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1,4-Dibromobenzene

    • Product Name 1,4-Dibromobenzene
    • Alias p-Dibromobenzene
    • Einecs 204-276-9
    • 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

    746406

    Chemicalname 1,4-Dibromobenzene
    Casnumber 106-37-6
    Molecularformula C6H4Br2
    Molarmass 235.90 g/mol
    Appearance White crystalline solid
    Meltingpoint 87 °C
    Boilingpoint 220 °C
    Density 1.86 g/cm3
    Solubilityinwater Insoluble
    Odor Aromatic
    Refractiveindex 1.613
    Flashpoint N/A (decomposes)
    Vaporpressure 0.12 mmHg at 25 °C
    Pubchemcid 7240

    As an accredited 1,4-Dibromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,4-Dibromobenzene is packaged in a 250g amber glass bottle with a tightly sealed cap and hazard warning labels.
    Shipping 1,4-Dibromobenzene should be shipped in tightly sealed containers made of compatible materials, protected from heat and direct sunlight. It is classified as regulated for transport and must be properly labeled according to hazardous materials regulations. Avoid inhalation and contact. Follow all local and international shipping, handling, and storage protocols for dangerous goods.
    Storage 1,4-Dibromobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Store at room temperature and label clearly. Follow all relevant safety guidelines and local regulations for storage of hazardous chemicals.
    Application of 1,4-Dibromobenzene

    Applications of 1,4-Dibromobenzene in Industrial Manufacturing

    1,4-Dibromobenzene has established its position as a specialty intermediate across several chemical industries due to its dual bromine functionality and aromatic stability. As an original manufacturer, we supply this material for direct use by formulators and processors in specialized downstream sectors, supporting stringent compliance demands and repeatable large-scale synthesis.

    1. Advanced Agrochemical Synthesis

    Major pesticide and herbicide formulators rely on this compound as a key starting material for the construction of complex brominated intermediates. Its high purity and predictable reactivity are favored in targeted substitution reactions for aryl-branched biocidal structures, supporting batch and continuous processes within regulated agrochemical manufacturing environments.

    Industry compliance standards

    • EPA TSCA Inventory (US)
    • REACH (EC 1907/2006)
    • China IECSC
    • ISO 9001:2015 (Quality Management for Agrochemical Manufacturing)

    Typical usage ratio

    • 0.15–0.28 molar equivalents relative to final active ingredient; adjusted based on targeted molecular substitutions and purity of crop-protection agent.

    Downstream process integration

    • Chlorination and coupling for brominated aryl anilines in pre-plant and post-harvest pesticide synthesis.
    • Reactant feed in bromination steps for pre-emergent herbicides.

    Final product types

    • Selective herbicide intermediates (aryl bromide-based)
    • Pyridine-containing insecticides
    • Fungicidal agents for cereal and soy crops

    2. Pharmaceutical API Intermediate Formation

    The material serves pharmaceutical manufacturers as a precise building block in the multi-step synthesis of select active pharmaceutical ingredients. It supports the installation of brominated aromatic groups essential for novel APIs with antimycobacterial, anticancer, and CNS-modulating activity. Controlled release and reproducibility are critical due to GMP oversight in the pharmaceutical supply chain.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP <467> Residual Solvents Testing (where applicable)
    • EDQM CEP Submission (Europe)
    • 21 CFR 211 (US cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.11–0.23 molar equivalents based on targeted coupling efficiency for aryl-bromine installation, balanced for batch or flow synthesis scales.

    Downstream process integration

    • Suzuki or Buchwald–Hartwig coupling for preparation of biaryl pharmaceutical scaffolds.
    • Bromoarene insertion in the penultimate or pre-penultimate synthetic step for advanced intermediates.

