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2-Bromo-1,4-Dichlorobenzene

    • Product Name 2-Bromo-1,4-Dichlorobenzene
    • Alias p-Bromodichlorobenzene
    • Einecs 221-053-2
    • 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

    519629

    Chemical Name 2-Bromo-1,4-dichlorobenzene
    Molecular Formula C6H3BrCl2
    Molecular Weight 240.90 g/mol
    Cas Number 7516-37-0
    Appearance White to off-white solid
    Melting Point 49-52°C
    Boiling Point 262°C
    Density 1.82 g/cm³
    Solubility In Water Insoluble
    Flash Point 113°C
    Smiles C1=CC(=C(C=C1Cl)Br)Cl
    Refractive Index 1.595
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place

    As an accredited 2-Bromo-1,4-Dichlorobenzene 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 2-Bromo-1,4-Dichlorobenzene, tightly sealed with a screw cap, labeled with hazard warnings.
    Shipping 2-Bromo-1,4-Dichlorobenzene should be shipped in tightly sealed containers, compliant with local and international regulations. It must be packed to prevent leaks and exposure, labeled appropriately as a hazardous chemical, and protected from heat and physical damage. Transport should follow hazardous materials guidelines, ensuring safe handling and delivery.
    Storage 2-Bromo-1,4-dichlorobenzene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat sources, direct sunlight, and incompatible substances such as strong oxidizers. Keep the chemical away from moisture and ignition sources. Use appropriate chemical-resistant storage cabinets and ensure containers are clearly labeled to prevent accidental exposure or misuse.
    Application of 2-Bromo-1,4-Dichlorobenzene

    Applications of 2-Bromo-1,4-Dichlorobenzene in Industrial Manufacturing

    As a direct manufacturer of 2-Bromo-1,4-Dichlorobenzene, we supply high-purity material for specialized industrial sectors. The compound supports advanced synthesis and strict quality requirements in regulated markets. Below, we detail key application pathways with compliance, formulation, production, and end-product specifics.

    1. Agrochemical Intermediate Synthesis

    Global agrochemical producers use this material as a halogenated precursor for building selective herbicides and fungicidal actives. It introduces specific functionality in stepwise coupling or substitution reactions, enabling the formation of target molecules with improved bioactivity and environmental behavior. Strict traceability and ingredient control form a core part of the supply chain due to regulatory scrutiny. The usage level adjusts depending on desired reactivity with downstream reagents, requiring close process monitoring and documentation.

    Industry compliance standards

    • REACH registration (EU)
    • 40 CFR Part 720 (US EPA PMN)
    • ISO 9001:2015 for traceability
    • China Pesticide Registration Regulation (ICAMA)

    Typical usage ratio

    • 5%–18% by weight in targeted halogenation steps, depending on the synthetic route and the type of crop protection molecule

    Downstream process integration

    • Charged at stage 2–4 of multi-step synthesis for acylanilides or substituted benzene-based actives

    Final product types

    • Selective herbicides (acetamide class)
    • Seed treatment fungicides
    • Intermediate key blocks for post-patent formulations
    • Custom research actives for field trials

    2. Pharmaceutical and Fine Chemical Building Block

    Pharma-grade manufacturers use this compound to introduce brominated and chlorinated sites for API intermediates and specialty drug building blocks, especially in oncology and anti-infective R&D. The compound enables controlled site-selective reactions under cGMP conditions with full batch traceability. Downstream integration often involves Suzuki or Buchwald couplings, and purification may require additional chromatographic steps. End users demand analytical documentation to meet regulatory inspections and robust quality management requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • USP/NF reference monographs (as applicable for intermediates)
    • EU GMP Vol. 4 Part II (Active Substances)
    • ICH Q3A/B: Impurities management

    Typical usage ratio

    • 2%–12% by mass, based on the specific API intermediate and the degree of substitution required in the medicinal scaffold

    Downstream process integration

    • Early-stage intermediate preparation, granulation or solution-phase coupling reactions, typically under cGMP in reactors with validated cleaning protocols

    Final product types

    • Brominated pharmaceutical intermediates
    • Precursors for oncology APIs
    • Batch samples for preclinical studies
    • High-purity fine chemicals supporting drug discovery programs

