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1,3-Dichloro-2,5-Difluorobenzene

    • Product Name 1,3-Dichloro-2,5-Difluorobenzene
    • Alias 1,3-Dichloro-2,5-difluorobenzene
    • Einecs 609-804-6
    • 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

    931379

    Iupac Name 1,3-dichloro-2,5-difluorobenzene
    Molecular Formula C6H2Cl2F2
    Molecular Weight 183.99 g/mol
    Cas Number 1435-49-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 174-176 °C
    Density 1.49 g/cm³
    Solubility In Water Insoluble
    Refractive Index 1.516
    Flash Point 64 °C
    Purity Typically ≥98%
    Smiles C1=C(C=C(C(=C1F)Cl)F)Cl
    Inchi InChI=1S/C6H2Cl2F2/c7-3-1-4(8)6(10)2-5(3)9
    Synonyms 2,5-difluoro-1,3-dichlorobenzene

    As an accredited 1,3-Dichloro-2,5-Difluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, tightly sealed, labeled "1,3-Dichloro-2,5-Difluorobenzene, 100 g," hazard warnings and safety instructions clearly printed.
    Shipping **Shipping Description:** 1,3-Dichloro-2,5-Difluorobenzene should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically transported as a hazardous material under UN 3082 (Environmentally hazardous substance, liquid, N.O.S.), with required hazard labeling and documentation. Store and handle in accordance with applicable regulations for toxic and environmentally hazardous chemicals.
    Storage Store 1,3-Dichloro-2,5-difluorobenzene in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sunlight and incompatible substances such as strong oxidizers. Ensure storage away from heat and ignition sources. Label containers clearly and avoid moisture contact. Use secondary containment if possible to prevent leaks, and always follow local regulations for hazardous chemical storage.
    Application of 1,3-Dichloro-2,5-Difluorobenzene

    Applications of 1,3-Dichloro-2,5-Difluorobenzene in Industrial Manufacturing

    1,3-Dichloro-2,5-Difluorobenzene serves as a critical intermediate in several specialized chemical sectors. Its structure enables precise functional group transformations, supporting manufacturers in pharmaceuticals, agrochemicals, liquid crystals, and polymer additives production. Below we detail focused, real-world downstream applications based on our years of direct supply and plant integration experience.

    1. Pharmaceutical Intermediate Synthesis

    Active pharmaceutical ingredients often require halogenated benzene derivatives for selective nucleus modification. Pharmaceutical plants use this compound to introduce chlorine and fluorine atoms in API syntheses such as for anti-infectives and CNS-targeted drugs. It enters reactions including nucleophilic aromatic substitution where control of halogen positions influences target molecule yields and purity, and enables compliance with multi-step synthetic requirements.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP monographs (where applicable for downstream API)
    • FDA 21 CFR Part 211
    • ISO 9001:2015 for quality assurance

    Typical usage ratio

    • Used as 0.15–0.22 molar equivalents in halogen exchange or nucleophilic substitution reactions; adjusted per route and scale
    • Stoichiometry modified based on targeted API and loss on handling

    Downstream process integration

    • Charged into batch reactors post-main skeleton assembly for late-stage halogenation
    • Often preceded by solvent drying and base addition to control moisture and byproducts
    • Monitored for residual levels in intermediate purification and final API release using validated HPLC

    Final product types

    • Active pharmaceutical ingredients for anti-infective drugs
    • Analgesics and CNS drug intermediates
    • Pesticide antidote drugs (specific APIs regulated in North America and Europe)
    • Specialty fluorinated precursors for metabolic studies

    2. Agrochemical Synthesis: Herbicide and Fungicide Building Block

    Agrochemical manufacturers employ this compound as a halogenated aromatic source for preparing key herbicide and fungicide actives, including triazole and pyridine derivatives. It reacts via selective halide displacement and cross-coupling reactions to construct molecules with improved potency and environmental persistence, supporting crop protection portfolios with regulatory-compliant formulations.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical material
    • REACH Annex XVII and SVHC controls for environmental release
    • China GB 2763–2021 food safety maximum residue limits (downstream monitoring)
    • ISO 9001 production and QC documentation

    Typical usage ratio

    • Charged at 0.08–0.16 molar equivalents per active ingredient depending on reaction route
    • Adjusted for catalyst loading in coupling reactions and side-chain introduction

    Downstream process integration

    • Introduced during the halogen exchange or Suzuki coupling stage
    • Combined with alkylating agents or nitrogen-based nucleophiles for ring closure
    • Crude product purified via crystallization or distillation prior to formulation

    Final product types

    • Triazole herbicide technical concentrate
    • Pyridine-based fungicide intermediates
    • Pre-emergent weed control actives
    • High-purity insecticidal co-formulants

    3. Electronics Industry: Liquid Crystal and OLED Intermediate

    Producers of liquid crystal and organic light-emitting diode components use this molecule for its controlled aromatic ring substitution profile. It supports synthesis of fluorinated and chlorinated biphenyls or terphenyls, enhancing dielectric performance and thermal stability in display materials. The compound is introduced during early functionalization steps, and strict trace impurity control enables compliance with ultra-pure electronic requirements.

