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5-Bromo-2-Methylaniline

    • Product Name 5-Bromo-2-Methylaniline
    • Alias 5-Bromo-o-toluidine
    • Einecs 610-047-4
    • 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

    178558

    Cas Number 578-58-5
    Molecular Formula C7H8BrN
    Molecular Weight 186.05 g/mol
    Appearance Light brown crystalline solid
    Melting Point 45-48°C
    Boiling Point 263°C
    Density 1.5 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Synonyms 2-Amino-5-bromotoluene
    Ec Number 209-423-0
    Smiles CC1=C(C=CC(=C1)Br)N

    As an accredited 5-Bromo-2-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-2-Methylaniline

    Applications of 5-Bromo-2-Methylaniline in Industrial Manufacturing

    As a specialized manufacturer of 5-Bromo-2-Methylaniline, we support international clients integrating this intermediate across multiple advanced chemical synthesis flows. Our focus is on industries where this compound proves essential for target molecule construction and end-use product performance. Below are the established, industrially validated scenarios for this raw material based on global practice.

    1. Pharmaceutical API Synthesis: Active Intermediate in Targeted Oncology Compounds

    Global pharmaceutical manufacturers employ 5-Bromo-2-Methylaniline during the multi-step synthesis of certain kinase inhibitors and other anticancer APIs. The material serves as a starting aromatic amine in regioselective coupling reactions, specifically in Suzuki or Buchwald–Hartwig cross-couplings, where precise halogenation dictates biological activity and patentable structure novelty. Process chemists adjust the input ratio according to stoichiometric requirements and impurity control protocols, guided by regulatory authorities.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP, EP, JP pharmacopoeial reference for residual solvents and impurities
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practices)
    • EDQM CEP certification protocols

    Typical usage ratio

    • 0.7 to 1.1 mole equivalent per target API intermediate, adjusted for percent yield and process losses; chemists optimize loadings based on impurity profile and scale-up batch verification

    Downstream process integration

    • Compound enters at Stage 2–3 amidation, amination, or aryl coupling, following initial halogenation and protection/deprotection treatments, handled under nitrogen blanketing with in-line GC/LC monitoring

    Final product types

    • Small-molecule kinase inhibitors (e.g., for NSCLC or CML targets)
    • Pyridine-based anti-infectives
    • Intermediates for analgesic and anti-inflammatory drugs
    • Custom reference standards for biopharma research

    2. Agrochemical Synthesis: Key Building Block for Novel Fungicidal Actives

    Within the agrochemical sector, formulators utilize this aniline derivative as a core aromatic unit for synthesizing azole or strobilurin-type fungicides. Its brominated ring enables selective construction of complex heterocycles through nucleophilic substitution, with careful control of incorporation ratios to ensure residual content complies with agricultural safety guidelines. Regulatory compliance mandates detailed tracking of all intermediates throughout the batch process.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius (residue and safety controls)
    • ISO 9001:2015 (Agrochemical Quality Management)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products Authorization)
    • China ICAMA pesticide certification for export production

    Typical usage ratio

    • 0.9–1.2 weight ratio per mole of fungicide precursor, variable based on product structure complexity and downstream coupling conversion; adjusted collaboratively with customer QC

    Downstream process integration

    • Dosed as a raw intermediate in Step 1–2 condensation or cyclization; often follows bromine-lithium exchange, then proceeds to controlled nucleophilic aromatic substitution; monitored for trace bromide residue

    Final product types

    • Triazole systemic fungicides for cereals and fruits
    • Strobilurin fungicides for horticultural and row crops
    • Seed-coating agents
    • Experimental bioactive screening compounds for discovery projects

    3. Dyes and Pigments: Intermediate for High-Performance Azo Pigments

    Producers of organic colorants draw on this compound for synthesizing diaryl and monoazo pigments used in plastics, fibers, and specialty coatings. Its methyl and bromo substituents enable precise color tuning via controlled diazotization and coupling routines, delivering pigments with high lightfastness and solvent resistance. Manufacturers manage additive ratios to balance color yield with purity and process efficiency, with all critical steps documented for customer audits.

