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2,4,6-Tris(Bromomethyl)Mesitylene

    • Product Name 2,4,6-Tris(Bromomethyl)Mesitylene
    • Alias TBM
    • Einecs 221-967-7
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    673760

    Chemical Name 2,4,6-Tris(Bromomethyl)Mesitylene
    Cas Number 80584-85-6
    Molecular Formula C12H15Br3
    Molecular Weight 437.87 g/mol
    Appearance White to off-white solid
    Melting Point 90-94 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.92 g/cm³
    Synonyms Mesitylene tribromomethyl derivative
    Purity Typically ≥ 98%
    Storage Conditions Store in a cool, dry place, tightly closed container
    Smiles CC1=CC(=C(C(=C1C)CBr)CBr)CBr

    As an accredited 2,4,6-Tris(Bromomethyl)Mesitylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tight-sealed cap, labeled “2,4,6-Tris(Bromomethyl)Mesitylene, CAS 1826-11-9, 25g.”
    Shipping 2,4,6-Tris(Bromomethyl)Mesitylene should be shipped in tightly sealed containers under dry, cool conditions, protected from light and moisture. Classified as a hazardous material, it requires proper labeling and documentation. Transport according to local, national, and international regulations for hazardous chemicals, ensuring compatibility and separation from incompatible substances during shipping.
    Storage 2,4,6-Tris(Bromomethyl)Mesitylene should be stored in a tightly sealed container, away from light, heat, and moisture. Keep in a cool, dry, well-ventilated area, separated from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and use secondary containment to prevent spills. Handle under an inert atmosphere, like nitrogen or argon, to minimize degradation and moisture exposure.
    Application of 2,4,6-Tris(Bromomethyl)Mesitylene

    Applications of 2,4,6-Tris(Bromomethyl)Mesitylene in Industrial Manufacturing

    2,4,6-Tris(Bromomethyl)Mesitylene is a specialty brominated aromatic compound widely used as a reactive intermediate in several advanced materials sectors. The following application scenarios demonstrate how our product integrates into key industrial verticals, supporting compliance, additive precision, and downstream process reliability across stringent manufacturing environments.

    1. Flame Retardants for Engineering Plastics

    Producers of high-grade engineering plastics incorporate 2,4,6-Tris(Bromomethyl)Mesitylene as a brominated flame retardant precursor. Its molecular structure enables efficient grafting into thermosetting resins and thermoplastics, especially where high thermal stability is a key requirement. Customers formulate blends to comply with international flame-retardancy standards for automotive, electrical, and appliance housings, while maintaining the mechanical properties of polycarbonate, epoxy, and polyamide matrices.

    Industry compliance standards

    • UL 94 Flammability Standard (Underwriters Laboratories)
    • IEC 60695-11-10 (Glow-Wire Test)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • EN 45545-2 (Fire Protection on Railway Vehicles)

    Typical usage ratio

    • 2–8% by weight in resin systems; adjustment based on target V-0 or V-1 flammability class and resin compatibility for balanced performance.

    Downstream process integration

    • Direct addition during polymer melt compounding, or pre-reacted as a monomer in cross-linked resin synthesis; included before extrusion or molding steps.

    Final product types

    • Enclosure components for consumer electronics
    • Automotive under-hood parts
    • Electrical switchgear housings
    • Industrial circuit board laminates

    2. Reactive Flame Retardant Intermediates for Epoxy Resins

    Chemical manufacturers employ this raw material to synthesize brominated epoxy intermediates, particularly where high-bromine content and stability under curing conditions are needed. Its unique configuration supports chain extension and cross-linking, offering downstream processors consistent bromine incorporation during advanced composite or electronic encapsulant production.

    Industry compliance standards

    • IPC-4101 (Base Materials for Printed Boards)
    • REACH Regulation (EC) No 1907/2006
    • EN 13501-1 (Fire Safety for Construction)
    • IEC 61249-2 (Materials for Printed Circuit Boards)

    Typical usage ratio

    • Reaction into epoxy intermediates typically at molar ratios designed to deliver 15–25% bromine content in the final advanced resin.

