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3-Hydroxy-2,4,6-Tribromobenzaldehyde

    • Product Name 3-Hydroxy-2,4,6-Tribromobenzaldehyde
    • Alias 2,4,6-Tribromo-3-hydroxybenzaldehyde
    • Einecs 259-709-0
    • 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

    655275

    Chemical Name 3-Hydroxy-2,4,6-Tribromobenzaldehyde
    Cas Number 7026-99-1
    Molecular Formula C7H3Br3O2
    Molecular Weight 375.81 g/mol
    Appearance Light yellow to beige powder
    Melting Point 209-213°C
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO
    Purity Typically ≥98%
    Iupac Name 2,4,6-Tribromo-3-hydroxybenzaldehyde
    Smiles C1=C(C=C(C(=C1Br)O)Br)C=O
    Storage Temperature Room temperature, dry place
    Synonyms Tribromosalicylaldehyde

    As an accredited 3-Hydroxy-2,4,6-Tribromobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed with screw cap, labeled "3-Hydroxy-2,4,6-Tribromobenzaldehyde, 10g," hazard symbols and handling instructions displayed.
    Shipping 3-Hydroxy-2,4,6-Tribromobenzaldehyde is shipped in sealed, chemical-resistant containers compliant with international regulations. The package is clearly labeled with hazard information and handled by trained personnel. During transit, it is protected from moisture, light, and heat to ensure stability and safety. Shipping documentation includes relevant safety data sheets (SDS).
    Storage 3-Hydroxy-2,4,6-Tribromobenzaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Use secondary containment to prevent accidental release, and ensure proper labeling. Store at room temperature and avoid heat or direct sunlight to maintain stability.
    Application of 3-Hydroxy-2,4,6-Tribromobenzaldehyde

    Applications of 3-Hydroxy-2,4,6-Tribromobenzaldehyde in Industrial Manufacturing

    3-Hydroxy-2,4,6-Tribromobenzaldehyde is a specialty intermediate supplied for advanced chemical synthesis across various industrial sectors. We supply this raw material with consistent assay and purity, integrated directly into downstream processes by formulators and manufacturers requiring reliable input for high-performance applications.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Major pharmaceutical companies utilize this compound as an electrophilic building block for synthesis of brominated benzene derivatives in API production. Its unique substitution pattern enables selective reactions for antibacterial and anticancer drug candidates in multi-step synthesis routes. Chemists often employ it for coupling reactions during intermediate assembly and late-stage halogenation modifications under GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia requirements for synthetic intermediates
    • FDA 21 CFR Part 210/211 drug substance regulations
    • REACH Registration under ECHA for pharmaceutical uses

    Typical usage ratio

    • 0.5%–3% by mass relative to final API batch, adjusted for route yield and molecular weight

    Downstream process integration

    • Introduced during key-step bromination or formylation as a limiting reagent; enters multi-step synthesis after core scaffold construction in batch or semi-continuous reactors under controlled atmospheres

    Final product types

    • Antibacterial agents with brominated aromatic cores
    • Investigational anti-neoplastic APIs
    • Intermediates for CNS-acting small molecules
    • Brominated imaging agents for contrast media

    2. Intermediate for Industrial Dyes and Pigments Synthesis

    Dye and pigment manufacturers incorporate this compound in the formation of specialty triarylmethane and azo dye structures. Its three bromine groups provide ortho-directing effects required for functionalized colorant backbones, leading to increased photostability and shade depth in industrial textile and ink applications. Color chemists leverage its high reactivity during condensation or coupling stages.

