyl(2-butyl)phosphonium bromide |
| Boiling Point | Decomposes before boiling |
| Iupac Name | butyl(triphenyl)phosphanium bromide |
As an accredited (2-Butyl)Triphenylphosphonium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (2-Butyl)Triphenylphosphonium Bromide, 25g: Supplied in a securely sealed amber glass bottle with tamper-evident cap and clear labeling for safety. |
| Shipping | (2-Butyl)Triphenylphosphonium Bromide is shipped in tightly sealed containers, protected from moisture and exposure to air. It is classified as a non-hazardous material for air and land transport. Store and ship at room temperature, away from incompatible materials. Standard shipping methods apply; special handling is typically not required unless specified otherwise. |
| Storage | (2-Butyl)Triphenylphosphonium bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. The storage temperature should be kept at room temperature, typically 15–25°C (59–77°F). Ensure the container is clearly labeled and protected from physical damage. |
Applications of (2-Butyl)Triphenylphosphonium Bromide in Industrial ManufacturingAs an experienced chemical raw material manufacturer, we supply (2-Butyl)Triphenylphosphonium Bromide for specialized production uses in advanced material synthesis, pharmaceuticals, electronics, and catalytic processes. Below, we outline distinct downstream segments where this compound drives critical performance and reliability, detailing industrial standards, recommended usage ratios, integration points in workflow, and resulting value-added products. 1. Phase-Transfer Catalyst in Organic Synthesis(2-Butyl)Triphenylphosphonium Bromide acts as a key phase-transfer catalyst (PTC) for nucleophilic substitution and alkylation reactions under biphasic conditions. Industrial chemical manufacturers select this material for its ionic character and compatibility with aromatic and aliphatic reactants. Accurate dosing enables controlled reaction kinetics, while robust purification protocols ensure trace removal of catalyst residues before product isolation. Industry compliance standards
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2. Precursor for Wittig-Type Olefination ReactionsDownstream synthetic units utilize (2-Butyl)Triphenylphosphonium Bromide as a phosphonium salt precursor in Wittig and Horner-Emmons olefination, especially for building substituted alkenes under controlled laboratory and pilot-plant conditions. Its capacity to form ylides upon deprotonation in the presence of bases is critical for process engineers achieving target product geometries. Industry compliance standards
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3. Intermediate in Ionic Liquid ProductionChemical processors engaged in manufacturing room-temperature ionic liquids (RTILs) employ (2-Butyl)Triphenylphosphonium Bromide as a customizable cation source. Subsequent ion exchange processes produce tailor-made ionic liquids with application-specific conductivity, viscosity, and thermal profiles, advancing electrochemical and materials engineering fields. Industry compliance standards
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4. Supporting Electrolyte in Organic ElectrosynthesisSpecialty manufacturers apply (2-Butyl)Triphenylphosphonium Bromide as a supporting electrolyte, improving ion transport and current efficiency in electrosynthetic setups. Its chemical stability and high ionic mobility make it essential for preparative-scale electro-reductions and oxidations, particularly in nonaqueous media. Industry compliance standards
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Day after day, chemists at our facility handle synthetic challenges that demand not just purity, but consistent material performance across every batch. Among the phosphonium salts we make, (2-Butyl)Triphenylphosphonium Bromide stands out for the reliable results it brings to a range of organic transformations. Our team spent years tweaking every part of this process, from raw material selection to precise crystallization monitoring, and we see exactly how these choices play out inside reaction flasks around the world.
Our most requested product model, structured as C28H30BrP, offers a measured balance of hydrophobic and aromatic character—distinct from methyl or benzyl-substituted triphenylphosphonium salts. In our typical lot, purity consistently measures above 99%, tested batch-by-batch with both HPLC and NMR to catch even faint traces of side-products. Crystal structure analysis has pressed us to refine particle size: most years, we hold steady within a 60- to 200-micron range to allow easy handling and fast solubility in common polar aprotic solvents. Melting points typically cluster tight, 220–225°C, which prevents surprises in storage or processing, even in humid conditions.
In our own synthetic labs and through feedback from long-term clients, (2-butyl)triphenylphosphonium bromide has become a standard component for Wittig reactions that call for steric tuning at the phosphorus center. Unlike bulkier or more basic phosphonium salts, this material provides a careful nudge for E/Z selectivity in alkene installation, especially when sensitive aromatic aldehydes or electron-poor partners enter the equation. The butyl group imparts subtle flexibility—not so bulky as tert-butyl, not as volatile as ethyl or methyl branches—creating a midpoint between reactivity and isolation convenience.
In comparison, we've seen that methyl and benzyl triphenylphosphonium bromides suit more aggressive, high-yielding reactions where speed trumps selectivity. (2-Butyl)triphenylphosphonium bromide seeks a different balance: it helps create geometrically defined alkenes or intermediates where minor structural shifts cause major downstream property changes. Several agrochemical research teams have sent back notes about crystalline byproduct suppression when they switch from benzyl to 2-butyl triphenylphosphonium salts under otherwise identical conditions.
