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2-Bromo-5-Nitrobenzotrifluoride

    • Product Name 2-Bromo-5-Nitrobenzotrifluoride
    • Alias 1-Bromo-4-nitro-2-(trifluoromethyl)benzene
    • Einecs 249-019-2
    • 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

    947545

    Cas Number 4461-77-0
    Molecular Formula C7H3BrF3NO2
    Molecular Weight 272.01 g/mol
    Appearance Yellow crystalline solid
    Melting Point 55-59 °C
    Boiling Point 252 °C at 760 mmHg
    Density 1.804 g/cm3
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Flash Point 107 °C

    As an accredited 2-Bromo-5-Nitrobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 250g amber glass bottle is labeled "2-Bromo-5-Nitrobenzotrifluoride," featuring hazard symbols, handling instructions, and batch details.
    Shipping 2-Bromo-5-Nitrobenzotrifluoride is shipped as a hazardous chemical and must comply with all relevant transport regulations (DOT, IATA, IMDG). It is typically packed in tightly sealed containers, protected from physical damage, heat, and moisture. Proper labeling, documentation, and safety data sheets (SDS) must accompany each shipment.
    Storage 2-Bromo-5-Nitrobenzotrifluoride should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store it at room temperature, protected from moisture and sources of ignition. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills.
    Application of 2-Bromo-5-Nitrobenzotrifluoride

    Applications of 2-Bromo-5-Nitrobenzotrifluoride in Industrial Manufacturing

    2-Bromo-5-Nitrobenzotrifluoride is an advanced halogenated aromatic intermediate engineered for demanding synthesis processes. As a direct manufacturer, we supply this compound to specialized sectors where precision, purity, and consistent supply underpin product quality at scale. Below we detail principal downstream applications, integrating technical considerations, regulatory requirements, and processing insights that guide industrial partners in specialty chemicals, agrochemicals, and materials science.

    1. Agrochemical Intermediates: Synthesis of Fluorinated Herbicides

    Agrochemical formulators use 2-Bromo-5-Nitrobenzotrifluoride to introduce trifluoromethyl and bromo functionalities in molecule scaffolds during the multi-step synthesis of modern selective herbicides. Derivatives deliver targeted activity against broadleaf weeds while enhancing environmental stability. Our material feeds into chlorination, amination, and Suzuki coupling reactions, supporting actives with tailored bioperformance and regulatory compliance in global crop markets.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • FAO/WHO JMPR Residue Guidelines
    • ISO 9001:2015 Quality Management System
    • REACH Regulation (EC) No 1907/2006 Substances of Very High Concern (SVHC) assessment

    Typical usage ratio

    • Raw material loading typically 10–25% w/w in herbicide intermediate step; selection and adjustment based on target molecule yield and process economics

    Downstream process integration

    • Batch or continuous-feed introduction during aromatic substitution under controlled inert atmosphere (temperature 80–150°C), following precise charge schedule for coupling/condensation reactions

    Final product types

    • Pre-emergent aryloxyfluoro herbicides
    • Nitro-aromatic weed control agents
    • Broadened-spectrum post-emergent crop protection products
    • Technical active ingredients for custom agrochemical blends

    2. Active Pharmaceutical Ingredient (API) Synthesis: Building Block for Benzotrifluoride Derivatives

    Pharmaceutical process chemists employ this material as a key intermediate in the preparation of specialized benzotrifluoride analogs found in experimental APIs and advanced intermediates for CNS and anti-infective drug candidates. Selective functionalization and fluorination patterns are essential for tuning pharmacokinetics, patent space, and formulation stability, with stringent control of impurity profiles mandated by regulatory authorities worldwide.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monographs (where applicable)
    • European Pharmacopoeia (Ph. Eur.) substance standards
    • Drug Master File (DMF) submissions to FDA or EMA where required

    Typical usage ratio

    • Included at 15–30% molar equivalents in route-specific synthetic schemes after route optimization; exact dosage determined by route efficiency and step yield

    Downstream process integration

    • Chemoselective aromatic nitration, subsequent halide exchange, and organometallic coupling in controlled GMP reactors, with final isolation and purification tailored to downstream API specifications

    Final product types

    • Investigational CNS drug candidates containing trifluoromethyl phenyl pharmacophores
    • Benzotrifluoride-substituted anti-infective intermediates
    • Specialty building blocks for patented chemical space
    • Advanced pharmaceutical intermediates for contract manufacturing organizations

    3. Electronic Chemicals: Synthesis of Trifluoromethylated Aromatic Materials

    Semiconductor and display materials manufacturers incorporate 2-Bromo-5-Nitrobenzotrifluoride into precursor blends for high-purity organic electronic component fabrication. The unique combination of bromo, nitro, and trifluoromethyl groups provides controlled reactivity, facilitating subsequent formation of electron-transport and hole-transport molecules used in photoresist, OLED, and optoelectronic layer chemistry. Ultra-high purity and low metal contaminant profile are critical for device reliability.

