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5-Bromo-6-Methylpyridine-2-Carboxynitrile

    • Product Name 5-Bromo-6-Methylpyridine-2-Carboxynitrile
    • Alias 5-Bromo-6-methylpicolinonitrile
    • Einecs 618-894-7
    • 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
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    Specifications

    HS Code

    233119

    Productname 5-Bromo-6-Methylpyridine-2-Carboxynitrile
    Casnumber 885275-07-6
    Molecularformula C7H5BrN2
    Molecularweight 197.04 g/mol
    Appearance Off-white to pale yellow solid
    Meltingpoint 81-85°C
    Solubility Soluble in organic solvents such as DMSO and DMF
    Purity Typically ≥98%
    Storageconditions Store at room temperature, tightly sealed, away from light and moisture
    Smiles CC1=C(C=NC(=C1Br)C#N)
    Inchi InChI=1S/C7H5BrN2/c1-4-6(8)2-3-10-7(4)5-9/h2-3H,1H3

    As an accredited 5-Bromo-6-Methylpyridine-2-Carboxynitrile 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-6-Methylpyridine-2-Carboxynitrile

    Applications of 5-Bromo-6-Methylpyridine-2-Carboxynitrile in Industrial Manufacturing

    5-Bromo-6-Methylpyridine-2-Carboxynitrile plays a pivotal role as an advanced chemical intermediate in various specialized industrial sectors. Our manufacturing expertise ensures consistent quality, enabling reliable integration across multiple downstream applications. Please refer to the following application scenarios for a detailed overview of practical industrial uses, integration stages, standard compliance, and final product categories.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    This compound serves as a key pyridine-based building block for the synthesis of anti-infective and CNS-active drugs. Pharmaceutical manufacturers incorporate it in multi-step organic syntheses where stringent impurity controls are critical. Its functional groups facilitate regioselective transformations, supporting regulated route-of-synthesis development in pre-GMP and full GMP environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, and JP monograph compliance for related substances (traceability)
    • FDA 21 CFR Part 211 cGMP for Finished Pharmaceuticals
    • EMA Guidelines on Manufacture of Chemical APIs

    Typical usage ratio

    • 0.2–1.5 molar equivalents depending on the target API and reaction sequence
    • Ratios adjusted for process yield, step economy, and byproduct management in each synthetic route

    Downstream process integration

    • Forms the core structure in early-to-mid-stage batch or flow synthesis steps
    • Used as a substrate in palladium-catalyzed coupling or nucleophilic substitution reactions
    • Integrated during stepwise construction of heterocyclic drug scaffolds
    • Subjected to purification, isolation, and quality control before downstream elaboration

    Final product types

    • Neurological disorder medications
    • Anti-infective agents
    • Anti-inflammatory actives
    • Intermediates for small-molecule generics

    2. Agrochemical Intermediates Production

    Major crop protection companies utilize this nitrile as a cost-effective intermediate for the synthesis of herbicides and fungicides. The methylpyridine core allows for targeted halogenation and further derivatization, aligning with high-throughput process development and patent-protected formulations. Consistent product specification supports downstream eco-toxicological assessment.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems for Agrochemical Manufacturing
    • REACH Registration for relevant chemical categories
    • OECD Test Guidelines for Environmental Risk Assessment

    Typical usage ratio

    • 10–30% weight of the total active ingredient precursor mass
    • Ratios are set according to stoichiometry of specific crop protection molecule synthesis

    Downstream process integration

    • Starts as a foundational substrate in chlorination or amination steps
    • Mainly used in continuous or batch multi-step organic synthesis for active pesticide matrices
    • Monitored for residuals and byproducts per registration dossiers
    • Enters downstream blending and formulation lines after conversion

    Final product types

    • Pre- and post-emergent herbicides
    • Fungicidal active ingredient bases
    • Intermediate precursors for insect resistance management products
    • Generic crop protection actives