    Downstream process integration

    • Used in the bromination and glycidylation stages of advanced epoxy manufacturing; intermediates are supplied to PCB and semiconductor packaging operations.

    Final product types

    • Flame-retardant laminates for printed circuit boards
    • LED encapsulation materials
    • Coating resins for electronics assembly
    • Epoxy prepregs for high-performance composites

    3. Crosslinking Agent in Ion Exchange Resin Synthesis

    Specialty resin manufacturers utilize 2,4,6-Tris(Bromomethyl)Mesitylene as a trifunctional crosslinker during suspension polymerization for anion or cation exchange resin beads. Its trifunctionality enables high cross-link density, controlling pore structure and mechanical strength, which is vital for resins deployed in chemical processing, power generation, and water purification applications.

    Industry compliance standards

    • NSF/ANSI 61 (Drinking Water System Components–Health Effects)
    • USP <643> (Total Organic Carbon in Water for Pharmaceutical Use)
    • ISO 9001:2015 (Quality Management for Resin Production)
    • Food Chemicals Codex (FCC) for some water treatment grades

    Typical usage ratio

    • 0.5–3 mol% relative to base monomers (styrene/divinylbenzene); ratio selected per required pore distribution and exchange capacity.

    Downstream process integration

    • Charged into aqueous phase of suspension polymerization; crosslinking for bead formation before washing, activation, and finishing.

    Final product types

    • Industrial-grade anion and cation exchange beads
    • Ultrapure water resin cartridges
    • Resins for catalysis and organic synthesis
    • Water softeners and deionization systems

    4. Synthesis of Specialty Pharmaceuticals Intermediates

    API manufacturers source 2,4,6-Tris(Bromomethyl)Mesitylene as a building block in the preparation of advanced pharmaceutical intermediates, particularly for macromolecule assembly and as a scaffold in select drug candidates. Its high-purity grade and defined halogen content make it suitable for regulated environments demanding traceability.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (Current Good Manufacturing Practice, US FDA)
    • European Pharmacopoeia (Ph. Eur.) specification for intermediates
    • ISO 13485 (for medical device intermediates)

    Typical usage ratio

    • Stoichiometric ratios in intermediate steps; amounts calculated precisely based on desired molecular framework assembly in multistep synthesis.

    Downstream process integration

    • Introduced at early-stage halomethylation or cross-linking in multistep syntheses; handled in controlled reactors with in-process analytical verification.

    Final product types

    • Pharmaceutical intermediates (custom synthesis contracts)
    • Precursors for medical imaging agents
    • Key fragments for antiviral actives research
    • Specialty monomers in biodegradable drug delivery polymers

    5. High-Performance Polymer Additive for Aerospace Composites

    Composite material engineers utilize this brominated mesitylene compound in the formulation of aerospace-grade prepreg systems, focusing on smoke density, toxicity management, and flame propagation resistance. It enables the synthesis of resins with high char yield, supporting rigorous fire performance certification for aircraft cabin and structural applications.

    Industry compliance standards

    • FAR 25.853 (Flammability of Aircraft Cabin Materials)
    • EN 45545-2 (Rail and Aircraft Interior Materials Test)
    • ISO 5659-2 (Smoke Production Test for Polymers)
    • SAE AS5127 (Aerospace Resin Processing)

    Typical usage ratio

    • 5–10% by weight in resin formulations; optimized to balance fire rating, mechanical strength, and resin matrix compatibility for aerospace standards.

    Downstream process integration

    • Added during prepolymer resin manufacture prior to prepreg impregnation; incorporated with continuous QA tracking per aerospace protocols.

    Final product types

    • Fire-resistant interior paneling for aircraft cabins
    • Composite seat structures
    • High-strength structural laminates
    • High-performance adhesive films
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    Certification & Compliance
    More Introduction

    2,4,6-Tris(Bromomethyl)Mesitylene: Insights from the Manufacturer’s Floor

    In the specialty chemicals space, every batch tells a story, and few products draw as much attention as 2,4,6-Tris(Bromomethyl)Mesitylene. As a manufacturer with years refining this compound, we have watched industries push its limits, each striving for higher performance and precision. Our own process started small, in a single facility dedicated to halogenated aromatic intermediates, and has now scaled across multiple lines, supported by teams who know the ins and outs of aromatic bromination.

