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HS Code |
526553 |
| Chemical Name | Diphenylphosphinic Chloride |
| Cas Number | 1486-21-5 |
| Molecular Formula | C12H10ClOP |
| Molecular Weight | 236.63 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.24 g/cm³ |
| Melting Point | 35-38°C |
| Boiling Point | 164-166°C at 15 mmHg |
| Solubility | Reacts with water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Refractive Index | n20/D 1.599 |
| Flash Point | 126°C |
| Un Number | UN 3261 |
| Storage Temperature | Store at 2-8°C |
| Hazard Class | 8 (Corrosive) |
As an accredited Diphenylphosphinic Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Diphenylphosphinic Chloride, 100g, is supplied in a tightly sealed amber glass bottle with hazard labeling and protective outer packaging. |
| Shipping | Diphenylphosphinic chloride should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and incompatible materials. It must be handled as a hazardous material, typically under UN 3265, and transported according to relevant local, national, and international regulations for corrosive substances. Appropriate safety documentation and emergency procedures must accompany the shipment. |
| Storage | Diphenylphosphinic chloride should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as water, strong bases, and oxidizing agents. It should be kept tightly sealed in its original container, preferably made of glass or corrosion-resistant material, and protected from direct sunlight. Storage under inert atmosphere, such as nitrogen or argon, is recommended to prevent hydrolysis. |
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Purity 98%: Diphenylphosphinic Chloride with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal by-product formation. Melting point 66°C: Diphenylphosphinic Chloride with a melting point of 66°C is used in organophosphorus ligand preparation, where controlled melting enhances process efficiency. Molecular weight 218.6 g/mol: Diphenylphosphinic Chloride with a molecular weight of 218.6 g/mol is used in catalyst development, where precise molar calculations facilitate predictable reactivity. Chlorine content 16.2%: Diphenylphosphinic Chloride with 16.2% chlorine content is used in flame retardant additive formulations, where effective halogenation improves fire resistance. Moisture content <0.5%: Diphenylphosphinic Chloride with moisture content below 0.5% is used in polymer modification, where reduced hydrolysis risk ensures product stability. Hydrolytic stability: Diphenylphosphinic Chloride with high hydrolytic stability is used in electronic chemical manufacturing, where minimal decomposition supports high purity deposition. Refractive index n20/D 1.592: Diphenylphosphinic Chloride with a refractive index of 1.592 is used in specialty optical material synthesis, where optical clarity is critical. Assay ≥99%: Diphenylphosphinic Chloride with assay ≥99% is used in agrochemical production, where high assay levels ensure consistency in formulation performance. Boiling point 181°C: Diphenylphosphinic Chloride with a boiling point of 181°C is used in high-temperature organic synthesis, where thermal resilience expands processing options. Solution stability: Diphenylphosphinic Chloride with superior solution stability is used in laboratory reagent preparation, where reliable shelf life enhances experimental reproducibility. |
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Diphenylphosphinic chloride has long been one of those chemical building blocks that keeps turning up in laboratories, pilot plants, and commercial facilities, always with a knack for making things just a bit easier—or sometimes possible at all. Mention the model CAS 838-85-7 to anyone who’s worked in organophosphorus synthesis, and you’ll probably get a nod. This compound usually appears as a pale yellow liquid, sometimes with fine crystals, and people respect it because it consistently does what they need in both research and manufacturing settings.
Phosphorus-based reagents often carry a reputation for being tricky to handle or unpredictable, yet diphenylphosphinic chloride is as close to reliable as these materials get. I've watched colleagues reach for it not out of habit, but because its reactivity is both well-defined and manageable, making it a staple for those working with ligands, flame retardants, and pharmaceutical intermediates. This chemical reacts neatly with alcohols, amines, and other nucleophiles, which lets chemists attach diphenylphosphinic groups onto other molecules with confidence. More straightforward reactions mean less wasted time and cleaner yields—the real-world kind of efficiency with a direct impact on lab budgets and project timelines.
Some of the most compelling parts of working with diphenylphosphinic chloride come from its ability to act as both a starting material and a reagent for key transformations. It's helped researchers push the frontiers of asymmetric catalysis by simplifying the synthesis of ligands used in pharmaceutical manufacturing. That’s the sort of application that demonstrates value beyond the beaker—value that ultimately trickles into everyday medicine for regular folks.
