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2,4,5-Tribromo-1-Methyl-1H-Imidazole

    • Product Name 2,4,5-Tribromo-1-Methyl-1H-Imidazole
    • Alias MBI
    • Einecs 249-046-9
    • 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

    228167

    Cas Number 35125-74-5
    Molecular Formula C4H3Br3N2
    Molecular Weight 334.80
    Iupac Name 2,4,5-Tribromo-1-methyl-1H-imidazole
    Appearance Solid
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles Cn1c(Br)nc(Br)c1Br
    Inchi InChI=1S/C4H3Br3N2/c1-9-3(6)2(5)8-4(9)7/h1H3
    Synonyms 1-Methyl-2,4,5-tribromoimidazole
    Pubchem Cid 230682
    Ec Number None available

    As an accredited 2,4,5-Tribromo-1-Methyl-1H-Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,4,5-Tribromo-1-Methyl-1H-Imidazole, sealed with tamper-evident cap and labeled for laboratory use.
    Shipping **Shipping Description:** 2,4,5-Tribromo-1-Methyl-1H-Imidazole is shipped in tightly sealed containers, protected from light and moisture. The chemical is packaged in accordance with hazardous material regulations, including appropriate labeling, cushioning, and documentation. Handling is restricted to trained personnel, and transport is conducted with care to prevent breakage, leaks, or exposure.
    Storage **2,4,5-Tribromo-1-Methyl-1H-Imidazole** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature unless otherwise specified. Properly label the container and ensure only trained personnel handle the chemical, wearing suitable protective equipment.
    Application of 2,4,5-Tribromo-1-Methyl-1H-Imidazole

    Applications of 2,4,5-Tribromo-1-Methyl-1H-Imidazole in Industrial Manufacturing

    2,4,5-Tribromo-1-Methyl-1H-Imidazole serves as a specialty intermediate in several highly regulated industrial markets, with its halogenated imidazole structure supporting distinct downstream chemistries. As a direct manufacturer, we support large-scale customers in pharmaceutical intermediate synthesis, specialty agricultural formulation, advanced material R&D, and fine chemical development. In each segment, regulatory compliance, precise formulation, and established processing protocols define its industrial application.

    1. Pharmaceutical Intermediate Synthesis (Anti-infective APIs)

    In active pharmaceutical ingredient (API) synthesis, our material is used in the manufacture of certain brominated imidazole intermediates, which play a role in the generation of triazole-based antifungal and antibacterial APIs. The brominated imidazole ring introduces halogen functionality required in the molecular structure of select advanced pharmaceutical intermediates, forming a key part of stepwise multi-stage synthesis under cGMP and ICH guidelines. Manufacturers utilize it during the heterocycle functionalization stage, benefiting from its high purity and consistent bromine substitution.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice)
    • EU GMP Directive 2003/94/EC
    • Chinese Pharmacopoeia (for local production)

    Typical usage ratio

    • 0.8% to 1.5% molar ratio per batch, adjusted by target intermediate yield and synthesis scale (ratio calculated based on imidazole structural equivalents in the required end-intermediate).

    Downstream process integration

    • Introduced during the halogenation and cyclization phase.
    • Used as a coupling component for further ring modification or condensation reactions.
    • Dosed under nitrogen atmosphere in stirred tank reactors to minimize hydrolytic loss.

    Final product types

    • Brominated triazole pharmaceutical intermediates
    • Advanced anti-infective API precursors
    • Imidazole-ring modified pharma intermediates

    2. Agrochemical R&D (Fungicide & Growth Regulator Intermediates)

    Research and formulation units in crop protection utilize this raw material in the synthesis of novel imidazolic intermediates for agricultural fungicides and plant growth regulation candidates. The molecular structure allows bromination points needed in triazole development pipelines, with a critical role early in lead compound generation and structure-activity relationship (SAR) analysis. Direct addition occurs prior to condensation or further halogen exchange reactions, allowing access to highly substituted experimental candidates. Regulatory laboratories adhere to strict inventory controls and traceability.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management Systems
    • China National Agrochemical Standards: NY/T 2795
    • REACH Regulation (for EU-bound intermediates, registration as required)

    Typical usage ratio

    • 0.5% to 1.2% by weight in pilot-scale research blends, adjusted by the structural requirements of the fungicide or growth regulator under investigation.

    Downstream process integration

    • Introduced post-initial imidazole synthesis as a key halogenation reactant.
    • Feeds directly into SAR screening runs or pilot-scale batch synthesis for activity assessment.
    • Handled in sealed R&D vessels for purity retention due to analytical traceability requirements.

