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3-Bromo-5-Nitrobenzotrifluoride

    • Product Name 3-Bromo-5-Nitrobenzotrifluoride
    • Alias 3-Bromo-5-nitro-α,α,α-trifluorotoluene
    • Einecs 235-911-0
    • 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

    413884

    Cas Number 328-75-6
    Molecular Formula C7H3BrF3NO2
    Molecular Weight 286.01 g/mol
    Appearance Light yellow crystalline powder
    Melting Point 56-58 °C
    Boiling Point 246 °C at 760 mmHg
    Density 1.76 g/cm³
    Purity ≥98%
    Solubility Slightly soluble in water
    Flash Point 102.3 °C
    Refractive Index 1.547
    Synonyms 3-Bromo-5-nitro-alpha,alpha,alpha-trifluorotoluene

    As an accredited 3-Bromo-5-Nitrobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a secure screw cap, labeled "3-Bromo-5-Nitrobenzotrifluoride," including safety and hazard information.
    Shipping 3-Bromo-5-Nitrobenzotrifluoride is shipped in secure, tightly-sealed containers to prevent leaks or contamination. The chemical is handled as a hazardous material, complying with international and local regulations. Packaging is clearly labeled, and transportation is conducted by certified carriers to ensure safety and environmental protection throughout shipping.
    Storage 3-Bromo-5-nitrobenzotrifluoride should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong acids and bases. Store in a tightly closed container, protected from light and moisture. Use chemical-resistant shelving, and clearly label the container. Follow all relevant safety guidelines for handling and storage of hazardous chemicals.
    Application of 3-Bromo-5-Nitrobenzotrifluoride

    Applications of 3-Bromo-5-Nitrobenzotrifluoride in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Bromo-5-Nitrobenzotrifluoride for a range of specialized industrial applications. Our customers rely on this intermediate in regulated segments where strict process consistency, compliance with international norms, and tailored integration into established workflows are essential. The following outlines key downstream uses, each with their own industry-specific demands for compliance, handling, and process optimization.

    1. Advanced Agrochemical Synthesis

    Major agrochemical producers use this compound as a halogenated building block for high-value active pharmaceutical ingredient (API)-grade crop protection molecules. Our partners formulate it in reactions requiring precise ortho-nitro substitution patterns to achieve targeted herbicidal activity. The compound integrates at early cyclization or coupling stages to ensure purity and correct molecular orientation in final pesticide formulations. Ongoing batch validation and traceability are required from delivery to the final registrable end-use product.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • European Crop Protection Association (ECPA) Guidelines
    • Agrochemical Active Substance Regulatory Review (EU 1107/2009)
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 5–25% as a primary intermediate, depending on targeted molecular structure. Adjustment based on output purity and desired crop protection profile.

    Downstream process integration

    • Introduced via controlled halogenation and nitration step in multi-step synthesis. Retained selectively before oxidative or reduction reactions. In-process QC required for each batch release.

    Final product types

    • Selective herbicide actives and ready-formulate crop protection agents
    • Pre-emergent weed control active ingredients
    • Specialty fungicide intermediates

    2. Pharmaceutical Intermediate

    This compound serves as a reliable front-line intermediate in the bulk synthesis of certain fluorinated and brominated pharmaceuticals, including anti-inflammatory drugs and CNS actives. The molecular structure enables efficient downstream modifications such as amination and reduction, which influence pharmacokinetic properties. Regulatory audits require tracked lot documentation linking raw material receipt, process conditions, and finished API release in accordance with cGMP protocols.

    Industry compliance standards

    • ICH Q7A: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210 & 211 (US FDA cGMP)
    • EU Regulation (EC) No 1252/2014 for Pharmaceutical Intermediates
    • Ph. Eur. and USP standards for pharmaceutical purity

    Typical usage ratio

    • 2–8% in reaction mass for initial functionalization. Ratio varies by route—higher loadings for direct coupling, lower for stepwise syntheses or when used in mixed-intermediate processes.

    Downstream process integration

    • Reacted in upstream stage for trifluoromethylated ring formation. Followed by controlled hydrogenation, coupling, or alkylation to yield advanced API intermediates. All operations under validated cleaning and analytical regimes.