    Industry compliance standards

    • SEMI C3 Standard for High Purity Chemicals
    • ISO/TS 16949 for Automotive Electronics
    • RoHS Directive 2011/65/EU on restriction of hazardous substances
    • Internal customer-specific Semiconductor Quality Control guidelines

    Typical usage ratio

    • 1–5% in specialty precursor formulations, adjusted based on target functional group density and required purity tier

    Downstream process integration

    • Charged to multi-stage solution-phase synthesis with rigorous filtration and distillation, followed by direct integration in the monomer or oligomer formation for device substrates

    Final product types

    • Trifluoromethylated OLED emitter and host materials
    • Photoresist mask chemicals for photolithography
    • Protective coatings with high electron mobility
    • Specialty intermediates for organic field-effect transistor components

    4. Dyestuff and Pigment Production: Precursor in Synthesis of Highly Stable Colorants

    Colorant manufacturers leverage the unique electronegative and electron-withdrawing properties of the compound to develop high-performance dyestuffs and pigments designed for demanding textile, plastics, and coating applications. The material imparts superior lightfastness, chemical resistance, and color vibrancy to azo and anthraquinone derivative pigment frameworks, supporting production targets for both liquid and solid colorant forms.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys – Migration of certain elements
    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) Product Stewardship Code
    • Oeko-Tex Standard 100: Harmful substances in textiles
    • ISO 14001:2015 Environmental Management for colorant plants

    Typical usage ratio

    • Raw feed concentration 8–16% by weight in diazotization or coupling phases, variable according to target chromophore intensity and pigment structure requirements

    Downstream process integration

    • Introduced in the initial coupling reaction for monoazo or anthraquinone pigment synthesis, with subsequent purification and blending in water- or solvent-borne formulation systems

    Final product types

    • High-stability azo and anthraquinone pigments
    • Fiber-reactive dyestuffs for textiles
    • Masterbatch and color concentrate products for plastics
    • Liquid and powder coatings colorants for industrial surfaces

    5. Specialty Polymers: Fluorinated Monomer Chain Extension

    Polymer manufacturers utilize this compound as a chain-extension intermediate in small-molecule fluorinated polymer synthesis. The combined nitro, bromo, and trifluoromethyl groups introduce desirable performance features, including solvent resistance, thermal stability, and adjustable dielectric constants in the final polymer matrix. Selective incorporation during the pre-polymer or curing stage ensures tailored properties for demanding engineering applications.

    Industry compliance standards

    • ASTM D638 Standard Test Method for Tensile Properties of Plastics
    • UL 94 Flammability Standard for Plastics Materials
    • FDA 21 CFR 177.1550 (for food-contact polymers, where relevant)
    • RoHS/REACH compliance for electrical and electronic use

    Typical usage ratio

    • Feed ratio typically 3–10% in prepolymerization batch; modified according to desired functional group incorporation and batch scale

    Downstream process integration

    • Added at early or mid-stage monomer incorporation step in polycondensation or radical copolymerization; performance validated by molecular weight and functionality testing before further compounding

    Final product types

    • High-performance fluorinated engineering polymers
    • Dielectric resins for electronics encapsulation
    • Solvent-resistant coatings for chemical tanks
    • Advanced composite matrix materials for aerospace components
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Nitrobenzotrifluoride: A Manufacturer's Perspective

    Understanding 2-Bromo-5-Nitrobenzotrifluoride

    2-Bromo-5-Nitrobenzotrifluoride occupies a unique spot on the workbench. In the lab, this compound rarely leaves the spotlight, prized for the way its three fluorine atoms shift the behavior of the benzene ring while the nitro and bromo groups open up synthesis routes that would otherwise stall. Our experience with this material stretches back over two decades, and we’ve watched the industry steadily shift toward compounds like these—each element on the benzene playing a different role, all working together to give chemists new tools.

