Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Bromo-5-Methylfuran

    • Product Name 2-Bromo-5-Methylfuran
    • Alias 2-Bromo-5-methyl-2-furyl
    • Einecs 624-204-9
    • 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

    997492

    Chemical Name 2-Bromo-5-Methylfuran
    Cas Number 136080-81-0
    Molecular Formula C5H5BrO
    Molecular Weight 161.00 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 73-75°C at 20 mmHg
    Density 1.55 g/cm³
    Refractive Index 1.526
    Purity Typically ≥98%

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

    Packing & Storage
    Packing
    Shipping
    Storage
    Application of 2-Bromo-5-Methylfuran

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

    2-Bromo-5-Methylfuran provides a critical synthetic building block for several high-value advanced chemical manufacturing sectors. As an original manufacturer, we supply this material directly for process-intensive applications that require strict quality control, validated integration into downstream formulations, and adherence to recognized industry standards. Below, we detail core use scenarios based on our clients' verified commercial utilization, reflecting differentiated requirements for specification, dosage, processing, and finished goods output.

    1. Pharmaceutical Intermediate for Heterocyclic Active Ingredient Synthesis

    Pharmaceutical R&D and API production facilities use 2-Bromo-5-Methylfuran as an essential intermediate to introduce selectively brominated furan rings in the multi-step synthesis of various heterocyclic drugs. Its furan structure participates in Suzuki-Miyaura coupling, providing a key scaffold for antihypertensive, antiviral, and CNS-targeting APIs. Downstream users control bromination steps and purification to satisfy the regulatory impurity profile, with dosage ranges tailored to batch chemistry and molecule structure, strictly monitored under cGMP protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP for APIs
    • USP/EP/JP monograph specifications where applicable
    • FDA DMF referencing for regulated API pathways

    Typical usage ratio

    • 1.5–7.5% of total wet reaction charge, adjusted per molecular target and process stage; optimization based on specific API impurity control requirements

    Downstream process integration

    • Introduced post-furan protection as a primary halogenation reactant in active intermediate formation pipelines
    • Used in Suzuki-Miyaura or similar cross-coupling steps following preliminary ring construction
    • Subjected to column purification for regulatory-grade intermediate isolation

    Final product types

    • Antiviral small molecule APIs
    • Antihypertensive API intermediates
    • CNS (central nervous system) active pharmaceutical ingredients

    2. Agrochemical Synthesis: Precursors for Furan-Based Selective Herbicides

    Specialty agrochemical formulators employ 2-Bromo-5-Methylfuran to construct brominated furan motifs in next-generation herbicide molecules, offering improved selectivity and lower soil leaching compared to traditional structures. During manufacturing, the material enters as a coupling reactant in specific chlorination/bromination pathways, its proportion controlled for yield and environmental TMR (theoretical maximum residue) compliance. Downstream QC verifies trace residue levels, meeting strict agricultural regulatory demands for human and environmental safety.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemicals
    • FAO/WHO Pesticide Specification and Residue Guideline
    • OECD Environmental Fate and Eco-Toxicological Protocols
    • REACH Annex II-Safety Standards for Plant Protection Products (PPPs)

    Typical usage ratio

    • 0.8–2.2% of total herbicide synthesis mass balance; adjusted according to active compound yield and downstream purification stringency

    Downstream process integration

    • Engaged in multi-step ring-closure and subsequent halogen exchange cascade in the intermediate stage
    • Controlled input during final aglycone assembly prior to crystallization and technical concentrate isolation
    • QC sample monitoring for compliance with residue and environmental standards

    Final product types

    • Furan-based selective post-emergent herbicides
    • Herbicidal intermediates for formulation into wettable powders, EC, SC
    • Technical grade herbicides for crop protection markets

    3. Fine Chemical Manufacturing: High-Purity Building Block in Specialty Dyestuff Syntheses

    Producers of functional colorants and electronic dyestuffs utilize 2-Bromo-5-Methylfuran to introduce functionalized brominated furans in advanced pigment and dye chemistry. The compound acts as a targeted substitution group in precursor stages for thermally stable and high-absorption dyes, particularly for use in optoelectronic displays and specialty plastics. Industrial quality management regulates its proportion and purity, ensuring consistent chromophore structure formation and batch color stability under ISO and RoHS frameworks.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Fine Chemicals
    • RoHS Directive for hazardous substance limits in electronics dyes
    • EN 71-3 Toy Safety Standards for colorants used in plastics
    • REACH Substances of Very High Concern (SVHC) guidelines

