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3,5-Bis(Trifluoromethyl)Bromobenzene

    • Product Name 3,5-Bis(Trifluoromethyl)Bromobenzene
    • Alias 1-Bromo-3,5-bis(trifluoromethyl)benzene
    • Einecs 221-222-0
    • 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
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    Specifications

    HS Code

    482546

    Chemicalname 3,5-Bis(Trifluoromethyl)Bromobenzene
    Casnumber 328-70-1
    Molecularformula C8H3BrF6
    Molecularweight 311.01 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 174-176°C
    Density 1.74 g/mL at 25°C
    Refractiveindex 1.451
    Flashpoint 61°C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents

    As an accredited 3,5-Bis(Trifluoromethyl)Bromobenzene 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 25 grams, tightly sealed, with hazard labels, chemical name, and manufacturer details clearly displayed on the label.
    Shipping **Shipping Description:** 3,5-Bis(Trifluoromethyl)Bromobenzene is typically shipped in sealed glass bottles or specialized containers to prevent leaks and contamination. It should be transported as a hazardous chemical, with appropriate labeling, documentation, and compliance with international and local shipping regulations for flammable and potentially toxic organic halides. Keep away from heat and incompatible materials.
    Storage 3,5-Bis(Trifluoromethyl)Bromobenzene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Use chemical-resistant shelves or cabinets, and label the storage area clearly to ensure safety and prevent accidental exposure or contamination.
    Application of 3,5-Bis(Trifluoromethyl)Bromobenzene

    Applications of 3,5-Bis(Trifluoromethyl)Bromobenzene in Industrial Manufacturing

    3,5-Bis(Trifluoromethyl)Bromobenzene serves as a critical fluorinated aromatic intermediate for high-value industrial synthesis. Its distinctive substitution pattern supports fine chemical development, agrochemical actives, pharmaceutical intermediates, specialty polymers, and advanced electronic materials.

    1. Pharmaceutical API Intermediate Synthesis

    Our 3,5-Bis(Trifluoromethyl)Bromobenzene is a preferred building block in the development of pharmaceuticals where electron-withdrawing groups are required for enhancing metabolic stability and bioavailability. It participates in Suzuki-Miyaura and Buchwald-Hartwig reactions for complex API intermediate synthesis, particularly in anti-inflammatory, oncology, and CNS-active molecules. Customers adjust stoichiometry based on target API structure, with stringent control over reagent identity, trace impurity profiles, and batch reproducibility. Purity, residual solvent analysis, and compliance with applicable pharmacopeias are key at every production step.

    Industry compliance standards

    • ICH Q7 for GMP manufacture of API intermediates
    • USP/EP/ChP for relevant downstream APIs
    • FDA 21 CFR Part 211 for pharmaceutical ingredient processing
    • ISO 9001:2015 for quality management in fine chemical production

    Typical usage ratio

    • Utilized at 1.0–1.5 molar equivalents relative to halogenated intermediates; precise ratio depends on coupling partner and process yield optimization

    Downstream process integration

    • Introduced after halogen-lithiation or direct coupling step; followed by palladium-catalyzed cross-coupling, then further derivatization or deprotection, under inert atmosphere with controlled temperature ramping

    Final product types

    • Fluorinated benzene pharmaceutical intermediates
    • Targeted small molecule APIs (oncology, anti-inflammatory)
    • Specialty CNS drug candidates
    • Advanced medicinal chemistry research tools

    2. Agrochemical Active Ingredient Precursor

    We manufacture 3,5-Bis(Trifluoromethyl)Bromobenzene as a raw material for the synthesis of selective herbicide and insecticide intermediates. Agrochemical formulators exploit its fluorinated moiety for increased hydrophobicity and environmental stability, fitting modern structure-activity requirements. Formulation chemists in the crop protection sector typically utilize it in nucleophilic aromatic substitution or metal-catalyzed bond-forming reactions, controlling input ratio based on desired biological profile and scalability constraints. Downstream integration emphasizes batch traceability and compliance with regulatory requirements for technical grade intermediates.

