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HS Code |
515035 |
| Chemical Name | 3-Bromo-2-Methylaniline |
| Molecular Formula | C7H8BrN |
| Molecular Weight | 186.05 g/mol |
| Cas Number | 6407-78-9 |
| Appearance | Light yellow to brown solid |
| Melting Point | 41-45 °C |
| Boiling Point | 262-263 °C |
| Density | 1.52 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Synonyms | 2-Amino-3-bromotoluene |
| Pubchem Cid | 78267 |
| Smiles | CC1=C(C=CC(=C1)Br)N |
As an accredited 3-Bromo-2-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tightly sealed cap, labeled "3-Bromo-2-Methylaniline," displaying hazard warnings and handling instructions. |
| Shipping | 3-Bromo-2-Methylaniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically transported as a hazardous material, following relevant regulations for corrosive and toxic chemicals. Appropriate labeling, documentation, and handling instructions ensure safety during transit and storage, with temperature and ventilation controls where necessary. |
| Storage | 3-Bromo-2-methylaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from direct sunlight, heat, and moisture. Appropriate safety measures, including chemical-resistant gloves and eyewear, should be used when handling. Store under fume hood if possible for added safety. |
Applications of 3-Bromo-2-Methylaniline in Industrial ManufacturingAs an established chemical producer, we supply 3-Bromo-2-Methylaniline for demanding industrial processes requiring precise intermediate performance and compliance with strict sector standards. Below, we describe the primary downstream markets where this specialty intermediate plays an essential role, detailing application specifics from compliance to finished product output. 1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (API)Downstream pharmaceutical manufacturers select this compound as a key intermediate in multi-step syntheses of APIs, particularly for targeted oncological, anti-inflammatory, and anti-infection drug classes. Process chemists value its ortho-bromo, para-amino functionalities for controlled coupling, halogenation, or amide bond formation in routes where impurity profiles and yield reliability must meet global drug standards. Each batch undergoes full traceability for process validation during upscaling and regulatory filings. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide FormulationsThis raw material enables the manufacture of specific heterocyclic intermediates imported into downstream agrochemical synthesis routes. Chemical engineers exploit its substitution pattern for constructing high-selectivity herbicide actives, requiring scalable reaction yields and tight byproduct controls for final formulation eligibility and international registration. Industry compliance standards
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3. Dye and Pigment Precursor in Specialty Colorant ManufacturingManufacturers in the fine dye and pigment sector utilize this aromatic amine to achieve targeted shade development and colorfastness in high-value dyes for plastics and fibers. The brominated amine structure allows for unique diazotization, azo coupling, or cyclization crucial to synthesizing colorants requiring regulated purity and thermal stability, tailored for critical applications such as high-performance automotive and industrial coatings. Industry compliance standards
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4. Intermediate in Electronic Industry Chemicals (OLED and Liquid Crystal Material Synthesis)Producers in the optoelectronic sector integrate this compound as a precursor during the development of arylamine-based charge-transport materials and advanced intermediates for OLED emitters and liquid crystal display additives. Laboratories and production lines require its isomer-specific substitution, which supports the creation of materials meeting electrical and purity standards vital for downstream manufacturing of stable, high-yield electronic components. Industry compliance standards
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As a chemical manufacturer with years spent on development, safety refinement, and plant-floor delivery, we know the crucial role direct handling and exacting standards play in specialty intermediates. 3-Bromo-2-Methylaniline, referenced by its CAS number 578-57-4, reflects a compound we’ve brought through substantial in-house iterations, from lab bench to industrial scale. Each batch has grown out of real feedback from downstream partners in pharmaceuticals and dyes, where precision and consistency shape every batch we deliver.
Our team designs this aniline derivative with an eye on every demand our clients put forth. We understand the usual struggles of scaling up aromatic bromoanilines. Moisture handling, consistent melting point, minimized impurities—each challenge gets direct attention. The 3-bromo substitution creates useful reactivity for cross-couplings and directs regioselectivity during further syntheses.
