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3-Bromomethylthiophene

    • Product Name 3-Bromomethylthiophene
    • Alias 3-(Bromomethyl)thiophene
    • Einecs 249-029-4
    • 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
    VTB
    Specifications

    HS Code

    925522

    Chemical Name 3-Bromomethylthiophene
    Cas Number 13220-95-2
    Molecular Formula C5H5BrS
    Molecular Weight 177.06
    Appearance Colorless to pale yellow liquid
    Boiling Point 96-98°C (19 mmHg)
    Density 1.59 g/cm³
    Refractive Index 1.570-1.572
    Flash Point 84°C
    Purity Typically ≥98%
    Smiles C1=CSC=C1CBr

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

    Packing & Storage
    Packing The 3-Bromomethylthiophene (25g) is supplied in a sealed amber glass bottle with a secure screw cap and appropriate hazard labeling.
    Shipping 3-Bromomethylthiophene is shipped in tightly sealed containers to prevent leaks and contamination. It must be stored in a cool, dry, well-ventilated area, away from heat and sources of ignition. Proper hazardous material labeling and documentation are required, and transport must comply with relevant local and international chemical shipping regulations.
    Storage 3-Bromomethylthiophene should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition or heat. It must be kept out of direct sunlight and incompatible substances such as strong oxidizers. Properly label the container and store it in a chemical storage cabinet, ideally under nitrogen or an inert atmosphere to minimize degradation.
    Application of 3-Bromomethylthiophene

    Applications of 3-Bromomethylthiophene in Industrial Manufacturing

    As a direct manufacturer of 3-Bromomethylthiophene, we support diverse chemical industries with high-purity raw materials. Our supply focuses on established downstream sectors where this intermediate delivers essential performance in synthesis routes for pharmaceuticals, agrochemicals, advanced materials, and electronic components. Below, we detail specific industrial scenarios where our material integrates into core processes, listing pertinent compliance mandates, process requirements, compositional guidance, and downstream applications.

    1. Pharmaceutical Active Ingredient Synthesis

    3-Bromomethylthiophene serves as a crucial building block in the production of active pharmaceutical ingredients (APIs), particularly in the synthesis of thiophene-based drug molecules such as anti-infectives and oncology agents. Downstream pharmaceutical customers compound this intermediate within tightly controlled manufacturing protocols requiring traceability and material characterization at each reaction step. The chemical’s unique bromomethyl functionality allows for regioselective introduction into molecular scaffolds, supporting the assembly of heteroaromatic systems essential for novel drug candidates undergoing regulatory review.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) general monographs for chemical intermediates
    • USP <823> for isotope and radiopharmaceutical precursors (if applicable)
    • REACH registration (EU Regulation No 1907/2006) for safety data alignment

    Typical usage ratio

    • 0.1–0.25 molar equivalents relative to core heterocycle, adjusted in 5–10% increments based on desired substitution levels in multi-step synthesis

    Downstream process integration

    • Integrated during nucleophilic aromatic substitution or palladium-catalyzed cross-coupling as the key electrophilic component
    • Charge-in step within closed-system reactors, followed by in-process yield validation via HPLC or GC analysis

    Final product types

    • Anti-viral API precursors (e.g., Thienopyridine derivatives)
    • Targeted oncology drug scaffolds containing thiophene moieties
    • Precursor intermediates for cardiovascular therapeutic compounds

    2. Agrochemical Active Ingredient Manufacturing

    Our supplied 3-Bromomethylthiophene is frequently used by crop protection formulators as an intermediate in the construction of thiophene-based herbicides and fungicides. The unique reactivity profile enables modification of agroactive molecules to enhance environmental persistence and biological activity, aligning with regulatory pesticide guidelines. End-users introduce this compound during the assembly of lead agrochemical structures where the thiophene motif contributes to soil mobility and plant uptake characteristics.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP)
    • EPA 40 CFR Part 158: Data Requirements for Pesticide Registration (US)
    • ISO 9001:2015 Quality Management Systems Certification

    Typical usage ratio

    • 0.05–0.2 molar ratios based on the target construction route, fine-tuned according to reaction scale and activity profile of the new molecule

    Downstream process integration

    • Added at the ring-extension or halogenation stage before the final coupling with active pesticide cores
    • Used in continuous processing or batch reactors, monitored via LC-MS purity checks

    Final product types

    • Selective pre-emergence herbicides with thiophene substructures
    • Broad-spectrum fungicide active ingredients for cereal grains
    • Synthetic intermediates for custom-designed agrochemical candidates

    3. Electronic Material Intermediates for Organic Semiconductors

    Large-volume purchasers in advanced electronics employ our 3-Bromomethylthiophene for the synthesis of high-performance thiophene-based materials used in organic thin-film transistors (OTFTs) and organic photovoltaics (OPVs). This raw material enters as a monomer precursor for complex conjugated polymers, facilitating the controlled introduction of side chains to boost charge mobility and film-forming properties. Consistent impurity profiles and batch reproducibility remain critical due to stringent requirements for optical and electronic component lifespan.