    The full chemical name sometimes feels clumsy in conversation, but behind it lies a model—CAS 328-75-6—where the trifluoromethyl group shares space with a bromine at the ortho position and a nitro group at the para. We spend a lot of time working with organic intermediates, and the specificity here matters. Subtle differences in bromination or the position of a nitro group can tip a reaction from stubbornly inert to reliable yield. Our in-house material has a purity typically above 98%, appearing as a solid at room temperature and packed to avoid contamination or moisture ingress. Small changes during synthesis or purification end up visible under chromatography, so we’ve built a system that controls each step—starting from the halogenation, measuring each batch, tuning the crystallization. Real experience with hundreds of kilos of product has revealed flaws not seen at the test-tube level.

    From Fundamentals to Applications

    Chemists know this intermediate appears in a wide range of advanced chemical transformations. Its electron-withdrawing property matters when building agrochemicals or pharmaceutical candidates. That makes our 2-Bromo-5-Nitrobenzotrifluoride more than a base-material—it’s an enabler that shapes the rest of the molecule. Certain aryl bromides hold back in cross-coupling reactions, but introducing electron-withdrawing nitro and trifluoromethyl groups flips the script. As a result, Suzuki, Stille, and Buchwald–Hartwig workups proceed with better yields and cleaner separations. We have run these reactions ourselves, guiding partner companies on solvent choice, catalyst loading, and temperature ramp rates, all because this compound sits at the junction of theory and real-world execution.

    This intermediate sees broad use when clients codevelop herbicides and crop protection agents. The trifluoromethyl group resists metabolic breakdown, giving downstream molecules greater environmental stability. Its combination of functional groups also makes it valuable for certain advanced materials—liquid crystals, specialty polymers, optoelectronics—where performance depends on precise molecular tuning. Traditional nitroaromatics often degrade under environmental or photo-irradiation, but fluorinated and brominated systems deliver a resilience that shows up in product benchmarks. Over years of pilot production, we’ve learned where theoretical advantages break down and which process parameters help maintain real-world advantages.

    We’ve also participated in numerous process transfer projects. Teams in both small-molecule pharmaceuticals and electronics sectors commission customized runs. Sometimes our chemistry team tweaks the mother liquor to shift crystallinity, at other times integrates extra filtration to lock out fine particulate. Whether the final need involves a downstream amination, substitution, or cross-coupling, the nature of the bromo and nitro handles reduces risk of byproducts and speeds up process optimization. It isn’t just a matter of supplying a reagent—our hands-on experience solving bottlenecks shapes our approach to each batch and each customer requirement.

    Quality, Reliability, and Process Optimization

    Quality control for 2-Bromo-5-Nitrobenzotrifluoride means more than standard instrumental runs. Every batch gets tested by NMR, GC-MS, and elemental analysis. Small trace impurities that might seem invisible in benchtop work grow into major headaches downstream. We invest in analytical capability because even a low-level isomer or residual halogen scavenger can poison a palladium catalyst or introduce variability that our customers—and our own teams—cannot afford.

    Our process evolved through repeated scale-up and iteration, beginning from decagram pilots and reaching hundreds of kilograms. Over these runs, minor heat spikes, solvent hydrolysis, and unplanned side-reactions sometimes led to unfamiliar peaks. Only direct experience—turning wrenches, monitoring process flow, repeating recrystallizations—has ironed out these issues. There’s no shortcut here. Meticulous documentation and feedback between our synthesis, purification, and QC teams keeps us ahead of potential pitfalls. We teach every new lab member about the consequences of an off-ratio halogenation or an unscheduled solvent switch, because robust process results in consistent product, batch after batch.

    Other suppliers may claim interchangeable product, but seasoned chemists know reality is not so simple. Slightly off-target melting point or trace instability under ambient humidity can signal problems. Over time, we saw how internal product—crystallized in-house, dried with the right conditions—outperforms externally sourced analogues. Our customers have confirmed this, sometimes returning to us after failed process validations or scale-up runs using competitors’ batches. The reliability comes from hands-on process tuning and fast responses when a question comes up—whether it’s analytical re-testing, support for regulatory documentation, or emergency troubleshooting in late-stage campaign production.

