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3,5-Dichlorofluorobenzene

    • Product Name 3,5-Dichlorofluorobenzene
    • Alias 1,3-Dichloro-5-fluorobenzene
    • Einecs 211-495-7
    • 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

    816358

    Cas Number 348-60-5
    Molecular Formula C6H3Cl2F
    Molar Mass 164.99 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.409 g/cm3
    Boiling Point 178-180°C
    Melting Point -24°C
    Refractive Index 1.548
    Flash Point 63°C
    Solubility In Water Insoluble
    Vapor Pressure 0.5 mmHg (25°C)
    Smiles FC1=CC(Cl)=CC(Cl)=C1

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 3,5-Dichlorofluorobenzene, sealed with a screw cap and labeled with hazard warnings.
    Shipping 3,5-Dichlorofluorobenzene is shipped as a hazardous material, typically in sealed, chemical-resistant containers such as glass bottles or metal drums. It should be labeled according to regulations, kept away from heat or ignition sources, and stored in a cool, well-ventilated area during transport. Handle with care to prevent leaks or spills.
    Storage 3,5-Dichlorofluorobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it away from heat, sparks, and open flames. Ensure proper labeling and store at room temperature. Use secondary containment to prevent spills and restrict access to trained personnel only.
    Application of 3,5-Dichlorofluorobenzene

    Applications of 3,5-Dichlorofluorobenzene in Industrial Manufacturing

    We manufacture 3,5-Dichlorofluorobenzene for established industrial applications where its specific reactivity and substitution pattern support complex synthesis. Below, we detail proven downstream use cases among specialty sectors, each with documented compliance, controlled formulation usage, direct process integration, and precisely defined finished product classes.

    1. Agrochemical Intermediate for Fungicide Synthesis

    This compound serves as a key halogenated aromatic intermediate in the multi-step synthesis of triazole and strobilurin fungicides, where its molecular framework enables targeted coupling reactions. Manufacturers in crop protection industries incorporate it in active ingredient formation, precisely controlling its content according to product registration requirements and environmental safety assessments.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • US EPA Pesticide Registration Requirements (40 CFR Part 158)
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Intermediate charge level at 0.8–1.2 molar equivalents in core synthesis step, adjusted based on the conversion yield and desired product purity

    Downstream process integration

    • Feeds into the nucleophilic aromatic substitution reactor for core building block assembly; post-reaction workup dictates downstream purification and isolation.

    Final product types

    • Triazole-based fungicide technical concentrates
    • Pyraclostrobin and related strobilurin actives
    • Water-dispersible granules (WDG)
    • Suspension concentrates (SC) for agricultural use

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Manufacturing

    3,5-Dichlorofluorobenzene acts as a controlled building block in synthesizing select APIs, where its unique halogenation drives regioselective reactions in medicinal chemistry. API producers require strict batch traceability and must optimize fluorobenzene feed ratios to ensure compliance with regulatory and pharmacopeial limits for impurities in the final pharmaceutical substance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • Used at 0.6–1.0 molar ratio relative to the main heterocycle scaffold, titrated based on specific API targets, impurity profile, and process yield

    Downstream process integration

    • Introduced during intermediate condensation or SNAr (nucleophilic aromatic substitution) steps in the API synthesis, followed by fine purification, and finally integrated into the API isolation scheme

    Final product types

    • Antihypertensive ingredient intermediates
    • Anti-inflammatory drug precursors
    • Final API crystals post-purification
    • Pharmaceutical-grade bulk intermediates for contract API producers

    3. Fine Chemical Intermediate for Dye and Pigment Synthesis

    In the colorant sector, 3,5-dichlorofluorobenzene provides a crucial halogenated nucleus for synthesizing specialty azo and anthraquinone dyes. Its selective reactivity supports precise substitution steps that impact hue, shade, and lightfastness in finished pigments, requiring exact stoichiometric control and adherence to both process and product safety criteria.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemicals)
    • REACH Regulation (EC) No 1907/2006—Annex XVII, colorant restrictions
    • DIN EN ISO 9001:2015 for pigment quality management
    • US FDA 21 CFR 74—Color Additives (applicable to food/contact colorants)