As daily operators of the full synthetic route, we invest in both starting material traceability and in-process controls. We rely on regionally sourced triphenylphosphine and n-butyl bromide, tracking each lot with strict in-lab documentation. Our reactors operate under nitrogen, and small deviations in stirring speed have led us to overhaul agitator design more than once. In every campaign, we faced the risk of bromide impurity carry-through; several years ago we replaced a generic quenching step with an inline solid-phase filtration to cut non-phosphine organics below 0.01%.
In packaging, we avoid chlorinated plastics, sticking to glass or heavy-duty PFA containers, which eliminate rogue leaching—important for pharmaceutical groups scaling up with our salt. Moisture grabs phosphonium salts fast, so every drum gets two layers of heat-sealed Mylar and a constant-cycle desiccant canister, which means nobody opens a jar to clumpy surprise. Our regular clients—pharmaceutical scale-up teams, university teaching labs, and contract research organizations—push us for transparency, so each delivery gets a full in-house quality analytics dossier, not just a PDF certificate.
One point often overlooked lies in handling outside large-scale warehousing. Unlike volatile peroxides or pyrophoric alkali reagents, (2-butyl)triphenylphosphonium bromide stores comfortably near ambient temperature, as long as relative humidity stays low. In regions facing monsoon or tropical climate swings, our clients have built custom dry rooms, but in temperate climates, a simple dry cabinet mitigates most issues. Several years back, one industrial user discovered routine caking issues after opening and closing their bulk containers in a coastal facility. After switching to our dual-sealed packaging, their material stayed flowable for months instead of weeks. Lessons like this filter back into our own warehouse practices: even on-site, we never store open product more than 24 hours.
Working directly with this compound, we pay special attention to dust control, since fine powders carry a risk of respiratory exposure if mishandled during weighing or transfer. Years ago, we moved away from manual spatula transfer, instead opting for closed-system powder hoppers during the final weighing step. This change not only reduced airborne particulates, but cut down cross-contamination between material lots—critical for anyone working with trace-sensitive syntheses or regulatory submissions.
Operators at our facility do not lean on automated controls alone; the day-to-day skill of experienced team members makes a visible difference. An operator who recognizes subtle shifts in reaction color or viscosity as the salt crystallizes can intervene and adjust, long before instrument readings flag a drift. We’ve met many visiting chemists who began as skeptical clients and became partners—each of them sensitive to minor inconsistencies in bulk material. Good chemistry demands human oversight as much as automated recording.
At the production level, human mistakes can cause as much trouble as imperfect reagents. Early production runs taught us the importance of regular retraining and careful check-in procedures. During one campaign, a substitution error at the loading station swapped n-butyl bromide with a similar alkyl halide, which nearly set off a month’s worth of rework before anyone spotted the shift through a routine TLC check. Since then, we run targeted audits at every new operator assignment and update procedures across both manual and automated reactors.
Wittig and related carbonyl olefination chemistry relies on subtle steric and electronic tweaks at the phosphorus atom. From our direct experience, the difference between a methyl and a butyl substituent might not show up in a textbook but becomes glaring in practical yields or product ratios. Butyl chains give phosphonium salts just enough bulk to slow side reactions in crowded synthetic targets, but not enough to create solubility headaches the way branched tert-butyl groups might. In published data and from partner site reports, we’ve seen over a 15% improvement in E/Z selectivity when switching to the 2-butyl variant in certain aromatic aldehyde conversions.
Benzyl triphenylphosphonium bromide, the classic workhorse for straightforward Wittig alkenations, excels in high-throughput settings where speed and cost win out. The 2-butyl version suits selective, fine-tuned chemical programs—flavors, fragrances, and pharmaceutical API precursors that command tight purity and isomeric control. By adding or deleting carbons in the phosphonium tail, a chemist doesn’t just affect the reaction rate, but the filterability, extractability, and workup timeline. Too much steric hindrance, and end-users report recovery drops; too little, and one sees creeping impurity formation that escapes even high-quality silica chromatograms.
Through hands-on synthesis and ongoing collaboration with downstream R&D teams, we've mapped how this single structural change influences dozens of cleavage, condensation, and substitution steps in the extended synthetic sequence. The butyl group fine-tunes both the physical handling and chemical reactivity, sometimes shaving days off purification or improving final product stability—details our technical support teams often discover only after rollout to a full pilot plant setting.
We field frequent requests for kilogram to multi-ton production, and scaling (2-butyl)triphenylphosphonium bromide brings its own headaches. Mixing and heat transfer become sticking points in larger batch reactors, particularly as exotherms spike during phosphorus alkylation. We spent years redesigning agitators and jacketed vessels to ensure uniform heat removal. Several times, we encountered “oiling out” effects where incomplete crystallization led to sticky, clumpy masses that couldn’t be filtered or dried efficiently. By working through these, we built in staged temperature ramps and controlled seeding from each prior best batch, making runaway exotherms or batch inconsistencies rare.
