Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Phenyl Dichlorophosphate

    • Product Name Phenyl Dichlorophosphate
    • Alias Dichlorophosphoric acid phenyl ester
    • Einecs 208-804-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    323765

    Chemicalname Phenyl Dichlorophosphate
    Casnumber 770-12-7
    Molecularformula C6H5Cl2O2P
    Molarmass 227.99 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.42 g/cm³
    Boilingpoint 259 °C
    Meltingpoint -30 °C
    Refractiveindex 1.543
    Solubility Reacts with water, soluble in organic solvents
    Flashpoint 131 °C
    Odor Pungent

    As an accredited Phenyl Dichlorophosphate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Phenyl Dichlorophosphate, 500g, is packaged in a tightly sealed amber glass bottle with hazard labeling and chemical-resistant cap.
    Shipping Phenyl Dichlorophosphate should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be handled as a hazardous material, typically under UN 3265 (Corrosive liquid, acidic, organic, n.o.s.), following all relevant local, national, and international regulations, using appropriate labeling and documentation during transport.
    Storage Phenyl Dichlorophosphate should be stored in a cool, dry, well-ventilated area away from moisture and incompatible substances such as strong bases, alcohols, and oxidizing agents. Store in tightly sealed containers made of glass or compatible materials. Protect from light and sources of ignition. Use proper chemical storage cabinets, especially those designed for corrosive or reactive materials. Ensure clearly labeled containers.
    Application of Phenyl Dichlorophosphate

    Applications of Phenyl Dichlorophosphate in Industrial Manufacturing

    We manufacture phenyl dichlorophosphate specifically for key industrial sectors, supporting large-scale formulations and integrated processes across the global supply chain. Our advanced production ensures compliance with international regulations required for each downstream application. Below we detail the core scenarios where this raw material delivers value in practical industrial operations, considering real compliance expectations and verified production methods.

    1. Synthesis of Organophosphorus Flame Retardants for Engineering Plastics

    Major engineering plastics manufacturers rely on phenyl dichlorophosphate when producing advanced phosphorus-containing flame retardants. The compound’s chlorophosphoryl group is essential for introducing fire-resistant properties, especially in polycarbonate, PET, and high-impact polystyrene (HIPS) systems, where thermal stability and non-halogenated performance are critical. The material reacts with polyols or aromatic diamines at the intermediate synthesis stage, allowing downstream production of additive masterbatches tailored to elevated regulatory requirements for electronics, automotive, and construction polymers.

    Industry compliance standards

    • UL 94 (plastics flammability standards)
    • IEC 60695-11-10/20 (test methods for fire hazard assessment)
    • RoHS Directive 2011/65/EU (restriction of hazardous substances)
    • EN 14582 (phosphorus content analysis for electronic materials)

    Typical usage ratio

    • 1.5–5.0% of total flame retardant batch; adjustment based on polymer type and target fire rating (V-0, V-1, etc.)

    Downstream process integration

    • Condensation or transesterification step to generate phosphorus flame retardant intermediates before incorporation during melt compounding or masterbatching with thermoplastics

    Final product types

    • Fire-resistant polycarbonate sheets
    • Flame-retardant ABS or HIPS resins for electronics enclosures
    • Non-halogenated flame retardant masterbatches for automotive and building materials

    2. Synthesis of Agrochemical Intermediates for Insecticide Production

    Leading agrochemical firms use phenyl dichlorophosphate in the controlled synthesis of organophosphorus intermediates found in commercial insecticides. This application demands precise reactivity to anchor phosphoryl groups onto aromatic or aliphatic scaffolds during the multi-step process, ultimately facilitating downstream functionalization for systemic or contact-active crop protection agents. Strict traceability and synthesis protocols apply due to regulatory scrutiny over pesticide precursors.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (FAO/WHO, ISO 23192)
    • European Regulation (EC) No 1107/2009 (placing plant protection products on the market)
    • US EPA 40 CFR Part 158 (pesticide data requirements)
    • Good Manufacturing Practice (GMP) for Agrochemicals (ISO 9001:2015, special process sections)

    Typical usage ratio

    • 0.8–2.5 molar equivalents relative to alcohol or phenol substrate in organophosphate core intermediate stage; strictly monitored to control phosphorylation level

    Downstream process integration

    • First-step phosphorylation of aromatic or aliphatic alcohols; intermediate then undergoes further derivatization (chlorination, esterification) prior to final product formulation

    Final product types

    • Phosphorothioate insecticides (e.g., chlorpyrifos technical grade)
    • Phenylphosphate-based acaricides
    • Intermediate pesticides with systemic action for seed treatment or foliar application

