Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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4-Bromothioanisole

    • Product Name 4-Bromothioanisole
    • Alias 4-Bromo-1-(methylthio)benzene
    • Einecs 242-162-8
    • 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
    VTB
    Specifications

    HS Code

    730049

    Name 4-Bromothioanisole
    Synonyms p-Bromothioanisole
    Cas Number 3446-11-9
    Molecular Formula C7H7BrS
    Molecular Weight 203.10
    Appearance White to off-white solid
    Melting Point 44-46°C
    Boiling Point 272-274°C
    Density 1.51 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractive Index n20/D 1.601
    Smiles Brc1ccc(cc1)SC
    Inchi InChI=1S/C7H7BrS/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3
    Storage Conditions Store in a cool, dry place, keep container tightly closed

    As an accredited 4-Bromothioanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Bromothioanisole is supplied in a 25g amber glass bottle with a secure screw cap and safety labeling for laboratory use.
    Shipping 4-Bromothioanisole is shipped in tightly sealed containers, compliant with relevant safety regulations. It should be transported as a hazardous chemical, protected from light, moisture, and incompatible substances. All shipments require appropriate labeling and documentation to ensure safe handling and prompt delivery. Use expedited, trackable shipping to minimize transit time and risk.
    Storage 4-Bromothioanisole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight. Keep away from sources of ignition, heat, and incompatible substances such as oxidizing agents. Ensure proper labeling and secure storage, ideally in a chemical cabinet designed for organic reagents, to prevent contamination and unauthorized access.
    Application of 4-Bromothioanisole

    Applications of 4-Bromothioanisole in Industrial Manufacturing

    4-Bromothioanisole is an essential chemical intermediate commonly utilized across specialized fine chemical and pharmaceutical sectors. Its distinct structural attributes support the development of complex molecules and advanced materials for critical downstream applications. As a direct manufacturer, we supply this compound for industrial customers who demand precise formulation support, transparent technical data, and strict compliance with relevant industry requirements.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical manufacturing, 4-Bromothioanisole acts as a key thioether-building block for the construction of sulfur-containing heterocycles and biaryl frameworks integral to various APIs. Medicinal chemistry teams rely on its brominated aromatic group for regioselective cross-coupling or substitution during multi-step syntheses, ensuring structural integrity in patented molecules such as kinase inhibitors and antifungal agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monograph Requirements (where applicable to intermediates)
    • EDQM CEP guidance (European Pharmacopoeia)
    • FDA 21 CFR Part 210/211 (as applied to ingredient sourcing and traceability)

    Typical usage ratio

    • Ranges from 0.5 to 3 molar equivalents in major coupling or substitution steps versus the primary substrate; adjustment depends on the target synthetic yield and impurity profile requirements.

    Downstream process integration

    • Introduced at the heterocycle assembly or biaryl construction stage, frequently via Suzuki or Buchwald–Hartwig cross-coupling reactions in batch or flow processes under inert atmosphere; used with a secondary base and catalyst system before subsequent downstream isolation and purification.

    Final product types

    • Small molecule kinase inhibitors
    • Anti-infective agents (antifungal APIs)
    • Intermediates for advanced oncology treatments
    • Heteroatom-modified drug scaffolds

    2. Agrochemical Intermediate Manufacturing

    Producers of next-generation crop protection compounds utilize 4-Bromothioanisole for introducing thioaryl groups into fungicide and insecticide intermediates. The compound’s chemical reactivity enables late-stage diversification necessary to optimize biological and field activity, assisting with patent protection for proprietary active substances.

    Industry compliance standards

    • FAO/WHO Guidelines on Pesticide Specification (JMPS)
    • ISO 9001:2015 for agrochemical raw material quality management
    • REACH Regulation (EC) No 1907/2006 for registration and safe use
    • Globally Harmonized System (GHS) hazard communication compliance

    Typical usage ratio

    • Implemented at 0.7–1.5 molar equivalents with respect to the halogenated precursor, with modifications depending on target compound yield and required purity for subsequent crop safety studies.

    Downstream process integration

    • Employed during the late-phase aryl thioether functionalization, typically through copper- or palladium-catalyzed coupling in jacketed reactors, followed by extraction and solvent switch for final active ingredient crystallization or formulation bases.

    Final product types

    • Novel fungicidal base structures
    • Precursor intermediates for pyrazole or triazole insecticides
    • Building blocks for oxathiin and related herbicide actives

    3. Advanced Material Monomer Sourcing

    Specialty polymer and materials manufacturers incorporate 4-Bromothioanisole as a monomer for introducing aryl-sulfur linkages into specialty resins, conductive polymers, and electronic materials that benefit from improved charge-transfer and oxidative stability. Its specific reactivity allows for controlled copolymerization or reactive blending.