    Industry compliance standards

    • FAO/WHO pesticide specification guidelines
    • ISO 17025 for laboratory chemical testing
    • Regulation (EC) No 1107/2009 for plant protection products
    • REACH registration for chemical intermediates

    Typical usage ratio

    • 0.8–1.2 equivalents per target agrochemical precursor, variable depending on downstream functionalization and target molecule

    Downstream process integration

    • Added during early-stage building block coupling or ring functionalization, prior to formulation of active ingredient concentrates or granulates

    Final product types

    • Herbicide and fungicide intermediates
    • Fluorinated insecticide core structures
    • Crop protection actives with enhanced photostability
    • Pest control research compounds

    3. OLED and Electronic Material Monomer Feedstock

    We supply this compound to electronic material producers specializing in organic light-emitting diode (OLED) technologies and fluorinated specialty polymers. Its strong C–F bonds ensure high chemical resistance and thermal stability, required for advanced monomer design in optoelectronic and dielectric applications. Materials R&D teams incorporate our product into synthesis protocols for arylated polymer backbones or hole-blocking layers, optimizing molar input and process flow to control chain length and electronic band gap properties. All shipments are traceable with batch release and purity specifications aligned with electronics industry standards.

    Industry compliance standards

    • IPC-4101 for base materials in printed electronics
    • RoHS Directive 2011/65/EU for hazardous substances
    • IEC 61249 for material characterization in electronics
    • ISO 9001:2015 for traceability and quality management

    Typical usage ratio

    • 5-25 wt% of total monomer feed, depending on target dielectric constant and processing environment (solution or melt polymerization)

    Downstream process integration

    • Introduced at early-stage monomer blending, followed by controlled polymerization under inert conditions, then converted to final films or device layers

    Final product types

    • OLED emitting and blocking layers
    • Fluorinated specialty polymers for electronics
    • Display and sensor device substrates
    • High-performance dielectric components

    4. Advanced Liquid Crystal Material Synthesis

    Leading liquid crystal display (LCD) material producers incorporate our product into the backbone engineering of mesogenic molecules, where the strong electron-withdrawing effect and molecular symmetry enhance birefringence. It is utilized during the formulation of custom liquid crystal mixtures to achieve targeted nematic, smectic, or chiral phase behavior, with precise management of composition to comply with electronic grade purity and moisture limits. Downstream QC covers advanced NMR, GC, and ion chromatography batch release criteria required for display applications.

    Industry compliance standards

    • IEC 61340 for electrostatic discharge management in liquid crystal materials
    • ISO 9001:2015 for quality management system
    • JEITA standards for display materials
    • RoHS and REACH conformity for chemical batch supply

    Typical usage ratio

    • 1–10 wt% in preformulated liquid crystal host; ratio adjusted based on final viscosity and phase requirement

    Downstream process integration

    • Mixed during mesogen synthesis, followed by blending and high-performance purification before cell assembly or polymer network introduction

    Final product types

    • Nematic and smectic liquid crystal compounds
    • High-speed display mixtures for LCD panels
    • Advanced optical films
    • Specialized chiral dopants for display tuning

    5. Active Ingredient in Fluorinated Phenyl Derivative Development

    Chemical manufacturers utilize 3,5-Bis(Trifluoromethyl)Bromobenzene for the synthesis of complex fluorinated phenyl derivatives, a critical component in advanced surface coatings and oil & gas extraction additives. The compound's structure allows site-selective coupling or substitution, aiding in the creation of molecules with high repellency and chemical hardness. Our technical support aligns shipments and formulation advice with customers’ pilot and commercial-scale process requirements, ensuring rapid resin or additive optimization, and strict regulatory conformity for downstream sectors.

