|
HS Code |
124936 |
| IUPAC_name | 2,6-dimethylpyridine |
| CAS_number | 108-48-5 |
| Molecular_formula | C7H9N |
| Molecular_weight | 107.15 g/mol |
| Appearance | Colorless liquid |
| Odor | Pungent, pyridine-like |
| Melting_point | -4 °C |
| Boiling_point | 144 °C |
| Density | 0.925 g/mL at 20 °C |
| Solubility_in_water | Slightly soluble |
| Flash_point | 38 °C (100 °F) |
| pKa | 6.99 |
| Refractive_index | 1.499 at 20 °C |
As an accredited 2,6-Lutidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, with a tightly sealed screw cap. Label displays "2,6-Lutidine," hazard symbols, and supplier details. |
| Shipping | 2,6-Lutidine is shipped in tightly sealed containers under well-ventilated, dry conditions, away from incompatible substances such as strong oxidizers. The transport complies with international regulations due to its flammable and irritant properties, and appropriate hazard labeling and documentation must accompany each shipment to ensure both safety and legal compliance. |
| Storage | 2,6-Lutidine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition. Keep the container tightly closed and protected from moisture, direct sunlight, and incompatible substances such as strong acids and oxidizers. Store it in a dedicated flammable liquids cabinet and ensure proper labeling to prevent accidental use or mishandling. |
Applications of 2,6-Lutidine in Industrial ManufacturingAs a dedicated chemical raw material manufacturer, we provide 2,6-Lutidine specifically for industries where its chemical properties support consistent downstream performance in key process routes. Below, we detail authentic sector-driven application scenarios, with a focus on formulation compliance, integration into established process flows, and the resulting end-use products. 1. API Synthesis: Pharmaceutical Intermediates and Fine Chemical PathwaysPharmaceutical producers use 2,6-Lutidine primarily as a mild sterically hindered base in multistep synthesis, including in the formation of active pharmaceutical ingredients where selectivity and side reaction control are critical. It suppresses undesired acylation and alkylation, which is essential most notably in nucleoside analogs, heterocycle construction, and selective deprotection procedures. The material is incorporated during defined condensation, acylation, or pharmaceutical salt formation steps, providing reaction control while maintaining the analytic and residual compliance necessary for regulated APIs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis: Crop Protection Active AgentsMajor agrochemical manufacturers use 2,6-Lutidine as a methylating agent precursor and process base within heterocyclic active agro-ingredients, notably in selective picolinic acid derivatives and pyridine-based herbicides. Its reactivity profile improves yield by minimizing N-alkyl side products in multi-step syntheses. It is usually introduced in process equipment before electrochemical transformation or in batch reactor setups for condensation reactions. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. High-Performance Polymer Additives: Catalyst and Process Agent for Specialty ResinsIn polymer manufacturing, especially for aromatic polyimides and polyarylene ethers, 2,6-Lutidine acts as a controlled basic catalyst and acid scavenger, supporting precision chain propagation and restricting hydrolysis during high-temperature processing. Leading specialty polymer formulators incorporate it to stabilize functional intermediates, prevent excessive coloration, and influence molecular weight distribution in linear and branched architectures. Its limited nucleophilicity suits sensitive monomers and advanced resin systems. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Electronic Chemicals: Precursors for Photoresist and OLED Intermediate SynthesisManufacturers for microelectronic and display technologies utilize 2,6-Lutidine as a precursor and strong base in fine chemical synthesis, vital for producing photoresist sensitizers and organic light-emitting diode functional intermediates. Its steric hindrance reduces side reactivity in preparation of electron donor materials and stabilizers, directly impacting product consistency demanded by high-purity electronic applications. Addition timing is engineered to coincide with lithography precursor activation and condensation routes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Solvent in Analytical Reagents and Chemical DiagnosticsProducers of laboratory and diagnostic reagents employ 2,6-Lutidine as a specialty aprotic solvent or mobile phase modifier, owing to its high selectivity and defined basicity, for analytical-grade derivatization, titrations, or detection of metal ions in HPLC and GC assay development. It additionally supports reagent stabilization for analytical supply kits subject to shelf-life and lot-to-lot consistency protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,6-Lutidine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In decades of hands-on chemical manufacturing, certain compounds prove indispensable across multiple fields. 2,6-Lutidine, with its chemical structure as 2,6-dimethylpyridine (C7H9N), shows up as a trusted option thanks to its specific properties and reliable results. To those who work daily with raw materials and synthesis batches, 2,6-Lutidine stands out not just by its formula, but by its practicality—especially in specialty synthesis and as a potent organic base.