    Industry compliance standards

    • REACH Annex XVII (restrictions on hazardous amines)
    • EN 71-3:2019 (Toys and children’s product pigment safety)
    • OEKO-TEX Standard 100 (Textile chemical safety requirements)
    • ETAD guidance relevant to pigment intermediates

    Typical usage ratio

    • 0.8–1.0 mole ratio relative to diazonium reaction partner; color strength and viscosity control require trial-based optimization at pilot scale

    Downstream process integration

    • Fed into diazotization vessel as limiting reagent for targeted pigment hue, followed by coupling and pH adjustment; isolated crystals or pastes then are post-treated for particle control

    Final product types

    • Azo pigments for engineering plastics (PP, PE, PVC)
    • Synthetic textile disperse dyes
    • High-stability printing ink pigments
    • Specialty coating colorants for automotive and industrial applications

    4. Electronic Chemicals: Precursor for OLED and Specialty Material Development

    Materials engineers rely on this building block in R&D and scale production of advanced organic electronic compounds, most notably as a precursor for hole-transport materials in organic light-emitting diode (OLED) displays and other optoelectronic devices. Its molecular structure assists fine-tuning of electronic properties when incorporated into small-molecule or polymeric systems. Precise input levels are calculated to match the targeted functional group modification, while downstream QC confirms low metal and halide residues as required for high-purity electronic applications.

    Industry compliance standards

    • JEITA ET-7304A (Guideline for OLED Material Evaluation)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances)
    • IPC-1752A (Material declaration for electronic products)
    • UL 94 (Polymer Flammability Certification for device safety)

    Typical usage ratio

    • 0.5–0.9 mole equivalent per functionalized monomer or polymer chain; further refinement required for each specific conduction threshold

    Downstream process integration

    • Reacted in solution-phase coupling, generally in the presence of transition metal catalysts, during early-stage monomer formation for subsequent deposition or spin-coating

    Final product types

    • OLED hole-transport luminophores and hosts
    • Photovoltaic cell polymers
    • Semiconducting films for flexible display substrates
    • Prototype organic transistor testing materials
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    Certification & Compliance
    More Introduction

    Introducing 5-Bromo-2-Methylaniline: A Closer Look at a Versatile Chemical

    Each time we dig a little deeper into the world of specialty chemicals, one thing stands out: details matter. Take 5-Bromo-2-Methylaniline, for example. This compound pulls interest not just for its formula, but for the ways it carves out a niche in everything from pharmaceutical development to professional-grade organic synthesis. With the chemical structure marked by a bromine atom on the aniline backbone and a methyl group adding extra nuance, subtle shifts in properties open up some unique possibilities. This isn’t the kind of chemical people talk about at dinner tables, but its value runs deep in the sort of projects that really push boundaries in research labs, pilot plants, and advanced manufacturing.

    Why 5-Bromo-2-Methylaniline Matters in Cutting-Edge Research

    Anyone who has worked long days in the lab knows the importance of building blocks that provide reliability mixed with a little flexibility. 5-Bromo-2-Methylaniline serves up both, anchored by its CAS number, 578-57-4, and a reputation built on stable, high-purity supply. The core attraction comes down to its bromo–methyl arrangement; that combination paints a new canvas for chemical transformations, thanks to the distinct reactivity brought by the bromine atom at the 5-position. The methyl group tweaks both steric and electronic effects, nudging reactions in ways that plain aniline derivatives just don't manage.

    Researchers gravitate to this compound when a synthesis pathway calls for a halogenated aniline that isn’t just reactive, but predictable. During my own time working on small-scale intermediate production for APIs, introducing a bromine atom meant our reactions stayed under tighter control compared to the hit-or-miss chemistry of chlorinated or iodinated analogues. 5-Bromo-2-Methylaniline melts at around 41-45°C and appears as light beige to yellow crystalline powder. These characteristics might not sound glamorous, but in lab glassware or industry kettles, you see the difference between nightmare clumping and smooth dissolving.

    Direct Applications Beyond the Standard Playbook

    Some chemicals just get tossed around in bulk to do menial background work. 5-Bromo-2-Methylaniline deserves a closer look. In pharmaceuticals, the compound helps build up key intermediates that lead toward more sophisticated targets. Synthesis of certain active pharmaceutical ingredients hinges on the careful introduction of bromoaniline derivatives to tune molecular frameworks or set up later coupling reactions. In agrochemical work, dropping a methyl group onto the structure adds just enough “push” to make analogues that hold up under tough climate conditions or resist early breakdown in soil.

    This aniline variant also draws attention in dye and pigment manufacture, a field known for stubborn chemistry and the need for subtle tweaks in color fastness. Brominated arylamines form the backbone of several azo and triarylmethane dyes, and the methyl group influences both shade depth and migration resistance. From personal experience, dialing in the exact tone of a purple or blue shade without a compound like this often pushes processes into expensive and wasteful rework cycles.

