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3-Ethyl-4-Methylpyridine

    • Product Name 3-Ethyl-4-Methylpyridine
    • Alias 3-Ethyl-4-picoline
    • Einecs 210-264-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    342531

    Cas Number 1126-09-6
    Molecular Formula C8H11N
    Molecular Weight 121.18 g/mol
    Iupac Name 3-ethyl-4-methylpyridine
    Appearance Colorless to pale yellow liquid
    Boiling Point 179-181 °C
    Melting Point -40 °C (estimated)
    Density 0.938 g/cm³ at 25 °C
    Refractive Index 1.510 at 20 °C
    Flash Point 59 °C (closed cup)
    Solubility In Water Slightly soluble
    Pubchem Cid 13232

    As an accredited 3-Ethyl-4-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL amber glass bottle with a secure screw cap, labeled "3-Ethyl-4-Methylpyridine, C8H11N, for laboratory use, flammable."
    Shipping 3-Ethyl-4-Methylpyridine is shipped in tightly sealed containers, typically glass or chemical-resistant plastic, to prevent leaks and contamination. It should be stored and transported in a cool, well-ventilated area away from sources of ignition, heat, and incompatible materials, following all applicable regulations for hazardous and flammable liquids.
    Storage 3-Ethyl-4-methylpyridine should be stored in a cool, dry, and well-ventilated area, away from heat, open flames, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from direct sunlight and moisture. Use chemical-resistant containers and secondary containment to prevent leaks or spills, and follow all relevant safety and regulatory guidelines.
    Application of 3-Ethyl-4-Methylpyridine

    Applications of 3-Ethyl-4-Methylpyridine in Industrial Manufacturing

    As the direct manufacturer of 3-Ethyl-4-Methylpyridine, we provide this intermediate to specialized sectors where its chemical structure delivers specific benefits to downstream synthesis and processing operations. Below are the principal industrial application scenarios, each detailed with actionable data for formulation, regulatory compliance, and process integration.

    1. Agrochemical Active Ingredient Synthesis

    Crop protection manufacturers utilize this pyridine derivative as a core intermediate during the preparation of heterocyclic agrochemicals, especially in the multi-stage synthesis of certain broad-spectrum herbicides and insecticides. It contributes essential scaffold structures, influencing both the target molecule's activity and selectivity, and is valued for its reactivity in alkylation and acylation routes within pilot and plant-scale reactors.

    Industry compliance standards

    • ISO 9001:2015 certified production traceability
    • Regulation (EC) No 1907/2006 (REACH) registration and reporting
    • OECD Guideline 407 (Repeated Dose 28-Day Oral Toxicity Study for Chemicals)
    • Chinese Pesticide Registration Standards (GB 4839, GB/T 1600 series)

    Typical usage ratio

    • 5–15% w/w of key reactant mass in the controlled feed stages, depending on target molecule and batch scale; process development teams adjust ratio based on desired intermediate concentration and yield optimization.

    Downstream process integration

    • Added during heterocyclic ring-closure synthesis after initial condensation stages; introduced into jacketed reaction vessels under nitrogen, preceding oxidation or halogenation reactions; subsequent removal via distillation if required for final purity.

    Final product types

    • Herbicide active ingredients (pyridine-based compounds)
    • Systemic insecticides for soil and foliar use
    • Plant growth regulators with heteroaromatic scaffolds
    • Key R&D samples for regulatory submissions

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    API manufacturers use 3-Ethyl-4-Methylpyridine as an advanced building block in the synthesis pathway for specific anti-hypertensive agents, CNS drugs, and hospital injectable actives. Its molecular configuration supports downstream functionalization, facilitating selective methylation or ethylation to achieve the drug target’s therapeutic profile. GMP and strict residual limits regulate every supply stage to ensure medicinal safety.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF and EP monographs for intermediates
    • FDA 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • EDQM Certificate of Suitability (CEP) validation

    Typical usage ratio

    • 2–8% w/w relative to core synthetic feedstock, based on molecule complexity and process yield; high-purity grades required to keep related impurities below 0.15% for EU and US finished drug requirements.

