|
HS Code |
817335 |
| Chemical Name | 3-Methylpyridine |
| Cas Number | 108-99-6 |
| Molecular Formula | C6H7N |
| Molecular Weight | 93.13 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Pyridine-like |
| Boiling Point | 143 °C |
| Melting Point | -17.7 °C |
| Density | 0.957 g/cm³ at 20 °C |
| Solubility In Water | Miscible |
| Flash Point | 34 °C (closed cup) |
| Refractive Index | 1.5068 at 20 °C |
| Vapor Pressure | 6.2 mmHg at 25 °C |
As an accredited 3-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250mL amber glass bottle with screw cap, caution label, UN hazard symbols, and product details for 3-Methylpyridine, laboratory grade. |
| Container Loading (20′ FCL) | 3-Methylpyridine is typically loaded in 20′ FCLs using steel drums or IBCs, ensuring secure, leak-proof chemical transport. |
| Shipping | 3-Methylpyridine is shipped in tightly sealed, chemically resistant containers, typically drums or bottles, to prevent leaks and contamination. It is transported under well-ventilated conditions, away from heat, sparks, and incompatible substances. Proper labeling and documentation in compliance with regulations for flammable and hazardous materials are strictly followed during shipping. |
| Storage | 3-Methylpyridine should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents and acids. Keep the container tightly closed and properly labeled. Store away from direct sunlight and moisture to prevent decomposition. Use approved, corrosion-resistant containers and ensure proper grounding and bonding for bulk storage to prevent static discharge. |
| Shelf Life | 3-Methylpyridine typically has a shelf life of 12-24 months when stored in tightly closed containers, away from light and moisture. |
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Purity 99%: 3-Methylpyridine Purity 99% is used in API synthesis, where high chemical purity ensures minimal by-product formation. Boiling Point 145°C: 3-Methylpyridine Boiling Point 145°C is used in solvent formulations, where controlled volatility enhances recovery efficiency. Stability Temperature 120°C: 3-Methylpyridine Stability Temperature 120°C is used in resin manufacturing, where thermal stability supports consistent polymerization. Molecular Weight 93.13 g/mol: 3-Methylpyridine Molecular Weight 93.13 g/mol is used in agrochemical intermediates, where precise molecular size enables accurate dosing. Water Content <0.1%: 3-Methylpyridine Water Content <0.1% is used in fine chemical synthesis, where low water content prevents unwanted hydrolysis reactions. Viscosity Low: 3-Methylpyridine Viscosity Low is used in catalyst preparation, where low viscosity facilitates uniform mixing and dispersion. Density 0.958 g/cm³: 3-Methylpyridine Density 0.958 g/cm³ is used in ink production, where consistent density results in stable print quality. Refractive Index 1.505: 3-Methylpyridine Refractive Index 1.505 is used in optical coating processes, where accurate refractive index ensures optimal light transmission. Melting Point -17°C: 3-Methylpyridine Melting Point -17°C is used in industrial extraction processes, where low melting point supports processing at sub-ambient temperatures. UV Absorption 265 nm: 3-Methylpyridine UV Absorption 265 nm is used in photoinitiator manufacture, where defined absorption enables precise activation under UV light. |
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Anyone who has ever spent much time among chemical supply shelves knows certain compounds spark immediate interest when their names come up. 3-Methylpyridine runs in this crowd, managing to bridge decades of chemical research, industrial progress, and hands-on practicality. Known by its chemical formula C6H7N, it owes its reputation to a unique blend of versatility and reliability.
As I’ve worked with various pyridine derivatives, I’ve come to recognize the subtle but important roles methyl groups play in shifting a compound’s personality. 3-Methylpyridine, identified by a methyl group at the meta position, offers properties that separate it from cousins like 2-methylpyridine or 4-methylpyridine. This basic fact changes how the compound interacts with other chemicals, including its solubility and reactivity, factors that matter deeply for chemists in both research and production settings.
Looking at this compound more closely, the substance appears as a clear to slightly yellow liquid under standard room conditions. The distinct, somewhat pungent odor sometimes becomes part of the laboratory backdrop, a familiar sign that pyridine chemistry is in progress. But more important than a whiff in the air, the methyl group’s placement at the third position impacts how this compound fits into processes that demand selectivity and precision.
