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2-Bromo-5-(Trifluoromethyl)Benzaldehyde

    • Product Name 2-Bromo-5-(Trifluoromethyl)Benzaldehyde
    • Alias 2-Bromo-5-(trifluoromethyl)benzenecarbaldehyde
    • Einecs 253-774-7
    • 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
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    VTB
    Specifications

    HS Code

    692391

    Productname 2-Bromo-5-(Trifluoromethyl)Benzaldehyde
    Casnumber 261949-10-0
    Molecularformula C8H4BrF3O
    Molecularweight 253.02
    Appearance Off-white to pale yellow solid
    Meltingpoint 49-53°C
    Boilingpoint No data available
    Purity Typically ≥ 97%
    Smiles C1=CC(=C(C=C1C=O)Br)C(F)(F)F
    Inchikey MARZGHBGZBGIJY-UHFFFAOYSA-N
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Storageconditions Store at 2-8°C, keep container tightly closed
    Synonyms 5-(Trifluoromethyl)-2-bromobenzaldehyde

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

    Packing & Storage
    Packing Amber glass bottle, 5 grams, sealed with a PTFE-lined cap, labeled with chemical name, hazard symbols, and batch information.
    Shipping 2-Bromo-5-(Trifluoromethyl)Benzaldehyde is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a hazardous material, requiring appropriate labeling and documentation. Transport complies with international regulations for chemicals, ensuring safe handling and transit. Suitable packaging prevents leaks or spills during shipment.
    Storage 2-Bromo-5-(trifluoromethyl)benzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it away from incompatible materials such as strong oxidizing agents. Protect from moisture and store under an inert atmosphere if possible. Ensure proper labeling and access is restricted to trained personnel.
    Application of 2-Bromo-5-(Trifluoromethyl)Benzaldehyde

    Applications of 2-Bromo-5-(Trifluoromethyl)Benzaldehyde in Industrial Manufacturing

    2-Bromo-5-(Trifluoromethyl)Benzaldehyde serves as a precision intermediate across several high-value synthesis channels. This section outlines key industrial applications, focusing on actual downstream use in pharmaceuticals, agrochemical synthesis, specialty polymers, electronic materials, and pigment production.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers incorporate this compound in multistep syntheses to construct advanced intermediates for active pharmaceutical ingredient (API) production, especially within the oncology and anti-inflammatory drug segments. Its electron-withdrawing trifluoromethyl group and ortho bromine substitution allow controlled introduction into heterocyclic frameworks and fine-tuning of molecular activity. Integration occurs during specific condensation or coupling stages and requires close attention to process validation and analytical traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) guidelines
    • USP <1116> Microbiological Control of Nonsterile Drug Production Areas
    • FDA 21 CFR Part 211 (US)

    Typical usage ratio

    • 0.6 to 1.2 molar equivalents per target intermediate, depending on stepwise yield and purification strategy
    • Adjustment based on specific substrate reactivity; excess often minimized to reduce downstream purification load

    Downstream process integration

    • Introduced at key coupling or cyclization steps in the API building block assembly
    • Used together with palladium or copper catalysts for cross-coupling transformations
    • QC performed after each batch through HPLC or LC-MS

    Final product types

    • Targeted anticancer drugs with aromatic structures
    • Antiviral pharmaceutical compounds
    • Intermediate building blocks supplied for custom synthesis firms
    • Precursor to specialty heteroaromatic APIs

    2. Agrochemical Active Ingredient Building Block

    Manufacturers of crop protection chemicals deploy this specialty aldehyde to generate key fluorinated and halogenated aromatic moieties within modern herbicides and insecticides. The introduction of trifluoromethyl and bromo substituents enhances biological activity spectra and environmental persistence, supporting new molecule registration. This compound is typically included in the early-stage condensation or oxidation reactions when assembling the final biologically-active scaffold.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 (EU)
    • US EPA 40 CFR Part 180 — Tolerances and Exemptions for Pesticide Chemicals in Food
    • ISO 9001-certified quality management system

    Typical usage ratio

    • 0.9 to 1.5 equivalents per batch, tailored as per molecule-specific synthesis protocols
    • Scaling parameters depend on pilot validation and target impurity profile

