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3-Bromoanisole

    • Product Name 3-Bromoanisole
    • Alias 3-Bromo-1-methoxybenzene
    • Einecs 210-360-8
    • 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
    Specifications

    HS Code

    620067

    Chemical Name 3-Bromoanisole
    Cas Number 2398-37-0
    Molecular Formula C7H7BrO
    Molecular Weight 187.04
    Appearance Colorless to pale yellow liquid
    Boiling Point 213-215 °C
    Melting Point -17 °C
    Density 1.529 g/mL at 25 °C
    Refractive Index 1.562
    Flash Point 92 °C
    Solubility Insoluble in water, soluble in organic solvents
    Smiles COC1=CC(=CC=C1)Br

    As an accredited 3-Bromoanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Bromoanisole, 100 mL, supplied in an amber glass bottle with a secure screw cap and clear hazard labeling for safety.
    Shipping 3-Bromoanisole is shipped in sealed, chemical-resistant containers, typically glass or HDPE bottles, to ensure safety and stability. The packaging complies with international regulations for hazardous materials. During transit, it is protected from moisture, heat, and sunlight, and accompanied by proper labeling and documentation, including Safety Data Sheets (SDS).
    Storage 3-Bromoanisole should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature and ensure the area is equipped to manage spills or leaks. Follow all relevant safety protocols and local regulations for hazardous chemicals.
    Application of 3-Bromoanisole

    Purity 99%: 3-Bromoanisole with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal by-product formation.

    Molecular weight 187.02 g/mol: 3-Bromoanisole with molecular weight 187.02 g/mol is used in agrochemical production, where precise stoichiometry enhances reaction efficiency.

    Boiling point 216°C: 3-Bromoanisole with boiling point 216°C is used in solvent recovery systems, where thermal stability allows for efficient distillation.

    Stability temperature up to 200°C: 3-Bromoanisole with stability temperature up to 200°C is used in organic electronic material processing, where heat resistance prevents decomposition.

    Moisture content ≤0.1%: 3-Bromoanisole with moisture content ≤0.1% is used in Grignard reagent synthesis, where low moisture content prevents unwanted side reactions.

    Colorless liquid form: 3-Bromoanisole in colorless liquid form is used in dye intermediate manufacturing, where product transparency ensures consistent coloration results.

    Refractive index 1.561-1.563: 3-Bromoanisole with refractive index 1.561-1.563 is used in analytical reference standards, where optical clarity aids precise measurement.

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    Certification & Compliance
    More Introduction

    3-Bromoanisole: A Closer Look at Its Role in Modern Chemistry

    Understanding 3-Bromoanisole: More Than a Building Block

    Stepping into any well-equipped laboratory, you’ll spot bottles marked with names that spark the curiosity of chemists and industrial practitioners alike. One of these labels is 3-Bromoanisole. This compound, with its signature combination of a bromine atom and a methoxy group positioned along a benzene ring, stands out not just for what it is, but for what it can accomplish. Speaking as someone who’s seen both the academic and practical sides of organic synthesis, I believe it’s necessary to dig beneath the basic formula—C7H7BrO—and see how this chemical supports complex, real-world innovation.

    3-Bromoanisole carries its own weight in the world of aromatic bromides. It doesn’t just sit in warehouses or catalogues; it makes crucial appearances on the benches of pharmaceutical researchers and specialty chemical makers. At room temperature, this compound takes the form of a clear, somewhat oily liquid with a faint, aromatic scent—an unassuming appearance that belies its function in high-stakes syntheses.

    The Shape and Quality That Matters

    To understand why chemists keep returning to 3-Bromoanisole, it’s helpful to look at its structure. With the methoxy group at the meta position relative to the bromine atom, the molecule offers routes that differ from its close relatives like 2-bromoanisole and 4-bromoanisole. This placement directly impacts its reactivity. From handling this molecule during graduate work—especially in cross-coupling projects—I noticed that the location of substituents on the aromatic ring often spells the difference between a successful reaction and wasted time.

    What sets 3-Bromoanisole apart is the way the bromine influences substitution reactions. Whether you’re planning Suzuki, Heck, or Buchwald–Hartwig couplings, the position of that bromine opens doors that other isomers simply can’t. Many large-scale drug discovery campaigns rely on this kind of versatility. For example, in creating intermediates for agrochemical products, the specific location of both the bromine and the methoxy group can change not just the efficacy of the synthesis, but also the safety and environmental impact of downstream products.

    Rethinking Its Usage: Where It Actually Fits

    It’s common to hear that “3-Bromoanisole is an important intermediate in organic synthesis”—but that statement barely scratches the surface. I see the compound turning up again and again where selectivity is more than a convenience. Say you’re aiming to add a functional group to an aromatic system. Starting from 3-Bromoanisole, the combination of electron-donating and electron-withdrawing effects creates a balance that can steer the next steps, producing unique substitution patterns that aren’t accessible through other isomers.

