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3-Bromothioanisole

    • Product Name 3-Bromothioanisole
    • Alias 3-Bromo-1-methylthio-benzene
    • Einecs 228-234-1
    • 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
    VTB
    Specifications

    HS Code

    738318

    Chemicalname 3-Bromothioanisole
    Casnumber 1530-73-2
    Molecularformula C7H7BrS
    Molecularweight 203.10
    Appearance Colorless to yellow liquid
    Boilingpoint 112-114°C at 15 mmHg
    Density 1.482 g/cm3
    Refractiveindex 1.610
    Solubility Insoluble in water, soluble in organic solvents
    Synonyms m-Bromothioanisole; 1-Bromo-3-(methylthio)benzene
    Purity Typically ≥97%
    Smiles CSC1=CC(=CC=C1)Br
    Inchikey DOEVNBKSEAMRRP-UHFFFAOYSA-N
    Flashpoint 110°C

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

    Packing & Storage
    Packing 3-Bromothioanisole, 25g, packaged in a sealed amber glass bottle with a secure screw cap, labeled with hazard and identification details.
    Shipping 3-Bromothioanisole is shipped in secure, tightly sealed containers to prevent leakage and contamination. It should be transported as per standard regulations for hazardous chemicals—protected from moisture, heat, and incompatible materials. Shipping follows DOT, IATA, or IMDG guidelines, and proper labeling, documentation, and handling procedures are strictly observed for safety.
    Storage 3-Bromothioanisole 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 oxidizers. Store at room temperature, and ensure the container is clearly labeled. Use proper protective equipment when handling and follow local regulations for storage of hazardous chemicals.
    Application of 3-Bromothioanisole

    Applications of 3-Bromothioanisole in Industrial Manufacturing

    We supply 3-Bromothioanisole directly to specialized chemical and pharmaceutical manufacturers worldwide. Each downstream segment utilizes this compound for precise synthetic transformations, meeting industry-specific quality and regulatory requirements. Our production processes guarantee consistent supply and strict lot traceability to underpin application-critical needs.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical companies integrate 3-Bromothioanisole as a key intermediate in synthesizing complex sulfur-containing and aryl bromide API scaffolds. Its chemical stability and defined reactivity make it suitable for Suzuki and Buchwald-Hartwig cross-couplings during early-stage API construction. In-house process chemists select this compound for controlled bromination and methylthio group insertion, enabling downstream synthesis of targeted molecular fragments. Batch-specific quality documentation supports regulatory filings and validation batches.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, ICH Q7A)
    • United States Pharmacopeia (USP) reference for intermediates
    • ICH Q3A/B guidelines on impurities and residual solvents
    • REACH (EC 1907/2006) pre-registration for chemical intermediates

    Typical usage ratio

    • 10–25% molar equivalent relative to core reactant, with adjustments for step yield optimization and impurity controls

    Downstream process integration

    • Added after solvent charging and base preconditioning, followed by controlled temperature application during coupling

    Final product types

    • Sulfur-containing heterocyclic APIs
    • Brominated small molecule drug candidates
    • Specialty API building blocks (for oncology and CNS indications)

    2. Synthesis of Agrochemical Actives

    Chemical formulators deploy 3-Bromothioanisole to introduce methylthio structures within active pesticide and fungicide molecules. Agrochemical research and production lines employ it during scale-up synthesis of aryl thioether core intermediates, meeting performance and selectivity criteria in newly registered formulations. Strict lot consistency and purity data support process validation and market authorization applications.

    Industry compliance standards

    • FAO/WHO Guidelines on Technical Grade Active Ingredients
    • ISO 9001:2015 certified supplier audit trail
    • OECD Guidelines for the Testing of Chemicals (for downstream safety studies)
    • National registration protocols (such as EPA FIFRA in the US, Regulation (EC) No 1107/2009 in the EU)

    Typical usage ratio

    • 5–17% by weight of organic reaction mixture, adjusted according to desired thioether incorporation and mitigation of by-product formation in key stages

    Downstream process integration

    • Charged as an initial aryl halide feedstock in controlled palladium-catalyzed coupling, monitored for complete consumption prior to hydrolytic work-up

    Final product types

    • Methylthio-substituted herbicides
    • Fungicide precursors
    • Safener and synergist molecules for crop protection

    3. Building Block in Fine Chemical Synthesis for Electronic Materials

    Manufacturers of organic electronic materials select 3-Bromothioanisole to build high-purity thiophene and aryl bromide derivatives. Its electronic properties and precise substituent pattern support development of organic semiconductors, charge transport layers, and specialty polymers for electronic device fabrication. Downstream processes require batch certification for elemental bromine and sulfur content, ensuring final material consistency at micro-scale patterning and device integration stages.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (control of hazardous substances)
    • IEC 61249-2-21 for brominated components in electronics
    • ISO 14001:2015 for environmental management in chemical processing
    • Customer-specific Quality Management Systems (QMS) for supply chain control

