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4-Ethylpyridine

    • Product Name 4-Ethylpyridine
    • Alias 4-Ethylpyridine
    • Einecs 202-599-6
    • 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

    532566

    Cas Number 5314-36-3
    Molecular Formula C7H9N
    Molar Mass 107.15 g/mol
    Iupac Name 4-ethylpyridine
    Appearance Colorless to pale yellow liquid
    Density 0.947 g/cm³
    Boiling Point 156-157 °C
    Melting Point -40 °C
    Flash Point 50 °C
    Solubility In Water Slightly soluble
    Refractive Index 1.512
    Smiles CCc1ccncc1
    Pubchem Cid 10746

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

    Packing & Storage
    Packing Amber glass bottle, 100 mL, tightly sealed with a screw cap, hazard symbols, manufacturer label, and product details prominently displayed.
    Shipping 4-Ethylpyridine is shipped in tightly sealed containers made of compatible materials to prevent leaks or contamination. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition. Compliant with relevant hazardous material regulations, appropriate labeling and documentation must accompany the shipment to ensure safe handling.
    Storage 4-Ethylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated place away from sources of ignition and incompatible substances such as strong oxidizing agents. It should be kept away from direct sunlight and heat. Store under inert atmosphere if possible, and ensure proper labeling and access to safety equipment in the storage area.
    Application of 4-Ethylpyridine

    Applications of 4-Ethylpyridine in Industrial Manufacturing

    Our 4-Ethylpyridine supports a range of specialized chemical industries as a functional intermediate. Below we detail its established downstream applications, defining technical use parameters and quality standards observed by end-users during integration into their production environments.

    1. Agrochemical Intermediate Synthesis

    Agrochemical formulators employ 4-Ethylpyridine as a building block when manufacturing specific classes of herbicides and fungicides. The heterocyclic structure enables selective derivatization, particularly for compounds designed to target weeds in cereal crops and rice paddies. Its integration in multi-step organic synthesis routes, typically during the construction of pyridine ring systems within active agrochemical molecules, requires strict batch consistency and impurity control to maintain downstream catalytic performance as well as regulatory acceptability in final products.

    Industry compliance standards

    • FAO/WHO Specifications for plant protection products
    • OECD Guidelines for the Testing of Chemicals
    • EU REACH registration requirements
    • EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) standards (USA)

    Typical usage ratio

    • In synthesis steps, typically 10–25 mol% relative to overall intermediate batch size, adjusted based on target yield and reaction route specificity.

    Downstream process integration

    • Used during nucleophilic aromatic substitution or alkylation phases; added as a primary reactant after initial solvent charging and prior to addition of catalyst or auxiliary ligands.

    Final product types

    • Selective herbicide actives (e.g., pyridine-based herbicides)
    • Pre-emergent weed control agents
    • Broad-spectrum fungicides for cereal crops

    2. Pharmaceutical Intermediate for Antihypertensive Agents

    Manufacturers in the pharmaceutical sector incorporate 4-Ethylpyridine as a core intermediate when constructing certain antihypertensive active pharmaceutical ingredients (APIs), most notably angiotensin receptor blockers (ARBs) containing a substituted pyridine moiety. Its high chemical purity supports stringent user requirements for backbone construction and side-chain modification steps, and batch traceability forms a critical part of process validation for each lot used in GMP production environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP and European Pharmacopoeia monographs for relevant actives
    • FDA 21 CFR Part 211 (current Good Manufacturing Practice) for finished pharmaceuticals
    • EDQM Certification of Suitability for intermediates (where applicable)

    Typical usage ratio

    • Ranges from 0.5–1.2 equivalents relative to related aldehydes or halides in key coupling stages, optimized to maximize conversion efficiency while minimizing residual starting material.

    Downstream process integration

    • Charged as a primary heterocyclic reactant during Suzuki or Buchwald coupling reactions in synthesis lines; introduced following solvent and catalyst preparation after in-process QC verification.

    Final product types

    • Angiotensin II receptor blocker APIs (e.g., valsartan, candesartan precursors where pyridyl units are present)
    • High-purity pharmaceutical intermediates for contract manufacturing

    3. Catalyst and Ligand Precursor for Olefin Polymerization

    Producers of high-performance olefin polymerization catalysts utilize 4-Ethylpyridine as a functionalized ligand precursor, enabling fine-tuning of catalyst activity and selectivity in polyolefin resin manufacturing. By reacting its pyridine ring with transition metal salts under controlled conditions, formulators can generate chelating complexes suitable for bulk or solution polymerization systems, influencing molecular weight distribution and stereoregularity of finished polymer products.