    3. Specialty Dye and Pigment Manufacture

    Pigment and dye producers apply this halogenated benzene for coupling and condensation reactions to produce high-performance organic pigments. It offers controlled electron-withdrawing effects critical for producing stable azo and anthraquinone-based colorants. The compound is primarily charged in batch reactors aligned with standardized color shade reproducibility requirements and must meet impurity controls specified by downstream textile or plastics customers. Batch documentation and compliance with ecolabeling standards remain essential in this sector.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Appendix 6 (textile applications)
    • ZDHC MRSL conformance (Zero Discharge Hazardous Chemicals)
    • ISO 9001:2015 for colorant manufacturing traceability
    • EU REACH Annex XVII (restricted substances)

    Typical usage ratio

    • 7%–15% in synthesis cocktails for target pigment molecules; exact dose depends on shade and purity required

    Downstream process integration

    • Key reactant in boiler reactors during primary chromophore assembly; followed by purification and finishing to customer technical grade

    Final product types

    • Solvent-stable organic pigments for plastics
    • High-lightfastness textile dyes
    • Special colorants for high-end inkjet applications
    • Masterbatch concentrates for fiber spinning

    4. Electronic and Liquid Crystal Material Production

    Leading electronics and display material manufacturers use this compound for the synthesis of substituted aromatic intermediates, which are essential in liquid crystal monomer and dielectric material production. Its dual halogenation pattern allows for controlled reactivity and specific physical properties, including dielectric constant and thermal stability in final materials. The compound must meet targeted electronic grade impurity specifications. Downstream customers require batch consistency with full analytical documentation, especially for safety and environmental controls in East Asian regulatory contexts.

    Industry compliance standards

    • IEC 61249-2-21: Halogen content limits (electronics)
    • RoHS Directive (EU, restricted hazardous substances)
    • ISO 14001:2015 Environmental Management
    • Chinese GB/T 26572 for hazardous material limits in electronics

    Typical usage ratio

    • 3%–10% in targeted monomer synthesis for downstream LCM (liquid crystal monomer) and precursor assemblies

    Downstream process integration

    • Added at core aromatic coupling steps for tailored substitution; typically processed in clean-room-grade reactors under tight environmental monitoring

    Final product types

    • Liquid crystal monomers for TFT LCD panels
    • Dielectric precursors for advanced semiconductor materials
    • Specialty photoresist intermediates
    • Functional coatings for OLED displays

    5. Polymer Modifier and Engineering Plastics Additive

    Producers of flame-retardant and specialty engineering plastics use this compound as a reactive additive to introduce bromine and chlorine into polymer backbones or to serve as a monomer unit for higher performance characteristics. Inclusion at polymerization or compounding stages offers enhanced flame resistance and supports regulatory compliance for electrical and construction materials. Manufacturers require batch-to-batch uniformity for safe integration, and the compound’s impurity profile must align with downstream certification and environmental requirements.

    Industry compliance standards

    • UL 94 (Flammability of plastic materials)
    • EN 14582 (Halogen content in polymers)
    • RoHS Directive and REACH compliance (electronics and E&E plastics)
    • IEC 60695-2-11 (Glow-wire flammability)

    Typical usage ratio

    • 2%–10% by polymer matrix weight, depending on target flame-retardancy class and base resin type (e.g., ABS, HIPS, PC blends)

    Downstream process integration

    • Fed into high-shear melt-compounding extruders as a masterbatch or directly into polymerization vessels; integrated during pre-blending for consistent dispersion

    Final product types

    • Flame-retardant ABS for electrical devices
    • Halogenated engineering thermoplastics for transportation parts
    • Polymer blend masterbatches for cable sheathing
    • Specialty molded housing components for electronic assemblies
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-1,4-Dichlorobenzene: Experience in Synthesis and Application

    Overview

    Synthesizing 2-Bromo-1,4-dichlorobenzene has been part of our production routine for more than two decades. As a chemical manufacturer, nothing compares to the satisfaction that comes from seeing the results of a well-controlled halogenation process, with pure white crystalline powder collected at the final stage. This compound has earned a reputation in specialty chemistry due to its clean reactivity and reliable structure. Here, we share our perspective on producing and working with this aromatic halide, the model types most in demand, and the differences that matter most for users in critical applications.

    Molecular Structure and Characteristics

    The molecular formula C6H3BrCl2, with a precise bromine and chlorine arrangement on the benzene ring, makes this compound a standout among halogenated aromatics. The chemistry at positions 1, 2, and 4 justifies the compound’s popularity for further functionalization. We respect how a well-aligned halogen pattern can open up unique synthetic routes; that's why attention to isomeric purity remains a recurring discussion among both our technicians and the chemists who order from us.