    3. Specialty Dye and Pigment Intermediate

    Dye manufacturers leverage halogenated pyridines such as this material for producing high-performance pigments and textile dyes. The nitrile functionality ensures effective coupling in condensation reactions, essential for developing strong and lightfast chromophores. Quality control for trace impurities is maintained for compliance with export and consumer safety mandates.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Certification for Textile Chemicals
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • REACH Annex XVII restrictions for aromatic amines and impurities
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL compliance

    Typical usage ratio

    • 5–15% of the total pigment precursor synthesis batch
    • Optimized for chromophore yield and intensity during pilot to industrial scale

    Downstream process integration

    • Reacted during primary coupling stages with diazo or condensation partners
    • Subjected to oxidative or reductive finishing depending on pigment class
    • Monitored through in-process QC for tinctorial strength and purity
    • Precipitated and isolated before standard pigment milling or blending

    Final product types

    • Disperse, acid, and reactive textile dyes
    • High-stability industrial pigments
    • Color additives for plastics and coatings
    • Electronic display pigment intermediates

    4. Veterinary Drug Intermediate Manufacturing

    This compound addresses the demand for animal health APIs, particularly for antimicrobials and ectoparasite control agents. Veterinary drug producers employ it in multi-step synthetic sequences, where structural specificity and impurity management align with regulated veterinary dossier submission requirements.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice for Active Substances Used as Starting Materials
    • Pharmacopoeia compliance (European Pharmacopoeia, Ph. Eur. monographs for veterinary APIs)
    • ISO 9001-based veterinary pharmaceutical quality management
    • EU Regulation (EU) 2019/6 on Veterinary Medicinal Products

    Typical usage ratio

    • 0.25–2.0 equivalents according to the required molecular scaffold and target activity
    • Adjusted to optimize yield and minimize process impurities specific to veterinary substances

    Downstream process integration

    • Initial substrate or side-chain precursor in heterocycle formation
    • Halogenation and condensation reactions prioritized for metabolic stability
    • WIP (work-in-progress) quality monitored for residual levels and proper identity
    • Passed through crystallization, drying, and subsequent API-forming reactions

    Final product types

    • Synthesized actives for oral or injectable veterinary medicines
    • Topical antiparasitic agents
    • Feed additive actives targeting microbial control
    • Intermediate components for specific animal health formulations

    5. Electronic Chemical Intermediate for OLED Materials

    Manufacturers of organic electronic materials utilize this pyridine-based nitrile in the synthesis of heterocyclic ligands and dopant precursor molecules. Its defined substitution pattern supports the design of high-purity emitter or transport materials, essential for OLED device performance in terms of efficiency and lifetime.

    Industry compliance standards

    • IEC 62321 standards for hazardous substance determination in electronic materials
    • RoHS Directive (2011/65/EU) for restriction of certain hazardous substances in electronics
    • ISO 9001:2015 QMS for electronic chemical production
    • IPC-5704 Guidelines for Cleanliness of Unpopulated Printed Boards

    Typical usage ratio

    • 0.05–0.5 molar equivalents in target dopant or host molecule synthesis
    • Tuned in lab and pilot production based on emission layer performance requirements

    Downstream process integration

    • Employed as a core intermediate during Suzuki or Buchwald-Hartwig coupling
    • Subjected to rigorous chromatographic purification for low trace-metal content
    • Integrated into organic layers after thin-film purity assessment
    • Verified through device-relevant photoluminescence and yield tests

    Final product types

    • Blue and green emitter molecules for OLED displays
    • Electron-transport materials for organic semiconductors
    • Host matrix components for lighting panels
    • Dopant precursors for flexible electronic applications
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    More Introduction

    5-Bromo-6-Methylpyridine-2-Carboxynitrile: Stepping Up in Fine Chemical Synthesis

    Every now and then, a compound grabs my attention because of how it shapes modern research and real-world applications. 5-Bromo-6-Methylpyridine-2-Carboxynitrile stands out for anyone making headway in pharmaceuticals or advanced materials. When you look at the model – C7H4BrN2 – you get a unique blend of structure and reactivity that stays a step ahead for labs and manufacturing teams determined to push beyond routine boundaries. Talking with friends in organic synthesis, I keep hearing the same thing: little shifts in a molecule’s design let researchers jump past old limitations in designing new drug intermediates and specialty chemicals.

