4-Chlorobiphenyl

    • Product Name: 4-Chlorobiphenyl
    • Alias: 1-Chloro-4-phenylbenzene
    • Einecs: 205-088-7
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    501227

    Iupac Name 4-Chlorobiphenyl
    Molecular Formula C12H9Cl
    Molar Mass 188.65 g/mol
    Appearance White to colorless crystalline solid
    Melting Point 48-51 °C
    Boiling Point 278-280 °C
    Density 1.17 g/cm³
    Cas Number 2051-62-9
    Solubility In Water Insoluble
    Flash Point 143 °C
    Smiles ClC1=CC=C(C2=CC=CC=C2)C=C1
    Pubchem Cid 6633

    As an accredited 4-Chlorobiphenyl 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 4-Chlorobiphenyl, labeled with hazard symbols, chemical name, purity, and safety precautions.
    Shipping 4-Chlorobiphenyl is shipped as a hazardous chemical, typically in sealed containers to prevent leaks and exposure. It should be packaged according to international and local regulations, with appropriate labeling for toxicity and environmental hazards. Transport must ensure stability, avoiding heat and shock, and include safety documents such as SDS.
    Storage 4-Chlorobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, or open flames. Protect from light and incompatible substances such as strong oxidizing agents. Ensure proper chemical labeling, and store separately from food and feedstuffs. Keep out of reach of unauthorized personnel and follow all relevant safety guidelines.
    Application of 4-Chlorobiphenyl

    Applications of 4-Chlorobiphenyl in Industrial Manufacturing

    4-Chlorobiphenyl is an aromatic organic intermediate that plays a crucial role in multiple industrial manufacturing chains. Our direct production ensures strict quality controls and consistent compliance, supporting downstream applications in specialty polymer processing, pigment synthesis, dielectric fluid manufacture, agrochemical intermediates, and liquid crystal material development. Every application follows sector-specific regulatory standards for safety, quality, and traceability.

    1. Engineering Plastic Additive for Specialty Polymers

    4-Chlorobiphenyl functions as a co-monomer and chain modifier in the synthesis of high-performance engineering plastics, such as modified polyarylates and high-temperature polyimides. Technical formulators incorporate this compound to adjust polymer glass transition temperatures, reduce flammability, and influence electrical insulation properties essential for automotive and electrical devices. Only specialized processing plants with enclosed facilities handle this material due to strict occupational and environmental safety compliance. Product consistency and purity directly affect resin melt-flow characteristics and end-use safety certifications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU, Annex II (EU)
    • Toyota Technical Standard TSC0354G for electrical insulation grade resins
    • UL 94 Flammability Rating for engineering plastics

    Typical usage ratio

    • 0.5–5.0% by weight, variable based on target flame retardancy and dielectric properties. Formulations adapt ratio depending on required ASTM D2863 limiting oxygen index and IEC 60243 dielectric strength.

    Downstream process integration

    • Co-feeding into polycondensation reactor during high-temperature synthesis. Addition occurs prior to chain termination to ensure full incorporation. Inline QC monitors conversion and homogeneity.

    Final product types

    • Electrical connector housings
    • High-touch automotive switches
    • PCB insulation components
    • Flame-retardant electronic device casings

    2. Intermediate for Advanced Pigment Production

    The compound serves as a critical intermediate for synthesizing diaryl-based organic pigments, especially yellow and green shades used in industrial coatings and specialty inks. Masterbatch makers rely on its specific aromatic structure to secure colorfastness and outdoor weathering resistance. The process requires careful metering, and traceability documentation for all raw material batches is mandatory by industrial pigment producers and paint manufacturers. Purity and isomer composition determine final pigment shade and process reproducibility.

    Industry compliance standards

    • EN 71-3:2021 Toy Safety standard for coloring agents
    • ISO 18451-1:2022 Pigments and extenders—Terminology
    • ASTM D5435-2023 Standard Practice for Preparation of Organic Pigment Dispersion
    • Chinese GB/T 21868-2008 Environmental labeling for coating products

    Typical usage ratio

    • 5–12% by mol in intermediate step for pigment synthesis, adjusted according to NMR-verified purity and targeted chroma intensity on CIE L*a*b* scale.

    Downstream process integration

    • Nucleophilic aromatic substitution with coupling agents in pigment synthesis reactors. Integration occurs before isolation and salt precipitation. Closed-system transfer tools used for operator safety.