In real-world applications, 3-Methylpyridine moves quickly from bench to bulk scale. It shows up frequently in the production of certain pharmaceuticals—antihistamines and even vitamin B3 run through this circuit at some point—unlocking pathways that other pyridine molecules fail to deliver with the same efficiency. Anyone who’s managed a chemical process line knows that even small advantages in yield, purity, or speed can cascade into serious savings and improved safety down the stretch.
Direct contact with industry colleagues sheds light on another trait: 3-Methylpyridine often serves as an important building block in the synthesis of agrochemicals. I recall a field project where an herbicide formulation hinged on the unique properties of this molecule, which not only boosted the effectiveness of the final product but helped to minimize the synthesis of unwanted byproducts. The meta-methyl placement steered the chemistry in ways that alternatives couldn’t match.
Choosing between 3-methylpyridine and a similar derivative isn’t just an academic question. Consider the environmental and regulatory pressures increasingly shaping the chemical industry’s future. 3-Methylpyridine’s relatively low melting and boiling points, coupled with its solubility profile, let process designers dial in the best conditions for efficient recovery, waste minimization, and energy conservation.
Product specifications do more than fill technical data sheets—they guide decisions everyday people make in labs, warehouses, and manufacturing plants. Purity, for instance, stands at the center of quality control. For 3-methylpyridine to drive reliable synthesis, producers routinely push for purity levels above 99%. That’s not just for show: trace levels of impurities may poison catalysts, slow reactions, or introduce hazards into end-use products. In labs where I’ve handled this compound, sources below that threshold led to more trouble than the apparent price savings ever justified.
Batch-to-batch consistency also counts. Colleagues up and down the supply chain, from inventory managers to chemists at the bench, find that certain suppliers recognize this need and invest in analytical technology—gas chromatography, NMR, or mass spectrometry—capable of sniffing out even trace breakdown products. This commitment supports not just safe operations but long-term reputation.
Talk to anyone who has worked with pyridines for long, and you’ll hear stories about both minor spills and more serious exposures. With 3-methylpyridine, the health profile demands respect but not fear. Exposure routes typically include inhalation or dermal contact, so standard precautions—fume hoods, gloves, splash-resistant eyewear—remain a daily ritual in workplaces that handle this material. The MSDS flags irritation and, at higher levels, nervous system effects, making good practice more than just regulatory box ticking.
Waste management and environmental release concerns follow as close companions. 3-Methylpyridine shows some persistence in water and soil environments. Many facilities install dedicated capture and treatment for pyridine-laden waste streams, both to stay within regulatory limits and protect community water resources. My experience has shown that integrating closed-system handling, along with proper storage in corrosion-resistant drums, keeps releases to a minimum—even during hectic production runs.
Chemists and industrial engineers don’t default to 3-methylpyridine without weighing other options. 2-methylpyridine, for example, holds a prominent spot in specialty chemicals and solvents, while 4-methylpyridine can sometimes substitute in pharmaceutical synthesis. The relative boiling points, reactivity, and how readily each one undergoes further chemical transformation matter greatly.
From my own work, I’ve seen 3-methylpyridine’s higher boiling point (around 144°C) compared to 2-methylpyridine (about 128°C), offering higher thermal stability when reactions climb in temperature. This means fewer losses to evaporation, tighter process control, and improved safety margins. Another difference, less obvious to those outside the field, is the pattern of substitution reactions—certain steps, such as nucleophilic substitutions, play out differently based on methyl placement.
Cost sits at the table, too. While certain applications justify the price premium for ultrapure 3-methylpyridine, others lean into more available or cost-effective compounds when the specific advantages don’t translate into real process gains. For example, in large-scale manufacture where minor yield variances matter less than raw material savings, process designers might choose a different methylpyridine or pyridine derivative entirely.
Over the years, hard lessons have emphasized the risks of taking shortcuts on sourcing. The right source delivers more than a drum labeled 3-methylpyridine; it brings a proven track record of transparency, documentation, and communication about impurities, batch test results, and relevant hazards. Whether working with a global supplier or a smaller custom source, I have always insisted on Certificates of Analysis for each batch.
Trust grows from open channels. When issues crop up—a slight off-odor, unexpected reactivity, or container corrosion—the best suppliers step in quickly. It’s not only a matter of service but safety. After an incident involving an off-spec batch in a contract manufacturing project, I learned firsthand how a responsive supplier could help trace problems back to shipping conditions or intermediate storage, preventing recurrence instead of just patching over the symptom.