    Industry compliance standards

    • ISO 14001 for environmental management in chemical synthesis
    • REACH Annex IX/X testing requirements
    • ASTM E2879 for analyses of fluorinated compounds
    • ISO 9001 quality management in specialty coatings

    Typical usage ratio

    • 0.5–2.0 equivalents per reaction batch, dependent on intended function group density in target molecule

    Downstream process integration

    • Reacted during initial aromatic functionalization, followed by further halogen exchange, alkylation, or ring modification prior to formulation into finished additive blends

    Final product types

    • Anti-fouling marine coatings
    • Surface repellent oilfield additives
    • Fluorinated resins for harsh chemical environments
    • Resistant paints and functional coatings
    Free Quote

    Competitive 3,5-Bis(Trifluoromethyl)Bromobenzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    3,5-Bis(Trifluoromethyl)Bromobenzene: Direct from the Production Floor

    Bringing Specialty Aromatics to Chemists Who Build the Future

    We work directly with 3,5-Bis(Trifluoromethyl)Bromobenzene every day, and each batch we produce reflects its own story of attention to detail, real-world chemistry experience, and practical application. This isn’t some out-of-the-box, standard aromatic compound. Its unique substitution pattern opens up routes not possible with other brominated benzenes, which is why it has earned regular demand from medicinal chemistry and advanced materials projects. As producers, we know what it takes to consistently deliver this compound at the purity and crystallinity that make it useful beyond just a lab curiosity.

    Quality at the Core—Why Every Detail Matters

    Our production of 3,5-Bis(Trifluoromethyl)Bromobenzene — modelwise we keep the focus on the molecular structure, C8H3BrF6 — is all about controlling the synthesis right down to the trace impurity level. In a field where a contaminant below 0.2% can side-track a coupling reaction or kill a catalytic cycle, manufacturers can’t afford indifference. We monitor each lot from the moment it leaves the reaction flask: NMR, GC and Mass Spectrometry are old friends. We see what others might miss, and we act on it, not later, but every step. Keeping water content under control, tightening up on halide purity, and screening for residual acids give scientists a reliable foundation to build the next round of transformation or scale-up.

    We don’t run faceless drum-filling lines. Our facility produces this compound using techniques developed over years of hands-on problem-solving. This is not just “stock” chemistry. Our chemists have refined the process to avoid troublesome byproducts, like symmetrical trifluoromethylbenzenes or halogen exchange residues. Every technical tweak reflects input from colleagues who have run their own Suzuki–Miyaura, Heck, or Ullmann couplings and know the frustrations of inconsistent starting materials.

    What Sets It Apart for Industrial and Lab-Scale Use

    Bromobenzenes come in many designs. What matters in 3,5-Bis(Trifluoromethyl)Bromobenzene is the patterning: two electron-withdrawing trifluoromethyl groups at the 3 and 5 positions, plus a brooding bromine at the 1. Not every aromatic system can make these transformations with the same stability and reactivity. The electron-deficient ring resists oxidative side-reactions, and the fluorines hold molecular geometry tight. That's a combination that stirs interest among those developing pharmaceuticals, OLED intermediates, or liquid crystal materials needing robust backbone scaffolds.

    One fact remains certain: substituent effects show up in yields, reaction temperatures, and product stability. In our production, the melting point runs tight—the sharp transition that trained eyes expect signals real purity. Feedback from our longtime users suggests that competing products can arrive with clouded, grayish tints, variable melting points, or suspicious odors—all hints something didn’t go right upstream. By working at scale and investing in continuous purification techniques, we deliver a crystalline solid that meets standards both for spectroscopy and for downstream process chemistry. We package with the researcher’s bench—not the shipping warehouse—in mind, because the few extra cents to avoid a leaky cap or a contaminated jar can save hours or days of lost R&D time.

    From Synthesis to Packaging—Lessons from Production

    Experience in the plant has brought a practical approach to each run. Handling 3,5-Bis(Trifluoromethyl)Bromobenzene, we see the volatility and recognize the irritant risk but also respect the need for a product uncontaminated by solvents or moisture. Standard bromobenzenes often emerge from plants with a laundry list of residue issues—from chlorinated solvents to decomposition acids, which sabotage downstream use. Through years of re-working process steps specifically for this molecule, we have adopted closed-loop systems that actively limit oxygen ingress, and our workforce is trained to spot subtle irregularities. A sight, a scent, a sudden shift in crystallization—these signal trends that must be corrected. Industry partners have occasionally sent us samples that “should have worked,” only to reveal micro-level contamination from poorly maintained piping, old containers, or suboptimal recrystallization.