    Final product types

    • Automotive OEM paint colorants
    • Industrial powder coatings
    • High-performance printing inks
    • Plastic colorant masterbatches

    3. Precursor in Agrochemical Active Ingredient Synthesis

    Chemical processing plants utilize this compound as a halogenated building block in downstream synthesis of selective herbicide and acaricide active ingredients. It functions in catalytic chlorination and coupling reactions, forming part of the core ring structure in end-use molecules. Regulatory bodies require validated cleaning protocols and impurity monitoring at each step. Our customers value analytic consistency and technical documentation support during regulatory submission and dossier compilation for new agrochemical registrations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation 1107/2009 for active substances
    • Japanese MAFF technical standards for agrochemical raw materials
    • Chinese GB 2763 pesticide residue limits for agro-products

    Typical usage ratio

    • 20–45% by mol in core coupling stage, with exact ratio established by downstream synthesis route and active ingredient registration specification.

    Downstream process integration

    • Charged into closed agitated reactors pre-coupling and catalytic halogenation. Batch process requires online GC/HPLC tracking. Waste streams sent to incineration units inline with local regulations.

    Final product types

    • Herbicide technical concentrates
    • Miticide emulsifiable concentrates (EC)
    • Seed coating formulations
    • Suspension concentrate crop protection products

    4. Synthesis Intermediate for Dielectric Fluids

    This halogenated biphenyl acts as a minor component in blending and synthesizing dielectric cooling fluids for transformers and high-voltage equipment, especially as a performance modifier for specialty fluids with enhanced stability at elevated temperatures. Only licensed facilities, under strict local and EU regulations, handle and blend these materials due to environmental controls surrounding PCB analogs. Customer audits review every batch record and emission control measure at our plant.

    Industry compliance standards

    • IEC 60296:2020 for unused mineral insulating oils
    • EN 61100:1992 Specifications for electrical insulating liquids
    • OECD Guidelines for Testing of Chemicals (Section 3: Environmental Fate & Behaviour)
    • Chinese GB 2536-2011 Technical conditions for transformer oils

    Typical usage ratio

    • 0.01–0.5% by weight in specialty dielectric blends, strictly capped under jurisdictional restrictions. Formulators adjust level based on arcing resistance and thermal degradation test data.

    Downstream process integration

    • Blending into base oil matrix during continuous or batch compounding step. Inline viscometric and dielectric loss factor test guides final ratio selection. Final blend filtered and filled under nitrogen blanketing.

    Final product types

    • High-voltage transformer dielectric fluids
    • Specialty capacitor oils
    • Arc-resistant switchgear coolant blends
    • Railway electrical insulator fluids

    5. Liquid Crystal Material Intermediate

    Display material producers leverage this aromatic intermediate to build complex rigid-rod molecules for use in liquid crystal displays (LCDs) and other flat-panel display applications. Proprietary processes require high isomeric purity and impurity profiling at each synthetic step. The upstream material controls molecular orientation properties, switching speed, and alignment in the final display layer. Production records, in-process controls, and end-use data traceability ensure regulatory documentation validity for export and brand customer certification.

    Industry compliance standards

    • IEC 62341–6–2:2015 for OLED and LCD device safety
    • China RoHS 2 and SJ/T 11364 electronic information product rules
    • ISO 9241-307:2008 for electronic visual display requirements
    • Japanese JIS C6109 (LCD panel manufacturing)

    Typical usage ratio

    • 3–10% by mol in the synthetic route, controlled based on NMR-verified purity, and adjusted per proprietary material performance requirements.

    Downstream process integration

    • Introduced during coupling or substitution reaction stages. Stepwise purification between reactions ensures targeted molecular weight distribution. Finished intermediates tracked by lot through to display material blending stage.

    Final product types

    • Twisted nematic (TN) LCD display materials
    • In-plane switching (IPS) LCD liquid crystal blends
    • Active matrix display alignment layers
    • Flexible polymer-dispersed LCD substrates

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    Certification & Compliance
    More Introduction

    4-Chlorobiphenyl: A Chemical Perspective from the Production Floor

    An Introduction from the Plant

    On the production floor, every batch of 4-Chlorobiphenyl traces a careful process from raw material to final product. This compound, known among chemists as 4-CB, stands out for its clear, stable crystalline form and reliable consistency in downstream uses. Over years of manufacturing, we’ve come to appreciate the subtle differences that define it against the many biphenyl derivatives on the market.

