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HS Code |
115047 |
| Chemical Name | 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One |
| Cas Number | 17608-52-7 |
| Molecular Formula | C6H4ClO3P |
| Molecular Weight | 190.53 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 69-71°C |
| Boiling Point | No data available (decomposes) |
| Solubility | Reacts with water, soluble in organic solvents |
| Density | 1.56 g/cm³ |
| Synonyms | 2-Chloro-1,3,2-benzodioxaphosphorin-4-one |
| Smiles | C1=CC2=C(C=C1)OP(=O)OC2Cl |
| Inchi | InChI=1S/C6H4ClO3P/c7-11-9-5-3-1-2-4-6(5)10-12-8/h1-4H |
As an accredited 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g chemical is packaged in a sealed amber glass bottle with a tamper-evident cap, labeled with hazard and product details. |
| Shipping | **Shipping Description for 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One:** Ship in tightly sealed containers, protected from moisture. Store and ship at ambient temperature unless otherwise specified. Handle as a hazardous chemical; complies with applicable regulations for transport of regulated substances. Suitable secondary containment and clear labeling are required. Consult SDS for further details on safe handling and shipping procedures. |
| Storage | Store 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one in a tightly sealed container under a dry, inert atmosphere, protected from moisture and light. Keep at cool room temperature, away from incompatible substances such as strong bases and oxidizers. Ensure storage in a well-ventilated, dedicated chemical storage area with appropriate labeling and secondary containment to prevent accidental release or exposure. |
Applications of 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One in Industrial Manufacturing2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One acts as a core reagent and building block for organophosphorus chemistry, supporting demanding industrial synthesis environments. As an original manufacturer, we ensure consistent quality for downstream clients across specialty chemicals, pharmaceuticals, advanced polymers, and agrochemical intermediates. Below are several key industrial application sectors, along with detailed requirements and integration methods for each. 1. Synthesis of Phosphorylating Agents for Nucleotide AnalogsThis chemical serves as a specific phosphorylating reagent forming activated phosphate intermediates used in nucleotide analog and oligonucleotide synthesis. Manufacturers in pharmaceutical and biotechnology segments depend on precise batch control to achieve high selectivity and reaction efficiency. The compound enters the phosphitylation step, activating hydroxyl groups to link phosphate backbones in modified nucleotide production lines. Industry compliance standards
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2. Advanced Flame Retardant Synthesis for Polymeric MaterialsThe compound functions as a precursor in the creation of phosphonate and phosphinate based flame retardants for high-performance polymers. Producers incorporate its reactive phosphorus moiety during the intermediate stage for engineering plastics requiring stringent fire protection. Mastery of feed ratio and reaction temperature ensures uniform substitution and polymer compatibility for electronics and transport sector requirements. Industry compliance standards
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3. Key Intermediate for Agrochemical Active Ingredient ProductionChemical synthesis teams use this phosphorus compound to generate phosphorylated intermediates for organophosphate and phosphonate agrochemicals. Its high selectivity enhances yield and purity during the phosphorylation stage. Regulatory documentation and on-site batch records are required to support traceability for food safety and environmental controls in crop protection markets. Industry compliance standards
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4. Preparation of Specialty Phosphorus Ligands for CatalystsSpecialty chemical producers use 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One as a phosphorus source in ligand synthesis for homogeneous catalysis and asymmetric synthesis applications. Quality control focuses on phosphorus purity, absence of residual chloride, and batch homogeneity to support catalyst production for fine chemical and API synthesis customers. Industry compliance standards
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Every batch of 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-one that leaves our facility represents years of technical expertise with phosphorus chemistry. In production scale, we've learned this compound isn’t just a reagent—it’s a modern tool that simplifies once-challenging reactions, gives cleaner conversions, and reduces waste. More than a specialty intermediate, it bridges synthetic ideas to industrial practicality.
Manufacturing this molecule means running tight controls across each stage, from phosphorus trichloride handling to oxidative cyclization and purification. Moisture pickup, exothermic profiles, and hydrolysis all put the process under scrutiny. Tuning every variable, we maintain assay levels above 98 percent and keep chloride byproducts to a minimum, proven by regular HPLC and NMR verification. What's on the label matches what’s inside—and that reliability only comes when you make large volumes yourself for years.