    We don't chase after every new formula that emerges from academic papers. Continuous feedback from commercial users, pharmaceutical developers, and materials scientists remains at the core of our process improvements. This is the backbone of why the melting point, moisture content, and residual solvent levels become more than numbers on a specification sheet—they become a testament to consistent synthesis and a sign that our team understands how downstream applications work.

    Model and Specifications

    Based on practical workflow, we typically produce 2-Bromo-1,4-dichlorobenzene as an off-white to white crystalline powder, delivering high purity models—over 99% by GC and frequently confirmed by HPLC. The melting range holds steady between 55°C and 58°C, a temperature window that aligns with textbook values and gives insight into batch quality and crystal integrity. Each batch runs through meticulous drying, leaving moisture content under 0.2%. Impurity levels, including related chloro- and bromo-derivatives, receive close attention. These trace analyses ensure the product will not introduce surprises in follow-up synthesis, especially in research arms where one wrong impurity can stall the entire process.

    We once tested a new purification column, only to find that the secondary halide contaminants—though reduced to a few hundred parts per million—altered the reactivity in a downstream Suzuki coupling. The lesson for us: pursuing lower impurity does not end at equipment upgrades. It happens with hands-on production monitoring and knowing how those details matter to our partners using the product in pilot or commercial synthesis.

    Production Approach: Batch-to-Batch Consistency

    Scale matters. It is easy to run a kilogram batch in a research setting, but translating that same purity level up to a metric ton challenges every process step. We do not believe in shortcuts when it comes to bromination. Side reactions, such as polybromination or uncontrolled chlorination, can slip in during large-scale runs. We mitigate these risks by sticking with time-tested glass-lined reactors and a team who has stood alongside us for years, not by pushing new hires straight onto the night shift.

    Many buyers ask us about the reproducibility of the product if they move from a sample jar to a full drum. The view from our factory floor supports the claim: controlling reagent addition rates, agitation speeds, and quench temperatures remains the only way to keep batch profiles predictable. If one batch starts drifting—identified by a melting point dropping below 54°C or an increase in GC-signal from off-target isomers—we halt, troubleshoot, and rerun before ever letting it near the shipping dock.

    Application Insights: Where 2-Bromo-1,4-Dichlorobenzene Makes a Difference

    Usage patterns keep evolving. Traditionally, this molecule finds a home as an intermediate in synthesizing pharmaceuticals, specialty polymers, and electronic materials—especially those needing halogenated precursors with robust regioselectivity. Medicinal chemists have used it to build complex bioactive compounds, while polymer specialists value it for introducing stability and targeted reactivity in specialty polymers.

    One project stands out: a customer in the OLED field pushed our product into a new domain, leveraging the ortho-bromo group for a cross-coupling sequence. Minute differences in halide arrangement—compared to 3-bromo or 2,5-dichloro analogues—meant every impurity counted. Our clean product profile gave their catalyst system the breathing room needed to reach target yields, ultimately speeding up their prototyping schedule.

    Not all chlorobromobenzenes behave the same. The 2-bromo group reacts more predictably in palladium-catalyzed reactions compared to other isomers. Taking the time to control isomeric content and minimize over-chlorination provides the difference between a reagent that helps discovery and one that frustrates it.

    Differences from Related Products

    Some customers initially think all chlorobromo benzenes look alike, and that one can simply swap material in most syntheses. Years of process experience say otherwise. 2-Bromo-1,4-dichlorobenzene brings two chlorine atoms, spaced para from each other, and a single bromine at the ortho position. This arrangement blocks some electrophilic substitutions, guides selectivity in cross-couplings, and can affect melting point or solubility compared to, say, 2-bromo-1,3-dichlorobenzene or 4-bromo-1,2-dichlorobenzene.

    During early customer visits, we fielded many queries about why 2,4-dichlorobromobenzenes from different factories showed inconsistent performance. After a deep dive, the culprit always turns out to be either unreacted starting material, non-target isomers, or excessive over-halogenation. Color alone provides a visual hint—impure material darkens after months, and subtle off-odors can clue you in to deeper problems.