    Final product types

    • Fluorinated non-steroidal anti-inflammatory drug (NSAID) APIs
    • CNS disorder active ingredients
    • Oncology synthetic intermediates

    3. Electronic Chemical Manufacturing

    Producers of specialty electronic chemicals use this intermediate in the controlled synthesis of materials for liquid crystal display (LCD) driver layers and organic electronic devices. The electron-withdrawing trifluoromethyl group and nitro functionality enable specific chemical transformations to tune dielectric properties. Strict moisture and metal contamination limits apply, with batch records traceable to each wafer spin or thin-film deposition lot.

    Industry compliance standards

    • SEMI C3 Standard for Advanced Electronic Chemicals
    • IEC 62474 Material Declaration Requirements
    • ISO 14001:2015 Environmental Management for Chemical Handling
    • RoHS 2 Directive (2011/65/EU) for electronic materials

    Typical usage ratio

    • 0.5–3% by mass in liquid mixtures or as a reactive monomer feedstock. Precise loading adjusted to achieve required permittivity and film thickness in final device architecture.

    Downstream process integration

    • Charged into reaction vessel for in situ coupling, nitration, or polymerization. Integrated with strict analytical control to avoid ionic or particulate contamination. Passage through inline filtration prior to wafer coating.

    Final product types

    • Precursor molecules for LCD driver chip passivation
    • Specialty polymers for OLED devices
    • High-performance thin-film transistor (TFT) materials

    4. Dye and Pigment Intermediate Production

    Leading dye and pigment producers blend this raw material as a controlled intermediate in the manufacturing of specialty colorants for high-temperature plastics, advanced coatings, and technical fibers. The bromo-nitro substitution facilitates development of pigments with enhanced lightfastness and chemical durability, especially in fluoropolymer and polyamide matrices. Our material supports critical chromophore extension and stabilization steps where impurity levels and batch consistency directly impact final color index registration.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of Certain Elements) for colorants in consumer products
    • REACH Annex XVII for chemical safety and usage in colorants
    • ISO 18451-1:2015 (Classification of Colorants)
    • GMP for colorant additives in plastics as per 21 CFR 178.3297

    Typical usage ratio

    • 1–10% in pigment synthesis, with upper end in dark shades. Modified per color target and substrate compatibility studies.

    Downstream process integration

    • Combined at condensation or azo-coupling stage in pigment build. Product processed under closed batching and subsequent high-temperature treatments to ensure structural stability and shade constancy.

    Final product types

    • Fluorinated azo and anthraquinone pigments
    • High-performance plastic colorants for automotive and electronics
    • UV-stable polymer fiber dyes

    5. Specialty Polymer Synthesis

    Polymer manufacturers incorporate this specialty intermediate into polymer backbones for fluoropolymer and high-performance engineering plastics. The unique substitution pattern aids in introducing functional groups for subsequent cross-linking or surface modification, thereby enhancing chemical resistance and thermal stability. Stringent lot acceptance, solvent trace monitoring, and in-process analytical verification must be maintained to match expected physical property specifications.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • ASTM D638—Standard Test Method for Tensile Properties of Plastics
    • RoHS and WEEE Directives for restricted substances
    • ISO 9001-compliant in-process QC systems

    Typical usage ratio

    • 1–6% by weight, depending on molecular weight targets. Fine-tuned for copolymer or terpolymer production and desired resistance profiles.

    Downstream process integration

    • Added at monomer blending or in situ functionalization stage—reactive blending ensures tight control over incorporation. Monitored using GPC and NMR to verify molecular weight distribution after polymerization.

    Final product types

    • Fluorinated engineering polymer resins
    • Heat-resistant composite materials for aerospace and automotive
    • Membrane materials for chemical and fuel cell applications

    6. Industrial Chemical Intermediate for Fine Chemicals

    Producers in the fine chemicals sector utilize this intermediate to access bromo- and nitro-functionalized aromatic compounds used in advanced synthesis routes for specialty solvents, analytical reagents, and complex ligands. The compound’s chemical stability and reactivity enable precision in scale-up reactions subjected to frequent inspection and strict impurity isolation demands.

    Industry compliance standards

    • ISO 17025 Analytical Testing Requirements
    • Controlled documentation under Responsible Care® Program
    • REACH Regulation (EC) No 1907/2006 for specialty chemical registration
    • Custom end-user Specific Certificate of Analysis (COA) per shipment

    Typical usage ratio

    • Variable: 0.2–5% depending on downstream compound. Adjusted according to the synthetic step—lower ratios in derivatization, higher for building bulk fine chemical stocks.