You’ll typically see diphenylphosphinic chloride offered with high purity, sometimes above 98 percent, in sealed glass bottles or steel drums, depending on the scale. The compound boils at temperatures north of 160°C under reduced pressure, and stores without much fuss if it's kept cool and dry. That stability means it doesn’t turn into another line item for expensive specialty handling. Many labs keep it in the reagent cabinet for months without any sign of breakdown.
For anybody sourcing this material with quality in mind, the better suppliers will provide details such as NMR, IR, and GC purity—not just a generic “98% pure” on a datasheet. Over the years, I’ve learned to never underestimate the headache that comes from working with chemicals that are a percent short of spec, especially in reactions where side products or trace impurities threaten to derail expensive multi-step syntheses. Reliable diphenylphosphinic chloride has kept plenty of reactions from ending up in the waste bin.
My first introduction to this reagent came during graduate school, trying to synthesize an exotic ligand for a palladium-catalyzed cross-coupling. It was the only thing that made the intermediates stable enough to carry through all the workup steps. Since then, I’ve seen it used across sectors—polymers, flame retardants, biochemistry, and even niche electronics. Diphenylphosphinic chloride’s knack for activating alcohols and amines makes it a crucial ingredient in creating organophosphorus compounds, which anchor a lot of the chemistry that underpins next-generation materials.
In pharmaceutical chemistry, there’s a growing appetite for structural diversity in drug candidates. Diphenylphosphinic chloride offers a straightforward route to phosphorus-containing molecules, many of which show increased metabolic stability or new modes of biological activity. Some pharma chemists lean on it to add phosphorus where it wasn’t possible before, taking advantage of its clean reactions and wide compatibility with other reagents.
Anyone in flame retardant application development may recognize how organophosphorus compounds help slow combustion in plastics, textiles, and other common materials. Phosphinic derivatives, often built from this reagent, have helped manufacturers comply with strict safety standards without giving up flexibility or performance. It’s been satisfying to see these real-world uses stretch far beyond the lab notebook.
Pick up a catalog and you’ll see several phosphorus chlorides lined up side by side. Triphenylphosphine and phosphorus trichloride often get more name recognition, but diphenylphosphinic chloride sets itself apart in more subtle ways. Its two phenyl rings add bulk and electronic properties not found in phosphorous trichloride or phosphorochloridates, giving chemists a tool for fine-tuning steric effects in catalysts and modifying solubility in organic solvents.
This specificity isn't about buzzwords or wishful thinking; it’s rooted in how the molecule behaves in reaction flasks every day. I’ve had projects hit a wall with bulkier or less-electron-rich chlorides, only to move forward again when switching to diphenylphosphinic chloride. Its performance is most obvious in ligand synthesis, where the steric environment makes or breaks the catalyst’s selectivity. Fewer unwanted by-products mean fewer purification steps, and that translates into less wasted solvent and a more environmentally friendly process.
Comparisons to diphenylphosphoryl chloride reveal another important advantage: increased selectivity without the harsh conditions that harsher reagents might demand. This opens opportunities to functionalize molecules that are sensitive to heat or acid, ultimately expanding the number of compounds a chemist can make without running into decomposition or ugly side reactions. I'm reminded of a scale-up project where boiling, aggressive agents kept decomposing our intermediates, while diphenylphosphinic chloride kept everything in line at lower temperatures.
Anyone with hands-on experience knows the potential risks that come with most organophosphorus chlorides, and this one is no exception. There’s a sharp smell to diphenylphosphinic chloride that always reminds me to double-check the glove selection and turn on every fume hood. Even so, its lower volatility compared to some others cuts back on fugitive emissions and accidental exposures, making it easier to manage safely during flask transfers and weighing. It still reacts with water to generate hydrogen chloride, so spills or splashes still need prompt containment.
On the sustainability side, diphenylphosphinic chloride participates in cleaner, high-yield reactions, which translates to fewer by-products and less process waste. In my experience, the clean-up after these runs is usually quicker, and downstream water treatments run more smoothly due to lower overall load of acidic and oxidizing contaminants. I’ve seen progressive labs increasingly choose this reagent for the lower downstream impact, and more organizations are starting to see this as a business advantage, not just an environmental checkbox.