    Standing Apart in a Crowded Field of Similar Chemicals

    Over time, chemists realize that not all substitutions on a benzene ring behave alike. If you put 2-methyl and 5-bromo on the ring, the electron density and the steric profile end up just right for specific coupling strategies that can falter with other halogen positions. While chlorinated analogues tend to offer slightly easier sourcing, they often drag out reaction kinetics or yield unwanted side products. The 5-bromo group keeps reactivity manageable, especially in palladium-catalyzed cross-couplings, such as Suzuki or Buchwald-Hartwig reactions.

    Safety data also shows a more manageable hazard profile compared to heavier halogenated anilines. Talking shop with colleagues in specialty synthesis, there’s a pretty clear consensus: we’d rather handle 5-Bromo-2-Methylaniline than the more unpredictable dihalogenated versions, which tend to create issues with byproduct formation or purification. Less off-gassing and easier containment translate to less headache during long pilot campaigns.

    Practical Insights: Working with 5-Bromo-2-Methylaniline in the Lab and Industry

    Whether you’re pipetting milligrams or scaling up to drum shipments, ease of use makes or breaks a project. Across the board, 5-Bromo-2-Methylaniline dissolves well in polar organic solvents. It stays stable under dry and cool storage, allowing stashes of stock material to last for months without losing purity—something that makes accountants and technicians equally happy. True, care is always needed in storing and handling; the amine group brings the usual need for gloves and good ventilation, but nothing extraordinary compared to related chemicals.

    Companies supply it in various grades, with purity hitting 98–99% in most reputable sources. Those working in regulated sectors usually request trace metal and residual solvent certificates. Reliable sourcing means researchers don’t have to pause work for extensive re-purification or lengthy QC checks. The bottom line is that more time goes into actual experimentation and less into damage control chasing batch variability.

    Comparisons With Common Alternatives

    Working with aniline derivatives, I’ve cycled through a range of bromo, chloro, and iodo substitutions. 5-Bromo-2-Methylaniline balances reactivity and safety in a way that remains tough to beat. Iodo variants bring increased reactivity useful in some challenging couplings, but they come with a higher price and less stability. Chloro analogues might be cheaper, but they slow down key reactions and often call for more forcing conditions—higher temperatures, longer times, and tougher workups.

    Purification steps stand as another separating factor. In day-to-day practice, you realize the finer details make or break your process: sticky residues or colored impurities can slow down purification considerably. 5-Bromo-2-Methylaniline, if sourced from solid suppliers, tends to behave better in both crystallization and chromatographic cleanup than other halogenated anilines. This streamlining trickles down to less waste and easier regulatory compliance, since you cut down on solvent use and byproduct management.

    Fact-Based Perspectives: Regulatory and Health Considerations

    Safety teams pay close attention to aromatic amines for good reason. While no chemical with an exposed amine and halogen should be handled casually, extensive studies show 5-Bromo-2-Methylaniline doesn’t present hazards out of line with similar compounds. Standard practice—nitrile gloves, lab coats, and fume hoods—suffices to keep risks minimal. That said, regular updates from safety bulletins reinforce the need for continued vigilance, especially regarding skin contact and inhalation of dust.

    Environmental responsibility sits front and center in chemical manufacturing these days. Waste streams containing halogenated organics demand careful tracking. The relatively simple breakdown pathway for 5-Bromo-2-Methylaniline makes disposal more manageable than some heavier halogenated cousins. It remains vital to follow local and international regulations when designing new synthetic routes or scaling up industrial usage.

    Potential Improvements and Future Directions

    Continuous improvement forms the backbone of any successful chemical operation. In the case of 5-Bromo-2-Methylaniline, newer synthetic methods aim to improve atom economy, reduce the use of toxic reagents, and curb energy use during production. Companies respond to calls for “greener” chemistry by investigating catalytic bromination and adopting closed-loop systems to capture emissions.

    One area with growing interest involves bio-based brominating agents that can deliver the 5-bromo function selectively, sparing the need for heavy-metal-based catalysts. As these methods mature, cost and environmental impact will swing even more in favor of this compound compared to costlier alternatives. From my experience, whenever a process cuts hazardous steps without giving up reliability, adoption follows quickly both in academia and industry.