    3. Production of Phosphorylating Reagents for Pharmaceutical Synthesis

    Pharmaceutical ingredient producers require phenyl dichlorophosphate as a controlled phosphorylating reagent during API synthesis, especially in protection-deprotection sequences or for creating phosphate ester prodrugs. The material’s reactivity enables selective mono- or di-phosphorylation of alcohol groups, forming intermediates for antivirals, nucleoside analogues, or kinase inhibitor APIs. Each production step must maintain rigorous traceability and compliance with global pharmacopoeias and GMP standards.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP <797> (sterile compounding)
    • European Pharmacopoeia 11.0, Monograph 0573 (Phosphate Esters)
    • Chinese Pharmacopoeia (CP 2020, Phosphorylation acceptance guidelines)

    Typical usage ratio

    • 1.0–2.2 molar equivalents relative to target moieties in the phosphorylation stage; adjusted according to protecting group needs or substrate steric hindrance

    Downstream process integration

    • Second- or third-stage reagent for selective phosphorylation during multi-step organic synthesis; product stream routed to downstream purification prior to crystallization or formulation

    Final product types

    • API intermediates for nucleoside or nucleotide analogue drugs
    • Intermediate phosphate ester prodrugs
    • Select phosphorylated building blocks for kinase inhibitor APIs

    4. Manufacture of Reactive Flame Retardants for Epoxy Resin Formulations

    Producers of reactive flame retardant additives for epoxy resins utilize phenyl dichlorophosphate as a key intermediate for introducing phosphorus units. This chemistry enables covalent bonding of flame retardant groups to resin oligomers, thereby enhancing charring and reducing smoke generation without plasticizer migration risk common to non-reactive systems. Application targets electronic potting compounds, circuit boards, and construction adhesives requiring both thermal stability and compliance with regional fire codes.

    Industry compliance standards

    • IPC-4101 (base materials for rigid PCBs)
    • EN 13501-1 (fire classification of building products)
    • NFPA 262 (fire and smoke of electrical wire and cable)
    • ISO 1043-4 (plastics classification—flame retardant designation)

    Typical usage ratio

    • 0.5–3.0% in reactive additive synthesis, adjusted for target phosphorus content (0.8–2.0% w/w in finished resin systems)

    Downstream process integration

    • Phosphorylation of epoxy resin hardener or resin prepolymer; additive introduced during resin pre-mixing before extrusion, cast molding, or impregnation processes

    Final product types

    • Reactive flame-retardant epoxy laminates for electronics
    • Low-smoke fire-protected structural adhesives
    • Flame-proof electrical potting systems and PCB substrates

    5. Synthesis of Phosphorus-Based Catalysts for Polymerization

    Chemical manufacturers engaged in specialty catalyst preparation employ phenyl dichlorophosphate as a phosphorylation agent during the fabrication of phosphorus-coordinated ligands. These ligands serve in downstream catalytic systems supporting ethylene polymerization, olefin copolymerization, and ring-opening metathesis. The material’s selectivity is integral to producing high-purity catalyst intermediates, meeting process and regulatory controls for both batch and continuous polymer manufacturing.

    Industry compliance standards

    • ISO 9001:2015 (quality management in catalyst production)
    • REACH Regulation EC 1907/2006 (substance registration and safety data)
    • ASTM D1601 (test methods for catalyst activity in polymerization)
    • Chemical Processing Good Practice Guidelines (company-specific SOPs)

    Typical usage ratio

    • 0.8–1.5 molar equivalents for ligand precursor phosphorylation, with adjustment for desired chelation and catalyst geometry

    Downstream process integration

    • Introduced at the ligand synthesis stage before final complexation with metal centers (e.g., Ti, Ni, or Pd); purified intermediate transferred to catalyst plant under inert transfer protocols

    Final product types

    • Organophosphorus metal catalysts for industrial polyethylene or polypropylene lines
    • Specialty coordination complexes for copolymerization plants
    • Chiral phosphorus ligand catalysts for fine chemical synthesis
    Free Quote

    Competitive Phenyl Dichlorophosphate 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 sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    Phenyl Dichlorophosphate: Practical Insights from Our Production Floor

    Focusing on Phenyl Dichlorophosphate

    Work in chemical synthesis depends on reliable building blocks. Among chlorophosphates, Phenyl Dichlorophosphate (CAS Number: 770-12-7), often referred to by its main structure, plays a unique role in laboratory and industrial-scale organic chemistry. As manufacturers, our focus rests not only on purity and efficiency but also consistency in reactivity since even small deviations can alter downstream results.

    Understanding the Chemical: Why Phenyl Dichlorophosphate?

    Across the years, feedback from custom synthesis labs and commercial production sites reminds us that consistent Phenyl Dichlorophosphate (PDC) output sets the stage for smooth processes—whether as a phosphorylating agent or as an intermediate for pesticides, flame retardants, and pharmaceuticals. Our reactors and distillation lines produce a clear, colorless to pale yellow liquid with a pungent, sharp odor, not terribly different from related chlorophosphates, but with properties shaped by the phenyl group bonded to phosphorus.