    Downstream process integration

    • Charged as a key step intermediate, participating in selective electrophilic or nucleophilic aromatic substitution. Followed by unreacted material removal and purification for subsequent coupling, oxidation, or reduction steps.

    Final product types

    • Nitroaromatic reagents for analytical chemistry
    • Ligand precursors for metal-complex catalysts
    • Industrial specialty solvent intermediates
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    Certification & Compliance
    More Introduction

    Unlocking New Possibilities with 3-Bromo-5-Nitrobenzotrifluoride: An Insider's Look from the Manufacturer’s Bench

    Our Commitment and The Journey of a Molecule

    Inside a chemical plant, the real work starts long before a molecule answers a customer's need. For years, we’ve been shaping specialty aromatics for a demanding market, witnessing firsthand how small changes in structure influence both process and performance. Among these, 3-Bromo-5-Nitrobenzotrifluoride stands out. Known in the lab by its CAS number 328-74-5, it offers a set of properties that meet challenges we see in fine chemical, pharmaceutical, and agrochemical synthesis.

    Every batch begins in reactors engineered to handle tricky substitutions—balancing temperatures, monitoring pressure, and keeping contamination below the strictest thresholds. The control room blinks and beeps; the team at every stage knows how this trifluoromethyl ring bolts to the benzene core, adding a bromo and a nitro group in precise steps. The Teflon lining may look plain, but it disciplines some of the most aggressive agents in organic chemistry. After years of hands-on optimization, we still respect every kilo we produce.

    What Sets 3-Bromo-5-Nitrobenzotrifluoride Apart

    With the inclusion of both a nitro group and a bromine atom on the same aromatic ring, alongside the trifluoromethyl anchor, this compound takes on reactivity not seen in simpler analogs. In our runs, we consistently achieve purities above 99 percent (GC), which directly influences the predictability and outcome of further transformations.

    Growers and drug chemists appreciate that the nitro group at the 5-position robustly deactivates the ring to electrophilic substitution, but leverages nucleophilic aromatic substitutions, especially in the presence of the electron-withdrawing CF3. On the other hand, the bromine at the 3-position gives the scaffold to Suzuki, Sonogashira, or Buchwald coupling partners. This combination provides unique access to pharmaceutically relevant heterocycles or crop protectant intermediates, especially where both electron-rich and electron-poor conditions need to coexist.

    Balancing Performance and Process

    We think through every variable: particle size distribution, bulk density, storage stability. The highly crystalline nature of our dried product allows for accurate weighing and reproducible reactions. During packing, the crystalline powder resists agglomeration, so workers avoid clumps and dust clouds that can spoil a blend and irritate operators. Over the years, we learned to cool product carefully after each run, avoiding brownish over-oxidized byproducts that complicate purification and sometimes produce misleading results for downstream analytical teams.

    Thanks to its high melting point and low volatility, the material is straightforward to store and handle, but calls for standard precautions. Nobody in the plant enjoys an accidental dust exposure—our best teams keep the rooms well-ventilated, suit up with respirators, and avoid static discharge. Routine monitoring of shelves rarely turns up decomposed product. While some halogenated aromatics show darkening or off-odors over months, our tight capping and regular rotation keep this problem at bay.

    Applications That Matter in Real Synthesis

    Lab notebooks and scale-up logs prove this molecule can open pathways inaccessible by other means. Early on, customers in advanced pharmaceutical R&D told us their teams struggled with meta-brominated arenes: some lack the right substituent, others give puling off-model side products. Here, the trifluoromethyl group not only shifts electronic profiles but also resists metabolic breakdown in vivo, driving interest in drug candidates involving nitrated aromatic scaffolds. Many blockbusters, from CNS agents to oncology leads, are designed using similar trifluoromethylated rings.

    On the crop science side, trifluoromethyl groups appear throughout modern agrochemicals, boosting both stability and the creature repellency profile, especially when coupled with nitro or halogens. Our partners report that this compound, as a precursor, simplifies routes to actives that otherwise required multi-stage protecting group strategies.