    Downstream process integration

    • Charged during multi-step synthesis at the pyridine-formation stage; involved in nucleophilic aromatic substitution or alkylation in high-pressure glass-lined reactors; monitored for residual solvent content before API isolation.

    Final product types

    • Anti-hypertensive bulk APIs
    • CNS pharmaceutical intermediates for clinical candidates
    • Sterile injectable bulk ingredients (following further synthesis and purification)
    • Generic drug intermediates for contract manufacturing

    3. Fine Chemical Intermediate for Dye and Pigment Precursors

    Specialty dye producers adopt this compound within multi-step syntheses to assemble functional chromophore groups, particularly when engineering color-fastenings for textile and ink applications. Its precise electronic effects enable control over hue intensity and stability, aiding the downstream acetylation or coupling reactions critical for pigment development in automated batch and continuous flow settings.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for dye synthesis
    • Colorants listed under REACH Annex IV and V
    • Oeko-Tex Standard 100 (for restricted substance controls in textiles)
    • EFfCI GMP (for fine chemicals used in cosmetics, if pigment is for personal care)

    Typical usage ratio

    • 4–10% w/w of pigment batch input at the coupling or cyclization stage; color strength and purity requirements drive minor ratio adjustments as confirmed by batch spectrophotometric analysis.

    Downstream process integration

    • Fed into reaction tanks during the precursor assembly, following diazonium salt generation or in situ catalyst addition; typically introduced just before final condensation or coupling to fix color tone and improve pigment yield.

    Final product types

    • Pyridine-derived azo dyes for textiles
    • UV-resistant organic pigments for printing inks
    • High-temperature stable dyes for engineering plastics
    • Specialty pigments for automotive and industrial coatings

    4. Chemical Intermediate for Flavors and Fragrances Production

    Flavors and fragrances formulators rely on this methylpyridine as a precursor in the construction of complex aroma molecules with high impact and stability, particularly those mimicking roasted, nutty, or smoky notes for food and tobacco flavourings. Strict traceability and low-odor profile requirements define quality acceptance and downstream blending operations.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association)
    • IFRA Standards for fragrance ingredients
    • US FDA 21 CFR 172.515 (Synthetic flavoring substances)
    • China GB 2760 (Food safety national standard for use of food additives)

    Typical usage ratio

    • 0.1–2.5% w/w of total batch input for flavor/fragrance synthesis, adjusting according to sensory impact and regulatory maximum residue levels; customized to comply with specific market entry standards for aroma chemicals.

    Downstream process integration

    • Enters reactor during the early construction of heterocyclic aroma structures after initial alkylation or cyclization step; process usually followed by distillation under reduced pressure and solvent-exchange to control purity and minimize unwanted notes.

    Final product types

    • Roasted and nutty aroma chemicals
    • Tobacco and beverage flavoring bases
    • Fragrance intermediates for perfumery compounds
    • Blended food flavoring concentrates for regulatory submissions
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    Certification & Compliance
    More Introduction

    Introducing 3-Ethyl-4-Methylpyridine: Experience, Expertise, and the Real Story Behind Its Production

    A Manufacturer’s Take on 3-Ethyl-4-Methylpyridine

    Within our production halls and labs, 3-Ethyl-4-Methylpyridine, known among chemists as EMP, represents more than just another pyridine derivative—it's a compound we’ve worked with for years and one whose every stage, from raw material selection to purification, reflects the standards and reliability our customers expect. There’s no substitute for actual hands-on manufacturing experience; we’ve seen how trace impurities or minor formulation tweaks can make or break a product batch when it reaches downstream processors.

    Unlike trade intermediaries, our perspective comes with a memory of every batch run, every flask, and even the precise challenges that each step brings. Building consistency into EMP output comes down to controlling not just the reagents and temperatures, but also understanding the minute-by-minute behavior of mixtures under actual plant conditions. That’s what we handle daily—and it’s where quality starts.

    What Sets 3-Ethyl-4-Methylpyridine Apart?