    Industry compliance standards

    • RoHS Directive (2011/65/EU and amendments) for hazardous substances restriction
    • IEC 61249-2-21 for halogen-free material specifications
    • ISO 14001:2015 (Environmental Management Systems) in materials industries
    • REACH SVHC requirements for polymer additives

    Typical usage ratio

    • Blended at 1–8 wt% relative to total resin formulations; concentrations selected based on performance targets for dielectric strength, chemical resistance, and final viscosity control in solution or melt-phase reactions.

    Downstream process integration

    • Dispensed during resin or oligomer synthesis steps in condensation or radical polymerization processes; often reacted with co-monomers in controlled environments (solution or melt), followed by in situ polymerization or extrusion into films and sheets.

    Final product types

    • High-performance printed circuit board (PCB) laminates
    • Conductive polymer composites for sensors
    • Specialty optical resin materials
    • Sulfur-modified engineering plastic grades

    4. Organic Electronic and OLED Material Development

    Manufacturers of organic semiconductors and electroluminescent materials employ 4-Bromothioanisole as an essential precursor for the introduction of thioether-type substituents in small-molecule or oligomer backbones, which are critical in modulating electronic and photophysical properties for high-efficiency OLED devices and functionalized organic transistors.

    Industry compliance standards

    • IEC 62341 for Organic Light Emitting Diode (OLED) device safety
    • RoHS Directive (2011/65/EU and amendments)
    • REACH Regulation (EC) No 1907/2006 for electronic chemical precursors
    • ISO/IEC 17025 for R&D materials traceability and quality control

    Typical usage ratio

    • Typically 0.5–2 molar equivalents incorporated in precursor synthesis steps, with the precise addition dosage determined by the desired electronic characteristics and target emission spectra in device design.

    Downstream process integration

    • Input during core skeleton assembly through cross-coupling or ring-closing reactions; subsequently purified via chromatography and used in thin-film deposition or ink formulations for device fabrication.

    Final product types

    • Blue- and green-emitting OLED molecules
    • Hole-transport or electron-transport materials for organic devices
    • Organic field-effect transistor (OFET) intermediates
    Free Quote

    Competitive 4-Bromothioanisole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Bromothioanisole: A Trusted Workhorse from Our Facility

    Demystifying 4-Bromothioanisole in the Lab and on the Line

    Few molecules shape advancement in fine chemical synthesis the way 4-bromothioanisole does. At our facility, we draw on years of manufacturing experience to craft this aromatic bromide to high purity, supporting professionals who rely on reliable building blocks for synthesis and research. Unlike all-purpose chemicals found on generic catalogs, our grade has been refined through continuous feedback from active laboratories and industrial clients who expect reliability batch after batch.

    The Fundamentals: What Is 4-Bromothioanisole?

    4-Bromothioanisole (also known as p-bromothioanisole or 1-bromo-4-methylthio-benzene) appears as a white or pale-colored crystalline solid, boasting a thioether group positioned para to a bromine on its aromatic ring. Chemists request this molecule for a straightforward reason: the para-bromo and methylthio arrangement opens distinctive routes for synthetic transformations. By anchoring a sulfur-methyl at the 4-position, one introduces a versatile handle for further functionalization. This orientation distinguishes it from its ortho and meta isomers, granting unique regioselective options during cross-coupling, halogen exchange, or nucleophilic substitution reactions.

    Our standard model often comes in kilogram or multi-kilogram packaging, sealed under inert gas or in moisture/barrier-protective drums. Typical assay runs above 99% by GC, minimizing the risk of side-product interference during downstream reactions. Trace-metal content remains low, with bromine byproducts and sulfur-based impurities tightly monitored. Having managed the full-scale manufacture for years, we prioritize not only nominal purity, but also realistic batch-to-batch consistency and shelf-life.

    Why Practicing Chemists Choose This Molecule

    Many research and commercial workflows rely on 4-bromothioanisole as a linchpin for making pharmaceuticals, agrochemicals, dyes, and advanced materials. As a starting point for Suzuki-Miyaura and Buchwald-Hartwig couplings, its aryl bromide moiety reacts predictably under palladium catalysis to forge complex C–C or C–N bonds. Clients frequently report smooth insertion into heterocycles, polythiophene-based semiconductors, and a variety of other organic scaffolds that require both the reactivity of bromine and the electron-rich twist conferred by the methylthio group.