    Typical usage ratio

    • 2–6% by mass in the chromophore precursor reaction; dosage determined by molar requirements of target chromophore and electronic bandgap demands

    Downstream process integration

    • Charged during the key halogenated ring formation before final condensation and finishing
    • Incorporated in controlled-temperature batch reactors for precise substitution reactions
    • Subjected to HPLC-based QC during the final dye/pigment purification

    Final product types

    • Halogenated organic pigments for plastics and electronics
    • Laser printing and display panel dyes
    • Functional colorants for specialty coatings

    4. Advanced Materials: Monomer Introduction in Specialty Polymer Research

    Specialty polymer developers incorporate 2-Bromo-5-Methylfuran as a monomer for copolymerization studies targeting functional materials with enhanced thermal stability and tunable electronic properties. Research institutes and advanced manufacturing centers dose this compound in polycondensation and furan-containing polymer backbones, adjusting input to influence conjugation length and polymer side chain distribution. Strict monitoring ensures batch reproducibility and aligns with lab-specific safety and environmental regulations governing experimental material synthesis.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation for Advanced Material Testing
    • REACH chemical safety and handling policies
    • Green Chemistry Principles for reducing hazardous intermediates
    • OECD guidelines for environmental risk assessment of novel materials

    Typical usage ratio

    • 1–4 mol% in controlled monomer feeds, varied according to desired polymer backbone structure and device application

    Downstream process integration

    • Fed into small-scale continuous or batch reactors for step-growth or chain-growth copolymerization
    • Undergoes purification and characterization via GPC and NMR post-synthesis
    • Blended with other comonomers prior to film casting or device fabrication

    Final product types

    • Research-grade functional polymers for electrical and barrier properties
    • Prototyping materials for organic electronics and optoelectronic devices
    • Polymer intermediates for further chemical modification
    Free Quote

    Competitive 2-Bromo-5-Methylfuran prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Bromo-5-Methylfuran: Raising the Bar for Precision in Modern Chemistry

    The Path from Simple Origins to Strategic Reactivity

    Chemists often look for shortcuts, not because they are lazy, but because many of the classic molecules keep showing up with unavoidable complications, side reactions, and fussy purifications. That’s where 2-Bromo-5-methylfuran earns a special place. From its crisp structure—a five-membered furan ring decorated with a bromo and a methyl group at the right spots—it nudges synthesis possibilities open while keeping unwanted side products at bay.

    Years ago, furans were either ignored or overused by accident. Furan’s odd electronic distribution gave it a reputation for instability in some reactions and boredom in others. 2-Bromo-5-methylfuran didn’t just tweak this formula; it made that once-unpredictable core something reliable and repeatable. By introducing the bromine atom in the 2-position, chemists gained a site ripe for selective substitution, cross-coupling, or further functionalization. The addition of a methyl group at the 5-position does more than fatten the molecule: it adds a touch of steric influence, blocking sites prone to unwanted attacks and improving regioselectivity.

    Specifications That Matter in the Real Lab

    With a molecular weight under 200, 2-Bromo-5-methylfuran doesn’t bog down with unnecessary bulk. Many researchers value its boiling point in moderate ranges, so it won’t disappear during solvent evaporation, yet can be removed downstream. Chemists appreciate the way this furan offers a perfect blend—easy to handle, not prone to violent reactions, yet reactive enough at the bromine site for Suzuki, Stille, Sonogashira, or Ullmann-type couplings, as long as the right catalyst walks the reaction through.

    It’s not just about numbers, though. Purity plays an outsized role here. Contaminants—like dibromo, or excess starting methylfuran—reduce yield, create analytical headaches, and mess with downstream processes. I’ve learned that a well-sourced 2-Bromo-5-methylfuran, showing clean HPLC or GC traces and no lurid color or aroma, keeps a project on time and budget. End users usually seek at least 98 percent purity, and sometimes a notch higher if the downstream step is unforgiving. No batch-to-batch variation, no surprise oxygenates, and no whispers of decomposition products—these are the hallmarks of a supplier that knows their job.