    This particular compound stands apart from its close relatives—like 4-ethylpyridine or 3-methylpyridine—because of its dual substituents that create unique reactivity and handling properties. Certain industry reactions demand specific electron densities or steric environments on the pyridine ring, which only this combination can offer. Engineers and bench chemists will immediately notice EMP’s particular odour and volatility, different from unsubstituted pyridine or even mono-alkylated versions.

    Our purification procedures have targeted these traits, allowing us to deliver EMP with minimal cross-contamination from other pyridine isomers. For example, while methylpyridines can cloud a desired reaction outcome, EMP’s specific arrangement suits advanced synthesis work involving pharmaceuticals, agricultural intermediates, or specialty dye development. Customers tell us that substitutions elsewhere on the ring don’t yield the same performance. We've even spent years fine-tuning the post-reaction separation to reduce byproduct formation so downstream processors get as little interference as possible.

    Manufacturing Mindset: From Raw Material Handling to Final Packaging

    Scaling synthesis of EMP means moving past textbook reactions to real-world, workable routines. Pyrolysis of carefully chosen precursors, monitored heat application, moisture exclusion, and precise control of atmospheric conditions prevent degradation and unwanted tars. One lesson learned after several harsh winters is the moisture sensitivity of certain intermediates—the compound won’t forgive lapses in humidity control. An undetected drip or leaky valve can lead to a week’s lost output.

    Handling this compound demands corrosion-resistant equipment, since both starting materials and EMP itself display a tendency for stress-corrosion on non-ideal steels. Our production floor uses a blend of glass-lined reactors and select high-grade alloys to avoid unwanted side reactions. Regular calibration and solvent purification routines form our daily rhythm. In our earliest runs, inconsistent glassware cleanliness led to colored byproducts; tightening up controls there nearly eliminated those issues.

    Our lab teams test every batch for trace isomers, water, and byproducts—knowing even minor deviations have caused headaches for end-users who need consistent outcome in their synthesis. Over time, we upgraded to GC-MS quantification to flag even low-ppm impurities, since organic functional groups found in pyridine rings can carry over and impact catalytic reactions or spectral purity downstream. Many resellers don’t see these effects directly, but problems show up in the hands of those who actually use the material.

    Specifications That Matter: Purity and Real-World Performance

    Most users ask one question: Does EMP from different producers truly perform the same way? Drawing on hundreds of test runs, repeated purification cycles, and customer feedback from several industries, we know the answer is no. The real-world difference lies in how slight differences in side-products, water content, or storage atmosphere can affect shelf-life and reactivity. Small jumps in water content, even by less than 0.05%, have fouled entire syntheses.

    Every EMP shipment out of our facility carries a guarantee for not just minimum assay, but for upper limits on methyl and ethyl side-products, residual ammonium salts, and color formation. Most end users don’t want surprises—cloudiness, unusual smells, or viscosity changes. Direct manufacturing means we can respond fast to out-of-spec results, recalling or replacing batches before an entire downstream process is disrupted. This is not the place for shortcuts—less rigorous purification costs time and money elsewhere, sometimes costing a plant a day’s production when something goes off.

    We don’t promise absolute theoretical yields, but our process delivers on reliability where it counts. Most recent batches run >99% purity (by GC), water content less than 0.03%, and no detectable chlorinated residues (which sometimes come from shortcut syntheses). In the rare case of unexpected results, our teams reach out directly—an advantage direct manufacturing brings.

    Application Side: Why EMP Stands Out in Use

    Serving both custom synthesis customers and volume buyers in pharmaceuticals, agrochemicals, and dyes, we’ve gathered plenty of feedback on EMP applications. Chemists report faster reaction times and fewer off-colors when working with our cleaner EMP, compared to broadly supplied monoalkyl-pyridines. In pharmaceutical synthesis, for instance, EMP’s pattern of electron-donating groups allows selective downstream transformation, especially in heterocyclic ring construction not achievable with 3-methyl or 4-ethyl analogs.