    Final product types

    • Advanced fungicide intermediates (e.g., brominated triazole precursors)
    • Prototype plant growth regulator intermediates
    • Lead compound analogue libraries for agrochemical patent registration

    3. Advanced Material Synthesis (Flame Retardant Precursors)

    Material science laboratories and polymer additives producers employ the compound in the development of flame-retardant additives, exploiting the high bromine content and imidazole core for enhanced char formation and radical quenching in thermoset resin applications. The substance functions as an essential synthetic precursor in the manufacture of high-performance brominated imidazole derivatives, which see integration into specialty flame retardant masterbatches for electronics, construction, and transportation markets.

    Industry compliance standards

    • UL 94 Flammability Standard (for component evaluation)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances, applicable for downstream flame retardants in electronics)
    • ISO 14001:2015 (Environmental Management Systems, for process emissions)
    • EU REACH Annex XVII (restrictions for brominated compounds as appropriate)

    Typical usage ratio

    • 0.6% to 1.0% by weight in resin additive precursor syntheses, with precise dosing dependent on desired bromine loading and end-resin compatibility.

    Downstream process integration

    • Added during multi-step synthesis of brominated resin modifiers, typically as the core halogenation substrate.
    • Integrated into inline blending units for flame retardant masterbatch compounding.
    • Captured and monitored for losses in closed-system process reactors (static mixers or twin-screw extruders for solid masterbatches).

    Final product types

    • Brominated flame-retardant monomers
    • Halogenated imidazole-based polymer additives
    • Masterbatches for polycarbonate, epoxy, and polyurethane composites

    4. Fine Chemical Synthesis (Specialty Heterocycle Building Blocks)

    Fine chemical manufacturers incorporate the compound as a building block for customized heterocyclic synthesis, where selective tribromination and the methyl group serve as tailored handles for further molecular elaboration. Small molecule development programs utilize this raw material when generating niche imidazole derivatives for catalysts, photoinitiators, or specialty ligands. The strict quality control and traceable batch records required in these applications restrict raw material acceptance to high-purity, low-residual impurity grades.

    Industry compliance standards

    • ISO 9001:2015 (chemical manufacturing and QC processes)
    • Chemical Facility Anti-Terrorism Standards (CFATS, US markets as applicable)
    • REACH Regulation (downstream notification for EU-market compounds)
    • Responsible Care® chemical management program

    Typical usage ratio

    • 0.3% to 0.8% by weight in custom synthesis projects, with the ratio based on the required heterocycle substitution pattern and product scale.

    Downstream process integration

    • Introduced during the stepwise formation of functional heterocycles, acting as a halogen source or reactivity site.
    • Employed in one-pot coupling, cyclization, or cross-coupling reactions, monitored by HPLC or GC for complete consumption.
    • Processed in jacketed glass or stainless reactors to control temperature and avoid product degradation.

    Final product types

    • Brominated heterocyclic fine chemicals
    • Specialty ligands for coordination chemistry
    • Photoinitiator and catalyst intermediates
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    Certification & Compliance
    More Introduction

    Introducing 2,4,5-Tribromo-1-Methyl-1H-Imidazole: Insights from a Manufacturer’s Perspective

    Understanding the Chemistry Behind 2,4,5-Tribromo-1-Methyl-1H-Imidazole

    Producing 2,4,5-Tribromo-1-Methyl-1H-Imidazole takes us to the core of halogenated imidazoles, with each bromine atom strategically bonded for meaningful reactivity. As a manufacturer, we see every molecule’s journey from raw components to the final crystal — this isn’t just chemical synthesis, it’s careful orchestration. This compound offers a molecular structure that provides chemists a unique platform for both research and application. No shortcut exists in handling three bromines on the imidazole ring; their placement matters for both stability and reactivity.

    Experience in the synthesis of halogenated heterocycles shapes our process. The 2,4,5-tribromo pattern doesn’t happen by allowing things to take their own course. Each step, from bromination to methylation, demands strict process control. Hydrated or impure ingredients can alter the quality; we invest heavily in refining not just yield, but batch-to-batch purity. Our production operates at a scale where quality checks begin before the reactants touch each other. A consistent melting point and absence of unwanted isomers is our daily benchmark, not just an advertised promise.

