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5-Bromo-1-Methylbenzimidazole

    • Product Name 5-Bromo-1-Methylbenzimidazole
    • Alias 5-Bromo-1-methyl-1H-benzimidazole
    • Einecs 629-490-9
    • 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
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    Specifications

    HS Code

    447711

    Product Name 5-Bromo-1-Methylbenzimidazole
    Cas Number 137324-17-9
    Molecular Formula C8H7BrN2
    Molecular Weight 211.06
    Appearance White to off-white solid
    Melting Point 148-152°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Smiles Cn1c2ccc(cc2nc1)Br
    Inchi InChI=1S/C8H7BrN2/c1-11-7-4-3-6(9)2-5-8(7)10-11/h2-5H,1H3
    Synonyms 5-Bromo-1-methyl-1H-benzimidazole

    As an accredited 5-Bromo-1-Methylbenzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-1-Methylbenzimidazole

    Applications of 5-Bromo-1-Methylbenzimidazole in Industrial Manufacturing

    5-Bromo-1-Methylbenzimidazole is a key chemical intermediate, supporting advanced molecule synthesis in specialty industrial fields. As a direct manufacturer, we supply this compound to global enterprises for integration into regulated downstream processes, especially within the pharmaceutical, agrochemical, and electronic sectors. Below are major real-world application scenarios where 5-Bromo-1-Methylbenzimidazole is required as a critical building block.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use 5-Bromo-1-Methylbenzimidazole as an intermediate for developing active pharmaceutical ingredients, particularly in antineoplastic and antifungal product lines. Its brominated benzimidazole scaffold serves as a crucial starting point in constructing heterocyclic core structures for patent-protected drugs. In regulated production facilities, sourcing and use adhere to established cGMP practices, requiring validated impurity profiling and traceable batch records at each transformation stage before API formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals
    • EU GMP Volume 4 for API and Intermediate Control
    • Pharmacopoeia standards (USP, EP, JP) for residual bromide and organic solvent levels

    Typical usage ratio

    • Ranges from 1.1 to 1.5 molar equivalents depending on the target heterocycle route; excess minimized to reduce downstream purification load
    • Adjusted based on efficiency of nucleophilic aromatic substitution or metal-catalyzed coupling efficacy

    Downstream process integration

    • Introduced in the initial heterocyclic scaffold assembly step via bromination or Suzuki coupling
    • Used as a core substrate in intermediate synthesis trains before stepwise functional group elaboration
    • Formulation control includes in-process HPLC monitoring for residue and by-product removal prior to final API formation

    Final product types

    • Antineoplastic actives—investigational and registered
    • Broad-spectrum antifungal APIs
    • Therapeutically targeted benzimidazole derivatives for proprietary pipelines

    2. Agrochemical Active Ingredient Manufacturing

    The agrochemical sector calls for this compound in the synthetic pathways of advanced pesticide, herbicide, and fungicide actives. As a halogenated benzimidazole derivative, it offers enhanced reactivity for introducing specific functional groups under controlled reaction parameters. Leading agrochemical producers run validated batch or continuous processes, checking conversion and isomeric purity by gas chromatography before further derivatization into formulation-ready actives.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems (relating to process documentation and traceability)
    • REACH Regulation (EC) No. 1907/2006—Registration and safety reporting for intermediate chemicals
    • OECD Guidelines for the Testing of Chemicals (analytical and residue methods)

    Typical usage ratio

    • From 0.9 to 1.3 molar equivalents per batch, based on target analogue demand and side-product minimization
    • Process engineers set stoichiometry according to desired halogen retention and coupling efficiencies

    Downstream process integration

    • Feeds into the core cyclization and halogen-exchange stage for ring-closure synthesis
    • Inline purification removes excess unreacted material before bioactivity screens
    • Intermediate must meet analytical specification for residual solvents and heavy metals, verified onsite

    Final product types

    • Selective herbicides for high-value crops
    • Broadleaf and grass fungicides
    • Pesticide actives for seed coatings and post-emergence formulations

    3. OLED and Electronic Material Synthesis

    Specialty electronics companies utilize 5-Bromo-1-Methylbenzimidazole as a molecular precursor for functional organic materials in optoelectronic components. Its bromine leaving group supports efficient aryl coupling and is a preferred module in constructing emitter and hole-transport materials in OLED stacks. Materials development teams specify precise impurity limits and work within ISO 9001-secured lines, documenting batch-level provenance and spectral analyses to ensure downstream device reliability.