    Industry compliance standards

    • Oeko-Tex Standard 100 for colorant toxicity limits
    • EU Regulation (EC) No 1907/2006 REACH for coloration intermediates
    • ISO 105/X12 for color fastness specifications
    • ETAD guidance for responsible dye manufacturing

    Typical usage ratio

    • 1%–8% per batch, adjusted for targeted pigment structure and required tinctorial strength

    Downstream process integration

    • Added post-condensation as an electrophilic coupling partner or during azo-coupling reactions, typically in closed vessel or semi-batch processes

    Final product types

    • Brominated triarylmethane pigments for inks and plastics
    • Functional textile dyes with enhanced UV stability
    • Specialty printing inks for security applications
    • Coating-grade pigments for high-performance industrial paints

    3. Synthesis of Flame Retardant Monomeric Additives

    This compound acts as a reactive monomer or intermediate in producing flame retardant agents for polymer and resin systems. The multi-bromine structure imparts high halogen content, essential for increasing the limiting oxygen index (LOI) in engineering thermoplastics and epoxy resin matrices. Flame retardant manufacturers rely on it for controlled synthesis of high-purity additives that meet strict regulatory requirements for building, electronics, and transportation sectors.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics Materials
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • National Fire Protection Association (NFPA) 701 for textiles
    • EN 45545-2 fire safety for railway applications

    Typical usage ratio

    • 5%–18% weight ratio in formulation, adjusted based on polymer matrix flammability and targeted LOI

    Downstream process integration

    • Introduced as a monomer during pre-polymerization blending or as a reactive additive during extrusion and compounding of polymer resins; often pre-dissolved into resin melt or master batching systems

    Final product types

    • Engineering thermoplastic pellets for wire & cable insulation
    • Epoxy-based fire-resistant coatings
    • Rigid polyurethane foam panels for construction
    • Flame-retardant electrical encapsulants

    4. Precursor for Agrochemical Active Ingredient Synthesis

    Agrochemical R&D teams adopt 3-Hydroxy-2,4,6-Tribromobenzaldehyde in the synthesis of brominated benzaldehyde-scaffolded actives for fungicide and herbicide development. Its unique substitution allows for downstream functionalization with nitrogen, sulfur, or phosphorus compounds, making it a critical intermediate for proprietary formulation work in crop protection. High-purity input is required for batch reproducibility in pilot- and production-scale plants.

    Industry compliance standards

    • FAO/WHO Specifications for agricultural pesticides
    • ISO 9001:2015 for agrochemical manufacturing QMS
    • EPA 40 CFR Part 158 for pesticide chemical registration
    • Chinese NY/T 1107-2020 pesticide product quality standards

    Typical usage ratio

    • 0.3%–2.5% per formulation batch, based on the target molecule’s stoichiometric requirements

    Downstream process integration

    • Charged as a core aromatic intermediate during the synthesis of candidate actives within multi-step batch or flow systems; added at selective aromatic substitution or nucleophilic addition stage to form unique brominated substituent patterns

    Final product types

    • Brominated pre-emergence herbicide molecules
    • Fungicidal actives for foliar application
    • Seed-coating agents for pest resistance
    • Agrochemical intermediates for custom blends
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    Certification & Compliance
    More Introduction

    3-Hydroxy-2,4,6-Tribromobenzaldehyde: A Reliable Choice for Demanding Synthetic Needs

    Among the various intermediates we produce at our plant, 3-Hydroxy-2,4,6-Tribromobenzaldehyde has carved out a special role. This compound stands out not just because of its structure, but also for how it brings consistency and value to a range of industries—especially those with tight demands on purity and traceability.

    Understanding the Product

    Every batch of 3-Hydroxy-2,4,6-Tribromobenzaldehyde rolling off our lines follows a process shaped by years of hands-on production experience. The benzaldehyde core, substituted with three bromine atoms and a hydroxyl, offers more than academic interest. Our teams zone in on both the ortho-bromo and para-bromo positioning to ensure clean reactions later down the chain. Manufacturing precision means our material consistently matches the required assay and meets low impurity thresholds, so researchers and factories don’t run into unexpected pitfalls.