We don’t roll out a new run of 3-Bromo-2-Methylaniline without firsthand inspection and retention sample analysis. At the beginning, we focused on 25-kg fiber drums. Over the years, larger lots for major pharmaceutical partners led us to install custom glass-lined reactors. Every run holds up to the rigorous standards expected by clients who can’t afford downtime or costly purification.
In process, our team adjusts each reaction keeping in mind the needs of pharma and agro-intermediate customers—water content, isomeric purity, and trace halide control. Each specification lies close to standard ranges demanded by fine synthesis: melting point, purity above 98%, and single spot on TLC in typical solvent systems. We avoid overbromination and minimize isomerization by using mild temperature profiles. There’s always a focus on downstream reaction predictability, since a clean aniline group remains crucial in multi-step aromatic building block chemistry.
Working with medicinal chemistry innovators, we’ve seen 3-Bromo-2-Methylaniline support synthesis of kinase inhibitors, fungicides, step-growth polymers, and high-performance pigments. The methyl group at the 2-position and the bromo substituent at 3 give this compound a reliable starting point for both Suzuki and Buchwald-Hartwig type couplings. This structural feature sets it apart from unsubstituted bromoanilines. The methyl group's electron-donating influence speeds up N-acylation or amide condensation. Whether scaling a clinical API route or producing developer components for color imaging, clients choose our product for reliable performance under catalytic or stoichiometric protocols.
We have sat down with chemists troubleshooting inconsistent yields from commercial anilines, always ending up with the same conclusion: purity and freshness change everything. Old or poorly handled 3-Bromo-2-Methylaniline sometimes brings about slow conversions and even product color issues. Our approach includes vacuum drying, moisture barrier packaging, and strict FIFO (first in, first out) logistics. We take personal responsibility, knowing a single batch that goes off-spec can disrupt entire campaigns down the supply chain.
Certificates from outside labs help, but certificates leave a lot unsaid in production-scale chemistry. We have traced problems in coupling reactions to minute traces of bromoanisoles and to thermal decomposition during sub-optimal storage. Many competitors rush material to market without stabilizing the shipment for long routes. We have learned not to cut corners, keeping our own retention samples for up to a year. If an end user calls about discoloration or poor crystallization, our team can trace actual lots and troubleshoot root causes.
3-Bromo-2-Methylaniline looks like a simple intermediate on paper, but plant-scale manufacturing reveals how batch-to-batch variations affect reactivity and product quality. We control residual solvents below the LOD (limit of detection) for common coupling catalysts, eliminating many failed reactions during scale-up. By following our own solvent recovery, washing, and drying protocols (developed through collaboration with QA experts and plant engineers), we cut down not just on impurities, but surprise events during complicated production schedules.
We’ve produced a library of halogenated anilines over the years—each behaves differently in the plant and in application. Compared to 4-bromo or 2-bromo analogs, this 3-bromo-2-methylaniline gives unique selectivity and reactivity. The proximity of the methyl group on the ring influences everything from the rate of Ullmann couplings to the yields seen in electrophilic aromatic substitution. We see customers routinely report improved isolations of ortho- and para-substituted derivatives. Our technical support team offers advice based not on literature alone, but troubleshooting from pilot facilities and feedback from collaborators.
Many clients ask about differences versus 3-bromoaniline. 2-methyl substitution impacts physical properties—melting point, solubility in NMP or DMF, and behavior in chromatographic purification. That methyl group offers more than a minor steric tweak; in catalytic hydrogenation, ring substituents can move reaction rates, selectivity, and even filtration steps. This real-world distinction shows up on the production floor, not just in academic texts.
