|
HS Code |
397806 |
| Cas Number | 770-12-7 |
| Molecular Formula | C6H5Cl2O2P |
| Molecular Weight | 226.99 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 263 °C (lit.) |
| Melting Point | -10 °C |
| Density | 1.405 g/mL at 25 °C |
| Solubility In Water | Decomposes |
| Refractive Index | n20/D 1.546 |
| Flash Point | 129 °C |
| Purity | Typically ≥98% |
| Smiles | C1=CC=CC=C1OP(=O)(Cl)Cl |
As an accredited Phenyl Dichlorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenyl Dichlorophosphate, 250g, is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | Phenyl Dichlorophosphate should be shipped in tightly sealed, corrosion-resistant containers, clearly labeled with hazard warnings. It must be handled as a toxic and corrosive substance, compliant with DOT regulations. Transport in a cool, dry, well-ventilated area, away from incompatible materials such as water, strong bases, and oxidizers. |
| Storage | Phenyl Dichlorophosphate should be stored in a tightly sealed container, away from moisture, heat, and incompatible substances such as strong bases and oxidizers. Store in a cool, well-ventilated, dry area, preferably in a designated corrosives cabinet. Avoid exposure to direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental spills or leaks of this moisture-sensitive, corrosive chemical. |
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Purity 99%: Phenyl Dichlorophosphate with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reduced byproduct formation. Molecular Weight 215.06 g/mol: Phenyl Dichlorophosphate at 215.06 g/mol is used in flame retardant manufacturing, where it delivers consistent reactivity and product quality. Melting Point 19°C: Phenyl Dichlorophosphate with a melting point of 19°C is used in pesticide formulation, where it provides precise phase control during process blending. Stability Temperature 70°C: Phenyl Dichlorophosphate stable up to 70°C is used in polymer modification, where it allows reliable incorporation without decomposition. Viscosity 1.5 cP: Phenyl Dichlorophosphate with viscosity of 1.5 cP is used in surface treatment applications, where it enables efficient film formation and uniform coverage. Water Content <0.2%: Phenyl Dichlorophosphate with water content below 0.2% is used in moisture-sensitive catalyst preparation, where it prevents hydrolysis and activity loss. Chlorine Content 33%: Phenyl Dichlorophosphate containing 33% chlorine is used in organic synthesis, where it provides effective chlorinating ability for target transformations. |
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Specialty chemicals like Phenyl Dichlorophosphate catch the eye for a good reason. Staring at rows of bottles and drums in the chemical warehouse, I soon realized not all reagents step up to the challenges of modern research or scale-up. Too often, so-called universal additives promise a lot and deliver very little when things get tough. Phenyl Dichlorophosphate, or PDP as many call it, shows a much stronger character in the real world of synthesis and material modification. For anyone serious about organic chemistry, custom pharma work, or advanced polymers, this compound often becomes a core tool—not a background player. There’s nothing flashy about its appearance, but there’s no mistaking its effect where it counts.
Consistent results matter more than theoretical purity. While other phosphorylating agents clog filters or invite all sorts of unintended paths during a reaction, Phenyl Dichlorophosphate offers clean, reliable conversion once the protocol gets dialed in. That means more usable product, less time babysitting separations, and fewer headaches from unexpected byproducts. The compound typically appears as a moderate-weight liquid—a detail that helps in handling but also gives more room for reaction control. This physical form isn’t just a footnote; it lets a lab tech measure, pour, and dose efficiently. Compared to crystalline competitors that clump, get stuck, or hydrate on humid days, this liquid form skips all the pointless drama.
As someone who’s slogged through endless purification columns, the true advantage isn’t obvious from textbook tables but from the memory of how fast a bench experiment can go wrong. Some phosphoryl chlorides, especially those bristling with halogen atoms or substituted backbones, behave like a bull in a china shop—aggressive, uncooperative, and sensitive to trace water or air. PDP displays a much less jittery temperament. In most standard reactors and even makeshift lab glassware, it tolerates routine atmospheric exposure with little fuss, provided standard precautions get followed. I’ve seen colleagues rush through rushed steps with other agents, only to circle back on bad yields and strange spots on their TLC plates. The comparative calm provided by PDP pays for itself in saved frustration and improved reproducibility.