    Projects that call for exact outcomes can’t tolerate drift in product profiles. Whether we're shipping grams for micro-scale pilot work or drums for factory-scale synthesis, our content and impurity profiles remain within agreed specs. Quality doesn’t lie in appearance alone; it comes out in every downstream reaction. To the chemist or engineer, differences in residual solvents, trace metals, or even moisture content can tip a reaction toward trouble. That’s why process stabilization and real-time monitoring guide our entire line—operators and supervisors know the risks of complacency.

    Why Choice of Intermediate Matters

    In specialty chemical synthesis, a missed detail at the intermediate stage can ripple out as failed batches far downstream. Unlike simple building blocks, 3-Hydroxy-2,4,6-Tribromobenzaldehyde often lands at stages where chemistries diverge: from pharmaceuticals and dyes to specialty polymers and even flame retardant applications. We’ve answered calls from researchers needing to scale up unexpected discoveries, only to find that off-the-shelf options failed to give reproducible yields. Our production plant’s batch records and archives get heavy use for this reason—we make sure there’s a clear trail back to the raw material lot and its analytical fingerprint.

    Over the years, we’ve watched labs struggle with material from uncertain origin. Unexplained reactivity, slow crystallization, odd tints after dissolution—each can point to trace differences in bromine substitution, small amounts of side-products, or incomplete conversions. Our own protocols take lessons from these stories. Each reaction, each finished batch, teaches us where to watch closer. In one recent season, a pharmaceutical customer flagged a low-level contaminant that had slipped by earlier equipment; after root cause analysis, we retooled filtration to trap the last traces, and reworked our solvent sourcing. There’s no way to guarantee outright perfection, but consistent improvements carry through to a more reliable intermediate for all users.

    Practical Applications

    In practical settings, the benzaldehyde’s high reactivity bridges key steps, such as forming crucial carbon-nitrogen bonds or introducing functional diversity at the aromatic ring. Most researchers using this material pursue synthesis routes leading to advanced pharmaceuticals, agrochemical actives, luminescent compounds, or performance materials. The tri-brominated skeleton lends itself to further functionalization; you get handles for Suzuki, Heck, or Ullmann couplings, and with care, the hydroxyl position unlocks protection, activation, or targeted substitution.

    Our collaborators often need predictable conversion rates when pushing these reactions forward. Minor differences in impurity content—whether unreacted mono-bromo derivatives, leftover acids, or trace metal ions—can throw off catalyst performance or dehomogenize reaction media. Our control over purity and lot certification, developed through routine collaboration with analytical chemists, helps avoid these headaches. For reference, we keep comprehensive retention samples and analytical reports. Customers request verification, and we can retest or track issues back to the original production logs. A lab can re-route a synthesis or optimize yields far more confidently when intermediates like ours perform as described.

    Comparison with Alternative Intermediates

    Some industry professionals suggest lower-brominated benzaldehydes or even unsubstituted forms, hoping to cut costs or sidestep regulatory constraints. But our customers explain, and our own tests show, that fewer bromine atoms often weaken selectivity in later steps, especially in multi-step processes requiring clean, directional transformations. Lesser brominated intermediates might appear attractive on paper, but in bench-top or factory settings, inconsistent side-reactions and purification headaches tend to erase these cost savings. Our backbone of tri-bromination, carefully monitored during synthesis and confirmed with NMR and mass spectrometry, translates to a more responsive, manageable intermediate.

    Take multi-step pharmaceutical routes: chemists might attempt to begin with 2,4-Dibromobenzaldehyde, hoping to tweak reaction conditions or add necessary groups as needed. They soon encounter issues: unpredictable by-products, lower yields, bottlenecks in purification. We’ve supplied samples for direct side-by-side trials and watched these differences in real time. One recent customer reported a clear batch-time reduction, shaving full days from their process after standardizing on our tri-brominated intermediate. Beyond pharma, similar stories echoed from polymer researchers and dye makers, who rely on efficient, high-yield reactions to keep project timelines intact.

