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1,4-Difluorobenzene

    • Product Name 1,4-Difluorobenzene
    • Alias p-Difluorobenzene
    • Einecs 216-367-7
    • 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

    155066

    CAS Number 540-36-3
    Molecular Formula C6H4F2
    Molar Mass 114.09 g/mol
    Appearance Colorless liquid
    Density 1.146 g/cm³
    Melting Point -1 °C
    Boiling Point 85-87 °C
    Vapor Pressure 35 mmHg (25 °C)
    Refractive Index 1.437
    Flash Point 13 °C
    Solubility in Water Insoluble
    SMILES Fc1ccc(F)cc1

    As an accredited 1,4-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, 250 mL, tightly sealed with a PTFE-lined cap; labeled with hazard symbols and product identification for 1,4-Difluorobenzene.
    Shipping **Description of Shipping for 1,4-Difluorobenzene:** 1,4-Difluorobenzene is typically shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and should be transported according to relevant regulations (e.g., DOT, IATA). Appropriate hazard labels and documentation must accompany the shipment, ensuring safe handling and compliance during transit.
    Storage 1,4-Difluorobenzene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from direct sunlight and moisture. Store at room temperature and avoid exposure to heat. Ensure all storage areas are clearly labeled and equipped for safe chemical handling and spill containment.
    Application of 1,4-Difluorobenzene

    Applications of 1,4-Difluorobenzene in Industrial Manufacturing

    1,4-Difluorobenzene serves as a critical chemical intermediate across several specialized industrial fields. Our manufacturing process achieves consistent purity and high batch-to-batch reliability, which enables downstream partners to meet demanding regulatory and technical requirements in advanced application segments.

    1. Agrochemical Intermediate for Selective Herbicide Synthesis

    Agrochemical producers use 1,4-difluorobenzene as a key building block in synthesizing specific phenoxy and pyridine-type herbicides targeting broadleaf and grass weeds. During multi-step synthesis, this raw material undergoes nucleophilic aromatic substitution or Friedel-Crafts acylation, introducing difluoro functionality for tailored activity and improved crop selectivity. Compliance with food safety, residue, and traceability standards is critical at every stage, driving precise input control and in-process analytical verification.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • European Union Regulation (EC) No 1107/2009 on plant protection products
    • ISO 9001 Quality Management for upstream handling
    • OECD Good Laboratory Practice for synthesis records

    Typical usage ratio

    • Batch input at 0.8–1.6 molar equivalents per targeted active ingredient unit; adjusted according to desired halogenation and substitution efficiency

    Downstream process integration

    • Charged into stage-1 or stage-2 reactors for controlled halogenation or coupling reactions; analyzed for unreacted residuals prior to downstream functionalization

    Final product types

    • Selective herbicides (e.g., difluorinated aryloxy acids)
    • Registered crop-protection mixtures for cereals and soybeans
    • Intermediate concentrates for post-patent formulation export markets
    • Precursor blends used by multinational agrochemical companies

    2. Pharmaceutical Intermediate for Fluorinated Active Ingredients

    The pharmaceutical sector harnesses 1,4-difluorobenzene as an aromatic precursor to introduce defined fluorine atoms into active pharmaceutical ingredient (API) scaffolds. These fluorinated moieties improve bioavailability, metabolic stability, and target specificity in cardiovascular, CNS, and oncology pipelines. All input usage requires full traceability, compliance with global pharmacopoeias, and rigorous impurity control throughout multi-stage synthesis workflows leading to API crystallization or salt formation.

    Industry compliance standards

    • European Pharmacopoeia (Ph. Eur.) monographs for starting materials
    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • US FDA 21 CFR Part 211 for drug substance manufacture
    • USP <467> Residual Solvents for testing

    Typical usage ratio

    • Applied at 5–15% w/w relative to core API precursor load; range varies per desired fluorination density in final structure

    Downstream process integration

    • Integrated into primary reactor trains for nucleophilic aromatic substitution or metal-catalyzed coupling prior to secondary derivatization; full trace documentation maintained in batch records

    Final product types

    • Oral and parenteral APIs featuring difluorophenyl motifs
    • Specialty contract-manufactured intermediates for regulatory filings
    • Investigational new drug (IND) clinical lots
    • Registered drug substances in major regulated markets

    3. Electronic Chemicals – High Purity Monomer for Fluoropolymer Synthesis

    Producers of electronic-grade fluoropolymers employ 1,4-difluorobenzene as a monomer or modifier for advanced coatings, insulating films, and high-performance dielectrics. Stringent purity, ultra-low metal, and particle standards must be met to prevent device contamination and degradation. The raw material undergoes catalytic polymerization or co-polymerization reactions, determining molecular weight and dielectric consistency of the end polymers used in microelectronics and semiconductor manufacturing.