We know 2,6-Lutidine best through use, not just through a catalog or online reference. We see it in drums being loaded, in chromatograms from QA labs, and in technical guidance provided to formulation chemists and process engineers. You find it as a pale yellow, stable liquid with a distinct odor—one that seasoned chemical technicians recognize. Supplied most often at purities exceeding 98%, we test each lot by GC and titrimetric analysis to confirm its basicity and absence of water and trace amines. The focus on consistency in each batch reflects years of learning about where challenges can arise—whether due to raw material impurities, storage conditions, or transport issues.
Where does 2,6-Lutidine offer advantages you cannot get from other chemical bases? The core reason comes down to its mild steric hindrance, elevated boiling point, and well-understood chemistry in handling specialized reactions. Many choose it for use as a non-nucleophilic base in organic synthesis—most notably for the selective deprotonation of moderately acidic protons or as a blocking base in alkylation, acylation, and condensation reactions. From Grignard reagent formation to intricate pharmaceutical intermediates, chemists prize its ability to facilitate the process while limiting unwanted side reactions.
Comparisons with other methylated pyridines matter in daily production. For instance, looking at 2,4-lutidine or 2,3-lutidine, both have different steric profiles and basicity, which ultimately change how they perform in various reactions. Compared to simpler bases such as pyridine, 2,6-Lutidine’s extra methyl groups reduce nucleophilicity. These groups limit its participation in side reactions such as alkylation or acylation, which safeguards target molecule yields when selectivity is critical. Over time, we’ve seen teams switch from other bases to 2,6-Lutidine after encountering unwanted byproducts or poor selectivity in specialized syntheses.
A key experience found in the plant—and echoed by research partners—shows that 2,6-Lutidine’s higher boiling point (over 140°C) allows for cleaner workups and easier solvent removal in most setups designed for laboratory or pilot plant use. In contrast, bases with lower boiling points volatilize quickly and complicate isolations, often costing time and materials to recover. Heating cycles during process scale-up often reveal the difference. Engineers appreciate the ability to run reactions at elevated temperatures without significant base loss or safety concerns related to evaporation or pressure spikes.
From manufacturing perspective, purity specifications never serve as a marketing checkbox. They stem from trial, error, and feedback from failures on the line or during QC. In practice, 2,6-Lutidine supplied for demanding syntheses arrives water clear, free from visible solids or haze. Moisture content matters: we continually monitor water levels using Karl Fischer titration, since even small percentages of water disrupt sensitive condensation or substitution reactions. Nitrogen bases with trace water not only run the risk of hydrolyzing downstream intermediates, they also create microphase separation issues, especially in anhydrous applications.
We run chromatograms on every outgoing lot to screen for related methylpyridines, known byproducts, and residual starting reagents. Any hint of isomeric pyridines above 0.2% triggers a retest and, if needed, fractionation until we hit the right profile. End users—particularly in pharmaceutical, agricultural intermediate production, or advanced electronic materials—report batch-to-batch consistency as the ground truth for reliable performance. For those downstream, using material with variable impurity profiles unravels consistency in API (Active Pharmaceutical Ingredient) synthesis or fine-tuned catalyst systems. We work with that reality daily, knowing that handoffs from raw materials to finished products leave no tolerance for excuses.