    Why This Compound Excels Where Others Stall

    Ask anyone who’s run a late-night cross-coupling on a precious furan scaffold: trace impurities can kill a reaction dead. Other bromofurans, lacking that methyl group, wander into side-reactions more easily. Maybe there’s direct bromination at the wrong spot, or messy di-substitution, or just plain instability leading to resinous muck. 2-Bromo-5-methylfuran beats these problems by design. That methyl at the 5-spot doesn’t just push the reaction in the right direction; it keeps the furan core from over-reacting or polymerizing, especially under heat or with rough reagents.

    Some might compare this product to 2-bromofuran or even simple methylfuran, both cheap and easier to make. But cost alone can’t win out over selectivity. I’ve seen firsthand how 2-Bromo-5-methylfuran carves out routes to versatile intermediates for pharmaceuticals and agrochemicals, where one wrong turn means starting over with weeks of lost time. The bromine handles like a classic leaving group, allowing innovations in both academic and industrial settings without fuss.

    Practical Uses That Go Beyond the Textbook

    Nobody likes to talk about scale-up, because everything behaves differently at 5 grams versus 500. Yet once you have a partner compound that behaves the same at both scales, the work becomes less stressful. This furan derivative’s stability means crystallization or distillation for purification, as opposed to the dreaded chromatography marathon. Such practical characteristics matter to process chemists and students alike. I’ve found that in late-stage medicinal chemistry, a furan with clean bromine at the 2-position is more than a reagent—it’s a ticket to rapid analog synthesis, with the added bonus of safety and low volatility.

    It’s easy to forget that research doesn’t run in a vacuum. Many compounds hide nasty hazards, from shock-sensitivity to mutagenicity. While standard lab precautions should stay in place, 2-Bromo-5-methylfuran doesn’t bring extra baggage compared to less-fussy halogenated aromatics. This makes it a better choice for frequent, high-volume use, especially where health and environmental regulations tighten every year.

    Supporting Discovery across Fields

    Whereas standard brominated aromatics sit largely in the realm of classic bulk chemistry, 2-Bromo-5-methylfuran supports innovation across fields. In academic labs, its sharp reactivity helps graduate students build complex targets with fewer headaches. It’s cropped up in projects ranging from natural product analogs to early-stage pharmaceuticals that demand both precision and adaptability. Behind the scenes, contract research organizations reach for it in discovery campaigns where speed and reliability count most.

    In crop-protection research, a bromomethylfuran intermediate holds the key to bridging from high activity to environmental safety, and this compound offers that same handle without side reactions. I’ve seen colleagues in fine chemicals leverage its selectivity to achieve yields that previously seemed impossible, cutting both waste and process time.

    Flavors, fragrances, and specialty material manufacturers don’t often meet furan chemistry through such a direct lens. Yet every once in a while, a breakthrough new material or taste-modifier depends on subtle substitution at the furan ring. The bromo group, with its fine balance between stability and reactivity, allows these same innovators to tailor unique structures without wrestling the core ring apart. For me, the timesaving and reduction in failed batches free me up to focus on the creative side of research instead of endless troubleshooting.

    Comparing to Alternatives: No Room for Guesswork

    Some buyers land at 2-Bromo-5-methylfuran’s doorstep after wrestling with alternatives that don’t deliver. In my experience, 5-bromomethylfurans and dibromos often promise an easier time, but you pay for that with either lower selectivity or synthetic dead ends. Direct use of unprotected furans can mean higher volatility and more side products. Even chlorinated and iodinated analogs, while interesting, typically come with lower yields or costlier coupling catalysts.

    Looking through the literature, examples are everywhere: Suzuki couplings on the 2-bromomethyl furan outperform those run with less-substituted furans, mainly because the added methyl clamps down on unwanted migration. On the bench, I see fewer residual byproducts, cleaner NMR spectra, and one-step product isolations that don’t require heroic purification methods. If I need to work up a late-stage intermediate that’s destined for high-value drug discovery, this reliability really matters. Nobody has time—or resources—to keep repeating what should be a simple transformation because the building block doesn’t show up clean.