    Comparing to Other Benzotrifluoride Derivatives

    Benzotrifluoride chemistry isn’t homogenous—a change in functional group position or type alters everything. We have worked with ortho-, meta-, and para-substituted derivatives, along with chlorinated, iodinated, methylated, and nitro-only analogues. 2-Bromo-5-Nitrobenzotrifluoride stands out because the combination of bromo and nitro directly activates the ring for further chemistry, allowing for high selectivity and low side-product formation. In contrast, an ortho-nitro-only variant lacks the handle for easy cross-coupling, whereas a dichloro system can resist transformation or require harsher conditions.

    Clients in the agrochemical sector rely on the robustness of this compound for halogen exchange or further nitration steps, many of which falter with similar benzotrifluoride scaffolds. Researchers in pharmaceuticals prefer the combination for direct arene functionalization, as the reactive positions align with many late-stage functional group installations. The bromo group at the 2-position lowers the activation energy for oxidative addition, while the nitro group maintains selectivity in multistep processes. Contrast this with a para-bromo or meta-nitro scaffold; each demands alternate conditions and often delivers lower yields. We’ve run this compound head-to-head in scale-up projects with similar halogenated aromatics, seeing faster turnover frequencies and lower byproduct profiles for the 2-bromo-5-nitro variant.

    Physical stability also differs. Many trifluoromethylated aromatics tend to sublimate or degrade after extended storage, especially with light or humidity exposure. Our proprietary handling keeps the product stable for long-term shipment and storage. We test material in actual storage and transport conditions, confirming that no detectable breakdown occurs in dark, sealed packaging over more than a year. Users who struggled with clumping or yellowing from other regional suppliers often report clean material after switching to our batches. This matters in production lines, where even small physical changes can clog feeders or disrupt automated weighing systems.

    Supporting Real-World Applications

    Our manufacturing site doesn’t just serve as a source for standard batches. We participate in application R&D with clients, transferring our bench-level synthesis knowledge to pilot production and regulatory validation. Whether a client needs a large lot for a proprietary herbicide synthesis or hundreds of smaller packages for a pharmaceutical research program, our experience enables us to adjust timelines and maintain quality at unexpected scales.

    In downstream chemistry, 2-Bromo-5-Nitrobenzotrifluoride serves as a building block for dozens of advanced molecules. Medicinal chemists working on fluorinated aromatics often rely on its diversity of reactivity. Our technical team went as far as running exploratory scale-ups under multiple reaction atmospheres—nitrogen, argon, dry air—to see which workup delivers the cleanest product for specific catalyst systems. We found minute differences in moisture levels could knock down product yield in Buchwald–Hartwig couplings. That drove us to redesign purification and packaging, screening each batch for water activity and surface adsorbates.

    Clients working toward registration batches or scale validation frequently consult us about impurity profiles, analytical standards, and long-term stability. We provide not just the COA and spectra but share troubleshooting advice drawn from thousands of hours in our own pilot plants. Chemical manufacturing sometimes feels like a collection of quick fixes, but real expertise comes from committing to quality and taking ownership of every detail that affects a downstream process.

    Sustainability and Regulatory Focus

    Modern chemical production doesn’t happen in a vacuum. Environmental compliance, regulatory scrutiny, and sustainable process choices drive many decisions behind the scenes. Our process for producing 2-Bromo-5-Nitrobenzotrifluoride has evolved since the early days when waste streams seemed manageable at smaller scales. As demand increased, so did the need for strict waste minimization, solvent recovery, and personnel safety training. Each change came from hands-on evaluation of real process bottlenecks and new local or international requirements.

    We redesigned halogenation and nitration steps to use closed systems, limiting volatile losses and enabling efficient scrubber operation. Fluorinated aromatics often raise concerns about environmental persistence, so we invested in tertiary containment and rigorous effluent monitoring. Trace halogen byproducts and nitration residues get neutralized with custom absorbents before any offsite transfer. Internal audits track raw material origins and waste transfer compliance, letting us guarantee downstream users reliable sourcing documentation for any audit or registration file.

    From a sustainability angle, we’ve worked with partners trying to recycle spent solvents and minimize overall carbon footprint for industrial campaigns. Our technical service staff support customers by providing detailed process flows and material balances, allowing alignment with internal sustainability reporting. Feedback from customers integrating 2-Bromo-5-Nitrobenzotrifluoride into biobased or green chemistry frameworks often prompts further process refinement or alternate sourcing of input chemicals. Real commitment to environmental impacts emerges only when a manufacturer closes the loop from design to execution and stays open to new scrutiny.

