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HS Code |
385961 |
| Product Name | 1,3-Dibromo-5-(Trifluoromethoxy)Benzene |
| Cas Number | 328537-21-1 |
| Molecular Formula | C7H3Br2F3O |
| Molecular Weight | 334.90 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 64-67 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as dichloromethane |
| Smiles | C1=C(C=C(C=C1Br)OC(F)(F)F)Br |
| Inchi | InChI=1S/C7H3Br2F3O/c8-4-1-5(9)3-6(2-4)13-7(10,11)12 |
| Synonyms | 3,5-Dibromo-1-(trifluoromethoxy)benzene |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 1,3-Dibromo-5-(Trifluoromethoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1,3-Dibromo-5-(Trifluoromethoxy)Benzene, sealed with a tamper-evident cap and labeled. |
| Shipping | 1,3-Dibromo-5-(Trifluoromethoxy)Benzene is shipped in sealed, chemical-resistant containers to prevent leaks and contamination. It must be labeled according to hazardous material regulations and handled with care. Transport typically occurs via ground or air, following all pertinent safety and environmental guidelines for brominated and fluorinated organic compounds. |
| Storage | 1,3-Dibromo-5-(trifluoromethoxy)benzene should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep the chemical separated from incompatible substances such as strong oxidizers or bases. Use appropriate personal protective equipment when handling, and ensure containers are clearly labeled to prevent accidental misuse or exposure. |
Applications of 1,3-Dibromo-5-(Trifluoromethoxy)Benzene in Industrial ManufacturingAs a dedicated manufacturer of 1,3-Dibromo-5-(Trifluoromethoxy)Benzene, we support advanced specialty synthesis across multiple industrial sectors. This compound provides essential functional groups for bromination and trifluoromethoxylation, enabling more complex molecular design for demanding downstream applications. Below are key industrial segments leveraging this material for high-value chemical production. 1. Agrochemical Intermediate SynthesisManufacturers use this aromatic compound as a core intermediate to prepare selective herbicide and fungicide ingredients. The controlled introduction of both bromine and trifluoromethoxy moieties enhances molecular bioactivity, hydrophobicity, and chemical stability. Process engineers incorporate it via direct coupling and further halogenation, achieving customized reactivity profiles for commercial plant protection products. Industry compliance standards
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2. Pharmaceutical API Building BlockThis brominated aromatic is routinely employed in the synthesis of advanced pharmaceutical intermediates, particularly for next-generation antihypertensive, anti-inflammatory, and oncology compounds. The combined electron-withdrawing effects support higher selectivity during cross-coupling and late-stage functionalization. Process chemists rely on its defined substitution pattern for constructing complex heteroaromatic scaffolds and tailoring pharmacophores. Industry compliance standards
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3. Electronic Materials PrecursorDownstream electronics and semiconductors industries depend on this compound’s aromatic framework during the fabrication of high-purity photoresists and specialty thin-film monomers. Its high electron-withdrawing capacity and halogen density are exploited in the design of resist polymers for advanced lithography and in high-performance dielectric materials. Process engineers integrate it through precision halogenation and controlled polymerization. Industry compliance standards
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4. Specialty Polymer Modification AgentPolymer producers incorporate this raw material to introduce bromine and trifluoromethoxy functionalities into aromatic backbone structures. Its reliable handling in Friedel–Crafts acylation and post-polymerization functionalization allows adjustment of glass transition temperatures, flame retardancy, and solvent resistance in engineering plastics. Technicians use precise feed rates and reaction controls to ensure property uniformity in high-performance formulations. Industry compliance standards
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This particular aromatic compound—known among chemists as 1,3-Dibromo-5-(Trifluoromethoxy)Benzene—continues to draw attention from synthesis researchers and R&D teams who wrestle with the shifting demands of specialty chemical development. In our facility, where we move from raw halogens to highly-engineered fluorinated intermediates, workers and engineers spend years refining processes for this molecule. Its structure features two bromine atoms and a trifluoromethoxy substituent, lined up on the benzene ring with precise geometry. The configuration opens pathways for targeted reactivity and selectivity that aren’t easy to achieve with other halogenated aromatics.