No one likes staring at vague numbers. Phenyl Dichlorophosphate arrives as a clear to light yellow liquid, with a density around 1.4 g/cm³—noticeably easier to handle than some clunky syrups. Its melting point stays well below room temperature, so there’s rarely any need to warm or fuss with special equipment. Boiling hovers just under 300°C, which means standard distillation setups can clean up crude batches or recycle excess. These physical traits matter when you tally up safety and efficiency—no one wants to wrangle a solidifying mass or deal with violent decomposition that some other phosphorylating agents spring on an inattentive chemist.
Chemically, PDP carries both promise and risk. The molecule brings a reactive dichlorophosphate group attached to a phenyl ring. This structure creates a strong yet selective agent ready for transfer reactions. But it doesn’t veer off uncontrollably if the pH shifts a bit, or if traces of moisture sneak into the flask. The dual chlorine components give enough activation to catalyze a range of bond-forming steps, especially in esterification and phosphorylation. I’ve found this flexibility refreshingly practical. Where PCl3 and POCl3 either over-phosphorylate substances or demand dry-box levels of handling, PDP settles into a much cleaner middle ground. Suitably reactive, but not a finicky diva.
Over time, my respect for Phenyl Dichlorophosphate grew with every successful experiment. In my field, researchers chase more efficient drug candidates, electronics, and coatings, usually under tight deadlines. One day stands out: our team worked to modify a high-value alcohol with a phosphate group for a pharmaceutical intermediate. Simpler agents burned through our substrate, making charred goo instead of coveted product. PDP stepped up—offering smooth, controlled reactivity that gave us high yields and an easy purification path. The difference wasn’t subtle. From crude isolation to NMR confirmation, every step fell into place, cutting hours off our usual timeline.
Many find PDP valuable for making phosphate esters and fine-tuning catalysts. In agricultural science, formulated products benefit from tailored phosphate groups, and PDP reacts smartly without nonsense byproducts that could hamper yield or require costly scrubbing. Within the polymer world, PDP lays the groundwork for unique crosslinked networks or surface treatments—a feature especially handy for specialty electronics. Medical labs use it to attach interesting labels or drug fragments to biologically active substrates, creating targeted prodrugs or diagnostic designs that regular phosphates just can’t deliver. I’ve seen advanced battery projects and flame-retardant research switch to PDP for the improved thermal and chemical stability it imparts to base materials.
That said, every tool demands skill. Mishandling PDP leads to waste and risk. The chlorine atoms onboard mean corrosive fumes can form if spill cleanup lags or ventilation fails. It’s a hazard, no question—but disciplined technique and proper setup turn this threat into a manageable challenge. Speaking from experience, routine safety: always gloves, goggles, and secure ventilation. PDP shouldn’t get poured mindlessly into unknowns without pilot runs—the same rule applies for any reactive phosphorus compound. Smart researchers check for compatibility, avoid mixing with strong bases until they run calculations, and store phenyl dichlorophosphate away from common lab water sources.
Comparisons sharpen our sense of what works. Many traditional phosphorylating tools—think PCl3, POCl3, and simple dialkyl chlorophosphates—come with trade-offs. PCl3 asks for painfully dry conditions and gives harsh side-products, while POCl3 eats glassware and can scar up even metal surfaces after repeated use. Dialkyl types often lack punch, forcing researchers to wait through endless cycles for reasonable conversion. The phenyl backbone of PDP doesn’t just look different in a chemical drawing; it grants a measure of selectivity that shaves pure product out of mixed soups, all while keeping a lid on runaway side-reactions.
Bench chemists, whether amateurs in a garage or advanced teams in a university cleanroom, soon recognize the value in time saved and mess avoided. Where resource efficiency rules—a few grams must stretch to many trials—a reliable, moderately aggressive agent like PDP handily outranks alternatives. The liquid format continues to reduce waste, since a dropper or pipette sees use right down to the dregs. There’s no reason to scrape vials or hammer bottles. Pulling from my own trial notebook, reactions using PDP have outperformed runs with both more exotic and supposedly more “advanced” chlorophosphates in every test I tried for customized surface modification. The tradeoff—needing routine safety checks and appropriate PPE—seems more than fair compared to the prohibitive glassware loss or hazardous off-gassing from more volatile phosphorus chlorides.