    Industry compliance standards

    • SEMI C3 Standard for Transistor Quality Raw Materials
    • IEC 61249-2-21 for halogen-free board applications
    • ISO 14001 Environmental Management (green chemistry practices)
    • RoHS Directive (2011/65/EU) for restricted substances

    Typical usage ratio

    • Dosed at 3–10% by mass as a modifying component; higher ratios possible for specialty co-polymer grades requiring elevated fluorine content

    Downstream process integration

    • Fed into continuous stirred reactors or microreactors, controlled by advanced process control systems to limit by-product generation and ensure repeatable polymer chain propagation

    Final product types

    • High-purity fluoropolymer resins for FPC and LCD films
    • Protective coatings on semiconductor wafers
    • High-frequency PCB laminates for 5G infrastructure
    • Insulating foils for ultra-low loss applications

    4. Fine Chemicals – Advance Material Intermediate for Liquid Crystals

    Manufacturers of liquid crystal materials utilize this difluorinated aromatic compound to tailor molecular structure, polarity, and phase transition behavior for display applications. The material is introduced in controlled amounts during organic synthesis of multi-ring, side-chain, or alkyloxyphenyl-based liquid crystal molecules, enabling custom alignment and electro-optical tuning for end-use in TFT-LCD and OLED panels. Batch processing is closely monitored for homogeneity and absence of ionic or metallic contaminants.

    Industry compliance standards

    • IEC 62321 for analysis of certain hazardous substances in electrical equipment
    • ISO 9001 Quality Management for supplier auditing and traceability
    • REACH Registration (EC 1907/2006) for European shipments
    • EICC/GeSI Conflict-free Sourcing Initiative for responsible sourcing

    Typical usage ratio

    • Integrated at 1.5–4.5 moles per 10-mole liquid crystal syntheses; precise ratio selected based on desired mesophase thermal range and viscosity control

    Downstream process integration

    • Dosed during condensation, etherification, or halogen exchange steps; in-process HPLC or NMR verifies structural incorporation before final blending

    Final product types

    • Nematic and smectic liquid crystal formulations for TV and monitor panels
    • Smartphone and automotive display liquid crystals
    • Low-temperature phase materials for IoT or e-paper segments
    • Chemical mixtures for fine-tuning refractive index and dielectric anisotropy

    5. Specialty Organic Synthesis – Precursor for Advanced Photoinitiators

    Specialty chemical manufacturers employ 1,4-difluorobenzene for synthesizing advanced aromatic ketone photoinitiators, supporting the printing, inks, and 3D additive manufacturing sectors. Its difluorinated structure imparts superior UV absorption and photoreactivity, facilitating rapid polymerization in high-throughput curing processes. Accurate raw material metering and contaminant screening are essential to achieving consistent initiator performance in downstream blends.

    Industry compliance standards

    • ISO 9001 for raw material quality and traceability
    • EN 71-3:2019 for migration of certain elements in finished products
    • FDA 21 CFR 175.300 for coatings contacting food (when applicable)
    • REACH pre-registration (if supplied into EU markets)

    Typical usage ratio

    • Feeds at 8–20% mass of total aromatic base for the photoinitiator synthesis; fine-trimmed depending on target absorption and quantum yield

    Downstream process integration

    • Charged in initial acylation or alkylation steps, followed by purification and direct blending into UV/EB cured resin pre-mixes

    Final product types

    • High-efficiency UV photoinitiators for digital and flexo printing
    • Photoinitiator packages for 3D printing resins
    • High-speed inkjet and LED-cured inks
    • Coating additive blends for sensitive food and pharma packaging
    Free Quote

