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2,5-Dibromobenzotrifluoride

    • Product Name 2,5-Dibromobenzotrifluoride
    • Alias 2,5-Dibromo-1-(trifluoromethyl)benzene
    • Einecs 216-857-6
    • 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

    693125

    Cas Number 328-75-6
    Molecular Formula C7H3Br2F3
    Molecular Weight 319.90 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 208-211 °C
    Melting Point -8 °C
    Density 1.86 g/cm3 (20 °C)
    Refractive Index 1.552
    Flash Point 93 °C
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Synonyms 2,5-Dibromo-1-(trifluoromethyl)benzene

    As an accredited 2,5-Dibromobenzotrifluoride 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 250 grams of 2,5-Dibromobenzotrifluoride, labeled with hazard symbols and detailed chemical information.
    Shipping 2,5-Dibromobenzotrifluoride is typically shipped in sealed, chemical-resistant containers, clearly labeled with relevant hazard information. It is classified as a hazardous material due to its potential health and environmental risks. Transport must comply with international regulations (such as DOT, IATA, or IMDG) regarding packaging, labeling, and documentation.
    Storage 2,5-Dibromobenzotrifluoride should be stored in a cool, dry, well-ventilated area, away from sources of heat, sparks, and open flames. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials like strong oxidizers and bases. Use chemical-resistant containers, and label them clearly. Handle with appropriate personal protective equipment to avoid exposure.
    Application of 2,5-Dibromobenzotrifluoride

    Applications of 2,5-Dibromobenzotrifluoride in Industrial Manufacturing

    As an established manufacturer of 2,5-Dibromobenzotrifluoride, we supply this specialty halogenated aromatic compound to customers operating in advanced chemical sectors demanding tight process control and consistent product purity. Below we outline its principal industrial applications, highlighting regulatory requirements, recommended formulation ratios, integration points within the supply chain, and the main finished product categories derived from each use case.

    1. Pharmaceutical Intermediate Synthesis

    API manufacturers leverage 2,5-Dibromobenzotrifluoride as a building block in the multi-step synthesis of targeted pharmaceuticals, including selective serotonin receptor antagonists and anti-inflammatory agents. Its high position-specific reactivity in palladium-catalyzed cross-coupling routes allows formation of complex aromatic scaffolds central to next-generation therapeutic agents, meeting the comprehensive requirements for process traceability and solvent residue benchmarks demanded by pharmaceutical regulators.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) specifications for related substances
    • EU Pharmacopoeia monographs where relevant
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals GMP)

    Typical usage ratio

    • 10–25 mol% relative to main aromatic ring substrates, adjusted per target API core size and required halogen density

    Downstream process integration

    • Fed into Stage II or III coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig type amidations, after initial halogen exchange reactions

    Final product types

    • Active pharmaceutical ingredients for CNS and anti-inflammatory drugs
    • Chiral intermediates for advanced small molecule targets

    2. Agrochemical Synthesis—Herbicide and Fungicide Building Blocks

    Producers in the crop protection sector use 2,5-Dibromobenzotrifluoride for the stepwise construction of heteroaromatic rings and halogenated benzene derivatives. These structures mark the core of modern herbicides and fungicides, where selective bromination and trifluoromethyl substitution impart improved biological activity and weather stability. This compound’s consistent isomeric purity supports compliance with traceability frameworks and environmental safety protocols enforced worldwide in crop protection engineering.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems (site qualification)
    • OECD Principles of Good Laboratory Practice for agrochemical R&D

    Typical usage ratio

    • 5–15% by weight of total halogenated benzene intermediates, dependent on the specific target structure’s substitution pattern

    Downstream process integration

    • Introduced in early halogenation stages and retained through condensation and cyclization steps for active ingredient assembly

    Final product types

    • Herbicide active ingredients with triazine or phenoxycarboxylic acid cores
    • Broad-spectrum fungicides for cereal and horticultural crops

    3. Advanced Electronic Materials—Liquid Crystal Monomer and Polymer Precursor

    Specialty chemicals manufacturers utilize 2,5-Dibromobenzotrifluoride as a precision intermediate for synthesizing performance monomers critical to liquid crystal display (LCD) alignment layers and other advanced organic electronic devices. Its trifluoromethyl group supports dielectric performance, while orthogonal bromines enable rapid functional group cross-coupling in precision polymer functionalization, all under strict electronic-grade material controls.