    Getting to Know the Compound

    Let’s put a spotlight on what really matters. In the world of pyridine derivatives, this compound stands out because both the bromo and methyl groups attach to specific spots on the ring. That C≡N nitrile at position 2 is not just a tag-on; it lets chemists branch out into new reactions and pathways, opening up novel functionalizations. For hands-on users, purity matters, and reliable suppliers offer this material in high grades – enough to match the premium needs of industry researchers who don’t compromise on results.

    Why 5-Bromo-6-Methylpyridine-2-Carboxynitrile Is a Gamechanger

    Researchers have learned that each modification to the pyridine ring can nudge a molecule’s personality in surprising ways. The bromo group at position 5 creates room for cross-coupling strategies that drive fast libraries of molecules – that pays off, especially when the clock speeds up on pharmaceutical lead optimization. The methyl group helps dial up selectivity and adjust solubility when you’re going from small-scale reactions in the lab to pilot batches in manufacturing. More than once, colleagues have noted how these changes help their routes work at lower temperatures, saving time, energy, and cost.

    Real-World Usage: Not Just a Lab Curiosity

    People sometimes get the idea that intermediates like this are only useful in textbook examples or specialty research. Most of the real work gets done at the bench. In advancing pharmaceutical research, this compound helps construct pieces of larger, more complex drugs. Medicinal chemists snap it into scaffolds that could eventually treat real human illnesses. Agrochemical researchers find similar value. The specific substitution pattern lets them finesse selectivity profiles for target molecules designed to protect crops without harming soil or water.

    Beyond health and agriculture, the building blocks created with this compound make their way into advanced materials – think electronic devices and specialty polymers. The electron-withdrawing effects of the nitrile, combined with the bromo and methyl substituents, let chemists tune physical properties, getting polymers or functionalized surfaces right where they need to be for the next generation of sensor technology or microelectronics. That’s not hypothetical; it’s happening in materials labs right now.

    Differences That Set It Apart

    It’s easy to think “another pyridine ring—seen one, seen them all.” Not so. The difference comes down to performance. Some pyridine derivatives lack the reactive bromo, so chemists can’t count on efficient cross-couplings or substitutions. Take, for example, 2-cyanopyridines without additional substitution—solid baseline materials, but you’ll hit a wall if your synthetic route needs a lever for downstream modifications.

    Compare this to a similar compound without the methyl at position 6. That small change affects not only sterics but also controls the reaction pathways available to chemists. A synthetic chemist told me how swapping a methyl for a hydrogen let them explore two pathways side by side, and the methylated route hit higher purity with fewer cleaning steps. Little differences translate into hours saved and less waste generated – which adds up quickly for teams managing tight budgets or running against a deadline for regulatory submissions.

    Why Purity and Reliable Specs Matter

    Anyone who’s worked in process chemistry can tell you: specifications make or break a project. Regular buyers of 5-Bromo-6-Methylpyridine-2-Carboxynitrile often discuss their purchases in terms of purity, often looking for 98% or higher. Impurities creep in through routes that use cheaper starting materials or slower crystallization steps. Run the same reaction with broader spec material, and troubleshooting starts to look like a full-time job, not an occasional headache. I’ve seen the charts and heard the stories—high-purity intermediates lead to better consistency in batch-to-batch work and reduce surprises during upscaling.

    This isn’t only about pretty certificates. Downstream users—think pharma quality officers and experienced process engineers—test incoming batches on mass spectrometry and NMR, pushing for full documentation so nothing gets overlooked. It’s become common practice not just to trust specs, but to ask for traceability and transparent sourcing all the way back to the raw materials. Transparency supports compliance and keeps timelines on track, especially with increased scrutiny from international regulators.

