Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One

    • Product Name 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One
    • Alias Phenyl dichlorophosphate
    • Einecs 219-239-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One

    Applications of 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One in Industrial Manufacturing

    2-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 Analogs

    This 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

    • cGMP (Current Good Manufacturing Practice, FDA 21 CFR Parts 210/211)
    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF requirements for pharmaceutical ingredient traceability
    • REACH Regulation (EC) No 1907/2006 register for raw material transport in the EU

    Typical usage ratio

    • Applied at 1.05–1.15 molar equivalents relative to the starting alcohol group in the nucleotide synthesis step
    • Ratio adjustment depends upon chain length and loading efficiency, characterized during pilot trials

    Downstream process integration

    • Added directly at the phosphitylation stage, in anhydrous solvent conditions, with strict moisture control
    • Removal of by-products via chromatographic or precipitation steps follows the coupling reaction

    Final product types

    • Modified oligonucleotides for antisense therapeutics
    • Phosphorothioate-linked nucleic acids
    • Nucleotide prodrugs for antiviral pharmaceuticals
    • Diagnostic PCR and sequencing reagents

    2. Advanced Flame Retardant Synthesis for Polymeric Materials

    The 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

    • UL 94: Standard for Safety of Flammability of Plastic Materials for Parts in Devices and Appliances
    • RoHS Directive 2011/65/EU for electrical and electronic equipment
    • ISO 1043-4: Plastics — Symbols and abbreviated terms — Part 4: Flame retardants
    • EN 45545-2 for rolling stock fire safety in rail applications

    Typical usage ratio

    • Used at 2.0–6.0% by weight in flame-retardant additive masterbatches
    • Final content determined by target fire performance (e.g., V-0 rating) and polymer compatibility

    Downstream process integration

    • Introduced at the copolymerization or reactive extrusion stage, ensuring in situ phosphorus incorporation
    • Followed by compounding and granulation to stabilize incorporation within thermoplastic matrices

    Final product types

    • Flame-retardant polycarbonate housings
    • Fire-resistant ABS or HIPS parts for electronics
    • Low smoke zero halogen (LSZH) cable compounds
    • Engineering resins for automotive and rail interiors

    3. Key Intermediate for Agrochemical Active Ingredient Production

    Chemical 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

    • FAO/WHO Specification and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 (Quality Management Systems for pesticide production plants)
    • EPA Title 40 CFR Part 158: Data Requirements for Pesticides (USA)
    • China GB 2763—National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Applied at 1.1–1.3 equivalents per functional group to ensure complete phosphorylation
    • Optimized based on precursor reactivity and process validation studies

    Downstream process integration

    • Employed at the intermediate synthesis step, typically under controlled temperature and inert atmosphere
    • Final agrochemical formulated by neutralization, crystallization, and dilution protocols

    Final product types

    • Active ingredients for insecticides and herbicides
    • Phosphonate-based fungicides
    • Plant growth regulator intermediates
    • Crop protection concentrates for formulation companies

    4. Preparation of Specialty Phosphorus Ligands for Catalysts

    Specialty 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

    • ISO 9001:2015 certified quality management for specialty chemical intermediates
    • Responsible Care Global Charter environmental and safety guidelines
    • Chemical Weapons Convention Schedule 2 substance reporting (if applicable)
    • National chemical inventory listings (TSCA, IECSC, REACH preregistration if exported to EU)

    Typical usage ratio

    • Employed in stoichiometric or slight molar excess (1.05–1.2 equivalents) to maximize ligand yield
    • Loading optimized as per the electronic/steric requirements of target ligand structure

    Downstream process integration

    • Added during step-growth synthesis of phosphorus ligands under inert gas
    • Subsequent purification by distillation or chromatography to remove unreacted precursor

    Final product types

    • Bidentate and tridentate phosphine ligands
    • Chiral phosphorus ligands for enantioselective catalysis
    • Catalyst complexes for pharmaceutical and fine chemical synthesis
    • Polymerization and hydroformylation catalyst precursors
    Free Quote

    Competitive 2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Chloro-4H-1,3,2-Benzodioxaphosphorin-4-One: Reliable Phosphorylation in One Step

    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.

    Proven Synthesis, Consistent Results

    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.

    What Sets This Compound Apart

    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.

    Real-World Applications

    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.

    Product Specifications from Our Own Lines

    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.

    Safer, Easier Handling Where it Counts

    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.

    Working Insights from Day-to-Day Production

    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.

    What Users Actually Experience

    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.

    Differences From Classic Phosphorylation Reagents

    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.

    Meeting Industry Trends without Gimmicks

    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.

    Scaling Production Without Shortcuts

    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.

    Challenges and Adaptations

    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.

    Direct Feedback and Future Outlook

    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.

    Summary

    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.