    Downstream process integration

    • Participates in the Grignard or Friedel-Crafts route for aryl ring derivatization
    • Employed in controlled batch reactors under anhydrous conditions
    • Isolated intermediate undergoes multi-step conversion to the active ingredient

    Final product types

    • Selective herbicide actives for cereals and rice
    • Aromatic-substituted insecticides with enhanced resistance
    • Intermediates supplied to global agrochemical majors
    • Fungicide precursors for cereal protection formulations

    3. Specialty Polymer and Resin Intermediate

    Producers of advanced functional polymers use 2-Bromo-5-(Trifluoromethyl)Benzaldehyde in the custom synthesis of fluorinated and brominated aromatic monomers. These specialized monomers introduce desired electronic, mechanical, and thermal properties to high-performance resins and coatings. The aromatic aldehyde typically enters the process as a core building block during condensation polymerization or via formation of imine/oxime linkage groups in engineered resin chains.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer production
    • RoHS 2011/65/EU (for electronics-compatible applications)
    • ASTM D638 for mechanical properties of plastics
    • REACH compliance for monomer import/use in Europe

    Typical usage ratio

    • 5–20% by mole in specialty monomer formulations, adjusted for molecular weight target
    • Bromine and trifluoromethyl content may be varied according to final resin specifications

    Downstream process integration

    • Integrated as a co-monomer or chain-extender during resin synthesis
    • Condensation polymerization under controlled temperature and catalyst system
    • Downstream blending with additional cross-linkers for property tuning

    Final product types

    • High-performance fluorinated resins for electronic encapsulation
    • UV-resistant coatings for industrial equipment
    • Brominated polymers for flame-retardant composites
    • Specialty adhesives for high-temperature applications

    4. Electronic Material Intermediate for Liquid Crystal and OLED Compounds

    Within the electronics industry, specialty material producers incorporate this compound as a structural unit in synthesizing advanced liquid crystal and organic light-emitting diode (OLED) molecules. The precise arrangement of trifluoromethyl and bromine substituents supports fine-tuning of electron mobility, display contrast, and chemical stability. Manufacturers add the compound during key steps of molecular assembly—often through Suzuki, Heck, or Ullmann-type coupling—prior to functionalization and device integration.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free electronic base materials
    • RoHS 3 Directive (EU) 2015/863 restriction of hazardous substances
    • IPC-4101C for base materials high-performance laminates and prepregs
    • ISO 14001 environmental management for electronic material factories

    Typical usage ratio

    • 0.2–0.6 mol/mol per chromophore unit in OLED/LC mixture design
    • Adjusted according to desired dielectric properties or solubility parameters in blends

    Downstream process integration

    • Enters as a key aromatic precursor in LC/OLED molecule formation
    • Coupled under inert-gas atmosphere using metal-catalyzed pathways
    • Intermediate undergoes further functional modification and purification prior to compounding

    Final product types

    • Liquid crystal display (LCD) and thin-film transistor (TFT) materials
    • OLED emissive layer precursors
    • Advanced dielectric components for flexible displays
    • Photoresist additives for semiconductor lithography

    5. High-Purity Pigment and Dye Precursor

    Manufacturers in the colorant sector employ this benzaldehyde for constructing high-purity fluoroaromatic pigment molecules. Its unique substitution pattern contributes to improved colorfastness, photostability, and chemical resistance in specialty dyes for plastics, fibers, and high-end printing applications. The raw material supports controlled condensation and cyclization routes, forming the chromophore backbone during the regulated manufacture of selective colorant series.

    Industry compliance standards

    • EN 71-3 for safety of pigment substances in toys
    • Oeko-Tex Standard 100 for textile applications
    • REACH Annex XVII for restricted substance content
    • ISO 18314-1 for colorimetric quality management

    Typical usage ratio

    • 0.5–1.2 equivalents per chromophore-forming reaction, adjusted relative to co-reactants
    • Ratio managed to control shade purity, stabilization requires further additives after synthesis

    Downstream process integration

    • Introduced during core aldehyde condensation step in pigment molecule synthesis
    • Subjected to high-purity distillation and crystallization for colorant-grade requirements
    • End product compounded with dispersants for finished colorant form

    Final product types

    • Specialty pigments for engineering plastics
    • High-performance dyes for fiber coloration
    • Inks for security and anti-counterfeit applications
    • Photo-stable toners for precision printing
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    Certification & Compliance
    More Introduction