    Industry compliance standards

    • IPC-4101B: Specification for Base Materials for Rigid and Multilayer Printed Boards (material grade requirements)
    • JEDEC JESD22: Reliability Test Methods for Electronic Devices
    • RoHS Directive 2011/65/EU (restriction of hazardous substances)
    • ISO/TS 16949: Automotive Electronic Materials (where applicable)

    Typical usage ratio

    • Up to 8 mol% in LCD monomer feedstock, subject to electronic film specification and desired physical property modifications

    Downstream process integration

    • Activated at the monomer coupling stage followed by polymerization or co-polymerization, prior to casting of films or deposition

    Final product types

    • Liquid crystal orienting agents for LCD manufacturing
    • Functionalized polyarylene ether resins for high-speed circuit substrates

    4. Specialty Chemical Synthesis—Aromatic Cross-Coupling Intermediates

    Practitioners in specialty dye, pigment, and advanced resin industries rely on the reproducibility of 2,5-Dibromobenzotrifluoride for targeted Suzuki, Stille, and Ullmann cross-coupling reactions. The specific electronic effects of the trifluoromethyl substitution combined with bromine atoms serve as a platform for the introduction of extended conjugation, tailoring chromatic and stability properties in the final pigment structure under tightly monitored process parameters.

    Industry compliance standards

    • ISO 9001:2015 (process control and traceability)
    • EN 71-3: Safety of Toys—Migration of Certain Elements (when pigments used in toys)
    • ELV Directive 2000/53/EC for coatings and plastics applications
    • ASTM D5443: Standard Practice for Determination of Color of Transparent Liquids

    Typical usage ratio

    • 1–6 mol% as a coupling partner in pigment/formulation batches; precise ratio determined by pigment system and required resonance extension

    Downstream process integration

    • Acts as a halogenated aromatic substrate during key coupling/polycondensation stages, influencing hue and stability

    Final product types

    • High-performance organic pigments for industrial coatings
    • Color-stable dyes for technical fibers and plastics

    5. Fluorinated Fine Chemical Manufacturing

    Producers of specialty fine chemicals use 2,5-Dibromobenzotrifluoride as a strategic fluorinated intermediate for downstream transformation into either further substituted benzotrifluorides or as an initiator for perfluoroalkyl side-chain synthesis. The molecule’s dual reactivity profile—enabled by its bromine functionalities and electron-withdrawing trifluoromethyl group—helps streamline the construction of custom fluorinated architectures essential for solvent, surfactant, and performance fluid markets operating under advanced regulatory controls.

    Industry compliance standards

    • REACH (EC) No 1907/2006 for new substance registration
    • OECD HPVC Data Sets for high production volume chemicals
    • ISO 14001:2015 Environmental Management Systems
    • Chemical Facility Anti-Terrorism Standards (CFATS, US DHS) as applicable

    Typical usage ratio

    • Variable: 3–12 mol% during select fluorination or Grignard exchange reactions, based on target molecule synthesis route

    Downstream process integration

    • Inserted at the initial halogen-magnesiation or substitution steps, feeding subsequent modification or chain extension units

    Final product types

    • Custom fluorinated intermediates for solvent manufacture
    • Precursors for high-performance surfactants and specialty fluids
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    Certification & Compliance
    More Introduction

    2,5-Dibromobenzotrifluoride: Direct from the Manufacturer's Perspective

    An Inside Look at 2,5-Dibromobenzotrifluoride Production

    Every manufacturer has a few core products that play a big role in what our customers make and accomplish. 2,5-Dibromobenzotrifluoride, which we know by its CAS number 328-84-7, stands out for its unique properties and value in a number of chemical sectors. As the folks who make this product at scale, we see its impact firsthand. Many technical data sheets in the market skim over the real-world reasons this compound gets tapped by chemical buyers and formulation teams. Here, from our perspective as the team making each drum and every batch, there’s more to 2,5-Dibromobenzotrifluoride than a chemical name.

    Distinct Properties Shaped by Experience

    Looking at its structure, 2,5-Dibromobenzotrifluoride brings together two bromine atoms on a benzene ring with a trifluoromethyl group. The bromines sit at the 2 and 5 positions, giving this molecule some interesting options for further chemical transformations. For us as a manufacturer, the positioning matters. Certain reactions rely on those bromines being at precise points around the ring. This means processes using 2,5-Dibromobenzotrifluoride get more predictable results than with some other halogenated benzenes.

    The trifluoromethyl group on the ring gives this compound its characteristic stability and compatibility with a broader range of organic reactions. In our daily lab and plant runs, we've found that this feature reduces the likelihood of side reactions and unwanted by-products—a benefit that cuts down on waste and provides more consistent, isolated yields. The product comes out as a white to off-white crystalline solid, not dusty powder nor sticky sludge, making it easier to handle in both manual and automated setups.