    In practical settings, PDC’s chemical structure—C6H5OP(O)Cl2—offers a reliable blend of reactivity and stability for users. While trimethyl or triethyl variants bring volatility, and alkyl mixed dichlorophosphates show greater instability under heat or moisture, our phenyl-based variant resists hydrolysis in the short term but offers a reactive dichlorophosphate group for condensation and substitution reactions.

    The Nature of Consistency: What We’ve Learned from Daily Production

    Spec production doesn’t start and stop with analytical numbers. As our operators refine the process for each lot, challenges from water control and air-sensitive packaging drive home the importance of closed systems. PDC's moisture sensitivity shows itself during transfer. Just a slight uptick in humidity, and we see trace hydrolysis products—phenol or phosphoryl acid residues—which shift the reaction balance for downstream users.

    To counter these effects, our team uses nitrogen-purged environments from the chlorination reactor through the glass-lined distillation columns. Regular inline monitoring with GC and NMR gives us real-time composition data. Batches register clear at 99%+ purity, with phosphorus content and chloride levels tailored to user demand. These numbers are more than just a label—they drive yield outcomes for chemical makers downstream.

    Performance Differences: Phenyl Dichlorophosphate Vs. Other Organophosphates

    A chemist may weigh PDC against trichlorophosphate or its dimethyl and diethyl analogues. Trichlorophosphate acts too aggressively for delicate substrates, especially in API intermediate manufacturing, often leading to side reactions and unwanted byproducts. The straight phenyl analog handles aromatic and heterocyclic substrates without the severe risk of overreaction or breaking sensitive functional groups.

    Colleagues on pharmaceutical intermediate production lines point out that phenyl dichlorophosphate stands out when used in phosphorylating amines, alcohols, or preparing activated esters. Nucleophilic substitutions run predictably, minimizing tar formation or side phosphates that demand extra purification. The phenyl group not only stabilizes the reactive phosphorus atom but also lowers the exothermicity of the initial step, making process scale-up feasible and safer on kilo or ton scales.

    PDC Usage: Beyond the Bottle

    We hear from R&D labs using PDC for synthesizing nerve agent antidotes and flame retardant precursors. Agriculture firms rely on it for manufacturing key pesticide actives. Handling depends on robust safety protocols since phenyl dichlorophosphate reacts strongly with water and alcohols, producing corrosive hydrochloric acid vapors. Our bulk containers come dry-inerted, and operators always suit up with full PPE, using fume hoods or sealed transfer systems.

    Out in the field, it often arrives through reduced-pressure transfer or closed-barrel systems that minimize exposure. Minor leaks smell unmistakable—an acrid, sharp note typical for aryl chlorophosphates—prompting immediate containment. Our end-users mention that PDC's slightly higher boiling point allows precise addition during stepwise synthesis, giving more time for safe handling and dropwise reactivity.

    Specification Choices and Their Effects

    Our production lines offer Phenyl Dichlorophosphate across a narrow purity range, but clients often request tailored impurity profiles. Water control is critical—the less water in a batch, the fewer downstream hydrolysis-derived side products. Specifications also define allowable levels of free HCl and phenol as these can interfere with sensitive pharmaceutical or electronic applications.

    When a batch approaches the end of its shelf life, we notice faint color changes: from clear pale to a faint yellow. This signals the start of minute degradation. Our tanks respond best to storage under nitrogen and at lower ambient temperatures. Some customers request ampoules or sealed glass bottles for applications where microgram impurities matter, such as oligonucleotide synthesis or complex peptide coupling.

    Process Improvements: Balancing Efficiency and Safety

    Every six months, our plant reviews solvent recovery and purification sections of the PDC line. We measure the balance between maximizing yield and minimizing thermal decomposition and chlorinated byproducts. The trade-off is clear: pushing reaction temperature too high burns off trace organic capacity but spikes tar and impurity formation. Every ton produced demands vigilance—instrumentation, pressure checks, and precise reagent loads.

    Working alongside our engineering team, we’ve recently adopted inline IR sensors on the distillation columns. They catch trace hydrolysis early, letting us intervene before a lot drifts off spec. This kind of intervention is only possible because our plant managers and operators work closely daily, adjusting valves, training new hands, and maintaining direct oversight over every run.

    Phenyl Dichlorophosphate and Environmental Responsibility

    Effluent from PDC production contains residual chlorinated organics, so the plant’s wastewater loops into a treatment train that uses activated carbon and careful pH control before discharge. Our choice to keep batch sizes moderate—never overshooting total capacity—directly cuts down risk in case of leaks or spills. Recycled solvents that come off the distillation lines are cleaned, tested, and, when possible, returned to early-stage reactions, cutting raw material demand while reducing landfill and incineration burdens.