    Specifications that Matter in Real-World Work

    For researchers and manufacturers who rely on 2,4,5-Tribromo-1-Methyl-1H-Imidazole, true performance shows up in the small details. We produce this chemical as a fine powder or crystalline solid, depending on real demand rather than convenience. Color, particle size, and handling properties change a bench procedure or industrial process. Moisture sensitivity, dusting, and batch uniformity can affect yields downstream. For us, rigorous loss-on-drying testing, spectroscopic analysis, and purity checks are part of production, not afterthoughts.

    Purity levels for our material routinely exceed 98 percent by HPLC and NMR confirmation. Impurities, especially lower brominated imidazoles or unreacted starting material, threaten unwanted side reactions in customers’ processes. Instead of accepting marginal grades, we optimize reaction and purification conditions to address these issues at the source. Filtration, recrystallization protocols, and rigorous vacuum drying form the baseline. Documentation isn’t a burden — it’s our map for identifying and correcting the rare deviation before it reaches your site.

    Where 2,4,5-Tribromo-1-Methyl-1H-Imidazole Comes into Play

    This compound rarely sits idle on laboratory shelves. Chemists choose it for its reactivity, tailored by its bromine substitution pattern and unshared electron density on nitrogen. The specific 2,4,5-bromination gives it different reactivity compared to simpler mono- or di-bromo imidazoles. It often acts as a precursor for cross-coupling reactions, particularly when creating more complex heterocyclic scaffolds. Suzuki, Stille, and other palladium-catalyzed routes leverage its predictable chemistry.

    Biotechnology, medicinal chemistry, and agrochemical developers reach for 2,4,5-Tribromo-1-Methyl-1H-Imidazole when alternatives fail to deliver sufficient specificity. In our experience, introducing the tribrominated motif can unlock unique bioactivity, hardness to electron transfer, and tailored hydrophobicity. Lead optimization projects in pharmaceutical labs have discovered that methylation of the imidazole nitrogen sometimes improves target affinity, while bromine patterns drive selectivity in more ways than a simple look at molecular weight suggests.

    Key Differences from Other Brominated Imidazoles

    Choosing between 2-bromo, 4-bromo, di-bromo, and this tribromo variant matters more than most anticipate. Through scale-up and pilot projects, we’ve seen the mechanical differences in reactivity first hand. Mono-substituted analogs are useful for milder reactions but lack the full range of derivatization possible with the 2,4,5-tribrominated form. Our own work and customer feedback have underscored that the added bromines significantly alter electronic distribution, making this molecule more suitable for stepwise transformations, especially in multi-stage library syntheses.

    From a practical standpoint, handling 2,4,5-Tribromo-1-Methyl-1H-Imidazole also diverges from lighter analogs. Shipping, storage, and workplace safety differ; this compound typically resists atmospheric degradation better than some mono-halo imidazoles yet remains sensitive enough that sealed containers and low-moisture handling make a difference. Operator training, extraction protocols, and even simple weighing procedures reflect the actual differences these structural changes bring.

    Facing the Challenges of Scale-Up and Process Control

    Moving this compound from gram-scale synthesis to regular production meant navigating pitfalls many underestimate. Reaction exotherms, byproduct formation, and crystalline slurry management do not scale linearly. Our team invested years developing process safety data, evaluating each risk point rather than pushing forward blindly. Modifying reactor design, improving agitation, and testing new isolation methods reflect lessons learned through practice. Waste management, especially concerning brominated byproducts, required investment in specialized treatment protocols — an essential commitment for modern manufacturers.

    No amount of specification sheets can replace hands-on process troubleshooting. During a spike in demand from pharmaceutical development, we learned to pivot from glass vessels to corrosion-resistant steel, managing both bromine load and pH changes. Outages due to clogging or sample loss weren’t classroom exercises; they affected real clients and drove us to create more robust procedures. Now, our scale-up failures inform our continuous training, so these problems become less common for us and our customers.

    Working with Customers: Solving Downstream Application Issues

    Half of the value we bring has nothing to do with the molecule itself, but how we help partners troubleshoot. One customer faced purification challenges due to an unexpected co-precipitate, causing headaches every batch. Our experience with crystallization and impurity diagnosis allowed us to recommend process tweaks that cut filtration time and minimize wasted effort. Direct conversations — not just emails — close the gap between lab-scale predictions and factory realities.

    We also encounter requests to adjust particle size or supply solvent-wet forms for highly sensitive syntheses. Our real-world knowledge lets us bridge the gap from chemical catalog to production line. Sometimes, it means trial shipments and frank discussions about process limitations. We consider process feedback essential, not an inconvenience, and openly address supply risk, stability windows, and process compatibility. Parties on both ends save time and money, avoiding expensive surprises after project launch.