    Understanding 2,4,6-Tris(Bromomethyl)Mesitylene

    This compound, known by its CAS number 80584-85-6, stands out for its structure: a mesitylene core substituted with three well-placed bromomethyl groups. Chemically robust and consistent in reactivity, we produce it in colorless to yellowish crystalline form. Strong, characteristic odor tells those on the line it’s being handled, and skilled workers rely on visual and olfactory cues just as much as instrumentation for real-time feedback. Each batch brings the same tight melting range and solubility profile, a level of reliability that our long-standing customers value.

    Specifications from Years of Experience

    Any product can meet a certificate of analysis. What counts on the manufacturing floor is recognizing when subtle variations might impact downstream applications. Our 2,4,6-Tris(Bromomethyl)Mesitylene consistently lands above 98% purity by HPLC, with controlled moisture content, residual solvents maintained at near-trace levels, and bromine content checked through titration on every production lot. Lower-purity byproducts, the inevitable challenge of aromatic bromination, undergo removal with custom chromatography systems we built after years of iteration. Secondary products from incomplete bromination occasionally crop up, but vigilance in temperature and stirring retards these unwanted impurities.

    Product is packed in lined drums or glass containers, with the material sensitive to moisture and light. Some clients worry about caking during transit; we counter this with careful pre-drying and vacuum sealing, steps developed after seeing clumping reported by old customers in humid regions. In our labs, every sample is tested for appearance, melting point, and trace color before it ships.

    Applications that Shape Expectations

    2,4,6-Tris(Bromomethyl)Mesitylene holds value across several industries, but we see most volume demand coming from the synthesis of tripodal ligands, flame retardants, and certain pharmaceutical building blocks. Out at the reactors, its three reactive bromines let users introduce branching fast, and it’s become a backbone in creating complex star-shaped polymers. Many clients choose it to anchor dendrimers or cross-link new materials, biting off two or more bromomethyl groups at a time in controlled fashion.

    Pharmaceutical researchers leverage the reactivity for stepwise alkylation of amine cores. This allows for creativity in drug design, stacking functional groups with fewer side-reactions. Specialized labs order our highest-purity grade for such synthesis, keenly aware that even a trace impurity can ruin a run that took weeks of planning. For flame retardants, polymer chemists use the compound to modify resin structures, seeking stronger thermal performance with less weight penalty than traditional additives.

    What sets the compound apart? Practical hands know that not all halomethylated aromatics behave the same. Single- or di-bromomethyl substitutions do not match the cross-linking efficiency of the tris variant. We’ve run side-by-side reactions in our pilot plant and tracked branching rates using pulse-field gradient NMR. Customers have confirmed our results in the field, noting that 2,4,6-Tris(Bromomethyl)Mesitylene integrates more smoothly into highly branched structures compared to ortho- or para-only alternatives.

    Lessons Learned Controlling Quality and Impurities

    Manufacturing this compound, bromination control matters more than with many simpler molecules. Early batches years ago taught us that unreacted mesitylene and dibrominated analogs sneak in unless you time the addition of brominating agent precisely and keep temperature gradients to a minimum. Our managers spent months troubleshooting reactor sampling points until impurity spikes fell within tolerances. Since adopting real-time monitoring with in-line FTIR, we stopped seeing unexpected color in the final product—one of those process improvements that’s now standard, but cost us thousands of dollars and overtime before we got it right.

    We also had to adjust our drying steps more than once. Early experience showed that gentle vacuum drying preserves product morphology better than aggressive heat cycles, which can cause degradation and create dust that’s hard on lungs and lab filters. Now, each drying batch is logged by operator initials, and spot checks with moisture probes keep residual water well below one percent. These “small” choices, invisible in written specs, become vital once scale-up brings shipments into new climates or storage for longer periods. One year, we had to recall part of a lot after unnoticed condensation skewed analytical results; since then, tracking container temperature during transit became our norm.