    What 4-Chlorobiphenyl Is at Its Core

    The backbone of 4-Chlorobiphenyl starts with biphenyl, a structure recognized for rigidity and stability. By adding a chlorine atom at the para position, chemical behavior shifts—including volatility, reactivity, and compatibility with other aromatic systems. These changes make 4-CB a preferred choice in specialty synthesis. Direct experience in the plant proves that subtle positional shifts on the biphenyl ring produce differences in melting point and solubility—consequences that echo in every downstream reaction.

    In terms of appearance, our 4-Chlorobiphenyl consistently emerges as a white to faintly off-white crystalline powder. We rely on advanced purification, not only because final customers demand it but because downstream reaction rates and purities depend on every trace contaminant being absent. Rigorous chromatographic controls and advanced distillation ensure a purity level above 99%, which continues to attract attention from researchers and industrial partners who know how stubborn unwanted byproducts can be.

    Why 4-Chlorobiphenyl Has Its Own Role

    Years of filling orders for 4-CB show that customers choose this compound for reasons not purely academic. In organic synthesis, 4-CB acts as a fundamental building block, setting the stage for creating complex liquid crystals, specialty polymers, and advanced materials. The para-chloro orientation delivers value during the Suzuki–Miyaura coupling or similar palladium-catalyzed reactions by reducing side reactions and giving higher yields compared with other biphenyl isomers.

    We have seen chemical engineers use our 4-CB to start new molecules that would later find homes in display screens, specialty coatings, and performance materials. Research teams repeatedly reported that the para-chloro setup improves charge transport in materials science, and makes purification easier—an attribute that cuts project timelines in half when mistakes happen.

    In addition, its structural resemblance to chlorinated polychlorinated biphenyls (PCBs) gives 4-CB a practical role in environmental research. Our plant occasionally supports universities and government labs by supplying reference-grade samples, used for GC and HPLC analysis to develop accurate environmental baselines, method calibrations, and investigative toxicology studies. By using a single, rigorously produced grade of 4-Chlorobiphenyl, these labs avoid contamination and cross-reactivity, improving the confidence of their results.

    We have watched 4-Chlorobiphenyl migrate from laboratories to application testing in fields such as additive manufacturing. This versatility stems from its robust aromatic framework and predictable chemical profile—qualities that have helped multiple R&D groups, start-to-finish, from early-stage trials to scale-up.

    Distinguishing Features in Production and Use

    The manufacturing process we use for 4-CB involves a direct chlorination of biphenyl, a procedure refined after years of trial and adjustment. Comparing 4-CB to other positional isomers, like 2-Chlorobiphenyl or 3-Chlorobiphenyl, reveals differences not just in molecular structure but in processing requirements and downstream properties. The para isomer typically presents a higher melting point and improved crystalline stability, which affects storage, transport, and blend performance in secondary synthesis.

    From the perspective of the plant, logistics take on real meaning. Our handling systems remain free-flowing across seasons because of 4-CB’s resistance to clumping and caking—issues that often plague ortho-chlorinated biphenyl isomers. Routine quality audits prove that with para substitution, product shipments leave the warehouse with the same physical qualities reported on incoming raw materials.

    Chemists in partner companies have noted that the substitution pattern of 4-Chlorobiphenyl leads to more predictable reaction kinetics when compared to other isomers. This benefit scales not just in laboratory glassware but in glass-lined reactors demanding careful heat transfer and mixing. The para-position, free from ortho steric hindrance, encourages clean coupling reactions—a fact well-known among those with experience in cross-coupling or electrophilic substitution methodologies.

    Our in-plant experience confirms that the nature of the chlorine atom at the para position reduces the risk of unwanted byproducts. Fewer impurities appear in final product assays, and batch-to-batch reproducibility remains one of our chief measures of quality. These advantages contribute directly to reduced costs in analytical testing and fewer delays from inconsistent reactivity.

    Applications Driving Demand

    Researchers routinely contact us requesting 4-Chlorobiphenyl for analytical standards, structure-activity investigations, and small-scale trial runs in specialty synthesis. Most projects fall under one of several headings: organic electronics, new materials research, or environmental method development.

    The transparency and high-purity standards of our 4-CB position it ideally for use in electronics. We have partnered with firms working on OLEDs, photoconductive films, and other niche applications where molecular uniformity makes or breaks product launch timelines. Specialists often comment that even a small deviation in isomeric purity increases the risk of charge-trapping sites, which ruin experimental results. Our experience meeting these specifications, under tight deadlines, has won trust across multidisciplinary teams.