    Typical usage ratio

    • 3–10 mol% per batch, adjusted for polymer block length requirements, desired dopant effects, and residual halide minimization

    Downstream process integration

    • Fed continuously or in charge batches for aryl coupling and monomer functionalization stages, monitored for trace residuals in solvent streams

    Final product types

    • Organic semiconductors and thin film layers
    • Specialty polymers for OLED displays
    • Charge transport materials used in solar cells and photodetector devices

    4. Aroma and Flavor Intermediate for Fragrance Ingredient Manufacture

    The aroma chemical industry uses 3-Bromothioanisole as a starting reactant in multi-step syntheses of sulfur-carrying aromatic compounds. Its bromine and methylthio functional groups allow for tailored modification into odorant molecules, especially those used in aroma profile balancing for foodstuffs and high-end perfumery. Manufacturers demand consistent purity and impurity profiles, as regulated by international flavor safety and hazard standards.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredient Safety
    • Regulation (EC) No 1334/2008 on flavorings and food ingredients
    • ISO 9001:2015 for quality system traceability
    • GHS/CLP labeling for hazardous components

    Typical usage ratio

    • 2–10% mass input per batch, adjusted for aroma precursor selectivity, targeted conversion rate, and minimization of sensory-impacting trace by-products

    Downstream process integration

    • Directly introduced during aromatic alkylation or substitution, with continuous sampling in fractionation and distillation post-synthesis

    Final product types

    • Sulfur-containing aroma chemicals
    • Precursors for food-use flavoring substances
    • Olfactory modifiers in luxury fragrance formulations

    5. Research Chemical for Advanced Materials and Custom Synthesis

    Leading R&D laboratories and pilot-scale custom manufacturers employ 3-Bromothioanisole in the design of functionalized aromatic thioethers and halides. It enables specialized, small-batch synthesis of new ligands, specialty monomers, and reference compounds for material science innovation. Researchers use it for target-oriented synthesis, method development, and pre-clinical evaluation, requiring detailed batch analytics and on-demand technical documentation support.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for research chemical processing
    • Chemical Safety Assessment Documentation (per REACH for EU)
    • Institutional Material Safety Data Sheet (MSDS) controls
    • ISO 17025 for analytical quality assurance

    Typical usage ratio

    • Ranges from milligram to gram per reaction, as determined by stoichiometric design and scale-up trial requirements

    Downstream process integration

    • Scheduled as first-step arylation component, or as selective functional group introducer in high-throughput parallel synthesis arrays

    Final product types

    • Novel aryl thioether reference compounds
    • Polyfunctional intermediates for material science evaluation
    • Custom chemical standards for analytical method development
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    Competitive 3-Bromothioanisole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Bromothioanisole: Precision and Reliability for Specialty Synthesis

    Our Manufacturing Perspective on 3-Bromothioanisole

    There is a unique satisfaction in synthesizing 3-Bromothioanisole batch after batch, measuring its clear, colorless-to-pale-yellow profile, and consistently hitting the purity demanded by advanced chemical work. As a chemical manufacturer with decades of experience in brominating thioethers, we've learned what keeps chemists coming back to this compound, and how even minor impurities can compromise an entire set of experiments or manufacturing goals. Producing this compound from start to finish on our own lines grants control over each step—selection of raw materials, reaction conditions, purification routes—and yields both tight material specifications and insight into the things only makers of chemistry notice.

    3-Bromothioanisole is not the most common name among sulfur-containing aromatic intermediates, but for labs developing new pharmaceuticals, advanced agrochemicals, and electronic materials, it stands apart for a few concrete reasons. As manufacturers, we see first-hand how small changes at the molecular level can ripple through downstream chemistry, leading to enhanced reactivity, selective transformations, or better process reliability. In our own daily work, we track which lots lead to successful couplings, which grades can tolerate storage for extended periods, and which preparation techniques minimize side-products. Over time, this experience shapes both our production methods and our understanding of the compound's practical value.

    Structure and Model Specifics

    The core structure of 3-Bromothioanisole, with a methylthio group at the para position and a bromine at the meta position on the benzene ring, gives it just the right balance of electron-donating and electron-withdrawing effects, making it an effective starting point for cross-coupling and functional group exchanges. Chemists rely on its reactivity profile, especially for Suzuki and Stille couplings, because the bromine atom presents a robust handle for palladium-catalyzed reactions, while the methylthio group acts as both a synthetic handle and a modulator of electronic properties—sometimes protecting reactive sites, sometimes acting as a leaving group after activation.