    Industry compliance standards

    • ISO 9001 certified polymer manufacturing quality systems
    • REACH registered intermediates for polymer catalysts
    • Food Contact Notification (FCN) regulations for polymers (when relevant)
    • ASTM D4101 for polypropylene resin classification

    Typical usage ratio

    • Forms 5–15 wt% of total ligand system in transition metal catalyst synthesis; precise loading depends on targeted catalyst performance profile and co-ligand selection.

    Downstream process integration

    • Reacted in situ with palladium, nickel, or titanium salts during catalyst compounding, prior to co-catalyst or monomer feed introduction in polymerization reactors.

    Final product types

    • Ethylene–propylene copolymers
    • High-density polyethylene (HDPE)
    • Specialty polyolefins with controlled molecular architecture

    4. Fine Fragrance Ingredient Synthesis

    In aroma chemical manufacturing, downstream processors use 4-Ethylpyridine to construct specific fragrance intermediates, especially pyridine-based aroma molecules for fine fragrance and flavor compounds. The ethyl substitution pattern imparts nuanced tobacco, roasted, or leathery notes sought after by perfumers working with high-impact base compositions and luxury fragrance formulations. Controlled addition limits off-notes and ensures consistent olfactory profile batch to batch.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Food Flavourings Regulation (EC) No 1334/2008 (for flavor precursor applications)
    • ISO 9235 (Aromatic natural raw materials—Vocabulary)
    • Allergen declarations according to EC 1223/2009 for cosmetic products

    Typical usage ratio

    • Commonly 0.2–0.8 wt% in perfume base concentrate formulations; adjusted to fit target fragrance accord and regulatory restrictions on pyridine derivatives.

    Downstream process integration

    • Introduced during aroma chemical synthesis prior to esterification, hydrogenation, or acetylation steps; integrated in the blending of top, heart, or base notes depending on end application.

    Final product types

    • Fine fragrance bases for luxury perfumes
    • Specialty flavoring agents (trace use only)
    • Compounds for tobacco-inspired fragrance compositions

    5. Corrosion Inhibitor Formulations for Oilfield Applications

    Engineers in oilfield chemical service companies deploy 4-Ethylpyridine in the synthesis of specialized corrosion inhibitors that protect downhole equipment from acidic media. The electron-rich pyridine structure facilitates formation of robust coordination complexes with metal ions, enabling effective surface passivation when blended with alkylthiazoles or imidazolines. Strict quality protocols ensure consistent active loading and impurity control for dependability under high-pressure, high-temperature field conditions.

    Industry compliance standards

    • NACE MR0175/ISO 15156 (petroleum and natural gas industries–materials for use in H2S-containing environments)
    • API RP 14E (Recommended Practice for Design and Installation of Offshore Production Platform Piping Systems)
    • REACH registration for specialty oilfield chemicals
    • ISO 9001 certified production and traceability systems

    Typical usage ratio

    • Usually compounded at 1–3 wt% of the inhibitor concentrate; field dosage rates are field-adjusted based on corrosivity profiles and system volume.

    Downstream process integration

    • Added during the quaternization or salt formation phase with surfactant actives, then post-blended into liquid corrosion inhibitor packages for batch or continuous injection into wellheads and production tubing.

    Final product types

    • Oilfield corrosion inhibitor concentrates
    • Acidizing additives for matrix and fracture treatments
    • Pipeline protection chemicals
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    Certification & Compliance
    More Introduction

    4-Ethylpyridine: A Chemist’s Perspective from the Production Floor

    Understanding 4-Ethylpyridine from a Manufacturer’s Viewpoint

    Years of making 4-Ethylpyridine in our reactors have shaped our view of what really makes this product stand out. Seeing every batch from raw material to drum reminds us that this isn’t just another basic building block for the catalog. Its molecular structure—an ethyl group at the 4-position on a pyridine ring—might sound simple, but small changes like this unlock very different chemical behaviors and market opportunities.

    What We Actually Make: Batch Practices and Model Consistency

    Each lot of 4-Ethylpyridine we produce follows a process adjusted across the years by feedback from our lab teams. We run controlled hydrogenation and careful phase-separation to yield material that consistently tests above 99% purity by GC. The tight control over water content, amine impurities, and color helps meet the demands from downstream industries like pharmaceuticals, agrochemicals, and specialty flavors. Over time, we’ve dialed in the process to keep metal ion trace levels below 5 ppm, which seems to make a difference for catalyst users.

    From our line, 4-Ethylpyridine usually leaves the plant as a colorless to pale yellow liquid with a characteristic mild nitrogenous aroma. We know that some customers require handling in glass or HDPE only, so our filling process prevents metal contamination right through to the final closure. Whether you see the model as “industrial-grade,” “research-pure,” or some other label, the consistency comes from hands-on batch verification, not just paperwork.