    2-Bromo-5-(Trifluoromethyl)Benzaldehyde: Sharpening Performance with Purpose-Built Molecules

    More Than a Catalogue Entry: Our Direct Experience Manufacturing 2-Bromo-5-(Trifluoromethyl)Benzaldehyde

    Our own hands and eyes guide every drum of 2-Bromo-5-(Trifluoromethyl)Benzaldehyde that leaves the facility. This isn’t a commodity to us; it’s a deliberate result of smart chemistry and laser-focused process control. Over years of refining our methods, every adjustment taught us about the stubbornness and subtlety typical of brominated aromatics. Many talk about product features, but making this compound day in and day out reveals every quirk and challenge. CF3 groups rarely play by simple rules, and the electron demands of an aromatic ring resist shortcuts. Nobody finds shortcuts here, and the final material reflects that stubborn honesty.

    Our technical team will tell you: each new batch teaches something about efficiency, stability, and purity. Impurities that might be shrugged off in less exacting manufacturing processes show their face in the reaction, sometimes tinting the crude product or tweaking the boiling point enough to warrant investigation. Several times, an off-spec shipment to a research client meant rooting through data and running trial purifications under different column conditions until purity ran above 99%. Because a single part per thousand of a persistent impurity can throw off a lead discovery program, we don't accept less. As manufacturers, the expectation from customers—especially those in pharmaceutical and agrochemical development—is simple: precise, reliable, traceable material, every time. Anything less doesn’t last long in the real world.

    Clarity in Design: How the Right Substitution Pattern Changes Everything

    Chemistry rewards those who respect the power of substitutions. Give a benzaldehyde molecule a trifluoromethyl group at the 5-position and a bromine atom para to the formyl, and you set up a different suite of physical and chemical behaviors compared to plain benzaldehydes. As a manufacturer who monitors reactions and final purity, the strength of electron-withdrawing groups means altered reactivity during further synthesis. The trifluoromethyl group bumps up lipophilicity, influences reactivity and introduces steric differences you can’t ignore. These features don’t just live on paper or in inventory; they change yield and cleanup in downstream chemistry. That's why project chemists ask for this specific substitution, even though it adds time and cost to every kilogram we make.

    Just about every run involves fine-tuning conditions to nudge selectivity, not only to install these groups, but also to prevent bromination from drifting onto undesired positions. Every raw material—bromine, trifluoromethyl source, or even the base aldehyde—forces us to test incoming batches. We see variability in reactivity or impurity pickup, depending on vendor or harvest date. Some may see this as a headache; to us, it’s the kind of detail that sharpens skills and feeds better process improvements. Those patterns reveal themselves only after hundreds of synthetic campaigns and many kilograms moved out the door.

    Real-World Usage: Stepping Beyond Academic Curiosity

    We know where this compound goes after leaving our plant gates. When pharmaceutical clients call, they expect this building block to sit at strategic points in heterocycle construction and fragment-based lead optimization. Agrochemical industry partners value it for late-stage diversification, where a strong electron-withdrawing group gives prodrugs or new pesticide candidates a fighting chance at stability and bioavailability. Sometimes we support advanced material customers shooting for high-performance monomers or specialty fluorinated polymers. Each application brings its own headaches: chemists after purification must adapt their conditions for the heavier electron drag of trifluoromethyl and bromine substituents. As a manufacturer, our role is to remove doubts about trace contamination or batch-to-batch inconsistency so end users don’t burn time troubleshooting the basics.

    We know researchers run sensitive reactions downstream—Suzuki couplings, nucleophilic substitutions, or condensation chemistry—where halogen and CF3 tolerance affects both yield and selectivity. A trace of residual solvent or an unexpected isomer in our product can throw out an entire library synthesis or high-throughput screen. Based on feedback and our own troubleshooting, we made it a point to control trace moisture below tight ppm levels, and we monitor for halo-aldehyde impurities that might sneak past ordinary analytics. There’s real pride in tracking dozens of analytics per lot, and knowing other suppliers rarely invest so much attention in a single intermediate. The trust we’ve built with buyers—especially those who can spot minor impurities by NMR or LC-MS—drives us to keep our operation ahead of the curve.