    Supporting Innovation in Pharmaceutical and Materials Science

    5-Bromo-2-Methylaniline isn’t only a background player; it takes center stage in many synthetic routes that yield life-saving drugs and high-performance polymers. Its versatility lies in how chemists can fit it into numerous frameworks. Whether in seed compounds for kinase inhibitors or scaffolds for new pigments, this molecule offers both stability and precision.

    Some projects in pharmaceutical discovery depend outright on having a reliable supply. Delays or purity issues echo downstream with product recalls or blown timelines. The confidence in 5-Bromo-2-Methylaniline’s performance, both in bench-scale work and kilo-scale campaigns, gives researchers a breathing room not always matched by less consistent options. That reliability breeds the kind of trust needed to jump from lab experiment to production without layers of contingency planning.

    Preparing for Shifting Global Demands

    Supply chain dynamics for specialty chemicals change rapidly. A few years back, intermittent shortages of key starting materials highlighted the need for diverse and local sources. Sourcing 5-Bromo-2-Methylaniline from multiple certified suppliers now stands as a common-sense move for anyone counting on uninterrupted research or manufacturing runs.

    Transparent documentation of origin and purity lets buyers make smarter choices while avoiding supply disruptions. Those running scale-up operations watch shipping routes, customs policies, and even domestic regulatory changes, since these can all impact timelines and costs. For the foreseeable future, stable materials like 5-Bromo-2-Methylaniline look set to hold their place in well-planned procurement strategies.

    Partnering with Users: Feedback and Continuous Refinement

    Feedback from users matters as much as metrics on product sheets. Over the years, direct conversations with bench chemists, plant operators, and research directors highlighted the value they place on having compounds behave predictably across batches. It isn’t just about purity; lot-to-lot consistency affects everything from batch records to patent filings.

    Stakeholders increasingly ask manufacturers to tweak particle size, packaging, and labeling for smoother operations on their end. Responding to this sort of direct input, rather than imposing generic standards, encourages better engagement. In this collaborative loop, both sides benefit—suppliers gain stable sales, and end-users shave hours off project timelines due to fewer surprises.

    Challenges and Practical Solutions for Today’s Users

    Like all chemicals used in rigorous applications, 5-Bromo-2-Methylaniline poses a few routine headaches—think dust control, precise weighing, and tracking trace impurities. Modern packaging addresses some of these issues with anti-static bottles, shatter-resistant containers, and tamper-proof labeling. In-house testing of every batch catches the rare outlier.

    Process engineers I know urge the importance of digital batch tracking and maintaining a real-time record of solvent compatibility. Traceability spares teams from labor-intensive troubleshooting, since any anomaly gets flagged and investigated before it snowballs. Emerging tech, such as RFID-tagged packaging and cloud-based logging, makes following aniline derivatives from warehouse to workbench less of a logistical puzzle.

    Expert Guidance for Safe and Effective Handling

    A molecule with as much potential as 5-Bromo-2-Methylaniline calls for diligence in daily handling. Well-trained staff who regularly refresh their knowledge on chemical-specific hazards keep accidents rare. Tailored in-house briefings beat generic safety sheets, since they account for actual equipment and layout found in each workplace.

    Waste minimization strategies pay off, not just environmentally but financially. Some plants now reclaim wash solvents that collected residual 5-Bromo-2-Methylaniline, recycling them into lower-value secondary products. Operators report both cleaner workspaces and a small but steady cost reduction—a smart approach for firms seeking incremental gains.

    Outlook and Ongoing Innovation

    There’s little doubt that demand for compounds like 5-Bromo-2-Methylaniline will keep climbing as pharmaceutical and specialty chemical industries grow more sophisticated. Cheaper, “rough” grades won’t serve where strict purity and documentation are needed; instead, ongoing refinement in production processes forms the backbone of steady supply.

    Future applications may drive entirely new handling or transformation approaches. For now, the compound’s track record supports continued confidence among those betting their timelines and safety on robust chemical performance.

    Conclusion: Why Details on 5-Bromo-2-Methylaniline Matter

    The deeper I’ve dug into specialty chemistry, the more I appreciate what separates routine success from major setbacks. No compound fits every need, but 5-Bromo-2-Methylaniline earns its status through a mix of reliability, adaptability, and long-term refinement in handling. As processes grow more demanding and customers raise their expectations, the companies and teams that lean into open, fact-based collaboration with their suppliers will push the real breakthroughs forward. For those who invest in understanding their key materials inside and out, chemicals like this one become more than a mere ingredient—they form part of the glue that holds the future of high-performance industry together.