    Beyond these, certain pigment and specialty polymer makers use 3-Bromo-5-Nitrobenzotrifluoride to tune refractive index or develop vivid colors that resist fading in harsh lighting or aggressive environments. During our collaborations with plastics engineers, we witnessed firsthand how the right building block leads to new resins that outperform previous iterations—improvements that start at the molecular level and ripple all the way to finished goods.

    Comparing with Other Halogenated and Nitroaromatics

    Chemists sometimes ask about switching from 4-bromo or 2-bromo nitrobenzotrifluorides. In our pilot trials, the meta configuration, as present in this compound, delivers distinct reactivity. For nucleophilic aromatic substitution (SNAr) reactions, the electron withdrawing effects of both the CF3 and the nitro group at 5-position accelerate displacement at the bromine’s 3-location. Similar molecules can stall or require harsher conditions; with this product, conversions push ahead at milder temperatures and with better selectivity.

    Other times, customers have weighed between using this compound or simpler nitrobenzenes. Yet, those lack the extra stability and metabolic features the CF3 offers, especially for licensing or regulatory review of pharmaceuticals and agrochemicals. The brominated analogs without a nitro group fall short when tuning downstream ring reactivity. After thousands of pilot runs and scale-ups, our records show this specific arrangement opens up transformations otherwise closed or uneconomic. For peptide and heterocycle synthesis, this difference translates directly into more robust yields, with fewer purification headaches.

    As the original manufacturer, we also fine-tune the drying and milling. Distributors selling similar-sounding intermediates rarely match the uniform crystalline consistency or the purity profile achieved from direct plant control. These aspects reveal themselves in process yields, kinetic predictability, and spectral cleanliness; operators downstream rarely thank us directly, but the absence of troublesome side peaks or greasy residues tells its own story.

    From Benchtop to Bulk: Scale and Quality Challenges

    On a kilogram scale, synthesis fine-tuning makes or breaks a project. We've hit pitfalls ranging from impure brominating agents to inconsistent reagent supply. Many years ago, we realized that reaction exotherms needed direct attention: even a few degrees off can turn a controlled batch into a brown mess. Setting up strict in-line monitoring, paired with automatic dosing, paid dividends. We linked retention times on analytical rigs directly back to modifications in run conditions, sharpening our ability to guarantee purity at every run.

    Waste management isn’t an afterthought. Our factory teams worked hard to adapt scrubbing systems and solvent recovery, reducing the environmental impact with every production cycle. Not every synthetic route tolerates change, but we have tucked incremental improvements into our process over the years, driving down the amount of halogenated and nitrated residue reaching field disposal. Responsible manufacturing underpins our long-standing customer relationships as much as any product certificate.

    How We Approach Customer Needs

    Vendor audits, deep-dive assessments, and the growing scrutiny on supply chain traceability have sharpened our approach. Process engineers, supply planners, and lab chemists want more than basic specs—they trace chromatography logs, impurity profiles, and batch stability over time. We run detailed QC and stability studies of every lot, pushing our analytical teams to detect even subtle degradation or contamination. We track the story of every drum, from raw material intake to the loading dock, because one uncertain kilo can trip up an entire pilot or registration filing.

    In critical applications, especially those bound for human or animal use, trace impurities can spark expensive headaches. We go beyond standard in-house HPLC and GC analysis, with periodic third-party checks and trending studies on storage effects. Trifluoromethylated nitrobenzenes, especially with halogen substituents, require careful documentation to meet international quality standards and scrutiny from global regulatory agencies. Our customers often mention that a tight impurity envelope saves time and trouble in both early-stage synthesis and final validation.

    Adapting to urgent logistical realities, we keep robust stocks, coordinating with operators so each batch leaves the plant within its freshest range of shelf-life. Seasonal variations and unpredictable customs events threaten delivery, so we invest in redundancy—our customers expect every shipment to line up with their plant schedules, and one late load can throw off an entire campaign’s timetable.

    Product Stewardship and Worker Wellbeing

    Handling this product responsibly means putting worker health front and center. The plant environment itself always throws up challenges. Even with decades in the business, we strictly control exposure, enforce PPE, and conduct regular training on safe handling and spill management. Out on the production floor, grounded drums and anti-static walkways aren’t just policy—they prevent serious accidents in a workplace where fine, reactive powders are in use daily.