We have produced this chemical to serve as a core building block in fields ranging from agrochemicals to pharmaceuticals and advanced materials. Our day-to-day experience with 1,3-Dibromo-5-(Trifluoromethoxy)Benzene has taught us about the practical challenges and advantages that rarely show up on glossy spec sheets. For chemists attempting to introduce both bromine and fluorinated groups to a synthetic route—and who need those groups in specific locations on the ring—this molecule earns its reputation for reliability and versatility.
Controlling consistency in each production lot becomes essential where tightly-regulated downstream processes depend on accurate substitutions and impurity profiles. To guarantee straightforward scale-up, laboratory procedures in our facility convert seamlessly into gloved full-scale operations. Every reaction is checked against rigorous standards, not simply for content, but also for color, moisture, and residual raw materials that affect subsequent yields for customers.
Physical characteristics of our product matter in the real world. Supplied as an off-white powder or crystalline solid, 1,3-Dibromo-5-(Trifluoromethoxy)Benzene dissolves in most organic solvents familiar to synthetic labs. If humidity enters the packaging, lumps and flow issues can crop up, so we take care to keep everything dry, sealed, and handled in temperature-controlled spaces. This feels like a minor detail on paper, but chemists who weigh out materials and load reactors day in and day out have reminded us: the difference between a smooth transfer and a damp brick can make or break a workflow.
Running a chemical manufacturing line means more than hitting a purity target. Trace impurities—especially isomeric or monobrominated byproducts—become stumbling blocks for downstream synthesis. Certain applications demand impurity levels under 0.2% for each possible contaminant. When an off-flavor material creeps above that limit, valuable intermediates can wind up as waste.
Our team attacks the problem by double-checking each batch through analytical tools, including HPLC and NMR, backed by operator know-how that only develops from years on the shop floor. We routinely chase down off-spec batches before a drum ships out the door, and consciously invest in instrumentation, not just in headline numbers but in workers who know what to do when a baseline wiggles or a color deepens.
As always, differences in structure drive the value and suitability of one product over another. Halogenated benzenes form the backbone of many chemistries, but this compound’s pairing—a combination of bromine (known for its reactivity and easy activation via metal-halogen exchange) with the electron-withdrawing trifluoromethoxy group—allows synthetic chemists to target unique pathways. Compounds that carry only one halogen, or lack the -OCF3 functionality, provide different reactivity profiles. For example, some halogenated benzenes give quick reactivity at the para position, but our material’s substitution pattern blocks certain side reactions, letting chemists install functions just where they want them.
Where our team has collaborated directly with formulation groups, we have seen this structure improve yields and selectivity in, for instance, coupling reactions or in the preparation of complex heterocycles. The impact becomes obvious when a customer can skip a purification step or move directly to the next phase of synthesis—saving not just time but real funds, solvents, and precious labor.
1,3-Dibromo-5-(Trifluoromethoxy)Benzene enters the synthesis stage for a broad spectrum of industries. R&D teams exploring next-generation herbicides and fungicides rely on this compound to add both halogens and fluorinated moieties in a single, efficient stroke. In pharmaceutical research, it serves as a core for building more intricate scaffolds, letting medicinal chemists explore aromatic substitutions that raise potency or modify metabolic profiles.
We regularly field requests from paints and polymers producers seeking improved dielectrics and weather stability; in these cases, the -OCF3 group helps lower surface energy and raise resistance to chemical attack. Our materials have found their way into specialty coatings and advanced composites where manufacturers need a balance of halogen reactivity and fluorinated hydrophobicity baked into a single molecule.
Research teams often require gram-scale samples before moving forward on commercial synthesis. In our shop, we maintain flexibility to turn out both kilo-lot and industrial-scale shipments for projects progressing from the bench to bulk. This means carefully adjusting crystallization parameters, altering the rate of bromination, and tweaking solvent choice at every level.