    Industry compliance standards

    • RoHS Directive 2011/65/EU and subsequent amendments (for electrical/electronic equipment)
    • IEC 61249-2-21 for halogen-free laminate applications (reference for allowable halogen content)
    • JEITA ED-4701 purity and cleanliness specification for electronic chemicals
    • ISO 9001:2015 production traceability and contamination control

    Typical usage ratio

    • Utilized at 0.12–0.19 molar equivalents in mixture reactions
    • Further refined for high-purity grades dependent on target contrast and switching speed

    Downstream process integration

    • Charged as a starting material during early-stage coupling with biphenyl synthons
    • Purified via distillation to sub-ppm contaminant levels prior to downstream blending
    • Strict batch-to-batch analysis for halogen content and residual metals

    Final product types

    • Biphenyl- or terphenyl-based liquid crystal mixtures for LCD screens
    • OLED display intermediates
    • Low-dielectric polymer blends for microelectronics
    • Specialty materials for photolithography resists

    4. Advanced Polymer Additives Manufacturing

    Leading producers of specialty polymers and engineering plastics incorporate this benzene derivative during functional monomer synthesis. Its halogen balance enhances flame retardancy and chemical resistance without disrupting processability. Used in small quantities, this intermediate enters polycondensation or copolymerization sequences where strict process and regulatory controls apply.

    Industry compliance standards

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • REACH SVHC candidate list review for polymer additives
    • ASTM E162 for surface flammability of materials
    • ISO 14001 environmental management for emissions tracking

    Typical usage ratio

    • Used at 0.03–0.10 molar equivalents relative to base monomer feed
    • Ratio optimized for target flame retardancy and mechanical performance per lot

    Downstream process integration

    • Mixed with polyol or polyester precursors prior to prepolymerization
    • Controlled feed via jacketed kettles to maintain temperature uniformity
    • Purity and residue halide monitored by GC for final formulation release

    Final product types

    • High-performance flame retardant engineering resins
    • Fire-safe cable insulation compounds
    • Modified thermoplastic elastomers for automotive parts
    • Low-smoke, low-toxicity building panel resins
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    Certification & Compliance
    More Introduction

    1,3-Dichloro-2,5-Difluorobenzene: Crafting Precision for the Chemical Industry

    A Closer Look at 1,3-Dichloro-2,5-Difluorobenzene

    Chemical manufacturing floors rarely stand still, and neither do the demands for specialty raw materials. Over years working with halogenated aromatic compounds, we've seen a steady rise in questions about 1,3-Dichloro-2,5-Difluorobenzene. As a molecule, its structure—two chlorines and two fluorines strategically locked on a benzene ring—gives it a unique profile for both reactivity and performance in advanced synthesis. Unlike its mono- or tri-halogenated cousins, the 1,3- and 2,5- placements create a symmetry that changes not just the chemistry, but the physical handling, solubility, and reliability during scale-up.

    Physical Properties with a Purpose

    The molecule’s dense, colorless to pale yellow liquid form reveals purity on sight. In practical terms, boiling and melting points remain stable through batches, so reaction engineers and plant operators gain an edge in predictable behavior—no unexpected crystallization, no vapor losses during transfer. These are the aspects we watch with every lot, not just because we value repeat business, but because consistency in physical parameters cuts unplanned downtime and wasted effort during reactions or downstream processing.

    Purity does not happen by accident. Each tonne—whether shipped in drums or bulk ISO containers—reflects our team’s attention to column conditions, feedstock sourcing, and analytical control. Analytical reports matter, but the interplay between human oversight and automation ensures the numbers on a certificate mean peace of mind at your reactor, not just in our labs.

    Model Variations: Not All Synthesis Routes Are Equal

    Moving into production, process design sets the stage. Chlorination-then-fluorination, or stepwise halogen exchange—each route bears its own implications for trace residues. We favor selectivity and quality, even if that means departure from the cheapest or quickest paths. Customers in pharma synthesis, crop protection intermediates, and high-performance materials value this. The resulting model, known throughout the customer base as C6H2Cl2F2, showcases a minimum purity above 99 percent by area normalization. No batch leaves the plant without passing these benchmarks.

    Our team remains aware of the temptation to cut steps or widen specifications to compete on cost. But lessons from scale-up disasters—side product build-ups, unexpected color changes, and resultant purification headaches—guide our choices. Staying on the tighter path saves heartache both for us and for formulators counting on predictable quality.