    Industry compliance standards

    • IEC 62321-7-1: Electrical and Electronic Equipment – Determination of certain substances
    • RoHS Directive 2011/65/EU substance restrictions
    • ISO 14001:2015 Environmental Management Systems
    • JEDEC JESD625C: Handling of Electrostatic Discharge Sensitive Devices

    Typical usage ratio

    • 0.12–0.35 mol per repeat unit in copolymer synthesis, tailored by end-use conductivity and solubility margin requirements

    Downstream process integration

    • Polymerization step via Kumada or Stille coupling using the bromomethyl handle for site-specific functionalization
    • Dispensed under inert atmosphere to avoid oxidative side reactions during monomer activation

    Final product types

    • Thiophene-based semiconducting polymers for OTFT layers
    • Conductive copolymer blends for OPV active layers
    • Functionalized oligomers for flexible electronic ribbon production

    4. Synthesis of Specialty Dyes and Optical Brighteners

    Chemical manufacturers focused on specialty dyes leverage 3-Bromomethylthiophene as a bridging intermediate in synthesizing thiophene-linked optical brighteners and fluorescent probes. These applications demand high purity and lot-to-lot uniformity to maintain essential photophysical properties. The intrinsic electron-donating characteristics of the thiophene motif influence absorption maxima and emission quantum yield, making careful control over bromomethyl functionalization essential during scale-up.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile dye ingredient safety
    • EN 71-3:2019 for heavy metal safety in colorants
    • CFR Title 21 FDA Chapter I Part 74 for color additive specifications (US market)
    • ISO 9001:2015 for documented quality assurance

    Typical usage ratio

    • 0.07–0.18 molar equivalents, modulated for target chromophore yield efficiency and desired spectral properties

    Downstream process integration

    • Introduced during the halogen-substitution or C–C bond-formation phase to link aromatic dye chromophores
    • Employed in solvent or water-based synthesis lines followed by high-vacuum isolation routines

    Final product types

    • Thiophene-based optical brighteners for plastics and textiles
    • Specialty fluorescent dye formulations for inkjet and security printing
    • Sulfur-containing colorants for automotive and architectural coatings
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    Certification & Compliance
    More Introduction

    3-Bromomethylthiophene: A Chemical Manufacturer's Perspective

    Real-World Performance from Synthesis to Application

    Producing 3-bromomethylthiophene takes more than just technical skills—it demands experience that only years on the reactor floor can teach. After many cycles scaling this molecule, watching it go from a crude precursor to its pure, clear state, I stand behind every drum we pack. Years ago, the rise in demand for substituted thiophenes caught our attention, and since then, we have focused on tightening every variable, not just for yield, but for the nuanced requirements our partners bring to the bench.

    Where some intermediates can tolerate minor impurities, thiophenes destined for fine chemical synthesis call for robust purification. Impurities never just vanish—they spread through the downstream process, leaving their mark on later steps, complicating separations, or even knocking out crucial catalysts. In pharmaceuticals, one unreliable batch ripples across a supply chain that can ill afford downtime. I’ve walked production lines to ensure the profile remains consistent from one kilo batch to the next, using up-to-date GC methods and lot-by-lot NMR to confirm both identity and purity every time.

    3-Bromomethylthiophene itself, with a CAS registry of 13221-33-1, falls into an active class of halogenated het­ero­cycles that saw early promise in agrochemical and medicinal chemistry pipelines. The model we have standardized for most customer lots, C5H5BrS, remains in demand by research organizations, scale-up labs, and formulation teams pursuing everything from plant protectants to building block explorations for next-generation active pharma ingredients. Substitution specifically at the 3-methyl group opens access to cross-coupling reactions or further transformation to aldehydes and alcohols without scrambling the aromatic core.

    Attention to Process Details

    Over the last decade, the approach to manufacturing 3-bromomethylthiophene matured beyond routine batch work. We witnessed unwanted side reactions at elevated temperatures, and we refined bromination so it delivered conversion, not charring. Aromatic substitution tends to attract trace colored byproducts. Cutting these byproducts at the source demanded precise timing, robust pH control, and frequent, hands-on in-process checks. Watching the color and consistency in each vessel during the run—experience reveals signs where theory cannot. We found even subtle changes in solvent quality or storage impacted yield. The active bromomethyl group, while valuable for forming C–C bonds or halide exchanges, proves sensitive to stray nucleophiles and water ingress. Our operators learned to anticipate shifts in process stability; a batch that looks well on paper can quickly sour if condensation creeps into the system.