    Final product types

    • Quinoline and isoquinoline-based APIs
    • Halogenated CNS therapeutics
    • Precursors for radiolabeled imaging drugs

    3. Liquid Crystal Material Synthesis for Electronics

    OLED and liquid crystal display producers use this raw material for synthesizing highly ordered, poly-brominated aromatic compounds needed in organoelectronic layers. Material consistency across lots and processability into higher-value monomers or dimers are essential for downstream device performance and regulatory approval of consumer display products.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU)
    • IEC 62474 (Material Declaration for Electronic Industry)
    • JPCA-ES-01 (Japan Printed Circuit Association Environmental Standard)
    • ISO 14001:2015 (Environmental Management in electronics manufacturing)

    Typical usage ratio

    • 5–18 wt% in precursor blends, with ratio determined by desired liquid crystalline mesogen length and degree of polymerization.

    Downstream process integration

    • Reactant charge for Grignard-type synthesis of pivotal liquid crystal rod-like molecules.
    • Precursor in high-temperature etherification and C–C coupling steps within custom monomer plants.

    Final product types

    • LCD and OLED panel intermediate monomers
    • Polyarylate-based display films
    • High-performance color filter additives

    4. Engineering Polymer Additive Manufacturing

    Producers of high-temperature performance polymers, particularly those in automotive and electronics sectors, use this compound for introducing aromatic bromine groups to boost flame retardancy and chemical resistance. Reliable supply and tight specification adherence support reproducible polymerization outcomes vital for end-customer acceptance and regulatory certification.

    Industry compliance standards

    • UL 94 (Flammability Standard for Plastics)
    • EN 14582 (Determination of Halogens in Polymers)
    • ISO 1043-4 (Plastics — Symbols and abbreviated terms — Part 4: Flame retardants)
    • RoHS Annex II (Brominated compounds for electrical products)

    Typical usage ratio

    • 3–13 wt% relative to total polymer mass, optimized after flame retardant testing in end-use substrates such as polyesters and polyamides.

    Downstream process integration

    • Direct feed in melt-polycondensation reactors for brominated poly(phenylene ether) synthesis.
    • Copolymerization blending for high-performance plastics with specified V-0 or V-1 rating targets.

    Final product types

    • Electrical enclosure housings
    • Automotive under-hood molded parts
    • Printed circuit board resins

    5. Dye and Pigment Intermediate Production

    Dye and pigment manufacturers utilize this compound for downstream bromination, facilitating color tuning and fastness improvements. The controlled halogenation supports the tailored synthesis of specialty pigments and drum-dyed fibers for demanding textile and industrial coloring applications.

    Industry compliance standards

    • GOTS (Global Organic Textile Standard) - applicable for certified dye intermediates
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 105-C06 (Textiles — Color Fastness to Domestic and Commercial Laundering)
    • OEKO-TEX Standard 100 (Textile Sustainability Assurance)

    Typical usage ratio

    • 0.07–0.21 molar equivalents in aryl bromination steps, percentage depends on target chromophore and batch synthesis scale.

    Downstream process integration

    • Initial halogenated coupling for azo or anthraquinone dye core modification.
    • Feed for vat dye synthesis and pigment condensation processes.

    Final product types

    • Reactive textile dyes
    • High-stability pigments for plastic and coating applications
    • Bright fastness dyes for industrial yarn
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    Certification & Compliance
    More Introduction

    Understanding 1,4-Dibromobenzene: More Than Just a Raw Material

    1,4-Dibromobenzene has established itself as an essential compound for a wide range of industries, from pharmaceuticals to specialty chemicals. Recognized for its chemical structure—a benzene ring substituted with two bromine atoms at the para positions—this solid, white crystalline powder holds far more value than its simple formula might suggest. The world of organic synthesis would feel a noticeable gap without this compound’s role in halogenation reactions and as a building block for more complex molecules. In the lab and on the factory floor, the physical traits like melting point and solubility in organic solvents pull equal weight alongside chemical reactivity. Its ability to act both as an intermediate and as a functional additive keeps it relevant even as industry demands evolve.