    Why 4-Ethylpyridine Holds Value Across Sectors

    Several chemistries demand a pyridine base that’s more than a brute solvent. Anybody who’s worked in heterocycle synthesis knows substituents can make or break reaction selectivity. The ethyl group at the 4-position shifts both the electronics and the solubility, which explains why some pathways simply give higher yield or cleaner workup compared to basic pyridine. We’ve supplied this to flavor and fragrance developers, who call out the slightly nutty, bready undertone for compound flavors. At the same time, it acts as a useful starting point for auxiliary chemicals in fungicides and herbicides.

    Not every base, and not every pyridine derivative, can stand up to aggressive alkylation or acylation. We keep hearing from customers using 4-Ethylpyridine in Suzuki and Negishi couplings who value the way it avoids some of the over-reactivity and background coloration issues seen with 2- or 3-substituted pyridine isomers. In pharmaceutical applications, we’ve seen trends where switching from 2- to 4-ethyl brings fewer byproduct complications, which makes downstream purification a bit less painful.

    How 4-Ethylpyridine Differs from Other Pyridine Derivatives

    We’ve put a few pyridines through their paces in production labs: pure pyridine, 2-ethyl, 3-methyl, even tert-butyl analogs. 4-Ethylpyridine stands out for a couple of reasons. First, the 4-positioned ethyl doesn’t create as much steric crowding around the nitrogen, making it a somewhat better ligand in coordination complexes. This has been a talking point with catalyst developers who are experimenting with non-precious metals. Second, its physical properties strike a middle ground: less volatile than pure pyridine, less pungent, yet not so hydrophobic that it resists dissolution in typical organic solvents.

    Something we’ve heard from flavor chemists is that 2-ethylpyridine can throw off an earthy, even musky aroma that doesn't blend well in most formulations. Moving the ethyl to the 4 spot smooths out the note, delivering a pleasing background without interference. Agrochemical folks, on the other hand, tend to highlight the stability and the relatively low boiling point, which supports more manageable process conditions.

    As for the big sibling—plain pyridine—there’s no avoiding its stench or its tendency to show up in regulatory flag lists. 4-Ethylpyridine, while still an aromatic base, sidesteps some of those restrictions due to its lower vapor pressure and improved handling safety profile.

    Practical Applications Seen from Production Experience

    Sitting in on technical calls with folks from pharmaceutical synthesis, we’ve noticed recurring themes. Pyrazole and triazine intermediates react more predictably when 4-Ethylpyridine serves as a base under controlled conditions, compared to some bulkier analogs. Lab staff often report smoother separations at work-up, especially in multi-step reactions. In peptide coupling, the mild steric bulk of 4-Ethylpyridine can tip a coupling from a sluggish, side-product-laden mess to a more selective process.

    We’ve seen a steady pull from companies working with complex nitrogen heterocycles in the crop protection sector. The product’s solubility gives more straightforward formulation work when blending actives for seed dressings and post-emergence sprays.

    Even though most outside the field won’t notice, flavorists appreciate the product for recreating subtleties in food aromas—bread crusts, roasted grains, and fermented profiles—effects that 2-methyl or 3-ethylpyridine analogs can’t quite capture without introducing undesirable bitterness.

    Practical Handling Experience and Laboratory Observations

    In our facilities, operators note that 4-Ethylpyridine doesn’t attack common fittings or storage tanks as aggressively as unsubstituted pyridine. This translates downstream into fewer equipment headaches, saving maintenance calls and improving uptime. We’ve addressed oxidation at the surface by sparging the headspace with nitrogen through the drum, which heads off peroxide formation—a small but important operational detail when preparing drums for export.

    Anyone scaling up from bench to pilot plant notices that heating profiles and off-gas scrubbing need tweaking compared to pyridine. The smell is less penetrating, and spill cleanup proves more straightforward due to lower volatility. We recommend basic PPE as with all pyridines, but few operators complain of the skin or nasal irritation that can happen with older, off-spec lots of bulk pyridine.

    Shipping stability depends on dryness, so our line includes a final pass using molecular sieves before packaging. The product’s low water content—consistently below 0.05%—sets it apart for moisture-sensitive applications like catalyst manufacture or solid-phase synthesis supports.

    Quality Control and Analytical Characterization: The Details Behind Reliability

    On the manufacturing side, we’ve put serious work into monitoring key impurities: residual solvents, high boilers, and metal traces. Our in-house analytical team uses GC, NMR, and Karl Fischer titration to keep the certificate of analysis meaningful. We also maintain reference spectra and benchmarks for side stream products, so issues get noticed before materials leave the gate.

    Throughout the years, we’ve seen how off-odor, high color, or trace metal impurities can throw off entire batches downstream. For users preparing pharmaceutical intermediates, a slight deviation in purity or residual solvent profile often comes through as yield loss or purification headaches. Active management of these details, along with transparent batch histories, provides an extra layer of trust for long-term polymer and pharmaceutical customers.