    Post-reaction workup takes patience. Distillation parameters can’t just be copied between shifts or seasons. Humidity, gentle vacuum application, and gradual cooling make for product purity that holds. R&D teams typically want consistent color, odor, and refractive index batch-to-batch, and honestly, it takes time to deliver that reproducibility as an everyday standard, not an exception. Our product control ensures a minimum purity of 98 percent by GC, and our lot documentation backs this up with the latest trace impurity data.

    Where 3-Bromomethylthiophene Fits In

    Synthetic organic chemistry offers a crowded toolkit of halogenated thiophenes, but 3-bromomethylthiophene occupies an important niche. Substitution at the 3-position impacts reactivity profiles, which often determines whether a downstream route proceeds cleanly or stalls. During cross-coupling, that bromo­methyl tail delivers more flexibility for Suzuki, Stille, or Sonogashira reactions than simple 3-bromothiophene or the 2-brominated analogs. Nucleophilic displacement and further oxidation or reduction routes open from here in ways unobstructed by the aromatic ring itself. Researchers who have wrestled with 2-brominated species know the difference in regiochemistry can make or break a scale-up.

    In medicinal chemistry, introducing methylated thiophenes runs the risk of metabolic instability. 3-Bromomethylthiophene lets molecule developers explore both direct modifications and side-chain elongations without disturbing the heterocyclic core. It’s not just about amassing new reference structures—sometimes, batch purity and predictable behavior mean the difference between a promising screen hit and a dead end.

    Comparing to Other Substituted Thiophenes: Why Choice Matters

    From the manufacturer’s side, we see the landscape of thiophene intermediates includes a series of related products: 2-bromomethylthiophene, 3-chloromethylthiophene, and simple methylated or brominated thiophenes. Differences in position and functional group have direct mechanical impacts on reactivity and downstream safety. For instance, 2-bromomethylthiophene sometimes suffers from greater side-product formation under standard conditions, which leads to heavier downstream cleaning requirements that drive costs up. Chloromethyl groups do act as useful handles in alkylation chemistry, but our experience shows that bromides release under milder conditions, improving yields and reducing over-alkylation risk.

    Customers sometimes ask whether it makes sense to swap 3-bromomethylthiophene for 3-chloromethyl versions due to cost pressure. In side-by-side trials, we’ve seen that while both compounds perform in alkylation steps, the bromo derivative consistently displays more complete, faster reactions across a broader range of catalysts. It’s these process and yield differences that dictate which product gets the green light for full-scale manufacturing. The market incentive, in our eyes, is clear: spend resources perfecting the material most likely to provide robust, predictable reactivity over shoulder alternatives. Money saved on raw costs evaporates quickly when additional work-up steps or re-crystallizations are required.

    Handling, Safety, and Real-World Storage Observations

    3-Bromomethylthiophene sits among those intermediates that demand respect in the warehouse and during handling. Small leaks and spills, if allowed to sit, emit a pungent odor and can cause irritation; we learned the hard way that early intervention and proper ventilation preserves both product quality and workplace safety. Labs that try to store open containers often find discoloration and tar formation in short order. Over the years, we shifted to packaging in sealed containers, with nitrogen blankets when volumes exceed a few kilos, and temperature-controlled storage to thwart off-spec behavior.

    Laboratory staff need reliable information on handling and emergency procedures. Though we provide detailed technical support, many customers find our real-world guides—compiled from incidents and resolutions over years in production—more helpful than documentation alone. Prompt spill response cuts loss, and attentive transfer avoids introducing moisture, which represents the main threat to quality. We do not rely solely on off-the-shelf protocols; each customer site varies, and sharing what’s actually occurred at the packing line prepares others to avoid common pitfalls.

    Supply Chain Realities and Customer Collaboration

    In the current world of globalized supply chains, even a mid-run hiccup at the plant can delay downstream partners. One lesson we’ve learned is that yearly forecasts rarely map perfectly onto actual project needs. As a result, we keep some production flexibility for urgent or scaled orders, and we've built direct lines between our in-house customer support chemists and our partner’s technical teams. Researchers with specialized requests—different purities, unusual solvents, non-standard packing—contact us directly. Listening to the technical intent behind each spec lets us adapt processes rapidly, shaving days off fulfillment times and building repeat trust.

    Shipping regulations for halogenated compounds shifted several times over the past decade, and we adapt. To keep supply running, we track regional classification rules—not just in our own country, but across all the destinations where our clients synthesize. Some colleagues in the industry try to stay lean at all costs, but from our experience, missing out on critical documentation or labeling cuts projects off at the knees. We devote resources to staying ahead of changing compliance measures because we’ve been on the customer’s side, feeling the logistical headaches firsthand.