Many early synthetic chemists overlooked phenyl-substituted chlorophosphates, assuming they were too similar to bulkier, less interesting variants. Direct experimentation cut through that myth. By bridging high reactivity and moderate stability, PDP occupies a unique spot. NMR studies reveal that the phenyl group stabilizes the otherwise edgy phosphorus-chlorine center, which means PDP shrugs off small handling errors but doesn’t stagnate when nudged into a reaction sequence. Seasoned operators—myself included—appreciate the margin for error. An extra minute on the stir plate, a touch of extra solvent, or a standard grade of starting alcohol: none of these minor tweaks throw PDP entirely off course.
The real strength comes from its ability to make phosphorus-oxygen bonds stick, a bedrock of any reliable esterification or polymer grafting experiment. Laboratory-grade batches of PDP show low impurity profiles, a detail verified by careful GC-MS and HPLC checks in published literature. This means what arrives in the container actually matches the label—a relief for anyone who’s gone a full day reconstructing someone else’s botched mixture. The safety profile demands respect but doesn’t overwhelm with unpredictability or nettlesome regulatory hoops, since it falls into established chemical classes with decades of industrial and research track records.
Sourcing specialty chemicals throws up occasional obstacles. PDP’s transport and shelf-life both emerged as points of concern over several decades. Its liquid state demands leak-proof packaging and intelligent labeling to curb accidental mixing or exposure. Institutions storing PDP share recommendations ranging from refrigerated units to dedicated, segregated shelves with spill trays, all with minimal inventory quantities at hand. In settings I’ve worked, capped amber bottles stand as the norm, since stray sunlight speeds up hydrolysis or causes darkening. Regular checks for slow leaks, corroded closures, or paper labeling degraded by fumes keep maintenance on schedule and law compliance straightforward.
Shipping across long distances or between continents presents hurdles connected not just to chemical stability, but also to regulatory frameworks. Many countries and states demand proper documents, trusted carriers, and sometimes pre-arranged import licenses, especially for kilogram-scale shipments. In practice, these steps weed out casual buyers but rarely slow legitimate researchers or manufacturers. The supply chain adapts, with warehouses and vendors specializing in short-turn orders of PDP. The more careful the institution, the less likely anyone finds an unscheduled hazard or unexpected bottle on the shelf. Organizations committed to ethical procurement and environmentally sound disposal fare best, since PDP, while potent and valuable, needs a lifecycle management plan just like any serious lab reagent.
No chemical story wins on brute force alone. As labs pivot toward greener practices, creative recycling and precise dosing come to the fore. To work cleaner, many chemists now pair PDP with catalytic supports instead of excess solution doses, eking out more runs from every bottle. Extraction solvents get selected for ease of recovery and reuse, shrinking the burden on the waste stream. From personal experience, careful scheduling—prepping enough material for a week instead of running fresh each day—brings down handling risk, improves cost efficiency, and cuts the total inventory needed on site.
On the broader scale, tighter training pays big dividends. Workshops tailored to phosphorus chemistry, scenario drills for accidental releases, and regular PPE refreshers all play a part in shifting the culture from reactive to proactive. Teams maintaining chemical inventories do well to update logbooks electronically, using barcodes and registry checks that flag nearing expiration or outdated containers. These safeguards mean freshmen and veteran team members both spot risks early and streamline emergency response in rare trouble spots.
Ethical sourcing matters as well. Individuals and firms that prioritize transparent supply lines avoid counterfeit or degraded materials on the black market—a chronic issue for specialty agents with value in illicit drug synthesis. Community engagement—responsible leadership watching for diversion or theft—completes the circle, making sure high-quality PDP finds its way only into legitimate research and manufacturing hands.
Innovation depends on access to reliable building blocks. Phenyl Dichlorophosphate combines precision and manageability in ways few others match. As more fields pursue custom phosphorus materials—think next-gen batteries, precision agriculture, biocompatible implants, or cybersecurity inks—PDP’s flexible reactivity and manageable safety profile guarantee steady relevance. Scientists pushing boundaries in slow-reacting or moisture-exposed environments will find in PDP a consistent partner, always favoring clean conversions over drama.
Where rigorous outcomes matter, this compound keeps proving its worth. Not as a mysterious black-box reagent with endless caveats, but as a straightforward, transparent partner in problem solving. For every glaring headline about new tech, there sits a lab bench, with glassware stained by years of missed cuts and breakthroughs alike. Choosing PDP, more often than not, means the scales tip toward successful, repeatable progress. The risk never vanishes—such is the nature of all potent chemistry—but experience, clear protocols, and ongoing education close the gap. Respect the bottle, trust the process, and Phenyl Dichlorophosphate rewards efforts with results that stand the test of peer review.