Sticking with familiar reagents can sometimes halt progress. In pharmaceutical research, for example, the search for new molecules often turns up cases where only a certain methylpyridine opens the right synthetic door. 3-Methylpyridine fits here, enabling regioselective reactions, allowing for specific functionalization that creates molecular diversity at a lower cost or with improved yields than older alternatives.
In academic circles, this flexibility gets highlighted in the literature—synthesis of new heterocyclic compounds, prototyping of catalysts, or development of more efficient agrochemicals use 3-methylpyridine as the starting block. Even beyond the academic and industrial benchmark, in smaller chemical startups or pilot projects, the ability to run exploratory chemistry with a consistent, well-understood starting material helps minimize the unknowns and reduce project risks.
Why does this substance matter today? According to reports from the European Chemicals Agency and research in journals like Chemical Engineering News, demand remains steady across life sciences and agricultural chemicals, with applications ranging from vitamin synthesis to specialized polymers. Recent years have brought more scrutiny to the environmental fate of pyridine derivatives, pushing research into greener production methods and improved waste management. The industry response has included investments in recycling and reclamation, which hint at a shifting mindset toward both environmental stewardship and long-term sustainability.
Yet, familiarity doesn’t mean unexamined comfort. Emerging health data sometimes shift regulatory benchmarks, requiring ongoing attention to storage, transport, and disposal best practices. In one regional facility, I witnessed active adjustments in inventory systems and improved ventilation after a safety audit cited new totals for allowable exposure—a reminder that regulations can and do change as knowledge grows.
With green chemistry now a fixture in industry planning meetings, demand rises for improved processes that minimize environmental risk and use fewer resources. Catalysts active at lower temperatures, for instance, cut both energy use and emissions. One project I consulted on replaced legacy reactors with modular, closed-loop systems, sharply reducing material loss and solvent recovery steps in vitamin production lines that use 3-methylpyridine as a key input.
Supply chain resilience needs special focus. Disruptions in raw materials, energy costs, or transport capacity—all experienced in recent years—can hit mid-stream producers hardest. Firms sharing accurate, real-time information about anticipated shortages or logistical snags help departments plan, avoiding frantic last-minute substitutions with less suitable chemicals. Few things create more downstream issues than materials with unexpected impurity profiles or unfamiliar storage requirements arriving without warning.
Another real point of progress comes from investment in people. Training new team members to recognize the signs of product instability or handle material safely arms workplaces with more than checklists; it builds a workforce with judgement. Early in my career, hands-on orientation reduced spills and waste far more than any manual. Putting trust in well-trained staff pays dividends long after audits and compliance reviews conclude.
Few conversations about industrial chemicals leave out the reality that knowledge remains incomplete. New findings about biodegradation rates, breakdown products, and long-term environmental persistence surface regularly, thanks to global research collaborations. One challenge for manufacturers lies in tracking these findings and quickly applying them, especially as public awareness and regulatory demands accelerate.
Research institutions and industry consortia serve a useful role here, moving data from laboratory notebooks into policy and practice. For example, adoption of new treatment processes for pyridine-laden effluents at plant scale relies on trials that tie together academic chemistry and practical engineering. Connecting the dots from bench to production line is not just beneficial; it’s become necessary.
With a world shifting toward more sustainable practice, every chemical, even one as established as 3-methylpyridine, receives renewed scrutiny. Environmental, health, and safety standards rise, pushing suppliers and users to stay alert. Missteps—whether in transportation, storage, or use—send ripples far beyond the fence line of any factory. Communities expect, and deserve, assurance that companies keep up with both today’s best practices and tomorrow’s anticipated requirements.
In my view, making smart, informed decisions about 3-methylpyridine use includes more than price comparisons or process diagrams. It means building long-term relationships with suppliers, investing in workforce skills, and supporting ongoing research to map uncharted risks. Success comes when cost, safety, performance, and environmental impact align. Each improvement—however incremental—keeps markets strong and communities safe.
Every day, thousands of decisions about chemical sourcing, usage, and disposal shape the world far beyond the walls of a laboratory or plant. 3-Methylpyridine stands as a model of how chemistry can stay both relevant and responsible when the right knowledge supports its use. For everyone who works with this material, experience combines with new data, and practical know-how blends with technological advances to keep outcomes positive. The ongoing commitment from users, manufacturers, and regulators will ensure that 3-methylpyridine remains an asset—never a liability—in a changing industry landscape.