    Safety, Environmental Responsibility, and Regulatory Commitment

    Our history with brominated compounds taught us that environmental and workplace safety bears directly on sustained supply. Scrutiny from regulators and downstream audits is a given. At our plant, every batch of 2,4,5-Tribromo-1-Methyl-1H-Imidazole starts with raw material traceability and worker training in exposure control. Fume management, spill prevention, and proper waste disposal are practices, not paperwork — we’ve faced unannounced inspections and know how quickly minor lapses snowball.

    Environmental policies are not external impositions but necessities for us and the communities in which we operate. We partner with certified hazardous waste handlers, monitor water and air discharged from our operations, and adapt practices in response to evolving standards. Investing in closed-loop processes and seeking safer solvents pays back in reduced regulatory scrutiny and improved employee morale. Responsible manufacturing builds trust with partners who track chemical stewardship upstream.

    Continuous Quality Improvement and Transparency

    As a manufacturer, our direct relationship with the production process keeps us close to the truth of each lot and shipment. Batch records, analytical data, and customer reports flow in both directions. Our laboratory equipment and techniques evolve in response to feedback and new technology, not as a marketing ploy, but as operational necessities. Each deviation, whether blamed on temperature swings or instrument recalibration, prompts immediate root cause analysis and preventative changes.

    Quality assurance isn’t a barrier process. Refining crystallization endpoints, monitoring impurity profiles, and updating hazard labels follow the complex reality of chemical manufacturing. Instead of hiding behind dense documentation, we provide customers with full access to supporting records, including certificates of analysis and up-to-date regulatory statements. This transparency builds long-term trust and forges deeper partnerships.

    Supply Chain Realities and Market Trends

    The demand for 2,4,5-Tribromo-1-Methyl-1H-Imidazole responds to both scientific trend and supply chain realities. New drug discovery avenues and material science applications often trigger surges in requests. From our viewpoint, the market shifts unpredictably, and real supply stability comes from strategic inventory, rapid batch changeover capability, and honest assessment of production limits. We keep extra raw materials on hand and train staff to swiftly adapt to urgent orders or specification changes.

    Global logistics have taught every chemical manufacturer hard lessons in resilience. Bottlenecks caused by port delays or regulatory checks can disrupt project timelines. Instead of leaving clients in the dark, we opened new communication channels that span purchasing, production, and logistics. If storms, customs holds, or regulatory changes might delay a consignment, we believe rapid disclosure keeps everyone aligned.

    Sometimes, scientific enthusiasm for novel halogenated heterocycles creates unrealistic demand projections, especially among startup clients. We actively discuss lead times, alternate sourcing options, and even technical feasibility barriers with our customers, enabling smarter project planning before material is required on the bench.

    Commitment to Long-Term Collaboration

    Decades of hands-on production experience with halogenated imidazoles have shaped how we see our role beyond simply making and shipping chemicals. From employee training programs to production audits and research partnerships, our goal is to foster collaboration rather than simply push product out the door. We routinely host technical workshops, invite process engineers to visit our facility, and seek out pilot project opportunities that deepen collective knowledge about these compounds.

    Our technical support doesn’t end once a drum leaves the warehouse. Partners often request process troubleshooting, impurity identification, or analytical method validation. We directly engage with on-site teams and share test results, even if they highlight process weaknesses. Openness to process improvement reduces both downtime and analytical confusion. Joint problem-solving with synthetic chemists and scale-up managers has saved projects and, in some cases, established new best practices.

    The Real Value of 2,4,5-Tribromo-1-Methyl-1H-Imidazole

    This compound holds value well beyond a line in a catalog. The science that surrounds these imidazoles continues to evolve alongside the needs of the researchers and manufacturers who rely on them. Whether acting as a molecular scaffold or as a highly functionalized starting point, the unique combination of reactivity, selectivity, and practical handling guides where and how to use it best. We view each kilogram we produce as a critical input to research aimed not just at profit, but at new therapies, advanced materials, and improved agricultural tools.

    Years of manufacturing experience reinforce a simple truth: complex chemistry rewards those who anticipate nuance. Details from powder flow to impurity profiles matter. Robust conversation with every customer widens our perspective. Regular investment in staff, equipment, waste management, and community relations supports not just continuity, but growth grounded in responsibility. Our product — 2,4,5-Tribromo-1-Methyl-1H-Imidazole — represents not just what we make, but the standards, values, and technical expertise we bring to every partnership.