    Our experience shows that minor tweaks—a longer condensation period or buffer tank—have an outsized effect on minimizing waste. Sustainability isn’t a vague goal; direct feedback from compliance audits and regulators drives incremental progress. The Phenyl Dichlorophosphate process embodies that push-and-pull between meeting technical need and upholding environmental standards. This respect for both lab outcome and site safety defines how we approach every product line, but it’s especially visible with moisture/hydrolysis-sensitive chemicals.

    End-User Support and Transparency

    Customers, especially those scaling up pilot projects, ask for more than just a shipping manifest. We supply detailed batch histories, impurity profiles, and storage recommendations—not out of regulatory obligation, but because unexpected reactivity losses or side reactions often stem from details in the production or storage chain.

    On-request, we discuss minor batch variations caused by seasonal weather, slight adjustments in cooling cycles, or changes in feedstock purity. This open-book approach helps users track even faint deviations in upstream processes that might ripple into their synthesis. Pharmaceutical and agrochemical partners report fewer process upsets and less need for error investigation when upstream communication focuses on practical manufacturing realities.

    Comparing Reaction Outcomes: Real-World Experience

    Veterans in intermediate synthesis line up data on product yields, cost-per-mole, and time in purification. Our in-house collaborations with outside process chemists often illustrate stark differences between PDC and simpler or more reactive chlorophosphates. Phenyl Dichlorophosphate enables a predictable formation of diesters or phosphate esters under controlled base and temperature. More reactive trichloride analogs often overreact, dividing a single desired product into several, each needing separation. Modified alkyl dichlorophosphates sometimes break down too quickly, especially in ambient conditions.

    In surface chemistry, especially when attaching phosphate groups to aromatic backbones, the phenyl group delivers better compatibility with nonpolar solvents and increases the selectivity of the phosphorylation step. This reduces downstream chromatography steps, simplifies workup, and conserves solvents. Feedback from academic labs notes that reaction exotherms also drop—a key factor when moving from gram-scale to kilogram runs or continuous flow reactors.

    Practical Safety Lessons from Plant Operations

    Handling PDC reminds us, every shift, of the need for constant worker vigilance. Chlorophosphate exposure doesn’t always announce itself with dramatic fume clouds; sometimes, a sticky gasket or faint discoloration around a manway signals potential leaks. Engineers and operators patrol the line with real-time monitors for airborne chlorides and keep spare absorbent on hand.

    Training new staff involves more than explaining hazard sheets. We walk the new hands through live transfer drills and run glovebox transfers. Regular “no shortcut” audits ensure that even veterans respect the sensitivity of the product to water and heat. Our insistence on sealed systems has paid dividends, with near-zero recordable exposures and uninterrupted supply to key customers.

    Adapting to User Feedback

    We don’t make small improvements for their own sake. Years ago, users pointed to bottlenecks in packaging that led to minor headspace condensation, dulling color and shifting acid number. It took several pilot runs to find a container linings and purge process that kept the product clean from fill to empty. Process improvement only works when plant and lab teams talk to users, swap stories about outcomes, and look for root causes rather than blame a checklist or standard spec.

    Some customers found value in prepacked break-bulk kits or smaller glass ampoules shipped under nitrogen, so we keep those lines operational for high-sensitivity applications. Learning from experienced users, we've refined equipment cleaning, operator rotation, and even switching sequence in our supply lines to curb potential cross-contamination.

    What Matters for the Future

    Market signals always shift. Over the last decade, the demand for PDC in flame-retardant development has grown as electronics safety standards tighten, while pesticide formulation calls for less impurity-sensitive product. Stable performance, tight impurity control, and honest service maintain steady orders during both peaks and lulls.

    Upcoming shifts include pressure for stricter emissions management and less hazardous transportation across jurisdictions. Our plant works to anticipate these demands—integrated vapor recovery, closed transfer improvements, container innovation and tighter on-the-fly process analysis. These adaptations don’t just comply with rules—they address the ever-present tension between industrial demand for reactive chemicals and social responsibility for safe, clean production.

    Closing Thoughts: Lessons from the Plant Floor

    From day one, making Phenyl Dichlorophosphate involves more than reaction equations and tank levels. Each batch captures hard-won lessons—respect for water control, care in closed transfer, and the continual refinements born of close partnership with users in pharma, agro, and specialty fields. The science doesn't stop at the fence; every production run is checked, tracked, and improved by people who recognize their work shapes the performance, safety, and environmental record of every downstream product. Our customers trust us because we live with these realities every day, and the commitment shows in the chemical, the batch sheet, and the result in their own plants.