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HS Code |
714891 |
| Chemical Name | 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene |
| Molecular Formula | C9H10BrNO2 |
| Molecular Weight | 244.09 g/mol |
| Cas Number | 77627-69-9 |
| Appearance | Yellow to orange crystalline solid |
| Melting Point | 71-74 °C |
| Density | 1.53 g/cm³ (estimated) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC1=CC(=C(C(=C1Br)C)[N+](=O)[O-])C |
| Inchi | InChI=1S/C9H10BrNO2/c1-5-4-6(2)9(11(12)13)7(3)8(5)10/h4H,1-3H3 |
As an accredited 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25 g amber glass bottle with a tamper-evident cap and a printed hazard label. |
| Shipping | 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene is shipped in tightly sealed, chemical-resistant containers. It is escorted with proper hazard labeling and documentation in compliance with international regulations. The package is handled by trained personnel, protected from moisture, heat, and ignition sources. Shipping must comply with relevant UN, IMDG, and IATA dangerous goods codes. |
| Storage | 2-Bromo-4-nitro-1,3,5-trimethylbenzene should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep it separated from incompatible materials such as strong oxidizers and reducing agents. Store at room temperature, and ensure appropriate labeling and access by trained personnel only. Use appropriate secondary containment for added safety. |
Applications of 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene in Industrial ManufacturingAs a specialized manufacturer of 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene, we serve advanced chemical sectors worldwide by supplying this raw material to critical downstream segments. Below, we detail genuine application scenarios drawing on the industrial practices and regulatory requirements of high-value chemical transformation processes where this intermediate plays a key role. 1. Synthesis of Active Pharmaceutical Ingredient (API) IntermediatesThis intermediate finds precise use in the stepwise synthesis of certain nitrogen- and halogen-containing API building blocks, particularly for kinase inhibitors and specialty heterocycles. Pharmaceutical manufacturers configure batch-wise or continuous processes where selective functional group modification is essential, and 2-Bromo-4-Nitro-1,3,5-Trimethylbenzene enables regioselective introduction of nitro and bromo substituents in complex synthesis schemes for next-generation drugs. Process control focuses on trace impurity profiling and scalability in compliance with regulatory filings. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisIn crop protection manufacturing, formulators use this intermediate in the creation of halogenated aromatic segments of selective herbicide and fungicide actives. Production recipes depend on aromatic substitution’s control for targeted activity and environmental degradability. Consistent impurity management is critical for field-application standards and regulatory submissions. Producers value its specific substituent pattern when developing novel actives or modifying existing molecules to meet shifting pest resistance trends. Industry compliance standards
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3. Electronic Chemical Intermediates (OLED/OPV Applications)Manufacturers in the organic electronics and specialty polymer segment apply this raw material for the synthesis of electron-deficient aromatic units in small-molecule and polymeric semiconductors, particularly for use in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. The compound’s substitution pattern allows fine-tuning of bandgap and charge transport characteristics in molecular engineering projects that require stringent control of synthetic route impurities and batch reproducibility for electronic applications. Industry compliance standards
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4. Dye and Pigment Intermediate ManufacturingThe specialty dye industry uses this aromatic intermediate when developing nitro- and halo-substituted colorants for plastics, coatings, and specialty inks, where consistent chromophore integration impacts lightfastness and color depth. The molecule’s structure is critical when precision placement of chromogenic groups is required, particularly in colorant production for high-value industrial and security printing, where trace contaminants may affect performance in demanding applications such as anti-counterfeiting inks and plastics labeling. Industry compliance standards
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5. Specialty Chemical Reference Standard ProductionQuality control, contract research, and advanced analytics labs use this chemical as a high-purity reference standard for validating analytical workflows involving halogenated and nitrated aromatics. Its unique structure enables precise calibration of method sensitivity and selectivity in mass spectrometry or chromatographic analyses required by regulatory authorities. In this role, purity certification and certified reference material (CRM) traceability form the foundation of production and client documentation procedures. Industry compliance standards
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After decades in the fine chemicals business, you start to see certain molecules stand out, not only for their chemistry but for the practical roles they play in production lines. 2-Bromo-4-nitro-1,3,5-trimethylbenzene (often listed under CAS 4277-43-6) is one of these substances our technicians have learned to respect. Once we recognized the consistent demand from process chemists and R&D teams worldwide, we invested in scaling up its synthesis—there’s nothing theoretical about what we do. We take crude materials from the very beginning and refine, crystallize, pack, and ship with direct accountability for every batch. For those with specific project goals, that directness matters.
Years of hands-on experience confirm that the combination of bromine and nitro functionality on a methylated aromatic ring offers unique benefits in custom molecule construction. This compound’s structure—a symmetrical benzene ring substituted at the 2-position with bromine, the 4-position with a nitro group, and three methyl groups at the 1, 3, and 5 positions—gives process flexibility not always present in plain bromo or nitro aromatics. These features aren’t simply decorative. The electron-withdrawing nature of the nitro group and the activating character of methyl substituents, combined with a single, reactive bromine, enable selective couplings, Suzuki reactions, and other classic C–C or C–N bond formations. Researchers reach for this compound when a less functionalized precursor just doesn’t cut through a synthetic challenge.