    Our experience shows that sound ventilation, comprehensive monitoring, and ongoing updates for safety data and training make all the difference. Product consistency begins with caring for the team that produces it. We review accident logs and near-misses, learning from every incident, no matter how small, and plug those lessons back into new SOPs and facility upgrades. Risk never disappears—but a solid safety culture and thorough system of checks keep it manageable and constantly improving.

    Anticipating Market Demands and Regulatory Trends

    In recent years, the pressure to comply with global regulatory frameworks has intensified. Regions like the EU and North America demand full traceability, defined impurity thresholds, and data transparency. As the original makers of 3-Bromo-5-Nitrobenzotrifluoride, we have adjusted both documentation and internal practices. Full batch traceability, integrated waste and emissions tracking, and expanded analytical capabilities now define every product release.

    We monitor patent landscapes and regulatory submissions closely. New science or legislative updates can tilt the playing field. Our internal teams review each new route, byproduct, and impurity, ensuring we keep pace with emerging needs. End-users, whether pharmaceutical R&D teams, agrochemical developers, or materials engineers, rely on that behind-the-scenes diligence to make their own breakthroughs possible and to avoid regulatory stumbling blocks that can appear overnight.

    Pushing the Boundary: Future Proofing and Scaling Up

    Increasingly, downstream partners want not only the kilo-scale batches but reliable, multi-ton consistency. Scaling a bench-scale process to a manufacturing plant demands both experience and open feedback from every link in the supply chain. We draw on years of digital process controls, high-frequency analytical runs, and head-to-head process trials to predict and stop scale-up pitfalls—not every synthetic approach that works in a 500 ml flask translates to a 2,000 liter vessel.

    Process chemists, when building out the route for a new API or crop chemical, often choose the building block that gets results, but they stay if a supplier delivers consistency and clarity batch after batch. As the direct manufacturer, each lot can carry detailed run conditions, impurity spectra, and stability profiles. We work closely with process teams, offering hands-on insight about best conditions, potential incompatibilities, and successful process adaptations using our product. That closeness, developed over years, keeps entire programs on track.

    Continuous Improvement: Lessons from Every Batch

    For decades, feedback has come directly from chemists in the field: requests for alternative lots, tighter impurity limits, or better size control. We learned early that openness to criticism sharpens not just product quality but also trust. Today, we run regular audits, both internal and external, benchmarking each batch against earlier lots, documenting every deviation, and drawing up clear plans for each improvement.

    Process waste, energy input, ILP (in-process losses), and yields—tracking these numbers over years, and learning from fluctuations, has let us hone the process, lowering costs and environmental impact. As a result, customers find fewer surprises, smoother scale-ups, and cleaner transitions into regulatory filings. The discipline to manage detail at all stages, from order to shipment to post-delivery support, reflects deeply held values—ones learned from navigating both successes and setbacks along the production line.

    Why Direct Manufacturer Experience Matters

    Out in the broader market, plenty of products appear under similar names. Only direct manufacturers, whose operators and quality teams touch every batch and solve every glitch, can promise the repeatable quality and transparency so necessary in critical applications. Markets expect low trace impurities, consistent supply, and direct technical support. Over decades, our direct interaction with diverse end-users—academic, industrial, and commercial—has driven us to adapt processes and documentation in real time.

    We work side-by-side with procurement teams, project managers, and R&D scientists, providing detailed support for process trouble-shooting, impurity identification, and scale-up challenges. Customers get more than a drum or bag—they tap into deep production insight, honest assessments of limitations, and a transparent look at both the product's strengths and its quirks. We respect that trust—the stakes are too high for anything less.

    Looking Forward: The Role of 3-Bromo-5-Nitrobenzotrifluoride in Innovation

    The value of this compound stretches from early lead synthesis in discovery labs to plant-scale manufacture of agrochemicals or advanced materials. Its unique structure, combining a meta-bromo with a para-nitro and a strong electron withdrawing CF3, ensures that chemists retain synthetic flexibility no matter the downstream transformations. In every field, the ability to manipulate reactivity, metabolic fate, and structural integration gives designers new levers to pull—essential as regulatory and environmental constraints tighten.

    Those of us who have made, packed, tested, and shipped 3-Bromo-5-Nitrobenzotrifluoride know that every detail matters. Experience on the shop floor—and the feedback loop from our customers’ own labs—shapes every improvement and guarantees a standard that supports real scientific and commercial progress.