    Applications: Beyond a Building Block

    On the surface, 1,3-Dichloro-2,5-Difluorobenzene acts as a multi-purpose intermediate. The molecule carves a niche in fields that push boundaries—agrochemical inventors, pigment designers, and pharmaceutical teams with targets unreachable by simpler halogenated benzenes. In the laboratory, chemists seek it out for its unique electron distribution and the way it holds up through radical and nucleophilic substitution. The chlorines and fluorines are more than substituents; they shape what gets built downstream.

    In crop protection, active ingredient invention projects often start with a halogenated aromatic skeleton. Having access to a difluoro-dichloro substitution pattern opens access to new patent spaces—new multi-use fungicides, herbicide candidates, and even anti-microbial agents. Research groups frequently approach us about scale-up support and impurity studies; we’ve built our technical advisory desk out of those collaborations by necessity, not just to check a box for customer service.

    Pharma process chemists—especially those following green chemistry mandates—look for high-purity halogenated intermediates to minimize downstream purification. By dialing in control over multiple process variables starting at chlorination all the way to storage, we’ve minimized the introduction of metal or halogen exchange residues. Over the last decade, we’ve noticed adoption by teams synthesizing kinase inhibitors, anti-infective scaffolds, and imaging agents, because they know this particular pattern doesn’t just change reactivity, it changes the biological profile.

    Colorant and pigment manufacturers demand particular attention to product hue and lightfastness. Subtle differences in ring substitution can create or destroy the target chromophore; we supply grades for pilot or production scale, working directly with application scientists to validate that the final pigment’s tone and stability pass both regulatory and market muster.

    Differences from Other Halogenated Benzenes

    Many clients—especially new entrants to halogenated chemistry—ask how 1,3-Dichloro-2,5-Difluorobenzene stacks up against related products. We’ve handled dozens of analogs from dichlorobenzenes to trifluorinated variants. The interplay of two chlorines and two fluorines on this core delivers a different spectrum of reactivity. Where 1,2,4,5-tetrachlorobenzene offers high thermal resistance, the dual fluorines in our product increase solvent compatibility and change how ring activation proceeds under catalysis or nucleophilic substitution.

    No two halogenated benzenes act the same in cross-coupling or halogen-lithium exchange. The 1,3- and 2,5- substitution means symmetry that can deliver cleaner regioselective downstream chemistry—and fewer headaches in column workups or distillation. Years of collaborative studies with both academic groups and industrial R&D have demonstrated fewer side reactions, lower by-product formation, and greater throughput when compared to single-chlorine or single-fluorine analogs.

    Another overlooked aspect sits in logistics. While more heavily halogenated benzenes often restrict options for container material or storage conditions, the intermediacy of our product—neither too light nor too heavy—simplifies handling. You don’t need exotic containers or special atmospheric protocols. With every shipment, we include practical advice drawn from decades of storage, transfer, and even accident inquiry. No need to relearn hard lessons about compatible gaskets and transfer lines when you rely on both our product and our support.

    Industry Experience and Customer Partnerships

    We understand that anyone can quote numbers from a technical document. Real trust builds over decades, not days. Our teams—from sourcing to plant technicians and application scientists—have watched trends in customer requests change with regulatory tides, new market entrants, or global volatility in raw material supply. In times of tight supply, partnership rises above transaction. We’ve kept customers running through port closures, currency shakeups, and multi-month force majeures. That resilience doesn’t show up in a product code, but it’s embedded in every drum.

    Collaborative technical development remains core. Plant redesigns often grow from direct customer discussion—what slows down a formulation line, what causes residue buildup in a high-shear mixer, which impurity spikes create compliance risk under evolving regulations. Decades of troubleshooting have convinced us to keep blending lab expertise with direct operator know-how. Those who call for batch-specific advice reach actual chemists who’ve crawled towers, not just sales scripts.

    Feedback has proven invaluable. Adjustments to particle size, residual solvent control, or shipping container choices come directly from the end uses. Our logistics team still remembers a pigment plant stoppage—caused not by impurity, but by a mismatch between drum lining material and local warehouse humidity. We invested in better storage coatings and shared the results across customer networks because one fix lifts the whole supply chain. The mark of a supplier committed to more than a transactional role rests in these daily details.

    Quality Control and Regulatory Confidence

    The importance of transparency and traceability keeps rising with every passing year. Audits grow more demanding, and data integrity forms the backbone of compliance. Quality assurance teams track every lot back to raw source. Every analysis leaves a digital trail—no exceptions, no gray zones. We understand the stakes when customers operate under ICH, FDA, or regional equivalents; regulatory submission cycles don’t stop for nonconformity or unexplained residues.

    Our plant maintains both legacy and newly commissioned instrumentation—GLC, HPLC, ICP-MS, and a steady calendar of calibration checks. These investments stem from customer site visits and third-party audits. We open doors to customer QC teams, not behind-the-glass tours but hands-on sample draws and paper-trail reviews.