As the original producers, we start from raw aromatic intermediates, running bromination and nitration under controlled, safe conditions. Each step reflects years of hazard analysis and troubleshooting. The target purity for this trimethylbenzene derivative regularly exceeds 99.5% by area (HPLC, GC, or NMR as the case requires). Manufacturing at this level isn’t a checkbox; it’s a commitment. We have walked plenty of clients through the simple reality: even a small impurity in an intermediate disrupts late-stage pharmaceutical or agrochemical synthesis. Several teams worked with us to root out a persistent trace of dibrominated by-product. After adjusting reagent addition and crystallization time, the issue faded. That is the stuff you only discover if you synthesize and analyze lot after lot, not by reading a spec sheet.
Most of our clients ordering this compound operate in two main spaces: drug development and pigment research. Custom coupling reactions for heterocyclic structures draw on the special pattern of electron density and reactivity here. It’s especially common in building blocks for kinase inhibitors, antifungal candidates, or novel dyes where classic bromoaromatics either lack selectivity or introduce unwanted side products. A few clients use this molecule as a core for advanced materials or performance polymers, benefiting from the thermal and chemical stability of the trimethylbenzene scaffold.
We have seen labs work with multiple halogenated nitrobenzenes, but after months at the bench (sometimes years), the attention comes back to this configuration for certain Suzuki–Miyaura couplings. The presence of three methyl groups on the aromatic ring helps reduce by-product formation under coupling and streamlines purification at scale. Our production supervisors support teams designing multi-kilogram runs because we know how much depends upon those subtle substitution effects.
Many buyers turn to us for guidance on how 2-bromo-4-nitro-1,3,5-trimethylbenzene performs compared to other methylated or halogenated benzenes. In the hands of synthetic chemists, the difference is obvious. Take unsubstituted 4-nitro-2-bromobenzene: lower molecular weight, but far less selectivity during functionalization, especially when aiming to introduce bulky side chains or manage regioselectivity. Mono- or dimethyl derivatives (for example, 2-bromo-4-nitro-1,3-dimethylbenzene) never offer the same steric profile; reactions trend toward ortho substitution or display poor yields due to side reactions.
Unlike simple 1,3,5-trimethylbenzene derivatives, the nitro and bromo groups here add not just synthetic interest but also open doors to applications in fluorescent tagging, redox chemistry, and catalysis—fields that require both electron richness and leaving group flexibility. Of course, we’ve also synthesized close analogues, including iodinated or chlorinated counterparts, but the bromo derivative hits a sweet spot for practical cost, yield, and versatility. Not every methylbenzene variant performs as cleanly under palladium- or copper-catalyzed conditions. Over years of production, we’ve seen far more customer re-orders for this specific substitution pattern than any of its close relatives.
Having handled and packed metric tons of this product over the years, we know it arrives at the bench as a pale crystalline powder, stable in normal storage, neither hygroscopic nor prone to rapid decomposition under ambient warehouse conditions. The product holds up well over time, provided it’s kept in sealed containers away from direct sunlight. We don’t use delicate language about product integrity because our business is keeping the integrity. Clients shipping to humid climates have relied on our proven packaging, which minimizes caking and clumping over long sea shipments. Our logistics crew packs every drum or bottle at source, and we know contamination or cake can literally ruin a production run abroad. Routine sampling always matches up: what we ship, what arrives, and what the receiving chemist weighs out on the bench.
We don’t wave around purity figures pulled out of thin air. Every batch ships with supporting GC, HPLC, and NMR data tracked to its unique lot code. Over years of manufacturing, we’ve seen enough analytical reports to spot trends in side-product formation or decomposition impurities. Our quality team keeps a running library of spectra, so if a client hits an unexpected result, we can trace and explain it. The reality in our lab is that consistent chromatography and clean NMR fingerprints matter more than tiered descriptions or certifications. Several customers have shared frustrations about batch-to-batch variation from aggregators or traders; we counter that by sticking with a process developed, scaled, and repeated in-house.
Any direct chemical producer answering to global customers faces the same realities in environmental and safety responsibility. For brominated aromatics in particular, waste management and air control present real engineering challenges. Over years of scale-up, we invested in closed-loop solvent handling, dedicated fume extraction, and persistent monitoring of workplace exposure. There are no shortcuts in modern chemical manufacture. Our operators use PPE, batch reactors stand under negative pressure containment, and our in-plant waste streams are monitored against regulatory thresholds. These aren’t abstract principles: our team has reworked entire plant sections after identifying shortcomings in early process runs. That’s what keeps our relationships with both local inspectors and multinational clients in good standing.