Pharmaceutical chemists lean into 2,6-Lutidine’s capabilities for building complex heterocycles, activating acids, or constructing intermediates that demand selectivity. In agrochemical synthesis, its use as a non-nucleophilic base helps generate herbicide intermediates, especially where subtle changes in basicity affect both efficiency and environmental release profiles. We’ve supported teams needing kg- or ton-scale production for these end markets, and the dialogue often becomes highly specific: a small increase in water triggers changes in process optimization, and so we work to consistently stay below the 0.05% moisture mark.
Outside pharmaceuticals and agrochemicals, the electronics sector now explores 2,6-Lutidine for custom molecular syntheses. Those developing OLEDs, specialty polymers, and other advanced materials employ it for its compatibility with sensitive substrates and controlled solvent systems. We have engaged directly with formulators who require assurance that our 2,6-Lutidine meets not just chemical purity, but clarity, color, odor signature, and low residual solvent content. This level of dialogue between manufacturer and processor helps avoid unknowns that could derail million-dollar pilot runs.
Anyone who has filled and shipped drums of 2,6-Lutidine knows its strong, unpleasant odor permeates easily. Proper packaging is not just a regulatory or QA demand, it is a lesson learned from experience—plastic-lined steel drums, vapor-proof seals, and clear labeling keep shipment rejections and warehouse incidents low. Teams storing 2,6-Lutidine for extended periods naturally worry about oxidation, venting, and polymerization; thus, we monitor for peroxides, regularly inspect seals and employ nitrogen blanketing where bulk storage is involved.
Temperature matters as well. Extended exposure above ambient temperature increases the risk of slow volatilization and, in rare cases, pressure rise in sealed containers. Warehouses stay ventilated, away from direct sunlight, and storage temps monitored to protect worker safety and chemical integrity. Customers counting on continuous supply for large-scale runs appreciate this diligence, knowing that a single leak can compromise a batch or incur costly site-level incident investigations.
Direct feedback from end users often shapes iterative improvements that data sheets rarely capture. For example, a customer formulating a chiral pharmaceutical intermediate encountered trouble with off-color and residual pyridine smell even after post-purification. We traced the issue to packaging materials and minor byproduct levels, then adjusted fractionation columns and drum liner specifications. Subsequent lots met their low color and odor standards, reducing downstream purification time, labor, and solvent waste for their team.
We see similar collaborations with process engineers scaling new reactions. Batch records sometimes indicate incomplete reaction or inconsistent yields. Upon investigation, variations in residual water or minor isomer contamination point back to our output, so QC responded by introducing more granular analysis at the blending and filling stages. Trust does not flow from certificates, but from a history of working directly to diagnose and resolve real-world production challenges.
Considerations between 2,6-Lutidine and its structural relatives often emerge in R&D meetings or troubleshooting calls. Chemists sometimes experiment with 2,4-lutidine (2,4-dimethylpyridine), which holds similar alkylation profiles, yet its spatial arrangement creates changes in hydrogen bond acceptance and basicity that may or may not benefit target transformations. Pyridine itself offers greater nucleophilicity but reacts more readily as a participant rather than only a base, compromising selectivity for sensitive substitution reactions. Triethylamine and diisopropylethylamine attract some for their stronger steric hindrance, but their higher cost and handling demands—such as their volatility and odor—place them on a separate balance of efficacy and practicality.
It’s easy to overlook how routine chemical choices affect multi-ton yields, waste streams, emissions levels, and workplace safety. The process of scaling up often uncovers subtleties that go unnoticed at the gram scale: a seemingly slight increase in isomeric impurity or solvent residue alters reaction profiles, afternoon GC analyses run long, and project deadlines slip. That’s why our focus on the specific properties of 2,6-Lutidine—steric hindrance, boiling point, water solubility, and odor—emerges from field problems, not just product listings. It becomes a strategic choice based on years spent responding to both lab-scale trials and full-scale plant logistics.
