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2-Bromo-6-Methylaniline

    • Product Name 2-Bromo-6-Methylaniline
    • Alias 6-Bromo-o-toluidine
    • Einecs 220-882-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    714072

    Chemical Name 2-Bromo-6-Methylaniline
    Molecular Formula C7H8BrN
    Molecular Weight 186.05 g/mol
    Cas Number 28320-31-2
    Appearance Light yellow to brown crystalline solid
    Melting Point 63-67°C
    Boiling Point 265-267°C
    Density 1.54 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC1=C(C=CC=C1Br)N
    Inchi InChI=1S/C7H8BrN/c1-5-4-2-3-6(8)7(5)9/h2-4H,9H2,1H3
    Synonyms 2-Bromo-6-methylaniline; 6-Methyl-2-bromoaniline
    Storage Conditions Store in a cool, dry place away from light and moisture
    Refractive Index 1.658 (Predicted)

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

    Packing & Storage
    Packing Amber glass bottle, 25g net weight, screw cap, hazard labels, white chemical label with “2-Bromo-6-Methylaniline” and safety information.
    Shipping 2-Bromo-6-Methylaniline is shipped in tightly sealed containers, protected from light and moisture. It should be labeled as a hazardous material and transported according to local, national, and international regulations pertaining to chemicals. Proper documentation and safety data sheets must accompany the shipment to ensure safe handling and compliance.
    Storage 2-Bromo-6-methylaniline should be stored in a tightly sealed container, away from sources of ignition, heat, and direct sunlight. Store it in a cool, dry, well-ventilated area, segregated from oxidizing agents and acids. Ensure proper labeling and restrict access to authorized personnel. Use secondary containment to prevent accidental spills or leaks, and consult the SDS for further safety instructions.
    Application of 2-Bromo-6-Methylaniline

    Applications of 2-Bromo-6-Methylaniline in Industrial Manufacturing

    2-Bromo-6-Methylaniline serves as a key intermediate in several advanced chemical production lines. As a direct manufacturer, we deliver high-purity material for critical downstream processes in fine chemicals, pharmaceuticals, specialty agrochemicals, and colorant synthesis.

    1. Pharmaceutical Intermediate Synthesis

    This compound plays a defined role in the synthesis of active pharmaceutical ingredients (API) for select antihypertensive and antineoplastic agents. Its brominated aromatic structure provides a strategic anchor for palladium-catalyzed coupling reactions, supporting the stepwise assembly of complex pharmaceutical molecules. Process engineers adjust the reaction conditions for nucleophilic substitution, ensuring regioselectivity and optimal yield without generating regulatory-restricted impurities.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapters — Impurities: General Considerations
    • European Pharmacopoeia (Ph. Eur.) purification requirements
    • FDA 21 CFR Part 211: cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 1.1 to 1.3 molar equivalents per target aromatic ring in multi-step synthesis. Mol ratio may vary based on target molecule complexity and required chemoselectivity.

    Downstream process integration

    • Input during initial carbon-nitrogen bond formation via Buchwald–Hartwig amination
    • Employed in subsequent halide-metal exchange and cross-coupling stages
    • Used for preparing substituted aniline building blocks in API assembly
    • Handled within closed reactors to ensure minimum contamination risk

    Final product types

    • Antihypertensive drug intermediates
    • Anticancer drug precursor compounds
    • Pyridine- and benzene-based pharmaceutical APIs
    • Custom R&D molecules for clinical trial material synthesis

    2. Agrochemical Active Compound Manufacturing

    Key manufacturers utilize this raw material in the synthesis of novel herbicidal and fungicidal agents, particularly within the aniline-derived phenylurea class. The methyl and bromo substituents facilitate structure-activity optimization for target selectivity against crop pests. Production teams use high-purity batches to avoid off-target crop toxicity and to maintain regulatory approval for downstream products deployed in global agriculture markets.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius limits for pesticide residues
    • ISO 9001:2015 certified quality management systems
    • EU Regulation (EC) No 1107/2009 – Plant Protection Products regulation
    • US EPA Pesticide Registration (FIFRA)

    Typical usage ratio

    • Typically 0.9 to 1.2 molar equivalents relative to chlorinated urea or triazine partners, adjusted based on desired biological efficacy and formulation route.