    Agricultural R&D teams have told us that certain crop-protection intermediates require substitution maps only found in EMP. Replacing EMP with other alkylpyridines alters biological activity and can drop yields or lead to regulatory headaches. Our dye manufacturing partners, who need consistency in chromophore formation, rely on EMP’s precise positioning for batch-to-batch reproducibility. Anything less, and color performance drifts—a difference you won’t see on a data sheet, but one that shows up on the production line.

    One overlooked use comes in catalyst and ligand construction. Many nickel, palladium, and copper complex formation reactions hinge on low-level impurities—sometimes traced back to the very EMP batch. Our investments in low-odor, high-purity EMP have allowed several customers to broaden their use into more sensitive ligand prep, pushing the boundaries of what metal-organic chemistries can achieve.

    Drawing the Line Between Us and Others

    Some chemical suppliers take pride in low prices driven by bulk imports or blends—but consistent customers often circle back to direct manufacturers like us after poor experiences. We’ve seen cut-price EMP containing high levels of regioisomers or with faint amine odors, which have caused problems ranging from shutdowns of continuous reactors to failed safety audits. Our name goes on every barrel and canister—we track source, storage, and delivery down to the batch. We build these safeguards into every process, starting with reagent choice and ending with pre-shipment inspection. It’s not marketing—it’s how we sleep at night, knowing the product we ship reflects on everyone in the plant.

    What competitors call acceptable, we often send for redistillation or blend into lower-purity grades. Some see that as waste—our teams consider it an investment in trust. We’ve managed recalls for less cautious suppliers, helping end-users resolve off-spec product issues, even when it wasn’t our material. Over decades, this has built deep relationships, especially with labs that need reliable performance, not just paperwork.

    Pushing for Solutions in Purity and Process

    A compound as particular as EMP doesn’t simply stand up to rough handling. Market pressure tends to reward faster, cheaper, and larger production runs. But sustaining top-tier EMP means ongoing investment. We’ve had to update reactors to handle rising demand without losing sight of purity. Newer distillation setups with expanded reflux columns (using nitrogen-sealed systems) have lowered impurity transfer.

    We keep pace with evolving regulations. Shifts in regional rules about pyridine derivatives require documentation beyond what most brokers even know about—batch traceability, usage logs, and even solvent disposal records. Our teams run regular training, so an operator on the floor knows not just the how, but the why of every procedure. The feedback loop—from plant floor to QC lab—lets us adjust SOPs faster, keeping EMP production both safe and reliable.

    Quality—Built on People and Continuous Improvement

    Quality here springs mainly from experience. Senior chemists, building on years of work, spot irregular crystallization before tests even finish. Operators can smell or see signs of a ketone or peroxide impurity almost before detection equipment. Newer hires train alongside them, picking up practical tricks that you’ll never get from a text or video. Equipment audits, regular shutdowns for deep cleaning, and robust cross-checks all play a role in safe and repeatable output.

    We chase incremental betterment, not some unachievable platonic ideal. Each year, small gains—one-tenths of a percent yield here, half-day scheduling there—add up. Those wins echo in tighter consistency from batch to batch. Some of our workflow improvements have even filtered to other lines—less waste in pyridine streams means cleaner EMP; better EMP leads to smoother downstream chemistry, and so forth.

    Trust Earned in Every Barrel

    Most of the time, a top-tier barrel or drum of 3-Ethyl-4-Methylpyridine never makes headlines. If it runs perfectly, nobody sees news about it. Yet, real quality shows not in brochures, but when things don’t go to plan. Rapid support, root-cause investigations, and live conversations with real chemists—not auto-replies—set us apart. We’ve resolved crisis after crisis that generic, distributor-supplied product simply can’t handle.

    We don’t substitute, dilute, or blend. Each unit ships with real paperwork, real data, and responsibility that can’t be dodged or whitewashed. For certain pharmaceutical or electronic-grade users, even our lot-to-lot stability presents a reason to stick with us through market swings. If the price wars push us to the wall, we refuse to cut corners. That decision has kept us relevant for decades—no fleeting bargain can replace reliability in the long run.