    Practical Challenges and the Path Forward

    Lab and manufacturing teams bump into classic headaches with specialty intermediates: inconsistent supply chains, questions about stability, and peaks in cost that pop up just when grants get tighter or procurement gets delayed. The logistics around this compound aren’t immune. Some teams, including those I’ve worked with in contract research, mention long lead times from certain suppliers or difficulty lining up the right documentation for regulatory submissions. Reducing “supplier risk” has become part of regular conversations at technical meetings, with suggestions ranging from dual sourcing to strategic in-house synthesis.

    Storage adds another practical challenge. Compounds with sensitive nitrile groups or halogens sometimes degrade under poor conditions. Storing in dark, cool, and moisture-controlled areas preserves integrity, but companies moving bigger volumes have started looking at more advanced packaging solutions. I’ve heard of teams shifting over to vacuum-sealed containers or adding in-line monitoring for sensitive batches. No one gets excited about storage, but anyone who’s had a batch degrade on the shelf will vouch for the investment.

    Comparing Bench Results and Manufacturing Scale-Up

    Running a reaction in a round-bottom flask teaches you one thing; seeing the same reaction in a 100-liter reactor teaches you a lot more. Bench scientists praise this compound for its dependable reactivity, even if they’re just running exploratory syntheses. Plant operators care more about whether results scale consistently, how easily the compound dissolves in common solvents, and whether side reactions create cleanup problems. That’s where small differences—like the methyl and bromo groups—show up in real financial terms. In one pilot program, a local pharma group reported that switching to this methylated derivative let them shave 15% off their solvent use, since reactions hit target conversions faster. In an era when environmental waste reporting keeps getting stricter, shifts like that are more than a footnote.

    Responsible Handling and Environmental Awareness

    The broader world has eyes on chemical manufacturing’s impact on safety and the environment. Chemicals with halogens and nitriles demand disciplined handling and thorough documentation, especially if downstream users ramp up to commercial scale. Teams now go beyond traditional PPE and look at closed systems, on-site scrubbers, and rigorous waste treatment protocols. Responsible stewardship gets rewarded; companies who lead with thoughtful, safe processes gain trust, which in turn brings repeat business from risk-conscious clients.

    Disposal approaches become part of regular discussion. Rather than treating spent intermediates as routine waste, more organizations opt for solvent recovery, product recycling, or developing secondary market uses. I’ve heard of research groups collaborating with local universities to validate greener transformations, turning what used to be waste into downstream feedstocks for other product lines. It’s not just compliance-oriented; it supports community and long-term sustainability, aligning with how the next generation of chemists wants to operate.

    Supporting Future Progress

    This compound rarely works in isolation—it joins a wider toolkit of reagents, developed in tandem with advances in automation, AI-aided synthesis planning, and green chemistry. Observing trends over recent years, it’s clear that investment in these specialized intermediates goes hand-in-hand with training and developing chemists to use them wisely. Savvy labs now build cross-functional teams who share experience. A synthetic chemist partners with a process engineer and an environmental health expert. Together, the trio optimizes not just the chemistry but the workflow—resulting in safer, smarter, faster project outcomes.

    Educational programs are beginning to highlight cases built around intermediates like this, offering students a hands-on progression from reaction design to real-world impact. As someone who regularly guest lectures to up-and-coming scientists, I watch how students light up when a theoretical topic connects to a compound they see repeated in patents or startup portfolios. The lesson sticks: subtle differences in structure create open doors to meaningful innovation, but only if the team knows which properties matter.

    Cross-Discipline Collaboration is Driving Innovation

    Synthesize, test, learn, repeat. That’s been the rhythm in most research organizations working with advanced intermediates. 5-Bromo-6-Methylpyridine-2-Carboxynitrile finds its way into medicinal chemistry, crop science, and electronics, sitting in the middle of cross-discipline collaboration. Chemists, engineers, and business strategists have started building direct lines of communication, sharing lessons as early as possible to head off process snags before they become costly hurdles.