For one long-term customer, a simple swap of solvents based on their feedback fixed a recurring filtration bottleneck. It brought down process time by several hours and consistently yielded a cleaner, easier-to-handle product. Flexibility on the manufacturing floor, coupled with open channels between technical support and operations, keeps pilots moving at pace without weeks of downtime between scale-ups.
Manufacturing halogenated aromatics draws scrutiny given the complexity and environmental risks inherent in the use of bromine and fluorinated reagents. In our own operations, we follow stringent guidelines set forth by local and international agencies, paying special attention to containment, recycling, and responsible disposal of waste streams. Teams trained to handle potential releases or spills focus on prevention, swift response, and accurate documentation for every stage of the process.
Where regulations shift, as they tend to with evolving understandings of persistent organic pollutants, our product management and regulatory teams work closely with laboratories to reassess methods or pivot to greener solvents, always maintaining performance needed by downstream clients. Sometimes that means updating process steps to minimize solvent residuals or reducing the use of high-impact reagents. Committing to this work has helped us continue exporting to demanding markets while protecting workers, neighbors, and ecosystems surrounding our manufacturing site.
Each fill, every seal, and each quality document attached to 1,3-Dibromo-5-(Trifluoromethoxy)Benzene owes something to continuous improvement initiatives adopted by our factory. For example, an improvement in sieve mesh sizing mid-run once led to a smoother, more uniform particle distribution, helping prevent clumping in larger shipment drums. That idea didn’t come from a manager’s desk; it originated with an operator tracking patterns during a particularly humid season.
Packaging matters more than most realize. Incorrect closure or poor barrier layers can ruin months of work. We take feedback from everyone on the supply chain—from those who empty our drums in sterile facilities to those who load pallets in the field—and adapt closures, liners, and outer drums in response. Over the last year, upgrades in packaging have led to fewer environmental complaints, less product loss, and a smoother ride across long distances and through variable climates.
Once the product leaves our site, technical service doesn’t just stop at the loading dock. If someone calls in with a solubility issue, unexpected reactivity, or even a lab result that doesn’t match paperwork, we start from our own lot samples, review reaction logs, and retrace any process variables that might play a role. In the past, customers facing hurdles with integration into scale-up chemistry have benefited from direct advice, whether that meant shifting solvent systems or adjusting heating curves.
Real transparency—not just a list of specs or a certificate on a file—has guided us here. We open up process narratives, share what went right, and get to the bottom of any hitches together. Successful outcomes, as shared with several long-standing clients, have established confidence and built long-term trust, both crucial in critical supply chains.
In routine discussions with R&D chemists and manufacturing leads, the most repeated feedback centers on predictability and functional flexibility. Other halogenated benzenes, even those carrying two bromines, rarely match the unique effect of the trifluoromethoxy group. The electron-withdrawing nature of -OCF3 combines with aromatic substitution, opening up new possibilities in metal-catalyzed couplings, nucleophilic substitutions, and direct arylation.
Some alternatives, such as 1,3-dibromobenzene, give high reactivity but lack site-selective control. By contrast, 1,3-Dibromo-5-(Trifluoromethoxy)Benzene’s substitution pattern brings both controlled reactivity and consistent outcomes across different processes. This translates, in practice, to fewer surprises and fewer rejected lots. Colleagues who have run comparative studies on scale, especially in pharmaceutical API intermediates, note the value in skipping additional purification or rework steps since byproduct profiles run cleaner batch-to-batch.
Nothing replaces lived experience at the reactor’s side. Our operators, through repeated campaigns, spot subtle shifts—a clear sign of reliable craftsmanship. Years spent on this product have taught us not just the chemical theory but also the hands-on adjustments that keep materials within spec despite fluctuating temperatures, humidity, or raw material changes. Our technical teams meet regularly to review process deviations and share what’s been learned, feeding improvements back into daily operations.