    Our own production runs have supported custom synthesis at dozens of university labs and pilot plants. We've seen this molecule used widely in medicinal chemistry when researchers pursue new sulfur-containing drug candidates or probe molecular interactions with target enzymes. Its stable crystalline form simplifies handling compared to some other aryl halides prone to decomposition or oiling out during storage. By offering reliable deliveries, we've helped customers avoid unpleasant surprises downstream—no solvent-freezing, stuck filters, or labeling errors stemming from off-white impure lots.

    Bench-Scale and Bulk: Responding to Real-World Demands

    Every chemist wrestling with a tough synthesis values consistency and traceability. We manufacture 4-bromothioanisole using purpose-selected solvents and reagents to control impurities at every stage—especially those brominated or sulfurous species that might escape basic washings or crystallizations. Our purification stream involves crystallization and thorough post-processing rather than relying on generic aqueous workups that can leave behind stubborn contaminants. We designed our workflow to minimize operator exposure and solvent emissions—less residual odor, fewer handling hazards, and better containment of fugitive emissions.

    In practical terms, the demand shifts between academic 100-gram bottle orders and bulk drums for commercial production. To serve both, we keep stocks at varied scales while using the same high-grade starting materials and rigorous process controls across all batch sizes. We don't dilute our specification just because the order size changes—every lot matches the same analytical profile. Documented batch history and transparent test results support regulatory requirements for GMP intermediates or reference standards, too.

    Not All Bromothioanisoles Are the Same: Subtle, Crucial Differences

    Those outside the lab might view 4-bromothioanisole as interchangeable with other aryl bromides or thioanisole derivatives. Decades of hands-on synthesis show how differences reveal themselves when it counts. For example, switching to the ortho or meta isomer shifts electronic effects and often destroys regioselectivity in coupling reactions. Dropping down from aryl bromide to the chloride tightens the reactivity window and leaves you fighting sluggish conversions or over-forcing reaction conditions.

    Our in-house experience confirms another pitfall: material from outfits who skip portions of the purification process, or who source raw inputs of dubious origin, delivers persistent off-notes—yellowing, sulfurous scent, and batch-to-batch unpredictability. These are more than minor cosmetic inconveniences; they slow downstream synthesis, introduce new workup steps, or generate persistent analytical artifacts in NMR or LCMS profiles. Years working alongside researchers have underlined that pure, odorless, accurately weighed crystalline product saves time and labor all the way through scale-up.

    Product Handling and Storage: Lessons from the Floor

    Day-to-day factory work brings plenty of pragmatic lessons on storage and shipping. 4-Bromothioanisole holds up well under dry, cool conditions. Yet even minor moisture exposure can erode purity or encourage slow hydrolysis—sulfur-based organics never appreciate excess water or acidic vapors. We seal our material promptly after processing, run moisture analyses before every shipment, and mark containers with expiration dating based on real-world stability tests, not guesswork.

    Operators avoid cross-contamination by dedicating glassware and process lines to thioethers, rinsing between runs, and recording every cleaning step. Solvent selection also matters: we use alcohols or ethers with minimal sulfur backbone attack, and skip aggressive halogenated solvents wherever possible. On the receiving end, we've trained clients to store drums away from heat and sunlight, and reseal portions immediately after use, even for short-term bench work. These small steps go a long way to keeping product in optimal condition, avoiding costly requalification or reworking.

    Regulatory and Downstream Impact

    Being a chemical manufacturer once meant just delivering on specs; now, environmental and safety demands drive continual process refinement. Thioethers can sometimes fall under enhanced surveillance for odor management, process VOC emissions, and hazardous waste tracking. We've retooled exhaust collection, adopted inline absorption and neutralization for sulfurous offgassing, and maintain traceability from raw incoming material through to finished lots. Outreach to our clients about split dosing, waste handling, and neutralizer selection helps them manage their EHS responsibilities.

    We’ve watched customers increasingly face tight scrutiny on ingredient origins, identity tracking, and contaminant profiles. Our own transparency lets research institutes compile reliable safety files and gives manufacturers credible data for their batch records. Our QC department runs spectral identification by NMR and HPLC, confirming no cross-over with other brominated or sulfur-containing contaminants. This streamlined documentation simplifies compliance and gives customers confidence that their audit trails will stand up under review.

    Putting Quality to the Test: Analytical Backing

    We analyze each lot using a battery of chromatographic, spectroscopic, and elemental techniques. GC and HPLC provide sharp resolution of the primary compound alongside any minor byproducts. NMR spectra confirm structural assignment—especially relevant for distinguishing isomers or detecting aromatic ring substituent impurities. ICP or XRF give us bromine content and inorganic residue levels down to single-digit ppm.