    Distinguishing Features from Other Bromomethyl Aromatics

    We get calls from chemists seeking alternatives to 2,4,6-Tris(Bromomethyl)Mesitylene, either to test a hypothesis or cut cost. Our technical team answers directly, pointing out that tris substitution on the mesitylene ring generates distinct reactivity. Most other products in this class substitute at only one or two methyl positions, producing intermediates less efficient in star-branched polymer synthesis or multi-site alkylation. The symmetric arrangement of all three bromomethyls enables faster and more controllable chain growth in dendritic and star polymers. Single and disubstituted variants introduce branching inefficiencies and cause broader molecular weight distributions.

    Competition sometimes promotes 2,4,6-tribromomethyl toluene or similar compounds as plug-in replacements, but our side-by-side application testing consistently finds slower reaction rates and less uniform product formation. We use strict analytical controls on our line, and years of NMR and GPC data from our own clients confirm that structural consistency of the tri-substituted mesitylene tracks directly with smoother, more predictable outcomes in both small-scale and bulk polymer settings.

    Handling, Storage, and Safety in the Real World

    Chemists appreciate theoretical safety, but those who move bags, pack drums, and load trucks want to see rigorous attention on the ground. Our site operates with full PPE requirements during filling and sampling, and air scrubbers run constantly. We learned this was necessary the hard way: in our early years, a minor spill forced an evacuation after brominated fumes spiked at one sampler’s workstation. The lesson stuck, driving our investment in modernized enclosure systems and air flow alarms. Our product ships with material safety sheets prepared by the same team that works with the substance daily—not farmed out to remote consultants. All containers go through double-seal checks and are stacked to avoid tipping or friction damage.

    Some competitors try cost-cutting by omitting desiccant or using thin-walled drums. Years ago we saw how a cheaper drum buckle led to a torn liner and subsequent contamination. Since then, our purchasing department never skimps on packaging. Day-to-day vigilance, shaped by hard-won experience, carries more weight than a blur of technical documents for anyone dealing with halogenated aromatics in bulk.

    Driving Innovation through Customer Partnership

    Feedback from our customers shapes more of our process than any text in a standard operating procedure. Not every client wants the same product grade: some want greater than 99% purity for advanced pharmaceutical research, others use slightly lower-purity grades to save cost without sacrificing function in polymer labs. We meet regularly with partner labs to map out new production targets and process improvements. More than once, a client’s application failure traced back to trace halide contaminants, which we then worked into our own in-process checks. One case involved a customer using our product to generate a three-armed ligand for a metal catalyst, only to find by NMR analysis that low-level chloro byproducts changed binding selectivity. We changed raw bromine sourcing, checked for solvent cross-contamination, and solved the problem within two generations of the process.

    Several partners in flame retardant manufacturing asked us for finer particle size, which wasn’t something we’d prioritized. After testing micronization on pilot batches, we now run additional screening for those orders, having seen how end-use testing at our customer sites yielded improved dispersibility and better final composite properties. Every incremental improvement brings us closer to a product line shaped by conversation, not just specification sheets.

    Regulatory, Environmental, and Supply Chain Challenges

    Producing 2,4,6-Tris(Bromomethyl)Mesitylene comes with a set of regulatory obligations. Local and international guidelines define not only raw material sourcing but also waste disposal and transport protocols. From the start, our plant design factored in closed systems for bromine handling and efficient neutralization tanks for acidic byproducts. Years back, inspector walkthroughs flagged volatile organic emissions higher than allowed; after installing advanced gas scrubbers, we cut total emissions below mandated levels and achieved better working conditions.

    Environmental sustainability takes center stage in every process update. Rather than accepting solvent-intensive steps, our R&D crew trialed alternative processes to recover or recycle solvents like dichloromethane. These trials saved thousands of liters a year and positioned us ahead of pending environmental rules. Multi-step cleaning cycles cut cross-contamination between product lines, another key lesson for robust compliance. Challenges remain—brominated waste is a tough problem worldwide, and we keep investing in new decomposition and reclamation methods to reduce landfill burden.