    Competitive 1,4-Difluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1,4-Difluorobenzene from the Manufacturer’s Perspective

    Understanding 1,4-Difluorobenzene in the Production Environment

    Those of us who work directly with aromatic fluorinated compounds know that 1,4-difluorobenzene stands out not just in its molecular structure but also through the role it plays in chemical manufacturing lines. Its formula, C6H4F2, describes a benzene ring carrying two fluorine atoms at the para position. For us at the plant, that subtle placement drives the properties that have made this molecule a staple among our customers who specialize in pharmaceuticals, agrochemicals, and specialty polymers.

    Each drum or tank that leaves our facility results from a careful process, not just in terms of synthetic chemistry but also operational discipline. We spend time focusing on the technical purity, trace moisture, and storage integrity, as fluorinated benzenes can be finicky about impurities and trace contaminants. Our continuous distillation methods help us hit purities ranging from 99% to ultra-high grades depending on the project needs. The technical spec matters a lot when you’re aiming for reliable performance in downstream organic syntheses or in electronics applications, where even minor byproducts can skew outcomes.

    The Practical Side: What Makes 1,4-Difluorobenzene Distinct?

    What separates 1,4-difluorobenzene from other difluorinated isomers or mono-fluorinated benzenes? To experienced operators, it’s both a matter of physical behavior and chemical reactivity. The para orientation gives the molecule a more symmetrical shape, which in practical terms affects volatility and solubility compared to ortho and meta isomers. This plays out in how the material vaporizes, how it handles in reactors, and even safety strategy—with fewer surprises during distillation or evaporation.

    Compared with compounds like 1,2- or 1,3-difluorobenzene, the 1,4- version offers more stable boiling range and predictable reactivity during halogen exchange and metalation reactions. In the lab and at scale, this translates to more reproducible yields. Users trying to introduce fluorinated motifs onto complex molecules often turn to this compound because it avoids unexpected side reactions that arise with less symmetric isomers. Anyone who’s experienced running hot pressure tubes with 1,2-difluorobenzene and traced back yield loss to ortho effects knows the value of the para variant.

    This product also distinguishes itself from heavier perfluoroaromatics and trifluorotoluenes through less aggressive reactivity. The presence of just two fluorine atoms gives a unique balance—stronger chemical resistance than simple fluorobenzene, not as stubborn or difficult to activate as pentafluorobenzene. Handling safety, waste treatment, and emission profiles benefit accordingly.

    Manufacturing Experience: Challenges and Solutions

    People unfamiliar with plant-scale chemistry sometimes assume all difluorobenzenes behave similarly or can be sourced interchangeably. In actual practice, making high-grade 1,4-difluorobenzene brings unique requirements to the shop floor. Our process engineers keep a close eye on fluoride source purity, avoid steel contamination, and maintain careful water removal from intermediates. Even minor hydrolysis during production or storage adds acids that foul equipment and reduce batch value; higher-end electronics manufacturers using the product as a solvent or precursor do not tolerate trace acidity. We address this with robust molecular sieving, inert gas blanketing, and constant monitoring.

    Our years of experience show that residual acidity or metal ions—byproducts often missed by less rigorous producers—will show up as pain points downstream, especially for our partners pushing reactivity in organometallic reactions. Customers who run repeated Suzuki couplings or lithium exchange appreciate that we prioritize ion removal before packaging. We have refined our filtration and distillation infrastructure to minimize cross-contamination and deliver material that doesn’t introduce unexpected catalyst poisons or hydrolyzable impurities.

    The logistics of storing and shipping 1,4-difluorobenzene also sets it apart. Operators at the warehouse know to monitor headspace pressure and temperature due to its volatility. In cold climates, drum handling, condensation, and pressure regulation all matter. We’ve learned to use specialty-lined containers for long-distance shipments to avoid unintended fouling—organic fluorides dislike long contact with some plastics and rubbers.

    Applications Driving Demand for 1,4-Difluorobenzene

    Much of the value associated with 1,4-difluorobenzene comes from its position as a critical building block. Pharmaceutical development teams often use it as a starting point for new active ingredients, taking advantage of the fluorine atoms’ influence on metabolism and biological activity. We’ve supplied countless batches destined for stepwise elaboration into anti-inflammatory compounds, radiolabeled diagnostics, and experimental oncology agents.