    Looking Ahead: Innovation and Sustainable Growth

    Our future challenge is to balance scale with precision. Markets don’t wait; neither do customer needs. Rising environmental standards, stricter waste policies, and new end-use applications keep refining what defines “quality” in EMP. For instance, we’ve pursued solvent recovery and recycling programs, not just to meet green credentials, but because it forces cleaner baseline processes, meaning better downstream EMP. Adjustments to byproduct recovery—turning what was once waste into feedstock for other lines—now keep costs in check without lowering material standard.

    We stay in step with industry, integrating new analytical tech for rapid impurity screening and adapting packaging to user feedback. Some of this comes from those in the field. Years back, a customer’s complaint about trace solvent residue during summer transport led us to overhaul seal checks and loading bay routines. Even our largest industrial shipments now meet the same scrutiny as our smallest research-scale bottles.

    Building EMP production that anticipates the unexpected means relying on both people and systems. We continue to invest in new reactor linings, solvent purification units, and atmospheric monitoring—not because we’re forced, but simply because it pays off with peace of mind for all involved. We expect more innovation at the molecular level as chemists find new EMP applications, each presenting fresh purity and logistics puzzles. That’s exactly the work we thrive on.

    Comparing EMP with Other Pyridines: Lessons from the Line

    Some newer chemists ask, can’t one just substitute another alkylpyridine when EMP isn’t on hand? Regular hands-on production has shown that’s rarely true over the long haul. Patterns of reactivity, substitution, and downstream yield regularly shift between EMP and its close cousins. For example, 4-methylpyridine might look suitable algorithmically, but nuanced differences in electron distribution alter reaction rates and byproduct spectra. Early on, we learned how even “iso”-labeled batches interfered with catalyst loads and affected final purity for our pharma customers.

    Even differences in boiling range, vapour pressure, or residual solvent carry-through influence both safety handling and shelf stability over time. This is particularly pronounced in EMP due to the combined methyl and ethyl substitutions. Standard drum fill, storage, and venting guidelines have needed adjustments for EMP compared to other pyridines. Our safety protocols reflect actual incident logs and observed hazards, not just theoretical hazard scores.

    Feedback loops from users keep us improving. New syntheses, especially at pilot or scale-up stage, highlight problems with competitor EMP batches—trace residuals, inconsistent color, or instability in storage. Fixing these often means returning to foundational steps: better distillation fractions, new filtration media, or improved sealing at packaging. Each time, lessons learned flow straight into process improvement for the next batch.

    Working Together: Support and Partnership Beyond the Bottle

    We see ourselves as more than just suppliers; our teams act as partners for every EMP customer. Support doesn’t end with order fulfillment. Our staff routinely take calls, walk users through unexpected analysis results, help troubleshoot reactions, and share insights on maximizing shelf life and minimizing waste. Unlike some remote supplier, we have a personal stake in the outcome of each shipment—it’s our chemistry, our product, our reputation.

    Collaborating with long-term clients, we’ve developed custom EMP grades, adapted storage recommendations for different climates, and run side-by-side analyses to benchmark our product against anything else on the market. It’s not just a transaction; years of shared success and learning drive both sides forward. We keep lines open for feedback, and actively explore customer-led suggestions for packaging improvements and sustainability practices.

    Final Thoughts: Real Manufacturing Means Real Value

    After years in the field, our approach to 3-Ethyl-4-Methylpyridine is more than just batch records and compliance sheets. It’s built on expertise, lessons from the floor, and honest engagement with customers large and small. The difference between direct manufacture and indirect supply isn’t invisible—it shows itself in every interaction, every consistently pure drum, every problem solved before it leaves the plant.

    Chemistry isn’t just about formulas; it’s about relationships and real-world consequences. For those relying on EMP as a tool in their synthesis, quality can never be left to chance. Our doors stay open, our teams stay sharp, and every corner of the process answers to those who actually use and depend on our product. In this field, trust and reliability deliver the real value—and that’s the way we do business, every day.