    Specifications Are Only the Start: How Manufacturing Choices Dictate Performance

    Actual performance doesn't come down to a checklist of melting point and purity digits. In manufacturing, the way you operate sets limits on achievable quality. For example, the syntheses for 2-Bromo-5-(Trifluoromethyl)Benzaldehyde produce byproducts typical of multistep aromatic substitution—difficult-to-separate minor isomers, over-brominated species, or polymeric gum. Removing those without losing yield takes skill at every distillation, crystallization, or chromatography stage. We've watched raw materials and workup conditions influence not just final color or odor, but also stability over storage and compatibility with downstream chemistry.

    Quality means something direct to us. We don't just hit a GC number and call it done. Downtime due to a batch failing impurity specs leads to overtime and extra solvent. We keep samples from every run and track how subtle differences in input materials or reaction temperature show up in the end material. Each change, even if suggested by a process engineer trying to optimize throughput, triggers full requalification down the line. This focus on vigilance separates usable product from wasted effort.

    Comparison to Other Aromatic Building Blocks

    Many buyers ask us why this molecule, and not a simpler benzaldehyde or a differently substituted ring, shows up as the best choice. After decades at the bench and on the plant floor, the answer always comes back to the properties baked into that substitution pattern. The brominated position enables direct metal-halogen exchange, idiosyncratic electrophilic aromatic substitution, or cross-coupling with respect for the lingering demands of the trifluoromethyl group. Trying to push the same chemistry with 2-bromo-benzaldehyde or 4-trifluoromethyl-benzaldehyde leads to frustrations: yields drop, selectivity suffers, or the downstream step introduces new headaches.

    Some partners with tight specs on downstream reactions have told us point-blank: other suppliers shipped “the same” compound but batches weren’t up to the challenge. Their process produced stuck columns, colored byproducts, or extra purification rounds just to reach pharma-grade purity. Consistency matters as much as raw purity; we see it with every returning customer whose time is worth more than a discount on paperwork-grade material. They need reliability, not a gamble on lot-to-lot variance.

    Trusted by Those Who Need More Than Just a Product

    Having worked with so many downstream partners building next-generation APIs and crop protection tools, we understand the stakes. Scientists don’t want just another bottle of material—they want transparency about process, impurities, handling, and storage. We’ve stood at the junction where research programs hinge on whether we can deliver product in time, at the level of purity demanded, and without the headaches of inconsistent results. Our approach has always focused on clarity and close communication, whether that means reanalyzing a material at the client’s request, or being honest about what our process can and cannot do.

    Material produced for general industrial supply looks different from what we generate for demanding med-chem projects. Reporting standards differ, and we’re transparent about which analytical tools we use (NMR, GC, HPLC), retention times, and impurity profiles to give customers insight that’s actionable. We’ve been asked to supply samples for unusual reactivity testing, or to hold product back from shipment to allow a customer to synchronize their procurement and scale-up. Our job involves adapting to these realities, not hiding behind standard specification sheets or generic answers.

    Manufacturing Process Insights: What Decades at Scale Has Taught Us

    In the daily grind, theory meets the messy side of real chemistry. Introducing the CF3 group and bromine in the right order, under controlled temperature and pressure, shows how easy it is to slip from desired product to worse side products. Down the hall, our team has learned every trick to coax crystal formation from tricky oil phases, eliminate colored contaminants, and maximize throughput without slipping below critical safety margins. These struggles drive the incremental process improvements that shave turnaround times, reduce solvent usage, and—most importantly—raise batch consistency.

    Scale presents its own lessons. Charging a reactor with a hundred liters for a kilo-scale synthesis demands respect for subtle but important issues like stirring rate, temperature gradients, and the fate of trace water in solvents. Operators track every variable, but still, each new run always offers something unexpected—a spike in a minor byproduct, a tough filtration, or a drift in reaction color. Instead of hiding these facts, we leverage them for process adjustment. Admitting mistakes and learning from them keeps our process robust long term.

    Troubleshooting and Support: Sharing Experience, Not Just Selling Product

    We don’t see ourselves as just the supplier of a chemical. When a customer’s downstream Suzuki reaction stalls, or a formulation expert sees inconsistent color, they call us directly. We walk through our own knowledge—maybe the CF3 positioning demands extra base, or a higher-purity solvent is advisable. Sometimes, we suggest alternate purification strategies based on what has worked in our own downstream labs post-manufacture. If we learn something new from these collaborations, we update our process or documentation, aiming to avoid repeating old mistakes.