    Typical usage ratio

    • 0.9–1.3 equivalents per foundational aromatic amine feedstock, calculated from targeted chromophore yield and solvent system parameters

    Downstream process integration

    • Charged into aromatic coupling and halogenation reactions, followed by intermediate isolation and finishing steps such as sulfonation or metallization for pigment performance adjustment

    Final product types

    • Azo dyes for synthetic fibers
    • Antraquinone-based pigments for inks
    • High-purity pigment dispersions
    • Specialty functional colorants for plastics and coatings

    4. Electronic Chemical for Liquid Crystal Material Synthesis

    Leading electronic material producers use this benzene derivative as an advanced intermediate in developing liquid crystal compounds and display-related specialty organics. The halogen and fluorine substituents enable precise engineering of π-conjugation and polarity, which are essential for phase behavior and dielectric properties in finished liquid crystal mixtures for digital displays and sensors.

    Industry compliance standards

    • SEMI Standards for Electronic Specialty Chemicals
    • ISO 9001:2015 for manufacturing quality systems
    • RoHS Directive EU 2011/65/EU (for hazardous substance limits in electronic components)
    • JIS C6109-3-2—Japan Standards Association for Display Chemicals

    Typical usage ratio

    • Feed ratio ranges from 0.5–1.5 mol/mol versus main cyanobiphenyl or terphenyl units; adjusted to achieve precise birefringence and viscosity targets in final blends

    Downstream process integration

    • Integrated into custom organic condensation or coupling synthesis, followed by multi-stage purification; material then undergoes blending and formulation into LC mixtures

    Final product types

    • Liquid crystal display (LCD) fluid mixtures
    • Specialty LC monomers for high-resolution display panels
    • Intermediate building blocks for advanced display technologies
    • Organic semiconductive materials for optoelectronic applications

    5. Chemical Synthesis of Fluorinated Aromatic Polymers

    Producers of high-performance polymers utilize this compound as a monomer precursor to synthesize fluorinated aromatic resins and specialty thermoplastics. It enables the controlled introduction of both chlorine and fluorine moieties, resulting in polymer backbones with tailored dielectric properties and environmental resistance demanded in aggressive applications such as wire insulation and high-frequency circuit boards.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • IEC 61249-2-7 for base materials in PCB manufacturing
    • ISO 14001 Environmental Management Systems (polymer production)
    • RoHS Directive (hazardous substances for electronics-grade resins)

    Typical usage ratio

    • Typically supplied at 1.0–1.2 equivalents per diol/dianhydride comonomer, determined by molecular weight targeting and required polymer performance

    Downstream process integration

    • Used in aromatic polymerization reactors, generally under high-vacuum or inert atmospheres, prior to isolation and extrusion or compounding into engineering plastics

    Final product types

    • Fluorinated polyarylene resins (for printed circuit boards)
    • High-dielectric thermoplastic resins
    • Specialty cable jacketing materials
    • Insulating sheets for electronics
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    Certification & Compliance
    More Introduction

    3,5-Dichlorofluorobenzene: A Reliable Building Block in Chemical Synthesis

    Understanding 3,5-Dichlorofluorobenzene

    In our years on the plant floor and in the lab, we've seen that 3,5-Dichlorofluorobenzene (CAS No.: 2506-38-3) stands out as a practical intermediate for industries that demand fine-tuned aromatic compounds. This chemical brings together chlorination and fluorination on a single benzene ring, which allows it to serve as a key precursor in pharmaceutical active compounds, crop protection ingredients, and specialty performance chemicals. Over the years, it has quietly become integral to many production chains without drawing much attention beyond those who work directly with intermediates like it.