Experience has shaped not just how we make the chemical but also how we approach customer pain points. For example, when feedback suggested that filtering fines clogged up customers’ lines, our plant reduced dust formation by fine-tuning crystallization. Each lesson instructs us to keep adding value not in abstract terms, but in the concrete improvements that show up on the receiving end of the supply chain.
One of the rarely discussed benefits of maintaining in-house manufacturing for specialized chemicals like 1,3-Dibromo-5-(Trifluoromethoxy)Benzene comes through stability of supply and independent process development. Relationships built over years with suppliers of halogens, solvents, and specialty raw ingredients give us control over lead times and lot quality. Sourcing teams form the critical backbone, making possible on-the-fly changes or back-to-back campaigns for urgent projects on a tight schedule.
By having complete control from raw materials through finished product, we avoid shipping delays, last-minute substitutions, or mismatched specs, all of which can derail an otherwise smoothly-running customer project. In recent years, where global supply chains have encountered more turbulence, customers have consistently called out the value of working with dedicated manufacturers who keep thorough records, communicate process changes, and stick to delivery timelines.
Recent events in global trade have reminded all of us in the supply chain about the need for robust, local capacity and thoughtful inventory planning. Where external turbulence affects raw halogen or fluorinated gas inputs, our purchasing and production scheduling teams work overtime to buffer customer projects. The value built up over decades of in-house development and careful supplier partnerships means we can provide transparency and certainty, where speculation or intermediaries frequently can’t.
We have added contingency inventories, built redundant utility lines, and forged agreements with logistics partners through experience gained the hard way—by enduring production slowdowns and delays that affect real delivery schedules for real people downstream. Sharing information openly and making joint decisions with customers ensures that as needs change, we adapt together, not through last-minute panic but out of mutual planning and review.
Though chemistry sits at the core of what we do, it’s the integration of expertise, process discipline, and clear communication that sets specialized manufacturing apart from trading or re-packing. For 1,3-Dibromo-5-(Trifluoromethoxy)Benzene, that means walking the product from synthesis through purification, packaging, and logistics, right down to the documentation handed over upon arrival.
Our technical team regularly reviews both customer and in-process feedback. Adjustments to reactor agitation or reaction time often stem from observed patterns in batch-to-batch variance or analytics. Detailed analysis, coupled with every operator’s note and observation, makes it possible to maintain quality where margins for error remain slim.
One of the clearest lessons from years in specialty molecule production: innovation follows from managing the details others might call small. We make a point to visit industry consortia, gather data from conference presentations, and pick up the thread of new regulatory concerns before they land in compliance audits. By approaching each raw material, each reactor run, and every QA check with readiness to improve, we keep our product at a standard that opens doors to new applications and fresh collaborations.
Customers benefit when the material they order matches not just a chemical formula, but the whole set of properties—handling, purity, appearance, shelf life, and downstream performance—that guide their own success. We find the real work comes in marrying technical mastery with operational humility, open conversation, and steady reinvestment in both people and process.
Specialty molecules do not earn a place in synthetic chemistry just by being novel. This benzene derivative, with its carefully-chosen arrangement of bromines and a strongly electron-withdrawing trifluoromethoxy group, has proven again and again that it can drive reactions, yield consistent intermediates, and streamline multi-step syntheses in a way unmatched by more basic alternatives.
The customers who come back year after year for our product teach us more than we teach them. Their exacting expectations, feedback loops, and direct conversations push us to reevaluate every process—whether on the reactor floor, at the packaging station, or in workplace safety meetings. This keeps us focused on delivering not only a technically excellent material, but the sort of transparency, reliability, and responsive support that makes business relationships last beyond the signing of an order.
The story of 1,3-Dibromo-5-(Trifluoromethoxy)Benzene is a shared journey, made not just through clever molecular design but through lived, day-to-day commitment on the line and in the lab. Meeting the needs of critical industries, keeping lines running smoothly, and fostering steady improvement all depend on unglamorous but essential work: open eyes, ready hands, and years of learning by doing. For us, this product isn’t just a code or a spec—it’s the result of persistent effort, careful study, and trusted relationships up and down the value chain.