    Supply chain hiccups occasionally ripple through the system. Bromine sourcing, always subject to market volatility, requires us to maintain safety stocks and hold standing supplier agreements. Disruptions in transport, especially with port slowdowns or regulatory holds, push us to communicate clearly with customers about possible delivery impacts. During peaks of global chaos, our foreman supervise extra shifts not to grow output, but to bring orders current for long-time partners. Trust builds best when those downstream know their orders are a top priority, even in uncertain logistics conditions.

    Continuous Improvement through Data and Operator Skill

    Technology evolves, but there is no substitute for skilled operators who spend years learning the product’s quirks. Data from continuous quality monitoring builds our protocols, and every year brings new instrumentation upgrades for faster, smarter production. Still, it is the shift supervisor’s judgment at midnight, the operator’s feel for the end of a distillation run, and the meticulous habits of the cleaning crew that keep quality deviations from ever reaching customers. Lean manufacturing initiatives work only if they add to—not replace—the hands-on know-how people accumulate batch by batch.

    Regular training on new equipment, and open debriefs on any out-of-spec discovery, tie our process together. Digital tracking drills down to the batch, operator, and even temperature probe used, but every dashboard data point also prompts a conversation or a corrective tweak by the team. Our labs hold weekly forums where technicians, supervisors, and engineers share findings and highlight recurring trouble spots. This keeps us nimble against evolving client demands, raw material variability, and shifting regulatory expectations. It turns a high-purity compound from a commodity into a specialty, shaped by dozens of small innovations over years.

    Advice for Users and Partners Developing New Applications

    Success with 2,4,6-Tris(Bromomethyl)Mesitylene doesn’t end with receiving the drums on your dock. Upstream purity and batch traceability matter less if storage falls short at the user’s site. We recommend storing this compound in climate-controlled environments, away from heat and light, and securely capped to block moisture ingress. Some customers underestimate the static charge buildup during handling, so we suggest careful grounding of all metal tools and filtration setups to avoid product loss or contamination.

    For R&D chemists trialing new synthesis routes, careful monitoring of reagent ratios and reaction times allows for full use of all three bromomethyls without runaway side reactions. Techniques like slow addition, overhead stirring, and spot TLC save hours of troubleshooting per run. Years of case studies in project debriefs point to the same root causes when things go awry: ambient humidity, insufficient mixing, or delayed workup. More collaborative clients now loop us in early, sharing pilot results so we can help tune their process for higher yield and fewer byproducts.

    The Value of Working with a Dedicated Manufacturer

    Those who handle chemicals only on spreadsheets miss the day-to-day unpredictability of the plant, warehouse, or research lab. Over time, we have built our processes for 2,4,6-Tris(Bromomethyl)Mesitylene on feedback from thousands of kilo-scale and gram-scale runs. Our own operators know the adolescent pang of a new product bringing hours of troubleshooting—tightening seals, cleaning scale from a jacket, or logging another impurity spike. These experiences aren’t abstract; they are part of every drum, every analysis, every end-use application developed in collaboration with our customers.

    Solutions to old problems never come from a single department or an out-of-the-box automation upgrade. Adjustment after adjustment—from waste minimization strategies to improvements in packaging strength—are all built on living experience. They come from innovators putting in extra hours, line workers swapping lessons about small changes that improved flow, and managers refusing to let an imperfect batch ship just because the clock says shift is over. No amount of technical jargon or third-party summary ever replaces the quiet confidence of a manufacturer who has put their own hands on the product, fixed small mistakes, and learned to anticipate downstream needs.

    Looking Forward: Ongoing Commitment

    Markets shift, end-uses evolve, and every year brings new challenges in regulation and customer need. Still, the demand for high-quality 2,4,6-Tris(Bromomethyl)Mesitylene holds steady, and we dedicate our future to continuous improvement through hands-on production, open dialogue, and analytical rigor. Standing behind our product means more than posting a purity figure; it means listening to feedback, watching for changes in global chemical trends, and investing in talent as much as in technology. In this way, every bottle or drum leaving our plant continues to reflect years of craftsmanship, accountability, and a drive to help our partners solve the next big challenge in synthesis, materials science, or discovery chemistry.