    Model and Specifications: Reliability at the Core

    Consistency is something every manufacturer aims to deliver batch after batch. Our in-house analytical work focuses on Gold-Standard GC and HPLC calibration to make sure our 2,5-Dibromobenzotrifluoride fits the tightest purity specs. Over time, we’ve seen that slight impurities can affect downstream processing—things like unreacted bromobenzotrifluoride or trace halides might interfere with demanding syntheses. That’s why we use a purification sequence designed to keep impurities well below the thresholds set by customers in the pharma, agrochemical, and advanced material fields.

    Standard purity for our production batches tends to sit at 98% minimum as measured by GC, often higher. From an on-the-ground point of view, our teams pay just as much attention to the moisture content, which can play havoc in certain coupling reactions. We ship the product in high-barrier PE-lined drums or sealed bags inside UN-rated containers to keep out atmospheric moisture during transit and storage.

    Other manufacturers sometimes blend grades or offer off-spec material. Over the years, we’ve opted for a single, tightly-controlled standard grade to reduce confusion and headaches at customer sites. Our experience tells us that customers care more about predictability and reliability in each delivery, not just the purity number printed on a certificate.

    Where 2,5-Dibromobenzotrifluoride Makes a Difference

    Most of the 2,5-Dibromobenzotrifluoride we ship finds use as a building block for other chemicals. We see it most often selected for creating intermediates that feed into pesticide actives, pharmaceuticals, and specialty polymers. The dual bromo groups make it especially useful for cross-coupling reactions, like Suzuki and Stille types, which require a consistent source of brominated aromatics.

    We also hear from R&D chemists developing custom molecules or scaling up pilot processes. 2,5-Dibromobenzotrifluoride fits best when they need a solid feedstock that adds both bromine and a trifluoromethyl group in a single synthetic step. This saves time and reduces the number of hazardous intermediates that labs need to manage.

    One area that doesn’t get enough attention is the use of this product in electronic materials—some advanced polymers and benchmarks for dielectric films now rely on structures that benefit from the electron-withdrawing effects of the trifluoromethyl substitution. We started to see this increase about five years ago, particularly as demand in Asian electronics manufacturing picked up. Direct feedback from plant floors highlights how consistent granulation and minimal dust matter for automated handling systems. This keeps production lines running without blockages.

    Comparing 2,5-Dibromobenzotrifluoride to Other Halobenzenes

    Many chemical buyers will ask about differences between our 2,5-Dibromobenzotrifluoride and other halogenated benzenes, like the more common bromotrifluorobenzenes or even chlorinated versions. Having run reactivity trials side-by-side in our own labs—sometimes with customer technical teams on site—we’ve seen some patterns.

    The twin bromines on our compound deliver better reactivity in metal-catalyzed coupling than monobromo versions, so you get more options for sequential functionalization. Chlorinated analogs are less reactive and require harsher conditions, which often means more solvent and longer run times. We’ve also noticed that other isomers, such as the 3,4- or 2,4-dibromo versions, behave quite differently in some palladium-catalyzed reactions. The 2,5 substitution pattern generally offers less steric hindrance during oxidative addition, letting chemists generate higher yields and cleaner products.

    The trifluoromethyl group in this model acts as a useful tuning fork for electronic effects. Where some users struggle with homo-coupling side reactions in other brominated benzenes, 2,5-Dibromobenzotrifluoride often solves that with its electron-withdrawing CF3 group. This extends the molecule’s usefulness into more specialized settings. A plant manager told us the shift to this compound cut their raw material consumption by about 15% compared to mixes of monobromo and bromochloro benzenes.

    Challenges and Lessons Learned

    Making and handling 2,5-Dibromobenzotrifluoride has taught our manufacturing teams plenty about both chemistry and logistics. There are risks working with heavy halogenated materials, especially when it comes to occupational safety and product stewardship. In-house training programs and strict PPE protocols go a long way toward keeping teams confident and safe.

    Shipping regulations can be strict for brominated products. We’ve invested in containment and leak-proofing, especially after a learning moment with a badly-packed drum a decade ago. Since then, we've switched over to drums with thicker linings and better tamper evidence, even if it costs a bit more up front.

    Storage and handling at customer sites matter too. Some clients used to store this product along with strong acids or oxidizers, which can pose risk. We found success working directly with customer safety staff, reviewing their storage rooms and providing handling tips based on lessons from our own production sites.