    Downstream process integration

    • Entry at condensation step to introduce aromatic nucleus to urea or carbamate backbone
    • Subjected to selective demethylation or further aromatic functionalization after coupling
    • Integrated with in-line purification to ensure low residues in final products
    • Continuous or batch processing depending on production scale

    Final product types

    • Selective herbicide active substances
    • Cereal and fruit crop fungicides
    • Soil treatment biocides for export formulations
    • Pre-mix technical concentrate for agrochemical R&D

    3. Specialty Dye and Pigment Intermediate Production

    Producers rely on this intermediate to develop high-performance azo and anthraquinone dyes, especially for textile and plastic applications requiring specialized color fastness and thermal stability. The methyl substitution confers improved affinity for polyester and polycarbonate fibers, while the bromo group enhances reactivity in subsequent diazotization and coupling reactions. Batch traceability and stringent impurity monitoring are enforced to meet international dye and pigment quality norms.

    Industry compliance standards

    • Oeko-Tex Standard 100 (Textile Chemical Safety)
    • REACH (EC) No 1907/2006 Substance Registration
    • ISO 14001 Environmental Management for pigment processes
    • ZDHC Manufacturing Restricted Substances List

    Typical usage ratio

    • 0.95–1.05 equivalents vs. diazotization agent, fine-tuned per shade, application method, and fiber compatibility.

    Downstream process integration

    • Entry during the base coupling step for azo dye formation
    • Available for further bromination or methylation when required by target pigment structure
    • Monitored and standardized in pre-dye blending stocks to ensure color reproducibility
    • Final filtration/clean-up to eliminate trace impurities prior to downstream pigment dispersion

    Final product types

    • Reactive printing dyes for polyester and nylon
    • High-purity pigment intermediates for engineering plastics
    • Fastness-enhanced dyes for outdoor textile applications
    • Chromophore units for specialty liquid ink jet

    4. Advanced Functional Material Synthesis

    Advanced material manufacturers increasingly deploy this chemical as a precursor in the synthesis of specialty ligands and organic electronic materials, particularly for optoelectronic and liquid crystal industries. The electron-withdrawing bromo group, combined with the ortho-methyl effect, enhances rigidity and improves hole-transport properties for high-value display and sensor products. Manufacturing adheres strictly to electronic-grade purity benchmarks, utilizing multi-stage crystallization and chromatography for impurity control.

    Industry compliance standards

    • JEDEC JESD 625B: Requirements for Handling Electrostatic-Discharge Sensitive Devices
    • IPC-6012DA for Rigid Printed Boards (relevant to final device QC)
    • IEC 61340-5-1 for protection of electronic components
    • ISO 14644-1 standards for cleanroom processing

    Typical usage ratio

    • 0.8–1.0 equivalents, calculated for maximal incorporation into ligand or organic semiconductor matrix, modifiable by specific device architecture.

    Downstream process integration

    • Introduced in early-stage ligand formation via Buchwald amination or Suzuki coupling
    • Further brominated for multi-substituted aryl intermediates
    • Subjected to chromatographic purification before final incorporation into device precursor blends
    • Maintained under inert gas conditions to prevent oxidative degradation

    Final product types

    • Organic light-emitting diode (OLED) ligands
    • Hole-transporting materials for display panels
    • Specialized liquid crystal alignment agents
    • Synthesis blocks for functionalized sensors and data storage films
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    Certification & Compliance
    More Introduction

    2-Bromo-6-Methylaniline: A Manufacturer’s Perspective

    Hard Lessons from Batch Synthesis: Why Precision in 2-Bromo-6-Methylaniline Matters

    Running a chemical plant that produces 2-Bromo-6-Methylaniline over countless campaigns quickly teaches that nothing about this compound can be left to guesswork. The compound—known by its CAS number 21898-43-9 in chemical circles—emerges only through a tight balance of reaction temperature, stoichiometry, and a resolute approach to purification. Operators must handle methylation and bromination steps with disciplined accuracy; neither raw material quality nor minor fluctuations in reactor temperature can be ignored. Over the years, we’ve fielded calls from research labs and plants who tried using less stable intermediates only to find batch failures or unreproducible yields. Not all aromatic amines tolerate the same variation. People who work the reactors meet the reality—and the off-odor of contaminated product—if slip-ups happen on a multi-kilo scale.