    Environmental Impact and Efficiency Redesign

    Chemical manufacturers today must grapple with environmental priorities alongside the hard realities of process engineering. Years ago, the standard synthesis for 3-bromomethylthiophene led to halogenated waste streams that cost more to neutralize than to produce the target compound. We overhauled our bromination step, integrating in-process capture to limit emissions. Proper solvent recycling and re-use of bromide-rich side streams translated not just into compliance but also into a sharper cost structure. This transition took effort, but it lowered our downstream waste burden, cut utility demands, and kept worker exposure as low as possible.

    Customers, too, care about green profiles. We now share these efficiency records with project owners for life-cycle assessments, whether they’re developing new API candidates or supply chemistries for agrochemical pilots. Open sharing of process data has become an expectation, and we find that delivering on these sustainability assurances often leads to deeper, longer-term partnerships.

    Solving Manufacturing Challenges with Direct Feedback

    Production-scale work exposes wrinkles missed by bench-scale chemistry. Over time, we mapped out reaction bottlenecks and built in checks for every quality point: bromine load, methyl group integration, off-gas absorption. We took feedback from frustrated process managers who spotted hairline leaks or persistent trace byproducts, and we acted on each note, one batch at a time. Problems like reactor fouling or demixing at large volumes led us to redesign impeller setups and to trial new antifoam protocols. Even small producer observations—like fragrance drift on hot days, or changes in product appearance across seasons—shaped our standard operating procedures.

    We make it a point to treat every inquiry about specification deviations as a chance to investigate and resolve—not to deflect or lay blame on the user. Transparency in our approach usually encourages users to share their hurdles openly, which arms us with key insights to improve upstream.

    Data Integrity and Certification: Building Real Trust

    In pharmaceutical and regulated markets, value grows from integrity and transparency. We have invested in upgrade cycles for both physical testing tools and electronic data management systems—barcoding, audit trails, validated LIMS entries. Each product lot comes with a reproducible, timestamped certificate of analysis generated directly from our instruments. We resist the temptation to cut corners because any shortcut in quality oversight ultimately costs more in lost trust—or worse, in failures at the customer's site when their own QC tests diverge from ours.

    Third-party audits and client site visits are routine and welcome. Open access to our raw data and QC logs never delayed a shipment—in fact, it speeds up qualification when questions arise. For clients working under strict GMP or ISO frameworks, we provide additional documentation and, if asked, custom process validation runs.

    Continuous Improvement in Fine Chemical Manufacturing

    3-Bromomethylthiophene production challenges us to innovate constantly. We stay alert to alternative synthetic routes, new halogenation reagents, and advances in separation technology. Collaborating with academic groups and industrial consortia, we test new catalysts, always with an eye on both process economy and downstream user impact—not simply on our own throughput.

    Our technical community believes in sharing process yields and impurity profiles, not hiding behind proprietary silence. Demonstrable context—why one route cuts work-up time in half, or how introducing an inert atmosphere eliminates a minor impurity—matters just as much as a clean product specification. We also learn every year that client-facing teams who check in post-delivery, whether to troubleshoot or optimize, keep the entire supply chain moving faster and with less waste.

    Adapting to Shifting Global Demands

    Changing regulatory or market pressures touch every performer in the thiophene sector. Trade restrictions, shifts in compliance norms, or the rise of domestic R&D capability all rewrite the landscape. Manufacturers best positioned to thrive adapt processes and documentation to fit these currents, rather than clinging to legacy routines. Investments in both people and equipment keep up productivity and safety standards.

    We monitor price movements and raw material availability. In the past, tightness in bromine supply placed stress on both pricing and delivery schedules, so we diversified sourcing and built up safety stocks for critical intermediates. Setting realistic expectations with clients early in every supply relationship helps. Sometimes, we advise against speculative double-buying cycles, showing past demand curves and discussing real-world batch run rates. Direct, data-driven dialogue leads to healthier, more resilient collaborations.

    Final Thoughts Born from Manufacturing Experience

    From the beginning, handling and producing 3-bromomethylthiophene revealed both the difficulty and the satisfaction of consistent fine chemical manufacturing. Each season brings a fresh challenge—shipping routes disrupted by weather, raw input variability, a new customer with unique regulatory demands. Yet each production batch teaches something new, often through direct, hands-on troubleshooting. The goal is always more than just filling orders—it’s about empowering research and formulation teams, being flexible to feedback, and remaining vigilant over both environmental and workplace health.

    Every lot of 3-bromomethylthiophene carries with it this spirit of direct engagement and continual refinement. Years in this business have proven that satisfied customers are best won not by low price tags, but by process knowledge, technical openness, and a willingness to adapt together. Meeting the needs of chemists searching for downstream breakthroughs, while running a responsible, lean, and safe factory floor—that’s the day-to-day reality behind every container we ship.