    As synthetic chemists, we understand theory, but we bring the lived reality of manufacturing to every consultation. For researchers used to single-gram prep, kilo-scale quirks come as a surprise. Slight variances at scale can snowball, and knowing what’s unique about this compound—its moisture sensitivity in storage, its susceptibility to light, or just its physical stability—makes the difference between smooth operations and wasted effort.

    Regulatory and Environmental Considerations: Balancing Progress and Responsibility

    Every chemical manufacturer sits under the growing weight of compliance and environmental stewardship. For brominated and fluorinated aromatics like 2-Bromo-5-(Trifluoromethyl)Benzaldehyde, this goes double. We restrict hazardous waste and employ closed-system handling for toxic reagents, not just for regulatory checklists but to ensure that our operators, the air, and local waterways aren’t impacted by our choices. Periodic audits and waste-stream analysis challenge our team to rethink every barrel of solvent and every kilogram of byproduct. Real impact starts in the plant, not just in the pages of a sustainability report.

    End users increasingly ask about the environmental footprint of our raw materials. We maintain transparency about sourcing, and we look for vendors who share these priorities. Improvements to solvent recycling and energy usage require up-front investment, and we’ve often chosen slower, more costly processes to ensure that our own standards meet or surpass local and international guidelines. This extends to shipment and packaging, where our logistics staff minimizes excess materials and matches container type to stability and regulatory requirements.

    Storage, Safety, and Viable Shelf Life: Our Lessons Shared Openly

    Batches stored in our warehouse go through monitored conditions, because we know moisture and light degrade some sensitive aromatics faster than anyone would like. Instead of relying on vague temperature and humidity ranges, we use data loggers at shelf level to track exactly what our material endures. From long-term storage, we’ve learned the visible and invisible signs of quality decline—changes in crystal appearance, small shifts in melting point, and new peaks in HPLC. Based on these lessons, we pass along detailed handling notes when shipping or consulting with customers, saving everyone time and reducing wasted material down the line.

    The very packaging—amber glass or high-integrity fluoropolymer containers—was chosen based on hard-won experience, not just regulatory paperwork. Overpacking sensitive goods, or underestimating customs conditions during shipment, can ruin a batch’s value before it’s even used. This kind of trouble-shooting and foresight only happens when the people making the product are also the ones fielding the angry phone calls if quality drops below expectations.

    Steadfast Attention to Quality with Every Batch

    Each new run proves that there are no shortcuts in manufacturing this specialty aldehyde. Maintaining purity, managing yield, and doing so at a speed and cost that supports discovery chemistry takes focus. We base our claim of quality, not merely on stated purity by GC or NMR, but on customer feedback, process control, and a level of transparency most intermediates rarely receive. And of course, as an experienced manufacturer—not a trader or distributor—we don’t shy away from complex or custom requirements, because our operations and relationships depend on getting details right the first time.

    Looking at the Future: Challenges and Opportunities in High-Value Aromatics Production

    The market signals clear trends—higher regulatory burdens, demand for greener chemistry, clients seeking increasingly exotic substitution patterns. Each of these pushes our process forward. We invest in automation and process analytics to spot deviations before they impact customers. Innovations in greener bromination conditions or alternative trifluoromethylating reagents come downstream only if real production experience validates their usefulness. We’re under pressure to reduce waste, improve throughput, and open new sourcing pipelines for rare reagents.

    One lesson shines through. The market rarely rewards lowest price over consistent, documented quality. Long-term customers return for the reliability, experience, and collaboration we bring, not just for a sharp quote per kilogram. We listen to evolving project requirements and invest not just in better equipment or analytics but in the people behind both the production and the research partnership. Through years of delivering molecules tougher than 2-Bromo-5-(Trifluoromethyl)Benzaldehyde, we’ve learned that trust, expertise, and resilience are the only guarantees in an industry that never stops changing. The everyday rigor of manufacturing isn’t glamorous, but the real innovation often starts with those who make—and stand by—the molecules on which new chemistry depends.