    Model and Specifications

    We produce 3,5-Dichlorofluorobenzene with a molecular formula of C6H3Cl2F and a molecular weight of around 164. This colorless to pale yellow liquid maintains a reliable consistency batch after batch, an important trait that process chemists and plant managers come to expect. Most of our lots typically test above 99.5% purity by gas chromatography, which helps downstream reactions start from a sound foundation.

    From a handling standpoint, shelf stability makes this compound preferable to other halogenated aromatics. It maintains its specification even after a season in warehouse storage, provided drums or IBCs remain well-sealed and shielded from sun and water vapor. The slightly higher boiling point compared to monofluorobenzene or dichlorobenzene means it withstands more robust operating temperatures in synthesis work, especially important for continuous operations that can't afford halts for side reactions or volatilization losses.

    On a production line, the compound responds predictably to common process controls. During distillation, it behaves much like its close relatives, producing a distinct but manageable odor and packing in a similar specific gravity to what seasoned operators expect for this class of chemicals. These properties may seem trivial, but in plants that run around the clock, dependable performance and predictability translate directly into cost savings.

    Applications and Benefits

    We see 3,5-Dichlorofluorobenzene used heavily in the pharmaceutical sector for active ingredient synthesis, especially in projects requiring unusual aryl halide scaffolds. Medicinal chemists appreciate the functional group arrangement when they need to introduce further substitutions in specific positions. It helps them push synthesis schemes past sticking points that stall out with other isomers, due to the distinct selectivity these halogens bring. Beyond pharma, agrochemical makers often use this compound to attach stable functional groups for advanced herbicides and fungicides.

    Another key usage comes in the realm of specialty material additives—particularly flame retardants and specialty polymers. Our partners in polymer chemistry describe that 3,5-Dichlorofluorobenzene gives them options for ring activation or deactivation, letting them dial in properties that would otherwise prove out of reach using unsubstituted or differently substituted benzene rings.

    At our plant, engineers regularly receive custom requests involving this molecule, as R&D teams experiment with ways to extract more performance from finished goods. These stories illustrate how versatile this compound is—its mix of chlorine and fluorine substitutions opens new reactions that either precursor alone may not support, such as cross-couplings, halogen-lithium exchange, or nucleophilic aromatic substitution.

    How 3,5-Dichlorofluorobenzene Stands Apart

    Compared to monochlorinated or monofluorinated benzenes, the electron-rich nature of this compound’s ring system makes certain transformations more straightforward—especially nucleophilic aromatic substitutions. Chemists on site have repeatedly told us that the ortho and para directing effects of the individual halogen atoms steer reactions down cleaner, higher-yielding pathways than unsubstituted or mono-substituted counterparts.

    Among dichlorofluorobenzenes, the 3,5-isomer offers a unique pattern of reactivity thanks to the alternating positions of substituents. This symmetry often improves process yields as well as selectivity in downstream modifications. For advanced pharmaceuticals, where precise substitution matters, these subtle differences in reactivity can determine whether a library of analogues becomes accessible—or never materializes on schedule.

    Technicians note another distinction: the boiling and melting points of 3,5-Dichlorofluorobenzene slot nicely into typical batch scheduling alongside its analogs. Some of our customers mention that this trait simplifies switching equipment between halogenated aromatic runs, reducing cross-contamination or residue problems during changeovers. We know a smooth switch between jobs cuts downtime, so this property saves effort and cleaning costs in the plant.

    Production Considerations and Experiences

    From an operator’s standpoint, 3,5-Dichlorofluorobenzene does not create the challenges associated with some other halogenated aromatics. It exhibits stable color, low volatility losses, and manageable odor, which minimizes regulatory headaches and neighbor complaints in chemical parks. Plant safety managers point out that compared to compounds containing heavier halogens or multiple fluorines, the substance presents fewer containment or corrosion issues, especially in vessels with modern fluoropolymer linings or glass-lined steel.