    From Basic Chemistry to Real-World Impact

    Over the past two decades, demand for halogenated benzene derivatives has shifted sharply. Rising standards in pharmaceutical manufacturing and the constant push for novel materials have many labs keeping 1,4-dibromobenzene on their shelves. Its key trait lies in the placement of its two bromine atoms, which aren’t just structural: the para orientation makes it especially useful for synthesizing complex organic compounds. I remember my first introduction to halogenated benzenes during college organic labs. The difference a small change in substitution makes on reactivity and product outcome always stood out to me. In today’s industrial chemistry setting, that difference translates into efficiency, selectivity, and sometimes significant cost savings.

    1,4-Dibromobenzene finds itself used in the manufacture of dyes, agrochemical intermediates, and, increasingly, advanced polymers that require well-defined halogen patterns. These industries prize reproducibility and clarity in chemical processes. The compound’s crystalline purity allows researchers to better isolate variables when developing new synthetic routes. Forget the image of chemistry as a guessing game—working with well-characterized reagents like this means predictable results and fewer surprises in yield or purity.

    The Specifics: Physical and Chemical Characteristics Matter

    The details mean everything in chemical manufacturing, and 1,4-dibromobenzene is no exception. Its melting point, which sits right around 87 degrees Celsius, turns out to be an asset. This temperature makes it easy to handle as both a solid and a melt, useful when casting or blending. Its molecular weight influences how it’s measured and manipulated in synthesis, while its solubility in organic solvents like ethanol or ether streamlines purification. A well-placed bromine atom isn’t just a theoretical talking point—it directly impacts reactivity in coupling reactions or Grignard reagent formation. Every synthetic chemist I’ve met values reagents that behave as predicted, and this compound rarely disappoints.

    Comparing 1,4-dibromobenzene with its relatives—such as 1,2- or 1,3-dibromobenzene—highlights its strengths. Ortho and meta isomers bring their own quirks in boiling point and reactivity, which can affect performance in polymer synthesis or dye manufacture. For example, ortho-derivatives sometimes suffer from steric hindrance, making reactions sluggish or incomplete. That sort of bottleneck can waste time and resources. Paring down inefficiencies matters, whether you’re tinkering at bench scale or mixing tons in an industrial reactor.

    Why Precision in Specification Drives Results

    Purity remains king in specialty chemistry. Most suppliers offer 1,4-dibromobenzene at a minimum purity of 99 percent, since even trace contaminants can complicate downstream processes, especially in pharmacological applications. Now, anyone with lab experience knows the headaches that “just good enough” raw materials can cause—ghost bands on chromatography, weird peaks on NMR, or low product yields that can’t be explained away. Years ago, I encountered a batch of lower-grade material while developing a synthetic route for a medicinal chemistry project. The difference was obvious—not only did reactions proceed unpredictably, but it took extra steps to remove unwanted byproducts. Ever since that lesson, I’ve cared less about price and more about the assurance that each batch lives up to its spec sheet.

    Careful control over physical characteristics, like crystal size and melting behavior, makes a real difference in production lines. In high-throughput manufacturing, consistency means more than convenience: it’s the linchpin that keeps scales tipped toward profitability. For those developing new drug candidates or specialty plastics, even minor changes in the input material can derail months of work.

    Safe Handling Reflects Responsible Chemistry

    Every substance comes with its quirks and risks, and 1,4-dibromobenzene deserves the respect anyone would give an industrial chemical. Its volatile organic nature calls for well-ventilated storage and serious attention to containment. Those faintly sweet, aromatic fumes can lead to headaches or, with enough exposure, irritate the respiratory tract. Gloves and goggles aren’t just window dressing—they mean fewer long nights spent dealing with chemical burns or missed shifts due to minor mishaps. From my own time in synthesis labs, I can vouch that cutting corners on safety only leads to more paperwork and less productive time in the lab.

    Beyond the walls of chemistry buildings, communities have become far more vocal about how chemical plants operate and what escapes into the atmosphere. Attention is turning toward how substances like 1,4-dibromobenzene are stored, transported, and disposed of. With more emphasis on green chemistry, responsible practitioners have begun to incorporate closed-loop systems and emission controls, limiting potential risks for both workers and the general public. It’s not just the right thing to do; tighter controls often line up with regulatory requirements and open the door for new applications that might have been closed by safety concerns in the past.