Custom derivatives, whether for labeled compounds or specialty intermediates, often challenge our upstream logistics chain. For example, isotopically labeled butyl chains require careful supplier partnerships, since even tiny switchovers in isotope content can result in false readings in GC-MS or qNMR. We collaborate directly with isotope suppliers and bring in external analytical testers at both material receipt and final QA steps, preventing substitution errors that could ruin a whole research run.
Our on-site purification system uses a blend of precipitation, recrystallization, and filtration, depending on target specification. If a downstream partner needs pharmaceutical-grade material with defined impurity profiles, we reroute the batch through additional fresh silica columns and double-support the QA testing. For those preparing research-grade batches, our base-stage purification involves a less aggressive filtration followed by oven drying, since over-manipulation sometimes degrades this otherwise robust material.
Our post-shipment service doesn’t stop at documentation or COAs. Over years, technical teams from different organizations have shared their field data, highlighting what works and what falls short. One university lab battling poor reproducibility found the culprit in slow product absorption of moisture after a new shipment of (2-butyl)triphenylphosphonium bromide arrived. Their feedback led us to strengthen the moisture protection protocol—internal vac-seals, indicator packs, and even a tweak to the drying oven schedule—to maintain the same free-flowing consistency they had grown to trust.
Industry-scale clients have influenced our drum and package sizing. Pharmaceutical partners often request single-use blister packs for one-step syntheses, which reduces both contamination and surplus waste. At the other end, fine chemical duplicators want drums, not jars, fitted for gravity feed. We remain open to these demands—engineering our packing line to support them without risk to batch-to-batch integrity.
In every process step, (2-butyl)triphenylphosphonium bromide lays groundwork that shows downstream, from pilot plant to commercial production. In the modern push for sustainable chemical transformations, minor gains in selectivity or purity compound over time, cutting both costs and environmental burden. One research group pointed out a 50% decrease in aqueous waste after switching from benzyl to butyl-based phosphonium salts, simply because crystallization and workup became more straightforward—filtration time disappeared, and with it, the need for aggressive organic solvents.
From a toxicity and process safety standpoint, the butyl group offers a reassuring profile. By comparison, certain shorter-chain or branched alkyl phosphonium salts produce trace volatile organic impurities on standing, whereas (2-butyl)triphenylphosphonium bromide remains stable for years under dry storage. Workplace exposure measurements in our own facility routinely come in below international phosphorus exposure thresholds.
Direct manufacturing pushes us to set and meet high regulatory standards, especially as global expectations around chemical safety and reporting rise each year. Many clients ask for EU REACH, RoHS, or similar documentation, and we supply full traceability on incoming and outgoing batches. Environmental reporting on bromide-containing chemicals increasingly requires transparency about process emissions and waste. To address this, we invested in a closed-loop water system for quenching, minimizing total halide output. All waste streams run through primary carbon and secondary ion exchange purification before disposal.
We continue to reduce our carbon and waste footprint through active solvent recovery and byproduct recycling. For example, waste mother liquors containing trace phosphonium or bromide cut through a custom reprocess route to recover useful intermediates; these changes go back into improvements on future production lots. By shortening the supply chain to direct-from-factory customers, we trim redundant packaging and costly, multilayer handling labor. Whenever possible, we ship direct for international partners to avoid unnecessary warehouse stops that can risk product damage or delay.
Production of (2-butyl)triphenylphosphonium bromide is more than just a recipe—it’s an ongoing process, shaped by hundreds of real-world variables. Our R&D team works with outside researchers on mechanism studies and improved reaction workflows. Collaborative trials have mapped subtle reactivity trends, pinpointing when the butyl group makes a functional difference in complex molecule synthesis. We regularly share anonymized data sets with trusted partners, contributing to precompetitive industry benchmarks and helping to lift technical standards regionally.
A culture of transparency lets buyers and end users pick up the phone directly to our technical staff, cutting through the haze of third-party brokers who can obscure the real chemical origins. Where needed, our support teams help troubleshoot both synthetic and workup challenges, and we share validated protocols for high-efficiency product recovery. Mistakes and surprises get documented, not hidden—so lessons learned travel faster across the community. Our goal is for end users to see our factory as a resource, not just a supplier.
In every batch that leaves our site, we build on the feedback, insights, and lessons of our own production teams and those of the chemists who work with our products worldwide. Charged with keeping every kilogram consistent, every drum dry, and every customer loop short, we stand by both the results and the work it takes to get there. As direct manufacturers, we believe success in chemical synthesis is a dialogue—reactive, ongoing, and rooted in hands-on practice. If (2-butyl)triphenylphosphonium bromide has become a staple for so many transformation strategies, it is because we have shared in that journey, refining everything from vessel maintenance to QA reporting along the way.
For chemists looking beyond routine transformations, this phosphonium salt offers more than a line-item reagent. It’s a bridge—a tested, responsive link connecting custom research to industrial application, supported by people who know firsthand how details shape discovery. We look forward to what the next synthetic challenge will ask of us and of our material, committed to quality at every scale and stage.