    Specifications Built from Real-World Demands

    We maintain product standards because customers run into issues when these lapsed. We produce 2-Bromo-6-Methylaniline as a faint yellow crystalline solid, typically reaching purities exceeding 99% by HPLC, and keep residual solvents far below 0.3%. Users in pharmaceutical or agrochemical research have zero patience for unclear melting points or “off” colors in a bottle, because those signs point to unwanted byproducts. Consistency isn't just window dressing: from filtration to packaging, even small impurities can trip up downstream reactions like Suzuki coupling or diazotization. Once, a collaborator shared how an amorphous brown spot in their chromatogram threw off weeks of medicinal chemistry work. Since then, we doubled efforts around activated carbon treatment and crystallization parameters, learning quickly that visible clarity usually follows meticulous control at each upstream stage.

    Comparison to Other Bromoanilines—Critical Differences

    Sometimes those outside the manufacturing side see 2-Bromo-6-Methylaniline as one option among many bromoanilines. Chemistry rarely lets such substitutions slip by unnoticed. For our process teams, the methyl group at the 6-position is more than a detail. During classic aromatic substitutions, the methyl group’s location creates distinct reactivity compared to relatives like 2-Bromoaniline or 4-Bromo-2-methylaniline. We’ve helped chemists who expected similar electrophilic or metal-catalyzed reactivity to find the methyl group can shield ortho positions, modifying both rates and selectivity. Down the line, high-speed coupling reactions might falter—or proceed with unwanted regioisomers—if the wrong starting aniline goes in the pot. 2-Bromo-6-Methylaniline’s selectivity patterns add genuine value in multi-step synthesis, and not every manufacturer or trader understands this distinction from casual catalog sales.

    The Technical Side: Synthesis Choices Matter

    Traditionally, production relies either on bromination of 6-methylaniline or methylation of 2-bromoaniline. We’ve learned after investing in both routes that each presents unique hazards and ergonomic headaches. Bromination often creates mixtures if unbuffered conditions prevail, requiring downstream clean-up with acidic washes or column purification. On the other hand, methylation frequently drags dimethylated byproducts, especially near the ortho position. We built our current process using a hybrid approach where tight controls on feed ratios and staged additions cut down byproduct formation. Regular GC-MS analysis and in-process color checks flag problems long before the batch is finished. Years in the plant teach that poor technique delivers not just yield loss but unpredictable operability, especially when production scales up beyond the lab synthesis described in papers.

    End-Use Applications: Feedback from Users

    We listen to chemists downstream who convert 2-Bromo-6-Methylaniline into heterocycles, pharmaceutical intermediates, or crop protection seeds. Many relay that other bromoanilines introduce unwanted reactivity or leave base-sensitive traces, ruining sensitive palladium-catalyzed or nucleophilic aromatic substitution steps. Building block selection sets the tone for the rest of a project, so hitting the right isomeric form and impurity profile early saves repeated troubleshooting. Several customers have found that switching suppliers mid-campaign led to a spike in side-reactions or catalyst deactivation, traced later to unseen trace contaminants—mostly residual halides or amines. Each complaint pushed us to revisit our own protocols for dehydration and vacuum handling, since dry materials and minimal residual acid make later transformations far more predictable.

    Batch Records and Traceability: Not Optional in Modern Chemistry

    Long before regulatory audits forced the issue, we kept meticulous batch records. Turns out, customers use our lot numbers to trace performance differences during scale-up—essential for troubleshooting in API development or registering crop protection ingredients. By archiving every reaction, filtration, drying, and packing step, we provide the confidence that product delivered last year matches today’s. Even for research segments, this transparency cuts downtime when a lab notebook somewhere in Europe pings us for spectra from an old batch. Documentation discipline supports reproducible results on both sides of the transaction; improvising on production logs leads not only to customer frustration but also internal confusion when scaling up a run.