    Our continuous improvement methods didn’t come from an outside consultant or some abstract regulatory expectation. Each tweak happened after observing how batch-to-batch variability led to real headaches: filter cake that clogs, unexpectedly high loss on drying, variations in HPLC retention. Addressing these, we developed tweaks to slow crystallization rates, or introduced inert gas blankets at practical stages, based on what operators learned hands-on. This sent our rejection rate plummeting and let us respond faster to customer’s purity or packaging requests.

    Supporting Synthesis—Not Just a Commodity Bromobenzene

    3,5-Bis(Trifluoromethyl)Bromobenzene has become a choice substrate where a more common halobenzene would fail or generate excessive byproduct. Medicinal chemists favor it for building fluoroarene motifs—an increasingly critical feature in improving metabolic stability of drug candidates. Its unusual substitution also helps in lowering aromatic ring activation, which in turn helps tweak bioavailability, a differentiator in the pharmaceutical business. Materials researchers, too, have reported that its symmetrical fluorinated pattern maintains high performance in next-gen device prototypes by improving electron mobility and preventing unwanted cross-conjugation.

    The majority of inquiries for this compound come from teams pushing into new territory—novel ligands in homogeneous catalysis, seed intermediates for complex molecule libraries, bridging units for organic electronics. Choosing the right brominated benzene matters, since differences in substitution patterns alter not only reactivity but also solubility, volatility, and storage profile. Our internal experience supports the view that a standard 4-bromotoluene or monofluorobromobenzene simply can’t substitute here: the symmetry, electronegativity, and steric profile are unique. Every gram made represents a step away from the routine and into the realm of advanced, specialty chemistry.

    Direct Feedback Loops with Users—Learning through Partnership

    Over the years, direct communication with customers has influenced far more than our internal specs. Lab technicians, research leads, and plant engineers have pointed us to bottlenecks or suddenly emergent needs: consistency in physical form, bottle sizes convenient for glovebox transfer, antistatic packaging for scale-up batches. Those working under tight deadlines can’t wait for excuses or restocked intermediate chemicals. So, we stay accessible, listening to what’s really needed on the ground, and modifying processes when it means greater convenience or efficiency for the working chemist or engineer.

    A few organizations even invited us into their pilot plants and synthesis rooms, allowing us to observe firsthand how small deviations in our product—particle size, static buildup, rehydration risk—rippled through their workflows. One notice from a customer struggling with static clumping in winter months spurred us to change our packaging and internal blending approach. We now modulate sieve drying times and container linings to cut back on static, making dosing more reproducible for even the most delicate microgram-scale reactions. What comes off the line is not just purer, it's adapted to living labs—something you won’t get when a trader sources from a dozen faceless producers.

    Meeting the Demands of High-Stakes Projects

    Anyone who has worked with multi-step pharmaceutical or complex materials synthesis knows the perils of switching suppliers. Small changes in supply chain can derail product launches, delay patent filings, or even introduce risks of regulatory review. Years ago, one partner failed to meet their contract requirements after discovering the bromobenzene intermediate sourced elsewhere didn’t align with analytical specs. Such stories remind us why in-house quality assurance and direct oversight at each production stage—right down to the drum or bottle—remain unyielding standards for us. Not everything asked of a specialty aromatic can be met through spot purchasing: the chain of trust has to start at the very reactor.

    Direct manufacturing means direct responsibility. Our record—built on traceable production runs, full spectral records, and transparent analytical data—stands behind each unit we produce. Because not every innovation can wait for a slow-moving supply chain, we work closely with planners to schedule flexible batches, guarantee forward order coverage, and support last-minute increases. Chemists have praised the lack of fracturing in our crystalline solids, a result of low-temperature grinding and vacuum-pack aging, which delivers a product ready for rapid weighing and introduction to sensitive vessels or automated dosing units.