    Consistency and Traceability Build Confidence

    A manufacturer’s reputation rests on keeping promises: if we say our 3-Hydroxy-2,4,6-Tribromobenzaldehyde meets a spec, it needs to. Our site never shortchanges routine controls, not just for compliance but because it’s the cost of trouble-free reactivity. Each batch’s documentation, whether related to melting point, appearance, moisture, or assay, travels with records accessible to both QC managers and lab partners. Raw material lots stay segregated; our tracking ensures that if a problem ever arises, we can roll back quickly and fully examine where things went sideways.

    We run regular audits not just on our line but with solvent and reagent vendors. Even minor changes at the source can cause headaches downstream—non-detectable contaminants or subtle batch-to-batch variation in bromine can have outsized effects in pharmaceutical production. Our team uses a mix of classic wet chemistry checks alongside modern spectroscopic methods, balancing legacy best practices with digital traceability so nothing slips past the net. Production engineers on our floor know the stakes, and pride themselves on spotting issues before the product heads to packaging.

    Addressing the Real-World Challenges

    Working directly as a manufacturer, we see research and market pressure from both ends—scientists pushing toward new targets, regulators requiring clear accountability, and customers needing speed as much as safety. A recurring challenge rests in balancing throughput with batch quality, especially as worldwide demand for specialty intermediates wavers with trends in pharma and advanced materials.

    Some customer projects run with minimal lead time. One week, we may field urgent requests from a biotech startup developing a new active ingredient; the next, a multinational relying on regular monthly shipments for established lines. Unplanned changes—a delay in bromine supply or an uptick in demand driven by regulatory changes—test our ability to source, produce, and ship with the same rigor as ever. We insulate production from such swings by holding strategic raw material stocks and working with a trusted supply chain network, rather than chasing the lowest short-term price. Our own production schedule flexes without sacrificing record-keeping or documentation.

    Shipping hazardous materials involves its own tangle of requirements. For a molecule like ours, with three bromine atoms, rules for packaging, storage, and transit stack up quickly. Our shipping group works closely with logistics providers, making sure every container meets the regulations—packed with the right absorbers, seals, and hazard label. These details aren’t just for peace of mind; they have direct impact on usability after arrival. Delayed or compromised material can cascade into project delays and cost overruns.

    Our customer support rests on technical know-how, not just paperwork. We field questions about optimal storage conditions and best practices for handling and reactivity, based on years running our own internal stability and reactivity tests. Labs run by early-career researchers might ask about minimizing waste or dealing with by-product formation, and we guide them using findings from our own troubleshooting. It pays off in user satisfaction—and often uncovers process improvements that feed back into our mainline production for everyone’s benefit.

    Adaptation and Future Improvements

    As reaction techniques evolve, so do the requirements for intermediates like 3-Hydroxy-2,4,6-Tribromobenzaldehyde. Automation and continuous flow chemistry hit the scene, bringing demands for finer control over impurities and particle size. We’ve taken these cues and developed in-line monitoring and real-time process adjustments that sharpen the product’s specs even further.

    Environmental standards have also tightened. Customers within Europe or North America—where REACH and comparable standards shape purchasing—insist on detailed records of every component and trace impurity. Our environmental and safety group works directly with the production team to adapt to these rules, substituting less hazardous reagents or recycling side-streams where technically feasible. These small efforts add up: we have managed to drop the waste output per kilogram produced through incremental changes, detail by detail.

    Ongoing projects focus on green chemistry, aiming to minimize reliance on reagents that leave legacy byproducts. Direct bromination used to be the weak point in the process chain, but research in the last decade now points toward oxidative processes that deliver selectivity with less risk. In our plant, we phase in newer catalysts as they prove robust in trial and don’t compromise the product spec or create new analytical uncertainties. Our customers benefit from the thoroughness, as their own green initiatives align with a supply chain that adapts rather than resists.