    Expertise Drives Continuous Improvement

    Manufacturing a specialized chemical like 2-Bromo-5-Nitrobenzotrifluoride doesn’t mean setting the process and ignoring the future. Every month, the supplier landscape shifts, raw material prices fluctuate, and regulatory bodies update guidelines. Our production managers meet weekly with R&D and QC to review not just batch results but feedback from incoming inquiries, failed applications, and competitor advances. The result is incremental but steady improvement in reliability, analytical control, and process safety.

    Customers benefit from this iterative improvement. It can mean tighter particle size specification one quarter, revised packaging to eliminate static buildup the next, or faster certificate turnaround to support a critical regulatory deadline. We field new requests every season: smaller trial lots for start-up companies, kilo-scale lots for process screening, or system validation documentation for global supply agreements. Each request feeds into the process, shaping next-generation internal standards. This back-and-forth with industry partners ensures that our material remains a leader for reliability, traceability, and documentation support.

    The difference between true manufacturing expertise and simple reselling becomes most obvious when complications arise. Whether it’s recovering from an off-grade raw material, supporting product recall tracebacks, or participating in joint troubleshooting for downstream process issues, we stand behind every batch we deliver. If a defect emerges, our approach isn’t limited to paperwork. Plant engineers and chemists review logs, run live diagnostics, and answer customer questions based on actual handling of the product—not just from a shelf or sales catalog. The trust built from open, responsive support endures even in a competitive field where commoditization pressures run high.

    Facing Market Changes and Future Developments

    Demand for trifluoromethylated aromatics continues to shift, influenced by changing agrochemical patent landscapes, evolving pharmaceutical priorities, and increasing regulatory scrutiny over perfluorinated compounds. Over the past five years, we’ve observed a gradual expansion of alternative synthetic routes and an uptick in pilot facility activity from smaller startups and regional competitors. This keeps us focused on process optimization, cost control, and continuous evaluation of feedstock reliability.

    On the research front, new catalyst systems and late-stage functionalizations open up fresh uses for 2-Bromo-5-Nitrobenzotrifluoride. We maintain collaborations with process development specialists, testing reactivity and selectivity across a library of related benzotrifluoride derivatives. This helps update our application guidelines and spot market shifts in real-time. We support emerging requirements for low-residual halogen or metal content, reaching deeper into purification and tracking steps to stay ahead of industry requirements.

    Supply security takes on new importance as global logistics face disruption and regional regulations change. We have learned that direct manufacturing not only secures our supply chain but grants flexibility for unplanned spikes in demand or specification changes. Our internal teams keep buffer stocks, and our plant can adjust batch sizes to fit unique requests. We also continue investing in solvent recovery, waste treatment, and emission reduction—not simply to meet minimum legal standards but to go beyond, supporting partners looking for audited green chemistry credentials in their own supply chains.

    Partnering with Industry and Academia

    Collaborative projects with universities and research institutes play a growing role in how we improve existing products and plan for new ones. Over the years, joint studies have benchmarked reaction conditions, identified new coupling or reduction strategies, and created opportunities for young chemists to understand how scale-up influences molecular behavior. Partnerships often deliver more than research data; they expand the talent pool, build credibility, and create innovation that spins back into our everyday operations.

    We share non-confidential best practices at industry forums and focused working groups. Our teams help draft practical guidance for handling and storing advanced halogenated aromatics, contributing in ways that build broader sector knowledge. Credibility in chemical manufacturing is built project by project, each batch underpinning the next publication or product. We see this mutual exchange as a way not just to sharpen our own work but to raise standards throughout the sector.

    Conclusion: Trust Built on Experience

    Offering 2-Bromo-5-Nitrobenzotrifluoride to the market involves more than standard process control or tight quality specs. Our story with this compound is one of learning through hands-on problem solving, solving real process issues, and adapting technology to evolving expectations. We approach every batch with an eye toward application, working not as a remote supplier but as an experienced partner who has walked through the same manufacturing, regulatory, and quality challenges faced by our customers.

    By remaining committed to transparent communication, practical problem-solving, and continual investment in analytical control, we maintain the confidence of innovators in pharmaceuticals, agriculture, advanced materials, and high-performance intermediates. As markets evolve and the science moves forward, we keep refining this commitment—standing behind every gram shipped and every question answered with the insight that comes only from true manufacturing experience.