    As a model compound, 4-Chlorobiphenyl plays an important part in PCB research. Regulations worldwide have phased out PCBs, but monitoring and remediation efforts continue. Scientists turn to 4-CB to calibrate analytical instruments, simulate behavior during waste treatment, and set baseline reactivity in bioremediation. Our consistent product quality supports these goals, helping partners build defensible data for publications, audits, and policy recommendations.

    In synthetic organic chemistry, 4-CB triggers unique transformations when exposed to activated catalysts. For example, 4-CB acts as a preferred aryl halide in C–C coupling, fluorodechlorination, and production of bithiophenes. Chemical producers prefer this product because cleaner reactions cut downstream purification costs. We hear consistent feedback from chemists comparing side-by-side processes using different isomers—yields jump, and impurity profiles simplify when 4-CB enters the flask.

    The compound also serves as an intermediate in the custom synthesis of agrochemical and pharmaceutical templates. While downstream applications depend on project specifics, demand continues for high-purity, reproducible batches scaled to kilogram or pilot-scale orders. The feedback loop from customer trials to in-plant improvements drives us to refine purity levels and address trace contaminants, tied directly to new regulatory and market needs.

    Why Specifications Matter to Us

    Years on the manufacturing side have taught us that not all specifications hold equal weight. Customers with routine needs want reliability over laboratory-grade purity, so we refined our process for easy upscaling if tighter specs are needed down the line. Each production run includes multiple checkpoints, confirming melting point, GC retention time, and elemental analysis. These procedures save time and reduce headaches since small variances in melting point serve as early warnings for contamination or isomer misplacement.

    Quality is not a marketing buzzword in our shop. The absence of moisture, dust, and unintended isomers has measurable impacts for our clients—affecting both safety and operational cost in their own plants. Handling characteristics like blendability and thermal stability draw from our decades tweaking everything from solvent system selection to storage containers. Purity checks, conducted in-house, prevent downstream surprises.

    Discussions with partners show that both the regulatory and end-market context shape demand. Regulations such as REACH and TSCA put pressure on traceability, full documentation, and impurity profiling. We prepare batches traceable to raw material lots, maintaining complete records to back each shipment. This transparency isn’t just required—it reduces risk for all stakeholders and simplifies audits during transitions or scale-ups.

    Safety and Environmental Point of View

    While 4-Chlorobiphenyl does not fall under the strict control categories assigned to PCBs, we keep strict controls during the synthesis, purification, and packaging stages. Years of safe handling in our plant support our confidence in routine operations, though we never assume complete risk elimination. Handling protocols address both chemical safety and environmental precautions. Our team always conducts closed-system transfer and secondary containment to avoid airborne exposure and minimize environmental release.

    Our end users often work under strict environmental controls, prompted by both regulatory compliance and internal safety procedures. We help by providing detailed batch records, COAs including impurity breakdowns, and guidance from our in-house environmental health specialists. It’s not rare for clients doing application-specific toxicology or fieldwork to share lessons that make their way back into our standard procedures.

    Transportation and packaging design have evolved with customer feedback. We upgraded from standard fiber drums to high-integrity, electrostatically shielded vessels for some sectors, making sure product safety starts at the warehouse and continues through to the customer. Minimizing risk at every step defines our commitment to quality and public safety.

    Comparing 4-Chlorobiphenyl with Similar Products

    From a production standpoint, 4-Chlorobiphenyl stands out among its close relatives due to both customer demand and process reliability. Isomer positioning leads to differences not only in reactivity, but in storage and process losses. We receive requests for 2-, 3-, and 4-chlorobiphenyl isomers; our experience growing and maintaining crystals under controlled conditions shows that, while all three offer structural similarities, only 4-CB forms crystals with minimal occluded solvent or mechanical entrainment. This reliability translates to lower maintenance costs and reduced rework.

    Our in-plant teams have noticed that para substitution offers improved chemical stability, a higher resistance to hydrolysis during wet processing, and greater compatibility with both organic and organometallic reagents compared to the meta and ortho forms. These features bring reproducibility, letting researchers and process chemists plan multi-step syntheses with greater confidence. Product managers at client companies have reported fewer headaches scaling up from bench to pilot plant when starting with our 4-CB, precisely because these qualities hold steady in scaled equipment.

    Not all differences are purely chemical. Even packaging and long-term storage bring distinctions. Ortho- and meta-chloro isomers can lead to clumping or slow phase transitions as humidity fluctuates; para-4-CB, by contrast, preserves its free-flowing nature over long storage periods, slashing equipment downtime and the risk of cross-contamination.