Lab chemists used to rely on phosphorus oxychloride or trichlorophosphate reagents for phosphoryl chloride transfer. Those classics bring their own baggage: complicated handling, higher water sensitivity, and tough separation from end-products. With 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one, selectivity jumps. The ring structure delivers a phosphoryl group with fewer side products compared to classic reagents. In our experience, this difference can pay for itself. You see sharper reaction endpoints and faster work-ups, not to mention a smoother offshore shipment with lower hazard premiums.
Bluntly, we used to see a lot of trial-and-error requests from custom projects. Labs wanted a way to functionalize nucleosides, phenols, or alcohols without risking high exotherms or ending up with emulsions at the quench. Once our operations shifted toward cyclic phosphorus reagents, complaints dropped. Retrospective QC data shows orders for this molecule generate about 60 percent fewer process deviation tickets compared to older phosphorus chlorides.
Our chemists and chemical engineers use 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one for phosphorylation where selectivity and manageable byproducts matter. In oligonucleotide synthesis, it lends precision: the site-specific introduction of phosphate groups ensures DNA and RNA strands don’t pick up extraneous isomers. Custom modification of pharmaceuticals and bioactive compounds also benefit. Out in the field, customers working with glass-forming agents, specialty polymers, and diagnostic intermediates have found the molecule fits reactions where thermal runaways or sticky residues torpedo batch yield.
Since we produce this in-house, not through a chain of traders, we track every specification ourselves. Typical lots arrive as a fine white to pale beige crystalline powder, melting near the expected 61 to 65°C. Each drum comes with our direct batch chromatograms, not copies provided by resellers. Chloride content, water, and phosphorus assays reflect actual observations from our latest runs, and individual COAs capture the subtle batch differences that can impact large-scale synthesis.
We’ve run kilogram to ton-scale lots across multi-month campaigns. NMR and GC-MS data from direct sampling show high isomeric purity; unlike some alternative phosphorus reagents, we rarely find lingering starting materials or intractable high-boiling residues. For those in pharma or biotech, that translates to repeatable downstream processing, fewer purification headaches, and less scrap.
This molecule’s ring structure holds the phosphorus center in a way that makes accidental hydrolysis less violent than with open-chain alternatives. Facility engineers report less corrosive vapor build-up and easier clean-outs in reaction suites. We still train all staff on PPE, local exhaust, and spill protocols, because no phosphorus halide belongs near an open drain, but handling here compared to POCl3 or phosphorus pentachloride runs smoother and with fewer alarms.
Customers often discuss “greener” chemistry. Using 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one, many routes become more sustainable. Cleaner conversions mean less contaminated washwater, and controlled byproducts allow for easier treatment or recycle. We've dropped total solvent and neutralizer consumption by about 30% in some campaigns using this reagent, without expensive process redesign. Shaving off clean-up costs and landfill-bound sludge appeals to both plant accountants and those who answer to environmental teams.
Large-scale synthesis is where quirks emerge. The molecule remains stable in sealed drums but shows some sensitivity to long exposures if kept unprotected. Running a big plant, we learned not to let granules sit out, especially on humid summer days, and we've built our QA system to spot minor changes in free chloride or melting point drift.
Operators appreciate the brief window from addition to full solution in standard solvents; solubility curves match well with acetonitrile, tetrahydrofuran, and dioxane, opening up direct substitution in established protocols. Unlike bulkier phosphoramidites or tert-butyl-based phosphorus reagents, this compound doesn’t gum up peristaltic pumps or form persistent emulsions on quench. The few times a line fouled, rinsing with moderate base cleared residues in short order.
Quenching this reagent doesn’t bring the same risk for peroxide generation or sticky solids as some cousins. That cuts downtime and helps us keep batch cycles on schedule. The difference from an efficiency perspective shows up after months—not hours—when comparing CIP (clean-in-place) cycles.
We watch our bulk customers closely, often visiting labs and plants. Synthetic chemists get sharper separation from byproducts, with fewer “dead-end” contaminants. If they run preparative chromatography, the typical tailing gets less severe. Our own kilo-scale teams took notice when glassware and reactors needed less acid cleaning after runs using this compound instead of traditional phosphorus chlorides.
Purchasing managers like knowing that we make this material and ship from our own warehouse. The pandemic years taught customers not to rely on promises from entities who themselves buy from another chain. Our documents track actual shipping lead times and QA logs, not repackaged numbers from unknown facilities.