    The role extends further into agrochemical development. Modern crop protection agents rely on selectivity and environmental stability conferred by aromatic fluorination. Chemists engaged in the design of new fungicides and herbicides count on 1,4-difluorobenzene’s clean substitution pattern to serve as a platform for further halogenation or side-chain introduction. In the plant, we sometimes see parallel orders for related isomers, but follow-up feedback consistently notes the superior downstream performance of material originating from our 1,4-specification, particularly regarding isomeric purity and stability.

    Another key sector draws on this compound’s physical traits. Electronic and specialty polymer producers use 1,4-difluorobenzene as a solvent or co-monomer. With melt behavior and strong solvency against polyelectrolytes, it supports processes as diverse as PI (polyimide) formation and advanced resins for circuit boards. Workers at our site know the clean-burning characteristics minimize soot and side residue in these applications, which reduces downtime for maintenance and improves end-product reliability.

    Practical Insights from Production Runs

    Our people who run and maintain the synthesis lines see trends in how 1,4-difluorobenzene consumption rises and falls depending on research cycles, regulatory changes, or shifts in global demand. Experience teaches us to keep production flexible—not every order requests the same volume or grade. Some customers emphasize the necessity of tightly specified water content, while others focus on isomeric purity. Adjusting batch size, distillation time, and packaging scale makes a noticeable difference. We keep close relationships with end-users, learning from their pilot-scale feedback when rare impurities or handling issues appear.

    Seasoned operators will tell you that, compared to handling more reactive perfluorinated aromatics, 1,4-difluorobenzene offers a more manageable hazard profile. Still, good practice always means routine headspace venting, leak checks, and solvent-suitable gloves in the bottling room. The team has developed site-specific procedures to minimize worker exposure and material loss; experienced handlers know to pre-flush lines, guard against static charge-up, and check for early signs of corrosion on older system parts.

    Not every plant runs into identical issues, but those producing for the pharmaceutical or electronics industries have to hold to a tighter set of specs not just for purity but shipping cleanliness. Since some customers use analytic techniques like GC-MS and ion chromatography that can spot hydrolyzable fluoride traces in the parts-per-billion, our crew takes a lot of pride in the cleanliness of our tanks and lines. This attention to detail results in fewer returns, better reviews, and longer customer relationships—outcomes rarely mentioned in product brochures but keenly felt by those on both sides of the order form.

    Comparing 1,4-Difluorobenzene to Related Compounds

    On the market, you’ll often encounter mono-fluorobenzenes or multi-fluorinated products like 1,2,4,5-tetrafluorobenzene. Each comes with its own pros and cons. Mono-fluorinated benzenes, for example, cost less to produce and handle but don’t always provide the same thermal and metabolic stability in downstream applications. The heavier tetra- or pentafluoro variants can yield insulation or specialty coatings, but manufacturers looking for both cost control and specific chemical reactivity often prefer 1,4-difluorobenzene.

    Those who’ve worked with 1,2-difluorobenzene know the ortho arrangement tweaks electron density on the ring, increasing reactivity at unintended sites—which complicates fine-tuned synthesis and increases waste. In contrast, the para arrangement on 1,4-difluorobenzene delivers more predictable selectivity, making it preferred for building functionalized aromatic cores where substitution patterns must be tightly managed.

    With other difluorinated benzenes, the thermal and chemical stability will shift along with the location of the fluorine atoms. For instance, the 1,3-isomer finds its main use in niche applications and often sees less demand. From our position as a producer, the global purchasing landscape for 1,4-difluorobenzene regularly outweighs both 1,2 and 1,3 versions—showing real-world preference among industrial chemists and R&D staff.

    Commitment to Quality and Transparency

    Making and supplying chemical building blocks such as 1,4-difluorobenzene gives us a unique view of how production controls support customer trust. Traceability, batch history, and timely technical support turn routine orders into long-term partnerships. Customers working on pre-clinical drug development or high-purity electronic components demand clean paperwork, access to historical testing, and clear lines of communication when an unexpected out-of-spec issue pops up.