    Feedback from end users highlights one more pronounced difference. Analytical chemists consistently report sharper, more reproducible peaks with our 4-Chlorobiphenyl during GC and HPLC workflows. We attribute this to our strict isomeric controls and rigorous solvent removal, which remain part of every batch. Environmental labs working on trace contaminant surveys rely on these properties for calibrations, trusting the reproducibility across year-long projects where reference standards must remain unchanged.

    Manufacturing Perspective: Challenges and Solutions

    Even with decades of steady production, challenges emerge. Chloroaromatic chemistry is never simple, and demand for higher purities or new regulatory limits brings continual adjustment. We’ve faced shifting expectations around trace PCB content, requiring us to adapt our distillation and column purification steps. Only by investing in new detection technology and quick in-plant feedback loops could we meet the evolving standards.

    Supply chain stability matters at every scale of operation. Global interruptions in precursors like biphenyl or specialty chlorine sources have forced us to diversify vendors, inspect raw materials more closely, and build buffer stocks to smooth sudden upswings in demand. Updates to our handling procedures, in cooperation with trusted suppliers, streamline incoming inspection and mitigate risk from off-spec input material.

    Partner feedback often redefines our priorities. If customers detect trace byproducts downstream, we return to raw data logs, microscope samples, and GC–MS profiles to ensure root causes are found and corrected. Commitment to these continuous improvement cycles has driven a steady increase in process robustness. Over time, production yields have grown, batch failures have shrunk, and the reliability of both technical and commercial relationships has strengthened.

    Human factors shape production just as much as process optimization. Training continuity, retention of experienced operators, and the involvement of on-the-floor personnel in troubleshooting distinguish our facility. The result shows up in greater batch reproducibility, fewer deviations, and better communication with long-standing clients.

    Experience with Diverse User Requirements

    Decades supplying academic and industrial customers have taught us to listen—sometimes the critical requirement springs from an unexpected end-use. Research groups working on pollutant fate modeling may require milligram quantities with ultra-tight impurity limits, while R&D operations in electronics demand large, repeatable kilo batches for pilot programs. Balancing these demands means variable production campaigns, dedicated cleaning protocols for line changes, and flexible sampling to address custom requirements.

    We keep records of customer feedback, bridging the knowledge gap between users in the field and production chemists on the line. These notes help shape new process controls, packaging upgrades, and communication methods—delivering practical value instead of generic claims. Our practice runs on evidence shared directly by users, whether from large multinational panels or small specialty labs.

    By supporting technical inquiries directly from our team (not through third parties), we cut time to delivery and solve problems quickly, building trust through practical engagement. This approach means the information we provide reflects real solutions—tested, refined, and put into practice from the plant floor.

    Looking Forward—Anticipating Change in the 4-Chlorobiphenyl Market

    The global landscape keeps shifting, whether through environmental policy, raw material availability, or technical innovation in downstream industries. Experience shows that plants producing 4-Chlorobiphenyl need not only chemical acumen but also flexibility and resilience. Staying ahead of regulatory scrutiny or technical obsolescence takes more than just running established processes—it requires engagement with the scientific, regulatory, and application communities shaping the next decade.

    New applications, such as sustainable electronics or analytic method validation, continue to grow. Demand for eco-friendlier derivatives, alternate production methods, and sustainable sourcing has begun to drive process development, pushing us toward greener chemistry and waste minimization initiatives. We invest in process simulation, pilot-scale testing, and real-time monitoring of environmental discharges— efforts that prove their value as industries demand better transparency and accountability.

    The environment for 4-Chlorobiphenyl production will only become more competitive and technically challenging. We believe that continuous dialogue with those who use our products forms the strongest bedrock for lasting quality and innovation. Through partnerships, transparent operations, and technical willingness to adapt, we keep ahead of shifting expectations while building lasting trust.

    Summary Reflections

    Seeing 4-Chlorobiphenyl through the lens of a chemical manufacturer reveals the daily decisions, continual improvements, and tight quality controls that define reliable production. Years of experience, direct customer feedback, and technical refinement have shaped our approach to making and serving this compound. Real-world application, scientific rigor, and practical engagement with stakeholders prove more useful than any abstract claim. We remain committed to safe, precise, and transparent production, prepared to meet future demands and support the innovative work our partners, researchers, and clients pursue.

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