    Industry compliance standards

    • IEC 61340—Electrostatics handling for organic semiconductor processes
    • ISO 9001:2015 (production traceability and documentation)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics)

    Typical usage ratio

    • 0.8–1.2 molar equivalents in coupling or polymerization processes
    • Fine-tuned according to the required electronic structure and target functional group density

    Downstream process integration

    • Used in pre-polymer synthesis before high-vacuum deposition or solution-casting to produce OLED layers
    • QC verifies residual halide and spectral absorbance before layer integration
    • Material lot numbers linked to device performance tracking

    Final product types

    • Emitter materials for high-brightness OLED displays
    • Charge transport layers for advanced electronic components
    • Organic semiconductor intermediates for flexible displays and lighting systems

    4. Dye and Pigment Intermediate for Specialty Colorants

    Chemical processing companies manufacturing advanced dyes and pigments integrate 5-Bromo-1-Methylbenzimidazole at key steps for high-purity, application-specific colorant molecules. The benzimidazole ring, functionalized by site-selective bromination, enables greater chromophore tuning and thermal stability, which is essential for textile, polymer, and ink system end-users. Facilities employing this material maintain sampling records and batch-wise traceability, complying with downstream VOC and heavy metal content limits.

    Industry compliance standards

    • OEKO-TEX® Standard 100—Product Class I–IV (for textile dyes)
    • REACH Annex XVII (specifically for azo dye intermediates and finished pigments)
    • ISO 14001:2015 Environmental Management (applicable to process emissions and trace impurity control)
    • Compliance with GB 18582—Chinese National Standard for Limits of Hazardous Substances in Coatings

    Typical usage ratio

    • Usage varies between 0.95 and 1.3 molar equivalents, depending on dye conjugation and incorporation efficiency
    • Adjusted during synthesis scale-up to manage reaction by-products

    Downstream process integration

    • Starts in diazotization and subsequent coupling stages in multi-step dye synthesis
    • Ensures ring structure integrity before further chromophore extension
    • QC measures color index strength, purity, and residual bromine content at stage completion

    Final product types

    • Application-specific dyes for synthetic fiber coloration
    • High-performance pigments for industrial coatings
    • Heat-stable colorants for thermoplastics and specialty inkjet formulations
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    More Introduction

    Introducing 5-Bromo-1-Methylbenzimidazole: A Chemical with Unique Performance in Advanced Synthesis

    What Is 5-Bromo-1-Methylbenzimidazole All About?

    Chemists and researchers have long looked for molecules that can deliver both selectivity and reliability in synthetic work. 5-Bromo-1-Methylbenzimidazole grabs attention for its versatility and the subtle power in its structure. Known as a high-purity reagent with the chemical formula C8H7BrN2, this compound brings confidence to projects centered around heterocyclic chemistry, building blocks for pharmaceuticals, and next-generation material science. It is recognizable by its crystalline, off-white to pale beige appearance, and its presence often signals a designer’s intent to push for tighter synthetic control or improved downstream properties.

    Stepping Into the Lab: Firsthand Experience with 5-Bromo-1-Methylbenzimidazole

    Years spent at the lab bench have taught me to spot the difference between a stock chemical that just gets the job done and one that helps solve complex problems. The methyl group at the first position of the benzimidazole ring and the bromine at the fifth position together open doors that are hard to match with more ordinary benzimidazole derivatives. Anyone familiar with the hunt for reliable starting materials knows how valuable a reagent with selective reactivity can be—it can reduce purification headaches and minimize byproduct formation. It is not unusual to see colleagues reach for this compound when working up new kinase inhibitors or optimizing ligands for metal-catalyzed coupling reactions.

    Comparing the Alternatives: Why Choose This Compound?

    In chemical development, the smallest tweak on a ring structure often means the difference between a successful reaction and a dead end. Take 5-bromo-1-methylbenzimidazole and put it next to 1-methylbenzimidazole. Adding a bromine atom at the fifth position creates an entry point for cross-coupling reactions such as Suzuki, Stille, and Heck. This difference grants it broader application compared to its unbrominated cousin, which lacks a useful handle for halogen-metal exchange or palladium-catalyzed activation. In my own projects, the bromo version integrated into structure-activity relationship studies, while the non-brominated type felt limited to analoging work without much flexibility.

    Meeting Demands in Medicinal and Material Chemistry

    Researchers in drug discovery find value in molecules with modular reactivity. By introducing a bromine atom, this compound opens multiple synthetic pathways, allowing for rapid exploration of analog libraries. Medicinal chemists, for instance, appreciate that the benzimidazole core brings bioactivity potential, while the bromine can be swapped out for more complex units using common cross-coupling techniques. I have seen research groups move seamlessly from the bromo starting material to thioethers, amides, and aryl derivatives in just a few steps. This streamlines target synthesis, cuts down on labor, and keeps focus on exploring new biological space.