    Industry professionals—especially in the pharmaceuticals and fine chemicals sectors—rely on this difference. Because many active pharmaceutical ingredients require specific aryl ether scaffolds, the choice between meta, ortho, or para bromine affects not just yield but also the biological activity of the end molecule. In practice, this means a production pipeline for a complex molecule is fundamentally different depending on whether the lab stocks enough 3-Bromoanisole rather than just any brominated anisole isomer.

    Having spent hours in synthetic labs, there’s a noticeable uptick in troubleshooting when the starting materials don’t match the demands of a particular method. For example, catalytic cross-coupling reactions—including those pioneered by chemists like Richard F. Heck and Akira Suzuki—depend not only on the nature of the catalyst but on the substrate itself. The placement of atoms in 3-Bromoanisole gives it a blend of reactivity and selectivity that’s hard to duplicate with alternatives.

    3-Bromoanisole Versus Its Isomers: Real-World Differences

    With dozens of aromatic halides available, people often ask what sets 3-Bromoanisole apart from the 2- or 4-bromoanisole variants. Chemists working in medicinal chemistry and materials science know there’s no one-size-fits-all. For example, 2-bromoanisole has a bromine and methoxy group right next to each other, which can create problems with sterics—that is, physical crowding blocks some reactions or lowers yields. Meanwhile, 4-bromoanisole positions them directly opposite each other, which can limit the types of ring substitutions or functionalizations possible in the next synthetic step.

    3-Bromoanisole, meanwhile, offers a compromise. Steric hindrance is lower than in the ortho isomer, but the methoxy group still activates the ring in a way that unlocks certain transformations. In making biphenyls, arylamines, or even more complicated polyaromatic compounds, this compound provides a starting point that’s often unavailable by other, more common brominated anisoles.

    The practicalities extend to purification and handling too. Compared to solid isomers, this one is a liquid at room temperature. I’ve worked in settings where that made a difference—a liquid substrate means easier measurement, more straightforward mixing, and less dust in air-sensitive environments. Cleanup and waste handling often go faster with fewer steps, which matters in industries bound by tight regulatory requirements and efficiency targets.

    Quality Control and Purity: A Matter of Trust

    Having been in labs where even minor impurities disrupt days of work, I can say the purity of 3-Bromoanisole plays a much larger role than just meeting a number on a datasheet. Many suppliers target purities above 98 or even 99 percent, which matters most for those working on pharmaceutical or electronic-grade projects. In my experience, trusted lots will come with detailed batch analysis, highlighting not only purity but possible contaminants. Such transparency reduces the risk of unexpected by-product formation, which in turn improves both reproducibility and safety.

    The nature of the impurities carries its own risks. For example, trace halogenated by-products, moisture, or residual solvents can derail sensitive palladium-catalyzed reactions. Chemists planning multistep syntheses need reliability in each bottle. I learned early on the frustration that comes from assuming all commercial sources are made equal. Building long-term, direct relationships with vendors who provide full disclosure on analysis goes a long way—especially when pilot runs move to commercial scale.

    Safety and Responsible Handling

    Though 3-Bromoanisole doesn’t pose the extreme hazards of many other chemical intermediates, safe handling is non-negotiable. Standard practice in laboratories calls for gloves, goggles, and good ventilation—this is basic training for any chemist, but absolutely essential when scaling reactions to multi-liter quantities in an industrial setting. Spills and contact risks never fully disappear with aromatic compounds. From personal experience, I once witnessed an early-career colleague suffer mild irritation due to a leaky septum and careless glove discipline; the lesson stuck with the team.

    Accurate labeling and tight storage controls curb both workplace accidents and environmental risks. Aromatic ethers are known for emitting persistent odors that signal leaks even at low concentrations. Quick access to MSDS and emergency protocols rounds out a safe workplace—anything less cuts corners not worth taking.

    Sustainability and Ethical Sourcing

    The chemical industry stands under increasing scrutiny, and this stretches to every bottle on the shelf, including 3-Bromoanisole. Modern buyers and technical leaders look for supply chains that source their raw materials without causing unnecessary harm. Brominated starting materials often come from large upstream chemical plants, and some regions continue to use processes with questionable emissions profiles or environmental oversight gaps.

    I’ve seen some manufacturers move toward greener bromination methods that cut waste and reduce energy usage. Life-cycle analysis and partnership with suppliers using closed-loop systems can directly reduce hazardous by-products. As a consumer, asking vendors about their procurement and environmental certifications is no longer an optional step—it’s become part of due diligence, especially for businesses that answer to customers and shareholders with green mandates.

    Driving Innovation: 3-Bromoanisole in New Applications

    Outside of standard pharmaceuticals, 3-Bromoanisole plays a part in developing new dyes, OLED precursors, and advanced agrochemicals. My own work with fluorescent probes for biological imaging required aryl bromides with the right electronic balance for developing tailored dyes. The unique ring-substitution afforded by 3-Bromoanisole enabled luminescent properties that other isomers simply couldn’t deliver.