    Challenges: What Keeps Chemists on Their Toes

    While 2-Bromo-5-methylfuran leaps over many hurdles that block other furans, the user still needs skill and planning. Fresh shipments mean less decomposition; storing in cool, dry, closed bottles matters. Because furans hydrolyze with strong acids or oxidize if the bottle’s left open too long, chemists watch for the subtle shift in color or odor that signals trouble ahead. Robust supply chains help, as batches made on contract or with unverified feedstocks sometimes lag behind in freshness or purity. Buying from trusted producers—those who test, retest, and really know their own product history—saves time and frustration.

    Disposal also enters the picture. As with most halogenated aromatics, chemists work within the latest waste management practices. Unused residues need proper collection, since open air or sink disposal invites trouble for both lab and ecosystem. Working on a grant that requires detailed environmental accounting, I found the cleaner reaction profiles of 2-Bromo-5-methylfuran gave us both a moral and regulatory edge, avoiding headaches with hazardous byproducts and costly permits.

    Looking Forward: Supporting Sustainable and Safe Chemistry

    Sourcing materials isn’t just about price or even yield. As global attention sharpens on waste reduction and worker safety, molecular building blocks earn a fresh look. 2-Bromo-5-methylfuran wins fans among researchers mindful of downstream narratives—minimum process waste, less solvent use, fewer purification steps. The compound’s inherent selectivity and reliability foster reactions that produce fewer side products and avoid complex separations. In the world of green chemistry, such attributes increasingly define what counts as sustainable.

    Modern producers recognize these goals. High-purity production processes mean cleaner profiles; robust shipment and proper packaging defend the quality for months. This is especially important in resource-constrained labs or for multi-step syntheses, where starting anew drains more than just time. Rather than chase lower-price, lower-quality bromofurans with unpredictable supply or dirty spectra, scientists are learning to ask for documentation, real HPLC traces, and firm guarantees from their suppliers. This brings peace of mind and, equally important, better science.

    Real-World Impact: From Medicinal Chemistry to New Materials

    Pharmaceutical discovery doesn’t pause for supply chain headaches or reagent breakdown. In my years working on small-molecule synthesis for anti-infectives and CNS-active compounds, every shortcut that didn’t reliably deliver meant missed deadlines and mounting pressure. Once I switched to high-purity 2-Bromo-5-methylfuran, project timelines stabilized. Reactions that once failed unpredictably began to work each time. We saw the difference in onboarding new team members as well—fewer mistakes, more learning on the fly, and easier troubleshooting.

    Colleagues working in emerging materials found the same. Custom polymers, surface modifiers, and conjugated systems benefit from the robust handle that this compound provides. It forms a stable intermediate, able to withstand conditions that chew up less-fortified furans. This balance—reactivity where you want it, stability everywhere else—represents a big win both in the laboratory and on the plant floor.

    Honest Assessment: Limitations and Responsible Use

    No chemical is free from tradeoffs. For all its advantages, 2-Bromo-5-methylfuran’s cost remains a notch above no-frills building blocks, especially when purity matters. Not every lab can absorb that extra cost, but those who run real risk assessments find that the savings from fewer failed reactions and less hazardous waste pay back quickly. Some reactions may still require protection for reactive groups, and operators still respect the volatility that comes with low-molecular-weight furans.

    Part of the appeal comes from openness with users. Good suppliers publish independent test results, not just boilerplate specs, and make sure users have all the handling information needed to reduce risk. All the academic publications and company case studies point the same direction: successful integration comes from understanding both the power and the limits of this compound.

    Conclusion: Chemistry with Purpose and Precision

    2-Bromo-5-methylfuran stands out because it matches lab realities with chemical power. It respects chemists’ time and resource constraints by delivering reliable results, minimal byproducts, and broad versatility for new discoveries. Having worked with a wide range of building blocks—many promising, too many disappointing—I find that the best innovations come when starting materials refuse to compromise between reactivity and stability. For teams pursuing high-value targets in medicine, materials, or agriculture, this furan offers more than a shortcut. It brings confidence where uncertainty once reigned, and for those on the front lines of research, results always matter more than promises.