    Key Specifications Driving Performance

    What sets this material apart, besides its molecular structure, usually comes down to its purity and form. Labs and production teams seek a reliable supply—high purity, consistent appearance, minimal byproducts. In my experience, good product flows from producers who understand the expectations of pharmaceutical and academic labs alike. Fine powders or crystalline material with high assay values (typically over 98%) save hours in post-reaction clean-ups, and good solubility in common reaction solvents—like DMF, DMSO, and acetonitrile—helps reactions proceed smoothly. Moisture and air stability have always added a layer of comfort, especially during scale-up or storage outside controlled-atmosphere boxes.

    Simple Adoption for Synthetic Innovation

    Synthetic chemists often gravitate toward reagents that cut down on steps or enable new bonds without complicated protection-deprotection cycles. One reason many labs embrace 5-bromo-1-methylbenzimidazole is how smoothly it integrates into alkylation, arylation, and heterocycle-extension protocols. Once, at a university combinatorial chemistry lab, I watched a new graduate student push out dozens of new analogs inside a single week by pivoting from routine couplings to using this bromo compound as an anchor. The shift didn’t require fancy equipment or proprietary reagents—just a smart choice at the starting line.

    Beyond the Spectrum: Where Bench Experience Meets Quality Control

    Seasoned chemists usually go beyond what's printed on a product data sheet. Reliability depends on how a compound behaves batch after batch. I’ve run TLCs and NMRs on material straight from the bottle, and the best batches always match spectra cleanly, without detectable impurities or shifting peaks. Minor impurities in this compound can significantly disrupt downstream processes, especially if moving toward regulated drug work. That’s why working with consistent, traceable suppliers is not just wise—it’s a necessity. I’ve seen time and grant money wasted with poor supplies, so clean material with traceable certifications always wins out.

    Differences That Matter: What Really Separates This Compound from Its Peers?

    A closer look at similar products highlights what makes 5-bromo-1-methylbenzimidazole practical. Compared to non-methylated or non-brominated benzimidazole derivatives, you gain both electronic and steric tuning. The bromine atom not only invites further functionality, it can change the compound’s electron density—a key factor impacting reactivity rates and the types of partners that handle it best. During a recent lead optimization project, the difference between the methylated and non-methylated versions became decisive, with the extra methyl delivering better metabolic stability in the screening assay. Distinctions like this are not always obvious from catalog tables but they emerge crystal-clear after several rounds of trial in both chemical and biological settings.

    Direct Uses in Applied Chemistry

    Researchers add 5-bromo-1-methylbenzimidazole to toolkits focused on building advanced molecules. Take its use in preparing complex ligands for transition metal catalysis. Bromo-substituted heterocycles turn into precious intermediates for embedding new functionality into pharmaceutical candidates and novel materials. In my work designing light-absorbing dyes for organic solar cells, this compound’s reactivity at the bromo position enabled rapid diversification, which brought improvements in panel efficiency. The same kinds of cross-coupling tools translate to device and polymer labs, where teams chase unique emission or conductance profiles by installing new groups onto a benzimidazole backbone.

    The Role of Structure in Activity and Reactivity

    Chemists build lasting solutions on the design of the right chemical frameworks. The addition of a methyl group at N1 and a bromine at C5 gives this molecule a distinct feel; it is not just about what reactions it can do but how it does them. The electron-donating nature of methyl pushes reactivity in subtle directions, favoring certain bond-forming reactions over others. Bromine, being a good leaving group, makes it possible to build out larger structures using standard synthetic methods. Colleagues working with DNA mimetics or novel enzyme inhibitors often comment on the ease with which this compound slots into several modular reaction schemes.

    Making Sense of Availability and Sourcing

    Demand drives availability, and this compound now finds a home on most established chemical supplier shelves. Reliable sources prioritize consistent purity and well-controlled packing to avoid cross-contamination with related benzene derivatives. Having a trustworthy source becomes even more important in regulated industries, where every raw material moves through documentation trails that must stand up to legal or regulatory scrutiny. In start-up environments where chemistry must move fast, the chance to pick up high-quality material in reasonable pack sizes—from gram quantities for discovery work up to kilograms for early process optimization—makes a significant difference in project momentum.

    Real World Performance: From Bench to Process Scale

    Starting in the academic setting, graduate students and postdocs pick up 5-bromo-1-methylbenzimidazole for focused structure-activity efforts. Once a hit or lead emerges, scale-up teams want to keep using the same reagent. My own push from bench discovery to pilot-scale synthesis taught me to value good handling properties—low hygroscopicity, stable shelf life, and a manageable melting point prove themselves every step along the way. Engineering teams often mention reduced risk of decomposition and manageable dust hazards compared to others in the same chemical class. Reduced handling issues mean less downtime and fewer reworks, easing scale-up headaches before they start.