    Waste management teams appreciate its inert character under ambient conditions and straightforward incineration profiles, which cuts hazardous waste costs. This compound does not form the highly persistent byproducts sometimes generated by polyhalogenated aromatics, so off-gas scrubbers and wastewater handling do not require much reconfiguration. For a compound in the halogenated aromatics family, this relative straightforwardness makes a difference in permit negotiations and long-term asset planning.

    In lab and pilot settings, technicians found that the liquid nature of this material—combined with its moderate viscosity—speeds up sampling and in-process quality checks. When time counts, as it always does in a plant, every small gain in sample turnaround impacts decision-making and process corrections. No unusual sampling equipment, heated lines, or extra pumps are needed, which simplifies infrastructure.

    Worker Safety and Environmental Responsibility

    Operators report that handling 3,5-Dichlorofluorobenzene brings lower acute risk compared to handling caustic agents, oxidizers, or polyhalogenated aromatics. Standard PPE, including splash-resistant gloves, goggles, and chemical-resistant clothing, has proven effective for regular work. The material's characteristic odor helps alert workers to spills or leaks, which allows for immediate response, and our teams appreciate any property that grants quick detection without complex sensors.

    Our environmental engineers stress that proper storage and predictable transportation make it easier to comply with local and international shipping codes. Drums and IBCs seal easily with standard gaskets, and ground crews value compatibility with usual warehouse practices, eliminating special needs for chemical-specific secondary containment.

    We review toxicity and aquatic persistence data each year as part of responsible manufacture, and so far, regulatory agencies have not found major cause for concern in monitored applications. That said, waste streams do require regular tracking, and ongoing dialogue with local authorities ensures good stewardship.

    Supply Chain Insights

    Across decades, our procurement teams have learned the value of stable upstream raw materials, as the halogen sources for 3,5-Dichlorofluorobenzene come from established suppliers. Seasonal swings sometimes affect costs, especially around major holidays or global trade fluctuations, but reliable supplier contracts have allowed continuity for both bulk and specialty orders.

    Managers highlight the value of local warehousing and distribution partners who understand this product’s nuances. Some distributors have reported better than average shelf performance, reducing loss or returns attributed to aged material. In times of logistic disruption, buyers typically find comfort in partnering directly with producers equipped to pivot production plans in response.

    Bulk storage at our own facilities has involved lessons over the years. For example, we have migrated away from old-style mild steel drum storage, switching to more robust HDPE-lined and epoxy-lined packaging to avoid trace impurities leaching into high-purity lots under heat stress. This upgrade has reduced customer complaints about color instability or minor odor changes, maintaining the rigorous standards needed for regulated industries.

    Regulatory and Quality Trends

    In recent years, demand from pharmaceutical and agrochemical sectors has driven a stronger focus on trace impurities and reproducibility, especially for those working under the ISO and GMP umbrella. Our QA/QC team follows routine chromatographic and spectroscopic checks throughout each production batch. Any process change—down to a different filtration aid or reactor agitator setting—must clear thorough validation before it reaches downstream processing. These habits, drilled in by audits and years of experience, keep the product quality up to expectations in every shipment.

    Some customers, particularly in North America and Europe, have called for detailed product lifecycle records and environmental impact analyses. Our plant keeps extensive batch records and waste-processing logs, giving partners confidence during facility inspections or when seeking international certifications.

    Process Adaptability and Customer Problem-Solving

    Over the years, researchers have reached out to us asking how to adjust processes when faced with yield issues or side reactions in downstream chemistry. Some describe how alternative chlorofluorobenzenes—or even unrelated halogenated aromatics—fail due to less predictable reactivity or incompatibility with their reactor setups. By reviewing historical plant data and drawing from previous case studies, we've helped multiple partners dial in optimal charge rates, heating profiles, and purity specifications for 3,5-Dichlorofluorobenzene.