    Handling and Packaging: Real-World Protection Ensures Usability

    Many chemical syntheses chalk their issues up to what happens before a bottle reaches the bench. We package 2-Bromo-6-Methylaniline in bottles or drums suited to the intended scale, using low-static plastics and multi-ply liners to protect the compound from light and ambient moisture. Plant teams found the compound tends to clump if packed too loosely, especially during humid summer weeks; this led to caking issues during weighing, which customers flagged as a handling problem. Our adjustments—benchmarked against real user complaints—not only keep the material pourable but also maintain homogeneity, which customers count on for automated batch dispensing.

    Regulatory Reality: Preparing for Submission-Grade Documentation

    Downstream users in regulated industries expect compliance-ready material fit for their documentation requirements. Years ago, we learned the hard way that a lack of full impurity profiling or an incomplete spectral library could delay an entire project’s regulatory submission. Now, besides HPLC and GC data, we offer 1H-NMR, 13C-NMR, MS, and IR records for each lot, along with certificates of analysis that don’t hide behind vague “pass/fail” designations. This approach meets the shifting goalposts for pharma or agrochemical applications, where old-school handwaves about “reasonable purity” no longer suffice.

    Practical Advice: Steric and Reactivity Considerations in Synthesis

    Developing 2-Bromo-6-Methylaniline at scale surfaced a slew of practical lessons around steric effects and reactivity. On a bench, the difference between a methyl group at the 6-position and, say, the 4-position might not stand out right away. Once reactions scale into multi-liter hydrogenators or kilo-scale palladium couplings, the impact of hindered ortho positions changes everything. Chemo-selective reactions become less predictable, and the margin for error shrinks dramatically. We’ve worked closely with synthesis teams stuck at an impasse—unreactive intermediates, sluggish couplings, or high ratios of regioisomeric byproducts. Improving the starting material—from purer 2-Bromo-6-Methylaniline to specific particle size ranges—often unlocked whole new campaigns. In short, nuanced structure-reactivity interplay learned on production lines rarely shows up in generic supplier data sheets.

    Safety and Environmental Considerations: More Than a Checklist

    Working with bromoanilines on a plant scale gives a different vantage point on health, safety, and environmental burdens than reading an MSDS in the abstract. Small exposures can sensitise operators, and the distinctive odor lingers without well-designed ventilation. Our safeguards include localized extraction at blending and packing, disposable PPE protocols, and careful wastewater treatment for mother liquors. We also pay attention to solid and solvent waste because brominated intermediates draw increased regulatory scrutiny. Years of handling spills and coordinating with local waste management taught us that even minor accidents ripple into lost time or regulatory fines. Thus, safety isn't a quarterly topic—it’s part of building trust among those who work the production line and those who run analytical checks.

    Cost Pressures and the Relentless Search for Efficiency

    Raw material volatility for bromine and toluene derivatives sends tremors through costs every fiscal quarter. As a manufacturer, we see how batch size, yield, and campaign length dramatically change unit economics. Minor upticks in reaction efficiency from cleaner solvents or greater conversion rates show up on the bottom line. Our process engineers committed to lean thinking learned to chase side reactions out—every fraction of a percent lost to an unknown byproduct impacts not only margin but also sustainability metrics. This pressure compelled us to automate certain steps, cut rework rates, and optimize inventory levels. By responding directly to user feedback on product quality and batch consistency, we’ve managed to keep competitive without undercutting on safety or regulatory requirements.

    End-User Trends: From Academic Bench to Industrial Scale

    Recently, demand for 2-Bromo-6-Methylaniline shifted as pharmaceutical and agrochemical R&D explores novel heterocyclic scaffolds and electronic application intermediates. Collaborations with university and industrial chemists highlight evolving use cases, including as a precursor in indole syntheses or ligand formation for specific metal complexes. Some customers push for even finer impurity control—demanding “ultra-high-purity” sub-ppm thresholds—driven by more sensitive catalysts or process regulations. Our R&D team works in tandem with those at the synthetic frontiers, adjusting protocols, and fine-tuning QC analytics. Staying close to user-driven expectations makes us agile: we chase after those reliability targets chemistry demands, instead of relying on broad-market solutions.