    Years of working with this molecule, from gram to multi-metric ton scale, taught us how subtle the balance of physical properties must be: purity above 98 percent guarantees that no contaminant disrupts catalyst performance or forms unwanted byproducts. The melting and boiling points, handled with rigorous quality control, enable confident storage and reliable measurement for preparing reaction mixtures. The sulfurous odor is a familiar side effect but can actually serve as a simple check for integrity, as any deviation usually hints at oxidation or degradation. Our favorite analytical signatures—sharp NMR aromatic peaks, a single molecular ion in mass spectrometry—confirm an authentic, well-prepared batch and signal readiness for further use.

    Real-World Usage Focused on Research and Manufacturing

    At the core of 3-Bromothioanisole’s commercial and research importance lies the niche intersection of organosulfur chemistry and halogenated aromatic synthesis. Our largest shipments go to pharmaceutical R&D, where structure-activity optimization often explores sulfur and halide substituents to achieve improved potency, metabolic stability, and target selectivity. Over the years, we've collaborated on preparing customized, GMP-ready batches for advanced drug candidates, finding that subtle differences in precursor quality can alter downstream product profiles and impurity patterns. In these settings, researchers often need to trust their building blocks without second-guessing trace impurities or inconsistent reactivity.

    Some of our most rewarding projects emerged from the agrochemical sector. There, 3-Bromothioanisole has helped speed up programs targeting new herbicides and fungicides, where the methylthio group often influences bioactivity. We've learned how the stability of this compound compared to many other brominated aromatics helps minimize unwanted decomposition during storage or reaction set-up—key for reliability. Because our processes keep oxidation to a minimum and reduce formation of byproducts like methylsulfoxides or sulfonium salts, our partners run reactions with less need for repeated purification, reducing waste and process time.

    In material science, the compound’s predictability carries even greater weight. For organic electronics and specialty polymers, the bromine and sulfur atoms both modify electronic properties and processability of the final product. As direct suppliers to electronics intermediates labs, we supply 3-Bromothioanisole with tight control over heavy metals and halide content, ensuring minimal risk of device failure or variability in electroactive materials. Formulators appreciate predictability; a reliable physical profile streamlines integration into larger syntheses, while uniform solubility allows straightforward scale-up. We’ve responded to feedback about solubility issues in mixed organic/aqueous processes by optimizing our crystallization methods, always tweaking parameters based on batch performance history.

    Differences That Matter in Practice

    One key benefit of 3-Bromothioanisole over similar halogenated thioanisoles, such as 4-bromo or 2-bromo analogs, stems from the electronic and positional effects of the bromine atom. Chemists who switch between isomers in SAR studies often report that swapping the meta-bromo variant enables unique coupling selectivity or downstream reactivity that would be much harder to achieve otherwise. We've scaled all three isomers over the years and found that the meta-isomer not only resists certain oxidation pathways better but also gives fewer mixed byproducts during palladium-catalyzed coupling, especially in the hands of less experienced users. This cuts back on purification headaches and batch rejections.

    Some customers ask why this compound stands out compared to 4-bromoanisole or 3-bromoanisole—two halogenated aromatics that lack sulfur. In hands-on synthetic work, aromatic methylthio groups often bring new flexibility and selectivity, permitting reactions that might fail or give mixed outcomes using only oxygen or carbon substituents. The thioether’s unique electron-donating ability influences both rate and regioselectivity of couplings. Years of batch traceability and performance data from client feedback show that the methylthio variant delivers cleaner reactions in metal-catalyzed couplings and fewer off-target modifications.

    Storage and handling logistics also matter more than most expect. Unlike some halides that tend toward rapid air-oxidation or polymerization, 3-Bromothioanisole’s stability in sealed containers means less loss and fewer surprises during long-term storage. In our own warehouses, we’ve set up climate-controlled units, but the compound’s performance history lets us safely ship even under less-than-ideal transport conditions with minimal impact to purity—something isolable by our own analytical review of arrival samples. Labs with frequent turnover of intermediates tell us that our precision in packaging and lot control makes their workflows less prone to process disruptions.

    Supporting Reliable Chemistry with Direct Experience

    By owning every stage of manufacturing, we have pieced together a deep logbook of “in the trenches” chemistry. We know which purification columns bind small amounts of sulfur dioxide byproduct, which local water supplies demand tighter controls on washing steps, and which storage protocols yield the longest shelf-life in practice—knowledge only possible after running thousands of batches and seeing how small supply chain shifts show up in the finished product. It’s easy to dismiss such details as marginal, but failures in downstream syntheses almost always trace back to trace contaminants, inconsistent particle sizes, or packaging defects. Our technical teams often field calls from scale-up chemists troubleshooting bottlenecks, and we trace the issue to material subtleties that only a manufacturer controlling the supply can resolve.