    Industry Demands and Regulatory Context

    A shift toward stricter regulations around hazardous solvent emissions has put all pyridine and derivative production under the microscope. 4-Ethylpyridine carries a better profile than pure pyridine for air emissions, due in part to its diminished volatility. Our lab keeps a close watch on REACH registrations and keeps track of changes under the Toxic Substances Control Act, since an update can change labeling or handling on short notice. While not considered a green solvent by environmental benchmarks, its more favorable handling and lower odor make it less likely to trigger complaints or require emission controls in typical uses.

    Pharmaceutical producers trust that we’re on top of food contact and residual solvent guidance, so our process runs with no Class 1 residual solvents. Our experience with flavor and fragrance users has shown that reliable composition and documentation mean fewer interruptions during audits and re-certifications.

    Technical Discussions: New Developments and R&D Insights

    The industry’s not standing still. There’s always someone in the field developing more selective catalysts or greener synthetic routes. Recently, we’ve fielded more questions about chiral auxiliaries based on substituted pyridines, with 4-Ethylpyridine serving as a precursor in several promising pilot projects. One active area is the preparation of fused-ring nitrogen systems, where selectivity and reaction scope rely on both the base strength and steric profile of the pyridine used.

    We see increasing attention to microwave-assisted synthesis, and 4-Ethylpyridine responds well to controlled heating, improving reaction rates with limited side reactions. In our own evaluation, batch reproducibility stands up to temperature ramping, which supports scale-up confidence for custom synthesis users.

    Another trend worth noting: flavor and aroma chemists continue to push for refinements that stem from extremely low residual tastes and off-notes. Our ongoing focus in this area involves extra purification steps and periodic evaluation with both analytical and sensory panels.

    Operational Challenges and Supply Chain Considerations

    No manufacturing line runs without setbacks, and volatile raw material pricing keeps us on our toes. The main cost driver comes from availability and purity of precursor pyridines and the associated cost for clean catalytic hydrogenation. By fostering relationships with reliable upstream suppliers for these building blocks, we buffer some of the volatility that downstream users feel in finished product prices.

    We’ve weathered logistical disruptions too—container shortages, changes in chemical transport rules, and unexpected customs slowdowns. Our response has been to keep safety stocks for regular users and to streamline packaging sizes to fit a mix of bulk isocontainers and small drum orders. Having flexible packaging lines helps us serve both high-volume agrochemical blenders and RP-lot size pharmaceutical labs.

    From the manufacturing floor, nothing guarantees continuity like clear communication with users: understanding whether a seasonal ramp-up or a regulatory change is coming allows us to plan more precisely and minimize the risk of running short or sitting on unneeded inventory.

    Supporting Innovation and Addressing Industry Hurdles

    On technical hotlines and at conference tables, collaborative problem-solving runs through the process. Sometimes a customer struggles with byproducts in a scale-up batch or encounters a regulatory bottleneck—we pull in our production engineers and QC team to help troubleshoot. More than once, we’ve developed incremental improvements like side-stream purification or custom blending to convert a near-miss project into a manufacturing success.

    R&D chemists on our staff join roundtable sessions to support the development of new applications or process tweaks that hinge on small changes in the pyridine ring. For example, switching from a methyl to an ethyl group in the 4 position can open opportunities for more nuanced performance as both a base and a building block.

    Customer Feedback: From the Plant Floor to the End User

    We hear regularly from users across sectors who share real-world notes—the pharmaceutical process chemist who saves steps in workup, or the crop protection formulator who needs a faster-dissolving base. Feedback loops run straight into our production meetings, pushing us to adjust cleanliness, packaging, or even process controls to better fit field realities. When a flavor and fragrance blender required extra screening for off-odor, we updated our QA protocol to catch a trace background note that only showed up at parts-per-billion levels.

    The long view comes from repeat buyers who’ve worked with pyridines in bulk for a decade or more. They tell us straight when a drum doesn’t match spec or a subtle shift knocks a new synthesis off course. Such input means more than lab analytics—it shapes tangible improvements in every following batch.

    Looking Forward: Keeping 4-Ethylpyridine a Reliable Choice

    In the end, making and shipping 4-Ethylpyridine becomes more than filling a slot in a chemical catalog. From our side, success means customers can count on each container to perform as expected, supporting both well-established and innovative new syntheses. We keep our lines running clean, our documentation transparent, and our focus on what actually matters to the users handling the product on their side. Changes in industry preferences and regulatory environments push us to adapt and refine year after year.

    Unlike broad summaries or generic product blurb, this is a view from behind the scenes—knowing how real-world requirements and direct experience in chemical manufacturing shape the way a compound like 4-Ethylpyridine keeps earning its spot in the toolbox of companies driving synthesis, formulation, and discovery.