Many plants started long ago with raw phosphorus trichloride or its oxidized derivatives. Those chemicals have earned their reputation, but using them often turns into a field of tradeoffs. With them, we faced rapid hydrolysis issues, higher chlorinated byproduct loads, and sometimes needed heavier PPE. Some open-chain phosphorus reagents cause persistent foaming or instability at higher temperatures. We rarely see that with 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one, even in 300 L jacketed reactors on multi-hour runs.
In head-to-head comparisons, we run pilot lines using exactly matched synthetic targets. Classic phosphorus oxychloride routes usually throw off more HCl and related volatiles, which stretches vent scrubbing. Our cyclic product emits far less of the sharp fumes, meaning less risk of accidental exposure and easier compliance with air rules.
Older reagents can also make downstream separation messier. Every kilo of product with stubborn phosphoryl byproducts meant extra solvent and more labor. The ring-locked cyclic structure of our product means faster purification and less solvent load. It carries into reduced product loss during crystallization or distillation.
Greener chemistry isn’t hype—our contracts with major pharma and specialty materials groups depend on real metrics. This compound gives end-users a wider operating window, from less stringent solubility limits to broader temperature tolerances. Less frequent maintenance and reduced chemical waste come from observed data on our own lines, not marketing claims. Long-term use in oligonucleotide and specialty monomer synthesis has shown us real savings, both in resource consumption and in final material QC.
Ongoing customer trends push for reduced hazardous byproducts, higher selectivity, and repeatable outcomes at scale. Direct user feedback points to this compound’s stability, rapid reaction time, and consistent output as reasons for their shift away from older phosphorus reagents. In one recent scale-up, a user switching from phosphorus oxychloride shaved two hours from their batch cycle and improved purity by 3 percent—enough to increase capacity without adding reactors.
Our in-house plant gives us immediate access to process control and fine-tuning. We revalidate protocols every time we boost scale, and full traceability on phosphorus, oxygen, and aromatic raw material means each shipment aligns to food chain and pharma standards, as required.
We invest in new containment and automation to reduce human error. That translates into dependable product in each lot. End users have told us that switching to this molecule cut their scrap rates and unscheduled maintenance. Meeting strict inspection—whether from customer auditors or regulatory reviews—relies on this consistency.
Producing this cyclic phosphorus compound isn’t trouble-free. Starting with raw phosphorus chemicals, slight changes in atmospheric pressure or air humidity can push up impurity levels. We installed high-accuracy environmental controls, and put protocols in place to intercept and correct drift before it reaches customers. On one occasion, we ran a night shift during an unseasonable hot spell; the dryer cycle ran too short and early QA flagged a sub-batch with off-spec moisture content. Having the production line in-house meant we could rerun the drying immediately, instead of returning questionable lots from a downstream packager.
Over years, we’ve also addressed occasional supplier outages for key raw materials. Because we anchor production here, not abroad, we stock primary precursors onsite, enough to buffer weeks of output. Users who rely on our compound get that security automatically; nobody wants an untimely supply disruption to put a six-figure campaign at risk.
Feedback loops drive improvement. By gathering data from both small-batch researchers and high-volume manufacturing sites, we strengthen our process and build relationships. A research group looking for alternative routes to problematic nucleoside phosphates found their batch yields improved by nearly 15% after switching. Others came with requests for custom particle sizing or tighter impurity thresholding, challenges we only take on because our technical and manufacturing staff interact daily.
The horizon for 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one pulls from both tradition and innovation. New drug modalities, gene synthesis, and bioconjugation rely on site-selective phosphorylation, and this compound sits firmly among those solutions. We continue to invest in quality systems, staff training, and analytical transparency because our own facility and staff answer directly for each shipment.
Years of hands-on manufacturing have refined our best practices around 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one. We get steady output, cleaner chemistry, and safer handling on the production floor, plus tighter control over supply and consistency for customers. By keeping synthesis, QA, and shipping internal, we avoid the risks that come with long supplier chains. Each bottle or drum ties right back to those of us who produced it. In a world full of generic phosphorus reagents, this cyclic compound demonstrates that the right molecule, made by the right team, still opens up new possibilities for industrial and research chemists alike.