    From a regulatory side, we remain vigilant about trace contaminants and solvent carryover. Halogenated aromatics attract scrutiny—regulatory submissions for pharmaceutical applications often bring up questions about specific process-related impurities. As a manufacturer, we appreciate a transparent paper trail, full batch-by-batch analysis sheets, and confirmation that each lot exceeds expectations regarding purity and trace elements. Product traceability means less troubleshooting down the line in scale-up or regulatory inspections.

    Handling and Storage: From Factory to User

    From the moment 2-Bromo-1,4-dichlorobenzene leaves our crystallization tank, minimizing exposure to air and light keeps the product stable for months, even in open storage drums. Our team lines each container with polyethylene and uses vacuum sealing to push oxygen out. No batch leaves with surface moisture or dust, which would affect stability during shipping or downstream use. Handling this chemical without proper PPE or training risks worker exposure, so every drum we send moves with supporting safety data and practical handling advice.

    We've seen storage mishaps at some customer sites, with product stored near steam lines or in unventilated rooms. The results: caking, yellowing, or cross-contamination. To avoid spoilage, storage below 30°C in a dry, shaded place always pays off. Logistics teams know that small errors in storage add up, spoiling hundreds of kilos of valuable product and setting back projects by weeks.

    Troubleshooting Batch Quality: Real-World Lessons

    No batch runs perfectly every time. We have poured over HPLC traces searching for elusive peaks after a worker swapped a reagent drum. In one case, trace iron contamination from a worn stirrer caused discolored crystals—identifying and replacing equipment took days, but that batch never left the factory. Sharing these stories with partners helps illustrate that product reliability doesn't just spring from good intentions but from years of diligence, maintenance, and honest reporting.

    Beyond equipment fault, we found that water ingress during monsoon months sharply increased hydrolyzed byproducts. The solution came from double-checking all seals and running regular Karl Fischer titration checks, not from blaming weather alone. Troubleshooting means listening to frontline staff who notice off-odors, cloudiness, or bottle cap damage before a spectrometer can.

    Supporting Customers: Beyond Selling a Commodity

    Our role extends beyond shipping out drums of material. Each customer inquiry, complaint, or suggestion returns full-circle into our quality improvement cycle. We open our doors to auditors, send technical representatives to observe pilot runs, and remain available for troubleshooting by phone or video call.

    Plenty of distributors promise the lowest price or fastest delivery, but only manufacturers who understand the quirks of their own process can stand behind batch consistency. Standing in front of the reactor, hearing the solvent boiling off, smelling the faint notes of halogen, it becomes clear—this isn't just a transaction.

    We work alongside those designing new molecules, validating new routes for generics, or scaling up specialty polymers. For us, the value comes from knowing how each drum of 2-Bromo-1,4-dichlorobenzene will enable those breakthroughs, reduce rerun costs, and keep ambitious research timelines on track.

    Looking Forward: Demand, Innovation, and Sustainability

    Demand for halogenated aromatics grows in tandem with high-end electronics, advanced materials, and pharmaceutical R&D. As new environmental regulations target halogen content and disposal, pressure mounts on manufacturers to minimize waste, optimize yields, and invest in greener alternatives.

    We meet this challenge head-on. Changing from high-chlorine solvents to low-toxicity replacements slashes the chemical footprint. Capturing vented gases for reprocessing, not just flaring, brings costs down and keeps our workflows sustainable. As halogen chemistry evolves, our R&D arm continually searches for catalyst systems that cut side-product formation and make post-reaction cleanups less demanding on both worker safety and environmental health.

    Our customers rightly demand more: better documentation, tighter purity specs, lower residual solvents, and more answers about supply-chain stewardship. By staying transparent, training new operators to the same standards upheld for years, and investing in measuring technology that keeps up with changing regulations, we run a production facility that answers these shifts directly.

    Your Partner in Halogenated Aromatic Chemistry

    Anyone with a credit card can source basic chemicals online. The difference is clear to those who use these materials every day in demanding applications where failure isn't an option. 2-Bromo-1,4-dichlorobenzene stands as a testament to careful synthesis, accumulated know-how, and an ongoing dialogue between producer and user.

    We invite partners who value stability, purity, and problem-solving guidance. Our track record proves that every batch tells a story—of process improvements, tough lessons learned, partnerships built, and the kind of technical confidence that only comes from manufacturing, not trading. Reach out to us; experience what decades of focused production, customer-centered adaptation, and straight talk can deliver for your next phase of innovation.