    Beyond the Label: The Value of Supplier Expertise

    Many researchers underestimate the complexity behind a bottle of 2-Bromo-6-Methylaniline labeled “99% pure.” We receive regular field questions on how different lots might react, or how to troubleshoot strange spots in downstream reactions. Front-line plant experience and cross-functional review of analytical data let our technical teams provide answers, not speculation. What makes a difference for users is not just traceability or logistics, but fast, chemistry-literate advice. Partnering with those who make the compound daily means dodging generic pitfalls and benefiting from developmental “war stories” few traders or general catalog suppliers can offer.

    Innovation and Continuous Improvement: Not Just Buzzwords

    Constantly refining the synthesis and handling of 2-Bromo-6-Methylaniline means more than meeting a spec sheet—it’s a mindset shaped by both failure and success. Over the years, we’ve retired entire process steps because process intensification or greener solvents improved throughput and reduced waste. NMR data review and root cause analysis keep every campaign cleaner, teaching us what works and what doesn’t. Batch failures stung but led to robust SOPs for monitoring reaction exotherms and spotting incipient emulsion formation. By embedding these lessons, future process teams inherit a culture that values actionable data and practical insight, rather than only formal compliance.

    Supply Reliability: Building Real Trust

    Anyone who ever ran out of crucial intermediate during a campaign knows the stress of unreliable supply. Over decades, we’ve invested in parallel reactor capacity, buffer stocks of key starting materials, and regular maintenance schedules to reduce unscheduled downtime. The value for end-users shows up not just in on-time shipments but also in actual continuity—users rarely face switched lots or unplanned substitutions. Our planning teams coordinate closely with major customers during long synthesis campaigns, sharing realistic timelines and any production risk far in advance. This builds the kind of trust that underpins long-term partnerships in the chemical supply chain.

    Supporting Sustainability: Practical Steps and Honest Accounting

    As calls for greener chemistry grew louder, we prioritized not just incremental waste reduction but also full-life cycle analysis. Solvent recovery, smarter reactor cleaning, and minimizing off-spec batch production made sense for both costs and conscience. Emissions to air and water remain visible metrics; every tonne saved year-over-year translates to less regulatory risk and a lighter environmental footprint. We tap into industry consortia and technical exchanges to benchmark and openly share better waste handling, safer process alternatives, and honest whole-cost accounting. We believe that practical, hands-on improvements outweigh glitzy greenwashing or vague pledges—every kilo cleanly made advances credibility with both regulators and customers.

    Real World Solutions: Overcoming Challenges Together

    Some of our most enduring customer ties grew out of troubleshooting sessions—helping scale up a reaction, finding a blockage in a filtration step, or advising on alternative solvents to solve solubility ruts. We know the road from synthesis to finished product winds through plenty of unforeseen hurdles. Because producing 2-Bromo-6-Methylaniline at scale means facing these head-on, our support teams share not only documentation and logistics but true process insight: unexpected impurity spikes, ways to avoid feedstock contamination, or even better ways to store and weigh out the solid in high-humidity environments. Facing these challenges with customers—treating every request as a chance to build something lasting—informs how we plan every campaign.

    Summary of Experience

    As an active manufacturer, our view of 2-Bromo-6-Methylaniline is shaped by daily real-world experience, evolving regulations, and close exchanges across the value chain. Whether troubleshooting a stuck reaction or simply guaranteeing enough material for the next campaign, every lesson shapes how we produce, package, and support this key intermediate. Quality, reliability, and informed chemistry are non-negotiable, and we keep improving because the markets and reactions we serve never stand still. Our role as manufacturers is to anticipate the next challenge with steady hands and practical know-how, delivering more than just molecules—delivering partnership and trust.