    Whenever we’ve run side-by-side trials against industry-standard references, our lots display cleaner baselines, crisper melting range, and steadier physical appearance on storage. Clients conducting structure-activity relationship studies or pilot plant de-risking appreciate being able to use and reuse their material without incremental deterioration. There’s satisfaction in knowing that cumulative feedback from hundreds of unique projects keeps raising our own bar.

    Customization and Flexibility: Meeting Evolving Challenges

    Innovation in synthesis sometimes brings the need for tailored material. Some clients have requested extra stringent drying, alternative micronization for thin-film deposition, or tighter specification on metal residue contents. Our manufacturing setup—combined with a willingness to collaborate—lets us run custom campaigns that address challenging needs without scaling hurdles or compromising quality.

    For instance, one project in advanced materials asked for low-sulfur, high-purity 4-bromothioanisole to serve as a monomer precursor. We reworked our steps, retuned purification, and initiated new lot testing, all while keeping shipment deadlines. This kind of flexibility grows out of continuous investment in our process and a willingness to treat each order as a partnership, not just a sale. Multiple repeat clients have come back with new specifications as their projects scaled, highlighting the value of a supplier who’s ready to adapt.

    Industry Context: Broader Significance of Reliable Supply

    Supply disruptions and material inconsistencies can grind a project to a halt. We’ve seen it happen when newly sourced lots from low-cost sellers show up contaminated or sub-par, causing wasted time and downstream troubleshooting. Our own philosophy puts stability of supply and documentation hand-in-hand with product quality. We maintain safety inventories for core clients, forecast raw material purchasing in close communication with them, and provide transparent ETA’s during high-volume campaign periods.

    Global sourcing stability for methylthio and brominated aromatics can become fragile in the face of regulatory change, solvent restrictions, or logistical challenges. Investing in local capacity, and building redundancy in solvent and raw chemical sourcing, keeps our timeline short and our batches repeatable. We keep our logistics agile—sea, land, or air—so our customers never face bottlenecks waiting on shipments, and can always speak to a chemist about unique packaging needs or just-in-time delivery.

    Safety Insights Based on Manufacturing Experience

    As a thioether, 4-bromothioanisole offers a more forgiving profile than some lower-weight analogs or more volatile bromides. It isn’t especially prone to spontaneous combustion or runaway exotherms, but dust and shavings can still travel and carry odor. Good manufacturing practice means ventilated hoppers, fine-mesh screens on bagging ops, and continuous air quality tracking. We keep an eye on local and international transportation rules to ensure all shipping meets updated codes and best practices. Clear labeling and SDS documentation come with every order, and clients with novel applications can speak directly with our safety and compliance team for application guidance.

    From past production campaigns, we know which reaction conditions create byproducts or unwanted side-reactions, and which polymer coatings or benchtop utensils resist absorption or contamination best. We recommend handling this compound in a standard fume hood, with gloves and goggles, to avoid any skin contact or long-term odor transfer. Disposal guidelines draw from our own plant procedures, supported by waste stream analysis and government safety advice.

    Building Trust Project by Project

    Over the decades, we’ve seen 4-bromothioanisole change from a specialty item for a handful of advanced projects to a regular lab staple for contract research and manufacturing everywhere. Its balance of predictable reactivity and strong electron-donating interplay with aromatic chemistry keeps it at the forefront of organic synthesis strategies. Whether labs reach for it at the bench or industrial clients fold it into multi-step syntheses, the trust comes from consistently delivered, clean material and open lines of communication.

    For every kilogram sent out, we welcome feedback—what worked, what could improve, and what new challenge a project faces next. Whether adjusting for new regulatory requirements, pushing purity thresholds for early-stage research, or scaling up for pilot manufacturing, we want our partners to know they get more than just a bag of white crystals. They get the backing of a factory team that’s lived through the ups and downs of real-world chemistry and understands that success is measured by more than a spec sheet alignment.

    Connecting on Quality and Real-World Solutions

    Reliable 4-bromothioanisole supply isn’t about checking boxes on standard paperwork. It means supporting a global network of scientists, scale-up engineers, purchasing teams, and safety specialists who expect every order to meet their expectations without causing havoc downstream. Our business grows by building those relationships—anticipating needs, fixing trouble before it arises, and drawing on every past batch to inform the next one. We work not just for a product, but for continuous improvement, shaped by decades of hard-earned lessons on the factory floor.

    Each batch reflects the combined insight of our production team, R&D chemists, quality control specialists, and shipping coordinators. Knowledge is cumulative—every issue solved feeds back into process optimization, every success confirms we’re on the right track. Our commitment is to the scientists and engineers who put our 4-bromothioanisole to the test, trusting not just what we make, but how we make it, every single day.