    Stories circulate about startup teams building out their own automated systems to screen dozens of intermediate combinations, with this compound repeatedly making the shortlist for high-yield, low-waste outcomes. As AI screening tools enter the scene, structures like this one provide a testing ground for combining traditional intuition with algorithm-driven predictions. The best results come from teams that treat the compound not as a black box, but as a versatile ingredient in a dynamic, open-ended process.

    Sourcing Quality in a Crowded Market

    The recent explosion in supplier options carries both promise and risk. Experienced buyers dig deeper than the price-per-gram sticker, looking for supporting data—batch test results, transparent sourcing declarations, and customer service that can answer real technical questions. Colleagues compare notes on forums and at conferences, steering each other toward companies who invest in research partnerships and reliable logistics. Not every supplier delivers on these points, and the difference comes out in the small details—faster troubleshooting, better documentation, and fewer interruptions as projects ramp up.

    Rapid shifts in global markets sometimes introduce interruptions in raw material supply or unexpected spikes in cost. Teams who plan ahead—lining up backup suppliers, even producing limited quantities in-house as a stopgap—end up better positioned when those hiccups crop up. I’ve seen organizations put together cross-functional teams, not just to monitor quality, but to carry out regular audits and competitor benchmarking. In the era of digital supply chains, the most adaptable survive, and the compounds that power tomorrow’s therapies and electronics must keep pace.

    Balancing Performance with Regulation

    Ongoing shifts in global chemical regulation keep everyone adjusting their playbook. The push for “compliance by design” means engineering better control at each step, from molecule design through to packaging and post-market surveillance. Pharmaceutical teams track trace impurities and demand explicit documentation; material science groups want full chain-of-custody details and validated “green” production routes. I hear more regulatory experts asking for early involvement in R&D, saving time and money by identifying compliance needs during discovery, not at the end of the cycle.

    The fine chemical field keeps evolving. Intermediates like 5-Bromo-6-Methylpyridine-2-Carboxynitrile have already shaped key advances. Now, the focus is shifting to “sustainability reporting”—how producers minimize environmental impact, protect workers and communities, and deliver robust, reliable results for their partners worldwide. Stakeholders across the value chain benefit from clear, science-based communication and practical case studies, showing what works and what doesn’t. As this trend continues, trust and collaborative problem-solving will only become more central to chemical innovation.

    What Sets Market Leaders Apart

    I’ve worked with teams who never accept “good enough.” They push to understand a compound’s character—from how it behaves under variable pressure, to what wash solvents make the cleanup faster, to which downstream partners see the best return on investment. In the process, they set expectations for their suppliers and regularly share performance reviews—celebrating fast responses, flagging unexpected hang-ups, and proposing new approaches tailored to emerging challenges.

    People-first leadership and open knowledge sharing keep this field moving. Market leaders build close links with academic partners, sponsor independent research, and remain transparent about both wins and failures. Instead of seeing supply chain hiccups as inevitable, they view each obstacle as a learning opportunity. Firms who’ve excelled with this compound often run in-house pilot labs, evaluating and refining every supplier sample before placing a larger order. That sort of discipline and openness to feedback drives higher quality—and it doesn’t only benefit the end users. Down the line, improved workflow supports safer, greener, and more cost-efficient production across the entire sector.

    Looking to the Future

    Real chemical progress depends on more than the molecule itself—it relies on the ability to adapt, connect, and learn. 5-Bromo-6-Methylpyridine-2-Carboxynitrile has become an important piece of that puzzle. Its specific physical and chemical properties allow teams to shortcut steps, minimize resource use, and accelerate both discovery and scale-up. It’s well suited for today’s fast-paced discovery environments, where rapid iteration meets climbing regulatory demands and growing attention to social responsibility.

    Advances in digital process control, machine learning, and analytics mean the story isn’t finished. Each project that uses this compound reveals new ways to cut cost, save time, shrink environmental footprints, and spark partnerships that last beyond a single research program. Going forward, chemists, engineers, and suppliers who treat each compound as an opportunity to innovate—not just another reagent—will lead the field forward.