    Industry Demands Change—So Does Supply

    One thing you learn over years in chemical R&D is that market demand drives everything, from the smallest research labs to the most sprawling chemical conglomerates. The push for high-performance plastics, better herbicides, or more precise dyes starts with raw materials that can walk the tightrope of purity and reactivity. 1,4-Dibromobenzene often finds itself at the crossroads of these trends. No one wants to start a scale-up campaign only to discover that critical input suffers from erratic supply or inconsistency.

    Global logistics networks, especially after the turbulence of recent years, play a big role in how easily manufacturers can get what they need. Companies that once sourced locally have dealt with delays, price spikes, or unexpected shortages. Those with a deeper bench of suppliers or alternate routes for raw materials tended to weather storms better. A compound like 1,4-dibromobenzene—clearly defined, widely used, but never immune to disruption—cuts to the core of debates about resilience in manufacturing supply chains.

    Some companies have started investing in back-integration, refining their own intermediates instead of relying on a handful of global producers. This vertical integration not only boosts their ability to ensure consistency, but it can help control costs, manage waste streams, and satisfy increasingly complex regulatory expectations. The decision isn’t always straightforward; balancing capital investments against short-term needs takes nuanced judgment and a clear sense for market demand.

    From Reaction Flask to Finished Product: Versatility at Its Core

    Few chemicals wear as many hats as 1,4-dibromobenzene. Its use as a brominating agent in organic synthesis is well-documented, but limiting the discussion to lab reactions misses the bigger picture. In polymer science, this compound helps tailor molecular weights and end group structures, affecting characteristics like flexibility and thermal resistance in finished materials. I worked briefly for a startup developing specialty films—switching from a lower-halogen to a para-dibromo feedstock cut our defect rates in half and simplified our quality control process.

    In pharmaceuticals, para-dibromo derivatives act as stepping stones for active drug molecules, influencing both yield and purification complexity in multistep syntheses. Crop sciences have also seen gains from brominated benzene intermediates, which appear in both established and next-generation agrochemicals. The consistent reactivity and cleanliness of reaction byproducts can mean the difference between a product passing stringent regulatory scrutiny or not.

    Peer for Peer: How 1,4-Dibromobenzene Differs From Related Products

    Many folks new to chemical supply wonder why different isomers—like 1,2- and 1,3-dibromobenzene—aren’t interchangeable. The answer comes down to reaction specificity. In Suzuki coupling, for instance, the para orientation of 1,4-dibromobenzene helps direct product formation in a way the meta or ortho forms cannot. That difference shapes the selectivity and, sometimes, the safety profile of the finished product. Ortho derivatives often bring more complicated product mixtures, requiring extra purification that can stretch both time and materials budgets.

    Other competitors, like monobrominated benzenes or heavier halogenated versions, offer their own sets of reactivity patterns. For certain high-molecular-weight polymerizations, the extra bromine atoms in tribromobenzenes might seem appealing. In reality, more isn’t always better—over-brominated compounds tend to be heavier, more expensive to handle, and prone to forming unwanted side products. Most process engineers I’ve worked with appreciate reagents that keep surprises to a minimum. For predictable outcomes and clear byproduct profiles, para-dibromo often wins the day.

    Sourcing and Sustainability Raises New Questions

    Attitudes toward chemical sourcing have shifted alongside wider societal concerns about safety and environmental impact. The last decade brought a surge in demand for sustainable routes of chemical production, and 1,4-dibromobenzene has not escaped scrutiny. New catalytic approaches, sometimes involving less hazardous or more renewable bromine sources, continue to undergo development. Promising alternatives have surfaced, such as flow chemistry setups that reduce waste and minimize human error by automating intermediate handling.