    REACH, TSCA, and local equivalents all add layers of reporting and data provision. Delivering only what fits the letter of a regulation misses the bigger picture. By building systems that exceed the strictest guidelines, we insulate downstream users from surprises during their own filings. In one recent market entry for a new pharmaceutical candidate, pre-shipment technical packages helped a multinational clear an unexpected audit hurdle within weeks, not months.

    Supply Chain Resilience and Sustainability

    Modern chemical industries face volatility in both logistics and social expectation. Pricing swings and geopolitics force adaptation—no secret there. Sustainability, meanwhile, is more than a label or a checkbox. As expectations for green chemistry, circular supply chains, and waste minimization increase, adopters of halogenated aromatics may worry about alignment with future regulations or brand image.

    Our operations do not stand still. We manage sourcing with an eye for both security and environmental impact; materials come from vetted partners over multi-year contracts, not spot buys. Waste minimization takes form through byproduct capture and solvent recovery, not just on paper, but through tangible reductions in wastewater discharge and emissions. Plant-wide audits—both internal and via independent agencies—identify energy sinks and safety gaps, driving average resource consumption down each year.

    Real sustainability comes not from loud promises but from open data and accountable improvement. We publish environmental impact scores when requested, provide full disposal and decontamination guidance, and cooperate with partners aiming to recycle or upcycle spent containers. Some customers operating under heightened ESG oversight ask for carbon footprint breakdowns and LCA data per batch—we supply it, not just to close a sale but to form a longer partnership in transparent operations.

    Technical Support: From Bench to Plant Scale

    Many of our technical conversations start with a research chemist and finish with a plant manager. Each link in that chain brings concerns about solubility, reactivity, compatibility with process fluids or downstream units. Our job doesn’t end at shipping dock. We answer questions on heating cycles, phase separation in mixed solvents, and even specialized advice on halogen management for effluent control. Every year, process troubleshooting cases from our partners become practical field notes that build both our in-house knowledge and industry know-how.

    Some clients operate kilo-labs or pilot plants with precise temperature controls and full environmental containment; others juggle legacy equipment and process uncertainties stretching back decades. We tune advice and process adjustments for both, aiming to cut process upsets, batch rejections, or yield drops. For recurring issues where bench conditions mismatch with tonnage, our technical staff are available to conduct on-site audits, not just by video or document review but through direct process observation.

    Collaboration never stops at compliance. For example, pigment producers working with 1,3-Dichloro-2,5-Difluorobenzene encountered issues with small-scale color profiling that did not translate to full mixing runs. Our staff brought batch-splitting studies and mixing regime recommendations, helping the team hit target specifications over several months. These stories happen quietly, but they validate the deeper relationship we seek with the industry.

    Safety, Storage, and Responsible Use

    As with any halogenated species, safety cannot take a back seat. Routine training, clear site signage, and support documents form the backbone of our commitment to safe handling—both at our sites and our customers. The molecule’s physical stability reduces many risks relative to more reactive analogs, but our team walks new crews through proper ventilation, fire control, and best loading practices every time a new site comes online.

    With dozens of customers operating from subtropical to Arctic climates, standard storage protocols may not suit every case. We provide actionable, context-specific guidance rooted in years of lessons on what works and what fails—a drum palletized too high in a winter dock, a blocked vent line in a summer heat wave. Our distributed network adjusts technical guidance both to regional regulations and practical field realities, not just rulebooks.

    In waste management, downstream users face tightening limits on halogen emissions and contaminated wash streams. We collect and summarize the best available abatement and treatment technologies—not just from open literature but from field trials and operational partnerships. This knowledge-sharing reduces user risk and helps maintain public trust in local operations.

    The Path Forward: Trusted Supply for Evolving Needs

    The future holds few guarantees but constant change. New applications for 1,3-Dichloro-2,5-Difluorobenzene continue to emerge, and regulatory definitions of "acceptable" shift unpredictably. Our experience proves that putting long-term trust, technical rigor, and open communication ahead of shortcuts pays off for all sides. Decades serving as a partner—rather than just a source—means our teams work to see problems before they grow, to answer calls when markets tighten, and to adapt with industry trends rather than react to them.

    Customers counting on 1,3-Dichloro-2,5-Difluorobenzene for reliable performance, regulatory clarity, and collaborative innovation find a steady partner with both deep bench knowledge and ongoing investment in tomorrow’s practices. Each shipment, each test, and every telephone call echoes our belief: specialty chemicals deserve serious stewardship, from feedstock to finished formulation. When complex synthesis and market uncertainty test your supply chain, you deserve more than a datasheet—you deserve a manufacturer who’s walked the road, learned the lessons, and stands ready to solve the next problem with you.