    A Track Record Through Industry Partnerships

    We didn’t arrive at today’s process overnight. Lasting relationships with industry clients in pharmaceuticals, dyes, and advanced materials provided feedback loops shaping our approach. Labs documented better yields and fewer purification headaches as they switched supply to our batches; returning customers confirmed that our focus on quality didn’t waver even as order volumes swung widely. More than once, early-stage feedback on process bottlenecks resulted in joint testing or shared analytical resources, drawing down costs for all sides and pushing efficiency up for future work.

    On-site visits by research partners—sometimes probing every step from raw bromine weighing through finished barrel filling—keep us on our toes and force honest evaluation of procedures. The mutual transparency between our team and these researchers means issues rarely sit unsolved for long. Not every result has been perfect, but persistent communication and learning from setbacks keep us sharp.

    What Sets Our Material Apart

    Some industry suppliers ship intermediates only by reselling commodity bulk product, purchased through traders and sometimes cut between multiple brokers. That approach does not fit with the reliability demanded in today’s synthesis. Our model means the same crew controls every step: from raw material check-in, through the reaction, purification, packing, and certificates released at shipment. We keep well-maintained, modernized reactors in-house, paired with decades of hands-on operator know-how that constantly shortens the distance from feedback to action.

    Each batch certificate matches actual QC testing—not generic data. This means the between-batch variation stays within tight limits. We know the importance of accurate NMR and GC-MS records to pharma and material science labs, so every report comes with full transparency. Multiple customers credit their switch to our direct-supply model with eliminating unexpected out-of-spec reactions, missed project milestones, and tedious troubleshooting.

    Careful control does not translate to inflexibility. Custom requests for specific particle size, alternate solvents, or even small-pack trial runs arrive here often—sometimes sparked by a new multistep reaction or regulatory request. Our technical team often collaborates directly with customer R&D to tweak processes, avoiding the frustration of one-size-fits-all supply. If a researcher encounters a persistent bottleneck, our in-house chemists test modified process steps, provide detailed analytical support, and push out pilot batches for real-world feedback.

    Real Stories: Value Beyond the Label

    Over the years, tangible returns from this direct approach kept our efforts sharp. An advanced materials customer working on OLED precursors faced recurring issues from a generic-purity intermediate; coordination with their R&D led to a joint pilot run at our facility, ultimately locking down reaction times and reducing waste. In another case, a contract pharmaceutical manufacturer flagged chronic drops in assay and purity from prior supply chains. Detailed examination of their synthetic route and blending techniques let us identify cause: a minor change in our drying protocol, made years earlier, didn’t interact well with their own isolation solvents. We amended our process; they reported step-increase in yield consistency ever since.

    Another researcher, based in the academic sector, needed minimal-level impurity content to avoid interference in an uncommon asymmetric transformation. Our team produced a micro-scale trial lot honed specifically for their setup. Over the following year those findings fed directly into process-language changes for larger customers, so the learning benefited more than the original requester. The experience of working side-by-side, instead of just delivering commodity batches, means breakthroughs and improvements don’t stagnate—they work back through the system.

    Conclusion: Trust Built In, Not Tacked On

    The backbone of our business lies not in simple product delivery, but in the trust built over years of transparent, hands-on manufacturing. 3-Hydroxy-2,4,6-Tribromobenzaldehyde, though just one intermediate among many, illustrates how this trust plays out in real results: smoother scale-ups, faster project completion, lower rates of unseen contaminants, and reduced troubleshooting for users both large and small.

    Each molecule leaving our line reflects the relentless focus on what matters: consistent quality, traceable origins, and reliable function. We produce for real outcomes, measured every day on lab benches and factory lines worldwide. For chemists, engineers, and researchers seeking a true production partner—not just a box on a manifest—our 3-Hydroxy-2,4,6-Tribromobenzaldehyde stands out as a tested, refined, and thoroughly supported building block, ready to meet the demands of next-generation chemistry.