    Understanding the Regulatory Landscape—Not Every Import Is Created Equal

    There’s no escape from regulatory expectations in specialty chemical manufacturing. 3,5-Bis(Trifluoromethyl)Bromobenzene often finds itself under strict eyes, particularly when destined for pharmaceutical or materials supply chains. Compliance to these requirements is not an afterthought during production. Our facility keeps thorough batch records, logs every cleaning cycle, and retains product samples from each lot for retrospective analysis. We have experience overlaying our methods with guidelines set by ICH Q7 and European Pharmacopoeia, supporting any requests for DMF-documented runs or traceability audits.

    A quick look at imported or repackaged alternatives often reveals gaps in documentation, undermining the confidence that innovators expect in a strategic intermediate. Several research groups have reached out after suffering unexplained yields or regulatory set-backs, only to find their “equivalent” product missed crucial impurity screens or lost its certificate history in the hands of re-packers. With direct manufacturing, these concerns land on our bench, where they can be rapidly addressed. Our chromatography records, residual solvent analysis, and assay documentation have resolved more than one production bottleneck or submission hold-up.

    Not Just a Reagent, A True Enabler

    3,5-Bis(Trifluoromethyl)Bromobenzene is more than a building block; it carries with it the reliability and insight that come only from dedication at the manufacturing source. Those who design new pharmaceutical scaffolds or engineer breakthrough display materials know nothing replaces direct, knowledgeable supply. From keeping water content under half a percent, to ensuring every batch achieves a clean melting point above 45 °C, our standards let researchers push boundaries without worrying about the building blocks crumbling beneath.

    There’s a reason our product consistently appears in patent filings and published syntheses for high-profile substances. Process repetition matters; so does willingness to tweak, adjust, and listen. Years of experience tells us that a tightly characterized, reliable aromatic intermediate makes the next step feasible, whether that’s making a clinical trial kilolab batch or scaling up a bench success toward industrial output. Day by day, our production lines prove the value of a direct, knowledgeable manufacturing source.

    Looking Forward: Challenges and Opportunities in Advanced Aromatic Synthesis

    Manufacturing specialty compounds like 3,5-Bis(Trifluoromethyl)Bromobenzene never grows stale. Each new grade, packaging tweak, or scale-up push launches new challenges but also reveals real opportunities to support progress in chemistry and beyond. The steady march of green chemistry is shaping our choices—optimization of reaction solvents, recycling fluorinated byproducts, and integrating more advanced waste stream purification all directly benefit both producer and end user.

    One ongoing challenge is the global availability and sustainability of fluorinated raw materials. Securing uninterrupted supply chains while keeping prices reasonable demands real foresight and the ability to pivot quickly. Our experience has taught us to invest in both upstream partnerships and contingency inventory, shielding our customers from raw material market volatility. This preparedness let us keep commitments even while others fell behind during times of global supply turbulence.

    Process safety is another arena where hands-on manufacturing pays dividends. Fluorinated intermediates can pose significant hazards if handled without intimate knowledge of their physical and chemical characteristics. Well-trained operators and well-maintained systems reduce risks of contamination, emissions, and personal safety incidents. Periodic audits and real-time process monitoring—developed in response to years of watching small flaws spiral into expensive problems—have minimized downtime and created a safer, more reliable plant environment. We see every improvement on the floor translate into confidence for those relying upon our product at the bench or in pilot scale.

    Why Direct Sourcing Makes the Difference

    No two shipments are alike unless every variable has been identified, traced, and locked down by those who truly understand the substance—right down to the molecule. Our commitment to direct manufacturing, backed by practical insight, keeps this specialty aromatic serving new science, safe scale-ups, and crucial technological progress. Each batch reflects partnership, knowhow, and a living, evolving process designed for those who push chemistry into unexplored territory. By sourcing directly from a dedicated manufacturer, research leads and industrial scale-up teams take control over their syntheses, shunning uncertainties that come from faceless intermediaries and ill-documented supply chains.

    3,5-Bis(Trifluoromethyl)Bromobenzene continues to play a pivotal role in shaping modern materials and compounds. Our experience as chemists and producers means we go beyond commodity thinking, investing in the craft, science, and quality needed to keep every project moving forward. This compound, and the expertise behind its manufacture, stands ready for the next breakthrough—delivered with integrity and a commitment sharpened by years in the field.