    Transparency goes beyond posting a certificate of analysis. We maintain open communication with our partners about process changes, safety incidents, or raw material sourcing updates that may impact their timelines or finished products. Years in business have proven that sharing real test data and operational insights builds confidence and helps teams on both sides of the supply agreement handle scale-up or regulatory review more smoothly.

    In chemical manufacturing, we see the value of investing in analytical upgrades—from GC and HPLC to trace ion analysis and NMR. Early detection of subtle byproducts or residual processing aids makes the difference between a batch that satisfies top-end electronics producers and one that falls short. Those of us on the operations floor know that what some call “overkill” in testing ends up saving everyone headaches in the long run.

    Environmental and Safety Considerations

    Nobody working near aromatic fluorides can ignore safety or emissions issues. 1,4-difluorobenzene brings risks more manageable than many more heavily fluorinated chemicals, but release into air or water still requires attention. Our plant’s venting, abatement, and recycling systems run according to regulatory guidelines, but also integrate lessons learned on the production lines. Small design changes—such as improved condensation recovery or automated vented solvent recapture—have increased yield and reduced off-site waste considerably over the past decade.

    Our technicians also monitor for low-level leaks and long-term exposure scenarios, not just for regulatory compliance but out of regard for co-workers’ health. Regular training and adoption of improved personal protective equipment—developed in partnership with frontline staff—increase daily safety and long-term well-being. The accumulated experience of plant personnel helps us anticipate issues before they become incident reports.

    Certain customers require documentation verifying environmental stewardship or life-cycle impact, especially those exporting to markets where extended producer responsibility or carbon tracking is the norm. We see increasing requests for data on production energy, raw material sourcing, and post-use disposal. Meeting these demands requires real investment, both in analytics and plant improvements, but matches our goal to stay competitive and responsible.

    Supporting Innovation and Meeting Market Shifts

    Shifts in markets for 1,4-difluorobenzene—from emerging drug candidates to new generations of battery materials—continue to shape both how much and what grade we make. We watch market signals, research papers, and regulatory updates to gear up for production shifts or to tweak our process when customers signal early signs of a new application. In our own experience, close coordination between R&D, production, and end users helps resolve material-related challenges before they threaten project timelines or budgets.

    Successful partnerships are built on more than competitive pricing. We see the best results when we support customer innovation, whether that means producing small batches with specialized purity control for an academic lab, or scaling to hundreds of kilograms for an industrial launch. Our daily work balances efficiency with nimble adaptation—a plant that invests in both process improvements and relationships stays relevant as needs change.

    In the years since we developed our original process line for 1,4-difluorobenzene, it’s become clear that consistent feedback—both positive and negative—drives our investment plan. Customers pushing frontier science keep us honest about quality and delivery, urging us to refine what others might call “good enough.” In turn, we encourage transparent dialogue on handling, storage, and process bottlenecks downstream. The end result is a higher-value product and fewer surprises for everyone, whether the final use is in a new diagnostic tool or a next-generation polymer.

    Looking Forward: Matching Supply with Real-World Application

    As chemists and operators at the source, we recognize our success rides on a steady grasp of end-use needs. Developing production protocols that anticipate the next regulatory twist or market-driven spec can seem daunting, but history shows this ongoing learning cycle keeps us competitive. 1,4-difluorobenzene shows up in patents and pipelines on a regular basis, testament to its flexibility and utility across technology sectors.

    We know that every specification on paper reflects hours of real work at the bench or pilot plant. Customers who choose direct-from-manufacturer supply often do so to gain these practical insights. Responding to requests for specialized packaging, rush shipments, or unique purity thresholds teaches us to see each order as more than just a transaction. These relationships help us refine not just product quality, but the whole organizational approach to safety, reliability, and innovation.

    Those of us on the front lines of chemical production apply our practical knowledge daily, from process troubleshooting to rapid response when a customer’s new formulation requires out-of-the-ordinary support. Our ongoing focus on pure, stable, and traceable 1,4-difluorobenzene acts as both a foundation and a challenge, continually pushing us to lead by example in the complex and ever-changing world of aromatic fluorochemicals.