    Potential Environmental and Safety Considerations

    Awareness of chemical safety and environmental impact has rightly moved to the front line of modern labs. While 5-bromo-1-methylbenzimidazole fits the design needs for effective synthetic schemes, safe handling and good housekeeping keep risk low. Proper ventilation, avoidance of skin contact, and diligent storage figure into every protocol. I’ve seen waste streams closely managed to avoid halogenated byproducts escaping into municipal systems; following solid waste separation and licensed incineration remains good practice. Emerging greener protocols sometimes use this molecule in catalytic reactions with reduced waste and milder conditions, which matches the drive for sustainability in research and production settings today.

    Navigating Regulatory and Documentation Needs

    Pharmaceutical and biotech users operate in tightly regulated frameworks where documentation and traceability of all ingredients are not optional. Batch certifications, adherence to country-specific chemical inventory lists, and transparent records on impurities matter. As more teams look toward clinical trials or product registration, secure documentation for every lot of material allows seamless audits and removes the uncertainty from regulatory submissions. I’ve seen talented teams stumble because supply could not match demanding paperwork; a robust audit trail from supplier to shelf can save months in the long run.

    Practical Guidance for Storage and Use

    Best lab practices favor storing 5-bromo-1-methylbenzimidazole in tightly sealed containers at controlled room temperature, shielded from direct light and excessive humidity. Clean tools, careful weighing, and swift transfer into reaction vessels help preserve both potency and purity. I have lost samples in shared labs to careless storage near bases or oxidizers, which underlines the importance of good habits in shared workspaces. Building a clear inventory system has helped keep research flowing smoothly without too many surprises from degraded or contaminated stock.

    Lessons Learned from Day-to-Day Use

    Every research group has those moments where a carefully selected reagent brings a project back from the brink. 5-bromo-1-methylbenzimidazole has been part of those stories more than once, especially for teams struggling with sluggish or messy couplings. In my experience, choosing the right substitution pattern on a benzimidazole ring sets up a win for late-stage diversification or hit-expansion projects. The difference in user experience compared to less functionalized or less pure analogs really comes through not just in yield, but in the speed and clarity of purification. The less time spent on column work or prep HPLC, the more productive the lab becomes.

    Fostering Creative Chemistry Through Solid Building Blocks

    Scientific progress depends on smart, reliable molecules that expand the range of what’s possible. 5-bromo-1-methylbenzimidazole fits this need by merging robust core chemistry with handles for deeper exploration. Its role as a starting point for new heterocycles sets up hundreds of possible downstream molecules for testing as drugs, materials, or catalysts. I have watched innovation accelerate in labs where the right building blocks come quickly, with proven consistency; talented teams need to focus less on troubleshooting raw materials and more on solving grander scientific questions.

    Reflections on Supply, Demand, and Progress

    Market trends show an uptick in both academic and industrial demand for versatile bromo-heterocycles. More start-ups in AI-driven drug discovery or organic electronics seem to tap into molecules like this as key search-space expanders. Ease of modification, strong support for fast SAR, and commercial supply chains keep this compound central in many current discovery platforms. Feedback from process chemists matches these experiences, with recurring reports of low impurity profiles and manageable process risk compared to less sophisticated reagents.

    Moving Into the Future of Synthesis

    The landscape of synthetic chemistry keeps evolving, with new tools, catalysts, and green protocols showing up each year. Building blocks like 5-bromo-1-methylbenzimidazole don’t disappear as new technologies arise—they become more valuable, supporting next-generation reactions that demand selectivity, stability, and creative extension. Open collaboration spaces and cross-disciplinary teams now use these types of molecules to build everything from protein-ligand interaction probes to components for flexible electronics and imaging agents. This compound’s track record supports its continued use in both routine and innovative settings.

    Ideas for Improvement in Commercial Supply

    Feedback from across industries nudges suppliers toward even higher purity, reduced trace metals, and larger range of packaging sizes. In my own teams, direct links between chemists and suppliers, plus clear batch histories, let us flag minor issues before they become big ones. Expansion of technical support, access to analytical data beyond the standard COA, or open communication channels with QA teams have already improved turnaround and confidence for users with strict specifications. These incremental improvements all tie back to smoother research progress and more reliable outcomes at the bench.

    Opportunities Ahead: Building on a Strong Foundation

    With the shift toward personalized medicine, green chemical processes, and smart materials, demand for reliable, multifunctional molecules like 5-bromo-1-methylbenzimidazole will only grow. At each stage in the synthesis pipeline, chemists need partners that bring both innovation and dependability. I see this compound moving further into screening cascades, probe design, and adaptive material synthesis. The core lesson remains that progress builds on dependable foundations, and this particular benzimidazole variant continues to show its worth, year after year, molecule after molecule.