Markets for phosphorus-based reagents have shifted in recent years, driven in part by fluctuations in phosphorus mining and downstream demand for high-performance polymers and specialty chemicals. Sourcing diphenylphosphinic chloride from reliable suppliers reduces the headaches that come from inconsistent purity or surprise shipping delays. The companies that survive in this space generally maintain strong quality and documentation practices, which helps end-users navigate everything from customs to internal safety audits.
Regulatory compliance gets more challenging every year, as authorities tighten controls on hazardous substances. Diphenylphosphinic chloride isn’t on the most restricted lists, but responsible users know to keep tight records and confirm registration status in every market where their products travel. European REACH regulations and similar frameworks in Asia and North America have raised the bar on safety and traceability—something I’ve experienced firsthand during joint projects with international teams. Those who treat documentation as an afterthought often find themselves left out of competitive bids and supply agreements.
Over the last decade, I’ve managed research projects ranging from early discovery to pilot scale-up, and diphenylphosphinic chloride has become a linchpin more often than I ever expected at the start. For ligand synthesis, the starting steps usually rely on attaching aromatic rings to phosphorus, and this compound lets us do that without heavy metals or harsh oxidizers, which means fewer downstream contaminants and less need for complex purification methods. The impact on project timelines is significant—projects move forward without weeks lost to troubleshooting or redoing entire reaction batches.
One of the more memorable projects involved scaling a reaction from grams to tens of kilos for a biotech application. The reaction demanded tight control over heat and mixing, and we tried several phosphorus reagents. Only diphenylphosphinic chloride gave predictable product quality and yield, batch after batch. When production costs matter, that kind of reliability transforms a lab curiosity into a commercial reality. Part of the credit also goes to its behavior during quenching and work-up; it doesn’t form emulsions or troublesome gels, so process operators can extract, wash, and dry product phases with fewer headaches.
I’ve also appreciated how much less clean-up there’s been, compared to other phosphorus chlorides that hydrolyze rapidly or create persistent byproducts. Teams can keep the focus on process improvement and product validation, not endless rounds of column chromatography or solvent distillation. For anyone measuring the true cost of a chemical, these downstream considerations make all the difference.
That said, no chemical is perfect. Handling diphenylphosphinic chloride still takes attention, especially in humid climates where ambient moisture can creep into bottles and lead to slow decomposition. Keeping containers tightly sealed, storing in desiccators, and scheduling regular checks on purity are simple but effective strategies. In multi-user settings, I’ve found it’s worth spending ten extra minutes reviewing handling protocols with new teammates—an hour of training pays back with months of clean, predictable chemistry.
Costs can add up, especially on industrial scales, and fluctuations in the phosphorus supply chain occasionally ripple down to this compound. Long-term contracts with reputable suppliers and ongoing purity testing remain the best advice I can offer from hard-won experience. Chemists who switch to cheaper—but dirtier—suppliers almost always regret it. The hidden cost of redoing failed batches far outweighs what’s saved at the time of purchase.
Innovation in the phosphorus chemicals field is steadily rolling forward, with researchers developing greener synthesis methods and safer handling protocols for diphenylphosphinic chloride and related compounds. Enzymatic approaches and low-waste routes could one day rewrite how we make these reagents on a large scale, so it’s worth keeping an eye on academic partnerships and government-supported consortia in the area.
I’ve seen the benefits of open technical exchange first-hand, where shared case studies reveal new tricks for running reactions more efficiently or minimizing environmental burden. Companies that bring these ideas to scale will shape the industry in the coming years. For new entrants in fields like pharmaceuticals, advanced materials, or electronics, understanding how diphenylphosphinic chloride fits into evolving sustainability frameworks ensures they stay a step ahead of competitors. People are already asking suppliers tough questions about provenance, chain of custody, and environmental impact. Those answers give buyers an advantage in a crowded field.
Diphenylphosphinic chloride doesn’t just check boxes on a supplier’s list. For many, it’s become the go-to answer for balancing reactivity, selectivity, and process safety across a variety of modern synthetic challenges. Chemists from graduate labs to global R&D centers have come to rely on it for the reliability and performance that real-world chemistry demands.
Years of experience, ongoing innovation, and responsible supply practices prop up its role in both current and emerging applications. Whether you’re scaling for industrial output or troubleshooting a stubborn bench-scale synthesis, diphenylphosphinic chloride provides a practical, proven edge. Experience in the lab and the broader market proves that some chemical tools really do stand out for the right reasons, and this is one of them.