No specialty chemical business goes long without running headfirst into storage and safety headaches. 3-Bromo-2-Methylaniline can suffer from discoloration if left with minor moisture or exposed to bright light. At one point, we had customer complaints about yellowed product in summer shipments. Re-investigating the issue, our teams found inadequate drum lining and closure issues—feedback that changed our shipment procedure.
We’ve transitioned to UV-blocking, tightly-sealed packaging to restrict oxygen and ambient humidity. Even so, we encourage customers to use sealed inert atmosphere containers in their own inventory rooms. Shelf life extends naturally if care is taken at every link. Over time, others in the industry have picked up similar practices, but our focus has always been, from the start, to solve problems before they reach the production chemist’s bench.
Feedback from users pushed us to adapt beyond the typical bulk processing. Early customers used our material in pilot batches and noticed difficulty in redissolving the product, hurting throughput. We started supplying more finely milled versions and improved lot screening for dust or small cluster formation. As synthesis moved to specialized routes with sensitive reagents, we added more robust drying and argon-purged packaging for clients with glovebox procedures. These are working solutions, not afterthoughts added to marketing brochures.
Our site engineers still run regular checks on column purity, customizing detection limits for trace compounds that sometimes slip into final product during scale-up. Each time a customer flags an issue—be it color change, residue, or off-odor—we replicate their complaint in-house, starting from the production batch in question. Talking directly with synthetic chemists abroad cuts resolution times, and our on-call experts follow up, offering small-scale resupply batches or practical recommendations. This dialogue between manufacturer and end user refines our processes and, in turn, the actual quality of each batch.
Academic and industrial partners increasingly demand unique molecules. 3-Bromo-2-Methylaniline finds use in creating custom ligands for bioactive screening, complex polymer precursors for coatings, and specialty dyes for advanced displays. We assist researchers by providing kilo-scale samples rapidly or suggesting purification tweaks based on prior knowledge, especially when developing new LC-MS or NMR analytics for trace contaminants.
We get involved in the early-stage conversations—helping to route around regulatory hurdles regarding transport, sharing our own thermal stability data, and offering to run extra stability trials for those pushing temperature or solvent extremes. Customers appreciate the directness: “Have you shipped this with a certain freight forwarder? Does it hold up after customs delays? What packaging avoids caking at 35°C?” Our lived experience with international logistics, customs, and safety rules provides confidence their order survives the journey intact.
The landscape for fine and specialty chemicals keeps shifting with each new regulation, raw material hiccup, or transportation price surge. Through sourcing diversification, we weathered key bromine supply shocks and aniline price fluctuations. Users feel the brunt of such swings, so we maintain both short-term and multi-year stocking strategies. Our warehouse decisions reflect more than spreadsheets—they answer the realities of tight project deadlines, erratic customs clearance, and line stoppages if raw materials go missing.
Handling specialty chemicals is not about one-size-fits-all solutions. We adapt granularity, moisture content, and purity requirements by working directly with teams overseeing pre-GMP and GMP pharmaceutical production lines. Their strict documentation needs empower us to invest in transparent batch tracking and generate full lot histories. This way, each kg reaching the customer comes backed by traceability and readiness for urgent, late-stage quality audits.
As primary producers, the greatest impact we offer comes not through slick advertising but through steady, thoughtful improvement in each manufacturing campaign. Dedicated chemistry teams, hands-on operations, and trusted shipping networks mean we answer both technical and practical questions about 3-Bromo-2-Methylaniline without layers of intermediaries. Sharing experiences from bench-scale synthesis to full commercial rollout, we help customers troubleshoot, optimize, and streamline their work. Each bottle, drum, or truckload matches the needs of the innovators who rely on it for the next big advance.
By embracing challenges—whether in supply chain disruptions, process hiccups, or demanding new reaction applications—we prove that manufacturing specialty chemicals remains a craft shaped by dialogue, diligence, and daily effort. Our mission: to fortify every synthesis, experiment, and process with product we know stands up under pressure, because we have spent years perfecting it for those who trust us to deliver.