Clients sometimes ask about REACH registration, TSCA, or other local compliance demands. Our experience tells us that anticipation, not reaction, prevents problems down the line. Early on, we prepared full dossiers on composition, stability, and potential exposure routes. For those running pharma or material science projects, we can provide supporting technical data to satisfy regulatory audit trails. Drawing from years of hands-on inspection and reporting, we stick with honest documentation—no half-answers, no surprises in the paperwork.
Working as the true source manufacturer doesn’t mean you’re immune to setbacks. Every so often, a process hiccup happens: crystallization doesn’t quite deliver, moisture creeps in when summer humidity spikes, or a new employee misjudges a filter change. Because we own the process from start to finish, we’ve seen each of these crop up over years in the business. Early in our production history, a filter press seal failed during a key wash, leading to a batch with higher inorganic salt content. This taught us the value of routine seal checks and post-filtration QC. Another time, a customer flagged increased tan coloration in one lot’s powder—our lab tracked it to over-extended exposure during drying. We reworked the drying procedure, later adding automated sensors for temperature and air flow. These lessons turn into permanent practice changes.
We share these missteps for more than transparency; we do it to help others avoid the same headaches. Anomalies aren’t swept under the rug but become daily checklist items. In our view, that’s what distinguishes a genuine chemical producer from those just moving drums across a warehouse.
After years supplying R&D chemists, process engineers, and scale-up specialists, we realize the value of keeping a two-way street open for feedback. Sometimes a client finds an outlier in melting point, moisture, or particle size that didn’t show up during our routine checks. Direct producers bear the responsibility of troubleshooting, not deflecting. If there’s a query or problem—delivery, performance, or technical support—our staff discusses it at a weekly production meeting and reaches out with a solution. We’ve modified milling protocols, tried out alternative packaging, and even tweaked crystallization schedules after customers in different climates gave us constructive criticism. The industry only grows stronger with these feedback loops.
One recurring discovery from our own lab and customer reports: solvent compatibility and process integration matter a great deal. This compound dissolves well in moderately polar solvents—ethyl acetate, acetonitrile, chlorinated hydrocarbons—something we confirm with each delivery by sending recommended solvent compatibility sheets, not just a generic MSDS page. We have run blending trials straight from production batches, so end-users know the material enters solution smoothly without lengthy stirring or heating. Having processed orders ranging from a few hundred grams to container-load shipments, we’ve built a storehouse of experience packaging, stabilizing, and shipping this material under various climate conditions. There is a real benefit in dealing directly with the originator—we aren’t passing the buck to unnamed sources or skirting around warranties.
Some of the most interesting work we’ve done, and continue to do, happens in partnership with innovative research teams. One pharma group used our bromonitro compound to build a new class of kinase inhibitors, relying on our support throughout process development. We worked with pigment manufacturers and advanced materials teams who demanded subtle tweaks in particle size and bulk density that traders simply could not promise. Historically, working directly with manufacturers shortens the feedback loop and speeds up innovation. We don’t just hand off a drum and disappear; we track product performance in bench and pilot runs, sharing process insights because someone in the field always finds a new use or limitation the lab missed.
QC doesn’t end with a clean analytical printout. We calibrate balances monthly, double-check every temperature probe, and scrutinize even the subtle differences in powder consistency. Years ago, an issue with foreign particulate showed up at the last minute in a visual check—one more reason we inspect at multiple stages, not just relying on analysis alone. Some teams in-house focus solely on re-verification: sampling from different bags in a lot, checking color, smell, flow, and taking photos for traceability.
The reality is that no large batch ever gets shipped without two independent sign-offs, and we maintain retained samples from every delivery for a full eighteen months. This backup system aids not only in our internal audits but also responds to external requests for reanalysis, stemming from non-conforming product claims that occasionally surface. Direct lines to our analytics staff keep communication quick, frank, and productive.
Textbook descriptions miss certain direct handling insights. There’s no substitute for learning how the powder flows, whether it clings to a scoop, mixes easily, picks up static, or compacts under pressure. These properties shift with batch size and seasonal changes, so process consistency takes more than routine lab data. Internally, we tune our particle size, density, and drying finishes based on repeated field feedback from trusted partners—not because it’s written in a monograph, but because it avoids slowdowns for customers pushing hard toward deadlines.
Having handled a wide range of bromonitrobenzenes, our synthesis operators, QC analysts, and warehouse packers keep running notes on quirks observed from run to run. The cumulative result for our end users: reliable product flow, consistent performance in both bench chemistry and pilot plant, and detailed guidance for every major variable affecting yield and throughput. This is what produces outcome differences in real-world reaction shots, scale-up efficiency, and clean downstream isolations.
After decades manufacturing 2-bromo-4-nitro-1,3,5-trimethylbenzene, we know the difference comes not from simply posting a spec online, but from living through each cycle of feedback, troubleshooting, and process refinement. It is the lived experience—resolving off-spec issues, optimizing blending and shipping, partnering on new uses, and investing in equipment upgrades—that creates genuine trust and superior product outcomes. For clients who care about predictability, accountability, and ready technical support, working with the source makes a difference that shows in every successful experiment, kilo-scale batch, and product delivery.