    One frequent customer question involves process waste and disposal. Our experience is that spent residues and wash waters from handling 2,5-Dibromobenzotrifluoride respond well to incineration at high temperatures, minimizing environmental risk. A few years back, regulatory focus shifted toward downstream user responsibility, and we now send updated disposal guidance complete with batch-specific data on trace impurities.

    Supporting Customers' Success

    Years in the business have shown us that our work does not end when the truck rolls out the factory gate. Some customers want more than a one-off order: they’re looking for a stable partner who understands not only how to make the product, but how it performs on a line or in scale-up. Test batches and on-site support let us see real-world challenges, like how a sticky climate in Southeast Asia influences product flow or how agitation speeds in a West European blend tank affect product incorporation. These stories make all the difference when it comes to troubleshooting or fine-tuning end-use processes.

    A good example from last year: a long-term electronics customer faced intermittent clogging in a dosing system. Analysis of their bulk storage showed trace clumping linked to humidity ingress, something we had run into years before. After reviewing handling logs and sharing best practices, they saw a sharp drop in downtime and waste. We keep these experiences in mind when discussing storage and dispensing with new clients, especially those who haven’t handled halogenated aromatics at scale before.

    The Role of Traceability and Batch Consistency

    In fast-moving sectors, traceability is no longer a bonus—it's required. Recalls, even in non-pharmaceutical settings, bring huge costs and hassle. So, we maintain a batch tracking system tied to every production lot. Audits, both internal and run by customers, confirm batch data and chain of custody. This backup comes into play in the rare event there is a downstream process deviation, letting our partners know they can trust what they’re putting into high-value syntheses or finished products.

    Across hundreds of campaigns, we’ve picked up on another key issue: consistency isn’t just a matter of purity, but also how well the product fits into end-user dosing equipment and reactors. Our technical team keeps logs from scale-up trials, watching for surprises in bulk density, particle size, or even stickiness under varying humidity. In a business where raw material hiccups can stall production for days, that kind of hands-on diligence has seen our customers through more than one crunch.

    Regulatory Responsibility and Supply Assurance

    Supply disruptions—even those beyond our control—can strain relationships and cost customers both time and money. Recent years brought attention to the importance of strong local and regional supply chains. Time after time, predictable supply from trusted manufacturers has helped customers avoid stockouts during global logistics crunches.

    On the regulatory side, our stewardship teams live and breathe compliance. Whether it’s the annual update to REACH dossiers or responding to new safety alerts about halogenated intermediates, the drive is always to keep abreast of changing standards. We keep GMP-inspired controls on critical steps even for non-pharma end uses. Regular site visits and communication with regulators allow for prompt response if new monitoring rules or thresholds roll out.

    Customers count on clear documentation and rapid support for customs or regulatory questions. Over time, we’ve learned to anticipate requests for origin and composition certificates, supporting smooth imports and helping downstream firms meet growing transparency demands in their own circles.

    Future Outlook: Innovation and Adaptation

    Chemistry doesn’t stand still, and neither do the needs of the industries we serve. As manufacturers, we invest in ongoing R&D aimed at making purer, safer, and more adaptable products. Part of this work looks at new process routes that give higher yields and minimize by-product formation, making our own production more sustainable.

    We also watch how downstream industries push for materials with even higher purity or with distinct particle properties. Over the past couple of years, there's been a push towards “greener” process routes for aromatic bromides, replacing traditional solvents or brominating agents with less hazardous alternatives. Our in-house teams run pilot studies with alternative solvents and explore catalysts that operate under milder conditions, learning from every campaign.

    Not all improvements make headlines, but the small changes—process tweaks and feedback loops with users—lead to better products, lower environmental risk, and closer supplier relationships. As demand shifts and new regulations appear, our direct connection to the chemistry keeps us agile and ready to respond.

    Conclusion: Continued Commitment to Direct Manufacturing Experience

    2,5-Dibromobenzotrifluoride stands as a reliable, carefully-produced building block backed by decades of manufacturing experience. We take pride in knowing the unique demands of both chemistry and end use. Each batch, every improvement, and each lesson learned contributes to a product that supports innovation, safety, and efficiency for our customers. In a landscape packed with intermediaries and shifting specifications, being the source lets us offer clarity, consistency, and practical support that goes beyond a line-item on a supply sheet.

    Working as the manufacturer means we see both the granular challenges and the bigger-picture opportunities. Our team’s focus remains on delivering a product that meets demanding process needs—batch after batch, year after year. That close contact with the reality of chemical manufacturing, not just trading or distribution, gives us the insight and adaptability customers rely on.