    We favor open dialogue with customers, sharing both strengths and quirks of 3-Bromothioanisole acquired over years of practice. For instance, operators handling the product for the first time often comment on the distinctive odor, an inescapable reality of sulfur chemistry. We recommend clear ventilation protocols, prompt transfer to reactors, and tight sealing—policy driven not only by regulation but by practical, boots-on-the-ground experience of minimizing loss and exposure. In large-scale manufacturing, static and dust control measures have become central to our shopfloor safety; small lessons born of repeated handling inform the setup guides we provide for handling and transfer.

    Analytical data never substitutes for experience. Our spectroscopists check identity and purity on each production lot, but we also track meta-data around storage, transport, and delivery. Lab leaders appreciate that our staff can discuss not just the numbers but also the context: how a slightly different storage temperature or cap type affects shelf stability, why we favor a specific bottle polymer for export orders, or which carrier logistics have the lowest incident rates for leaked shipments. These seem like outside-the-lab concerns but shape chemistry outcomes as much as purity metrics do.

    Solutions for Sourcing, Customization, and Batch Consistency

    New research teams and production chemists often ask how we solve the problem of scaling up rare intermediates like 3-Bromothioanisole. By keeping almost all key syntheses in-house, we avoid risk of contamination or inconsistency from third-party sourcing. This gives us direct control over temperature gradients, agitation rates, and quenching protocols—details that affect both yield and the impurity fingerprint. Our process engineers spend significant time on in-line monitoring and process optimization, validating that each parameter change helps, rather than hinders, overall product quality. Through this approach, we address issues like slow scale-up, uneven particle sizes, or unwanted crystallization during high-volume packaging.

    We’ve also developed custom production campaigns to meet atypical needs: pharmaceutical companies demanding ultra-low impurity traces, electronics manufacturers seeking halogen level corrections, researchers needing odd container sizes. Each time, our technical teams sit down with clients, review route feasibility, and offer sample lots for evaluation, then tweak the process to fit, collecting real-world feedback and shipping test-scale quantities. By being manufacturer-direct rather than through brokers or traders, we have flexibility and can bring technical tweaks to market in a matter of weeks instead of months, a pace appreciated by fast-moving R&D teams. Many of our long-term customer relationships grew not from initial price points but from solving one-off purity or supply chain issues together—lessons unteachable outside the factory floor.

    Another frequent challenge comes from regulatory shifts and environmental management. Because 3-Bromothioanisole contains both bromine and sulfur, it sits in regulatory crosshairs for waste water and process venting in many regions. From early days, we’ve invested in in-house waste management, using both off-gas scrubbing and internal effluent neutralization to reduce emissions. Working with local regulatory teams, we collect feedback to ensure smooth movement across borders and through compliance checks. This internal control, paired with aggressive quality assurance, means fewer surprises for our clients as regulations evolve—something barely visible up close, but crucial for large projects and multinational supply chains.

    Experience-Driven Reliability and Outcomes

    Producing, storing, and delivering high-purity 3-Bromothioanisole every day sharpens both practical skills and a deeper respect for details. We field frequent technical requests—from adjusting crystal size ranges to matching color standards set by downstream partners. Design choices on packaging, capping, and labeling grow out of ongoing production knowledge: we know which container types best prevent static buildup, which labels adhere under refrigeration, which closures resist leaks during air-transport. Chemists in the field see only the well-labeled bottle; we see the months of process validation, vendor auditing, and technical tuning that bring each batch safely to their bench.

    Our experience also drives honest feedback. Not every process works for every custom need, and some transformations—especially at massive scale—face challenges best solved with collaborative troubleshooting. We’ve never shied away from sharing pitfalls encountered during scale-up, or warning a partner away from a suboptimal downstream step based on our records. Time and again, these candid conversations led to process tweaks or new analytical controls that prevent surprises later. For us, transparency about real-world product performance instills trust and leads to better project outcomes.

    For those tackling next-generation synthesis, 3-Bromothioanisole serves as both a precise tool and a benchmark for consistency. Our manufacturing team tracks client feedback, builds it back into ongoing process development, and continually upgrades production lines to stay a step ahead of new demands. This approach anchors our difference—not just as a chemical supplier, but as a partner grounded in the daily realities and challenges of specialty synthesis.

    Conclusion: Putting Chemistry into Practice

    Every bottle of 3-Bromothioanisole leaving our warehouse reflects years of hands-on chemical engineering, process troubleshooting, and responsive partnership with innovative scientists. It’s easy to overlook such a molecule—just another aromatic halide, gone in a flash during a coupling step—but behind it stand layers of effort and technical knowledge, each tailored to deliver results in real labs, real factories, and real product lines. Whether used for a single pilot run or as a backbone to an ongoing manufacturing campaign, quality and reliability are non-negotiable. Our path as a manufacturer—the lessons learned, the mistakes corrected, the optimizations perfected—shine in every batch we produce. Those who work with 3-Bromothioanisole not only get a compound but also a full measure of our expertise, tuned and refined by every reaction we have helped make possible.