    A pharmaceutical customer once encountered byproduct formation during a late-stage coupling step, which created costly chromatographic separations downstream. By switching the order of addition for their base and solvent, guided by our process chemist, their team improved selectivity and reached target purity on the first try. These hands-on collaborations, based on mutual trust, highlight the real value manufacturers bring to tricky synthesis challenges.

    In another project, an agrochemical innovator aimed to replace an older dichlorobenzene intermediate classified as persistent and bioaccumulative. We offered to trial 3,5-Dichlorofluorobenzene as a substitute in their synthetic route. The new process cut reaction times and produced less tangling waste in post-filtration, which helped the customer fast-track field trial approvals. Stories like these surface regularly—illustrating how incremental changes at the intermediate stage can ripple into wider improvements on product performance, regulatory clearance, and sustainability metrics.

    Reliability and Flexibility in Bulk Production

    Our facility runs multi-purpose reactors built for halogenation and fluorination under strictly monitored conditions. Over time, plant operators have refined process control schemes to minimize side reactions and maximize product yield. By carefully managing temperature ramps and feedstock purity, we've supported consistent production runs scaled from the multi-ton level down to kilogram samples for research. Operators report that the relatively simple workup and distillation steps keep cycle times short.

    Through close collaboration with logistics teams, we have developed reliable shipping schedules for both standard and custom packaging. International customers often schedule shipments in advance, knowing that our output levels match published lead times. This approach helps project managers plan R&D, pilot, or commercial-scale campaigns without costly delays.

    Long-Term Value and Industry Feedback

    Over the span of our manufacturing history, 3,5-Dichlorofluorobenzene has shown a steady rise in both demand and reputation. Repeat partners from various regions return to us year after year, sharing updates on the successes and lessons learned from their own product launches. Some customers who originally started with small R&D bottles now pull regular bulk shipments as their own product lines mature.

    We have watched trends evolve—early on, most inquiries came from pharma labs in need of niche intermediates; now, agrochemical startups, advanced materials researchers, and established fine chemical makers all join in demanding high-purity, consistently shipped 3,5-Dichlorofluorobenzene. The compound’s flexibility in both traditional synthesis and newer applications (like specialty coatings or UV-resistant resins) keeps opening new doors for savvy chemists.

    Continuous Improvement: Listening and Adapting

    At each stage of production, we solicit active feedback—whether that’s through plant walkthroughs, post-shipment check-ins, or troubleshooting calls with R&D teams. Ideas from line operators, maintenance technicians, warehouse staff, and even truck drivers play a role in fine-tuning workflow, packaging, and documentation. This culture of listening and stepping up to solve problems is the true backbone of reliable chemical manufacturing.

    We constantly re-examine analytical methods, looking for faster turnaround or improved sensitivity in detecting trace impurities. In the last few years, we have adopted higher-resolution chromatography and in-line analyzers on several lines, which shortens release cycles and improves reporting accuracy for customers with strict technical transfer requirements.

    As regulatory frameworks shift and demands for traceability increase, we keep our documentation, certificates of analysis, and SDSs up to date. Our technical team spends time with customers reviewing batch data and even welcomes lab audits or virtual inspections. Part of manufacturing’s promise rests in trust—not only technical skill.

    In Perspective: Real-World Value

    The utility of 3,5-Dichlorofluorobenzene in today’s chemical landscape can’t be shrunk to just numbers or purity specs. Its true worth emerges when a project engineer, after a long day troubleshooting, finds that the intermediate worked as expected or when a plant QA manager relaxes knowing another batch matches the previous 20 runs. Over the long haul, customers realize that steady, conversational feedback with a manufacturer solves as many problems as any new certificate or analytical report.

    From raw material sourcing and reaction optimization to packaging, regulatory tracking, and shipping, our experience manufacturing 3,5-Dichlorofluorobenzene has taught us that attention to detail, honest communication, and a willingness to learn from every challenge set the stage for lasting partnership. Each barrel, tote, or tanker we send out carries not only a trusted chemical—but a shared commitment to keep projects on track, goals met, and new discoveries within reach.