    Beyond technical tweaks, more suppliers have turned to life cycle analysis to get a fuller picture of this compound’s journey from feedstock to finished consumer product. Reducing the environmental burden doesn’t always grab headlines but makes a significant difference in the long run. From responsible waste management to lower emissions during production, even incremental improvements matter. Users casting a critical eye toward each step in the chemical supply chain help raise the bar for everyone.

    What the Future Holds: Innovation, Regulation, and Demand

    The intersection of innovation and regulation continues to set the stage for how 1,4-dibromobenzene is used, shipped, and ultimately disposed of. New guidelines from both local and international agencies increasingly call for cleaner processing, tighter emissions controls, and better worker protection. Many in industry see these changes not as hurdles but as chances to refine longstanding processes. For every new restriction, smart operations find creative solutions—be it safer packaging for storage, advances in reactor design, or updated protocols for handling and disposal.

    Advances in analytical instrumentation, like real-time NMR or inline HPLC sampling, have simplified quality control. Consistently high standards let processing plants move faster from incoming raw material to clean, well-documented finished product. Buyers in pharmaceutical and specialty chemical sectors have grown less tolerant of vague provenance; full batch traceability is becoming the norm, not the exception. Suppliers who step up with transparent records and better customer support tend to see more repeat business.

    Researchers exploring new applications for halogenated aromatics often circle back to well-characterized reagents as their foundation. Recent developments in organic electronics, for example, show promise when using halogenated conjugated systems—areas where 1,4-dibromobenzene fits in naturally. Its symmetrical structure and predictable electron distribution allow engineers to build up complex architectures for semiconductors or photovoltaic materials. Not every groundbreaking invention makes the news, but progress marches forward on the shoulders of dependable building blocks.

    Lessons From the Field: What Experience Teaches

    Working with a staple like 1,4-dibromobenzene teaches the value of dependability. You soon learn that small lapses—an impurity left unchecked, inconsistent crystal habits, lack of documentation—create ripple effects. Imagine scaling up a promising lab procedure, only to spend months troubleshooting side reactions caused by a reagent that quietly slips out of specification. In my own career, the difference between frustration and success often came down to picking suppliers who valued integrity, communication, and rigorous batch testing.

    Peer-reviewed literature keeps reinforcing the lesson: reproducibility starts with the inputs. Recent surveys in synthetic chemistry echo the headaches that arise when switching suppliers or encountering unexpected shifts in manufacturing routes. The global marketplace introduces strengths—better pricing, wider access—but also real headaches if consistency isn’t baked in at every step.

    Better Chemistry Comes From Informed Choices

    Whether making new medicines, refining specialty dyes, or forging stronger plastics, those at the bench rely on more than textbook knowledge. Choices about raw materials set the trajectory for what’s possible. 1,4-Dibromobenzene, with its straightforward properties and reliable reactivity, gives chemists, engineers, and product developers a running start.

    By championing higher standards in sourcing, insisting on full transparency from suppliers, and staying alert to regulatory shifts, users of this compound stake out a stronger position in a competitive market. The real competitive edge doesn’t come from racing to the lowest price or turning a blind eye to environmental impact—it comes from foresight, experience, and a willingness to demand more from the basics. Whether in academic experimentation or high-volume production, the lessons hold: quality input creates quality output.

    Looking Ahead: Opportunity for Progress

    Change in chemistry rarely happens by accident. Improvements emerge when users question established routines and push supply chains to keep up with evolving standards. The story of 1,4-dibromobenzene is hardly static; every year brings fresh developments—whether new reaction applications, advances in process safety, or tighter environmental regulations. Those who engage with the material closely, lean into collaboration, and share best practices are the ones who will seize new possibilities.

    At a glance, this compound might seem like just one ingredient among many. Peer beneath that surface, though, and you’ll find a nexus of expertise, innovation, and experience, all converging on the drive for better results and safer, cleaner operations. Users who ask hard questions about process, provenance, and performance elevate not just their own work but the wider industry, setting standards that others will follow.