    Technology transfer from academic research to industrial-scale manufacturing often starts with this type of building block. As demand grows for specialty compounds—especially those used in devices, polymers, and crop protection products—reliance on distinct isomers increases. Forward-thinking suppliers keep pace by maintaining stock and investing in the synthesis of high-purity batches.

    Points of Improvement: Reducing Waste and Maximizing Efficiency

    With every bottle of chemical comes the question—how much is wasted, and can the steps be improved? During the years I spent trouble-shooting failed syntheses, it became obvious that batch variability from one supplier to another led to more by-product in downstream processing. Analytical investment, especially routine NMR and GC-MS checks, helps labs flag subtle differences before they create waste. The ability to trust what's inside a bottle, whether it's for a small-batch library or multi-ton production, can save thousands in waste management and product recall costs.

    Waste doesn’t just come from impurities; inefficient reaction conditions can turn a straightforward process into a complex, expensive clean-up job. Publishing and sharing real-world process improvements—whether it’s on a chemistry forum, at a conference, or in company knowledge bases—allows the entire industry to leap ahead while avoiding repeated errors.

    Alternatives and Trade-Offs

    No chemical exists in isolation. Chemists always have choices, and new synthetic routes sometimes make switching to a completely different starting material appealing. Direct C–H functionalization, for example, occasionally bypasses the need for aromatic bromides altogether. In practice, though, the reliability and established performance of compounds like 3-Bromoanisole make them a mainstay for work that’s both time- and cost-sensitive.

    Switching to greener, more benign alternatives requires testing and buy-in—not just from technical staff, but the regulatory, compliance, and environmental teams within an organization. Some new cross-coupling technologies further reduce reliance on hazardous metals or solvents, but the change takes time and resource commitment. Until those methods are fully deployed across industry, molecules such as 3-Bromoanisole hold their spot as versatile, reliable tools in the chemist’s toolkit.

    Real Situations: Lessons Learned and Shared

    There’s an enormous difference between reading about a compound in a textbook and seeing it deployed in the field. Through hands-on projects in both academia and industry, I’ve seen how different teams adjust their use of 3-Bromoanisole to fit their unique workflows and output demands. This is not a generic tool for theoretical problems—it’s a practical answer to specific, high-value challenges in organic chemistry and allied fields.

    One notable case: a team attempting to scale up a complex aryl ether synthesis found that switching to high-purity 3-Bromoanisole halved the number of purification steps required and improved assay yields by a measurable margin. This translated not only to less solvent waste, but also to faster time-to-market—key in a sector where weeks or even days can mean lost revenue or missed regulatory deadlines.

    Continuous Improvement: What the Future Holds

    Chemistry, like any science, keeps moving forward—sometimes through large leaps and sometimes through the steady march of incremental improvement. For 3-Bromoanisole, future improvements will likely come in three areas: safer production, tighter quality assurance, and a larger move toward renewable feedstocks. Some innovative companies have begun exploring biosynthetic pathways for brominated aromatics, looking to nature for inspiration rather than relying solely on legacy chemical processes.

    Improving communication between suppliers and end-users continues to reduce delays and mistakes. Rather than generic product listings, real partnerships—where technical support answers questions quickly and transparently—help maximize the impact of every shipment. More open sharing about both success stories and roadblocks can speed the entire sector’s adoption of best practices.

    Solutions That Work: Making the Most of 3-Bromoanisole

    The lessons learned from years of working with this compound can be distilled into clear takeaways. Prioritizing supplier relationships, verifying each batch, and investing in both safety and sustainability never pay off as temporary fixes—they become ongoing commitments. Labs just starting to explore cross-coupling chemistry with aryl bromides benefit from networking with those who have navigated issues before them. Sharing process data, especially about solvent use, workup optimization, and waste reduction, helps everyone get a little further, faster.

    Putting real resources into sustainable sourcing, cleaner production technologies, and knowledge transfer doesn’t just improve the bottom line. It ensures that when demand rises—whether for a new drug candidate or a next-generation material—the supply chain will be ready, the chemistry will perform, and the environmental cost will be smaller.

    Why 3-Bromoanisole Holds Value for Today and Tomorrow

    Every generation of chemists faces materials that become the backbone of entire industries. 3-Bromoanisole, through its unique balance of properties and proven track record, stands as one such material. From my perspective, its importance only grows as discovery cycles shorten and demands for quality, safety, and responsibility tighten. Relying on old habits or ignoring the benefits of transparency and continuous improvement only limits what future chemists can accomplish.

    Real-world experience supports the role of 3-Bromoanisole as more than just a commodity. It is a platform for building, innovating, and delivering results in a sector where precision, safety, and resource stewardship set the tone for progress. By focusing on careful sourcing, smarter applications, and rigorous QA—from bench to bulk—the chemical industry can use this trusted compound as both a benchmark and a springboard toward even more ambitious achievements.