Handling 2,6-Lutidine in large quantities brings up regulatory and safety demands. The compound emits a strong, persistent odor and can cause respiratory and skin irritation. Staff training includes appropriate PPE—nitrile gloves, splash protection, effective ventilation, and, for poorly ventilated spaces, cartridge respirators. Drains and sumps must remain protected since even small leaks create odor and contamination issues. Where process engineers or facility designers need support for material compatibility or incident mitigation, our experience can guide choices in handling equipment, vent scrubbers, and sensing systems.
Concerns around environmental emissions drive regular reviews of waste handling. Incineration or specialized solvent recovery capture processes feature in most disposal protocols we provide. Storage vessels get inspected for vent integrity and signs of polymerization. Collaboration with waste handlers and downstream users ensures safe management from start to finish. For us, these controls don’t stem only from compliance—they stem from the risks and lessons picked up counseling teams through unexpected leaks or off-spec shipments over the years.
Every lot of 2,6-Lutidine carries a story—documented through raw material sourcing, process notes, and analysis records. Because pyridine derivatives display sensitivity to slight changes in source chemicals, we maintain traceability from incoming feedstock through final packaging. Machine-readable batch codes map back to every processing step. Regular internal audits tackle gaps found through customer complaints or our own return samples. Our analytics team routinely re-examines historical trends, catching drifts in specification adherence before they disrupt shipments or product performance.
We see growing requests for documentation, not just for purity but for specifics on heavy metal residues, trace solvents, and even energy usage associated with manufacturing steps. This shift stems from clients with strict supplier qualification programs and sustainability goals. Rather than a burden, we view transparency as a tool to build long-term partnerships. R&D teams receive answers quickly, plant managers obtain detailed run histories, and regulatory officers get complete trace files to simplify audits. Trust builds with every resolved question—not with opaque certificates, but with clarity and openness.
The market for 2,6-Lutidine continues evolving. Custom syntheses and stricter purity standards push manufacturers to invest in better refining equipment, automation, and sustainable practices. Green chemistry drives demand for process intensification, solvent reduction, and closed-loop waste management—especially from customers in pharmaceuticals and electronics. Our team spends significant effort developing improved recovery columns, choosing lower-impact reagents, and piloting new solvent-exchange techniques to shrink our environmental footprint.
Rising expectations push us to offer not just chemical performance but responsible sourcing, minimal waste, and energy-efficient processing. We see this as a natural progression rooted in daily practice—responsibility grows from watching production lines run safely and efficiently, as well as minimizing waste and emissions that workers and communities feel directly. Choosing which markets to serve, and which innovations to pursue, comes from this balance: reliability, safety, environmental responsibility, and technical alignment with end user needs.
Bulk buyers and specialty users raise further requirements beyond purity or yield. Questions around controlled substance status, shipping restrictions, and in-country labeling change the conversation from pure chemistry to holistic supply security. Keeping pace involves not only technology upgrades but sustained dialogue—supporting a customer shifting from one base to another for new process routes, or working with regulators on documentation needed for new market entries. In this way, adaptability and transparency become as important as technical properties.
Year after year, we see why 2,6-Lutidine keeps its place among core chemical bases. Its balance of moderate strength, distinct selectivity, and manageable handling remains valuable for well-controlled, scalable synthetic work. Not every batch runs without a challenge, and real-world logistics—from sourcing to delivery—test the limits of our processes. Yet each success story, each troubleshooting win, deepens our understanding and strengthens our process controls.
To us, 2,6-Lutidine represents more than a commodity or line item. It carries the lessons of real-world synthesis, daily QC testing, technical problem-solving, and honest conversation with customers navigating high standards. No certificate or specification sheet stands in for the ongoing work to improve purity, traceability, and impact on both users and the environment. Each barrel or drum shipped out reflects our continuous commitment to supporting innovation, one reaction at a time.