|
HS Code |
726372 |
| Cas Number | 591-22-0 |
| Molecular Formula | C7H9N |
| Molar Mass | 107.15 g/mol |
| Iupac Name | 3,5-Dimethylpyridine |
| Synonyms | 3,5-Lutidine |
| Appearance | Colorless to yellowish liquid |
| Boiling Point | 172-174 °C |
| Melting Point | -16 °C |
| Density | 0.925 g/cm³ |
| Solubility In Water | Moderate |
| Flash Point | 52 °C |
| Refractive Index | 1.504 |
As an accredited 3,5-Dimethylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 500 mL of 3,5-Dimethylpyridine; sealed with a screw cap, labeled with hazard and product information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Approximately 13.6 metric tons (drums or IBCs) of 3,5-Dimethylpyridine, securely packed for export shipping. |
| Shipping | 3,5-Dimethylpyridine is typically shipped in tightly sealed containers made of compatible materials, such as glass or high-density polyethylene, 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 substances, following applicable regulations for flammable liquids. |
| Storage | 3,5-Dimethylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep away from incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Clearly label the container and ensure proper grounding when transferring to prevent static discharge. Store in accordance with local regulations. |
| Shelf Life | 3,5-Dimethylpyridine has a shelf life of several years when stored tightly sealed in a cool, dry, and well-ventilated place. |
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Purity 99%: 3,5-Dimethylpyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity formation. Boiling Point 171°C: 3,5-Dimethylpyridine with a boiling point of 171°C is used in organic solvent extraction processes, where it provides efficient phase separation and selectivity. Molecular Weight 107.16 g/mol: 3,5-Dimethylpyridine with a molecular weight of 107.16 g/mol is used in catalyst formulation, where it affords precise stoichiometric control. Low Water Content ≤0.2%: 3,5-Dimethylpyridine with water content less than or equal to 0.2% is used in moisture-sensitive reactions, where it minimizes hydrolysis of reactants. Stability Temperature up to 120°C: 3,5-Dimethylpyridine stable up to 120°C is used in high-temperature polymerization, where it maintains chemical integrity and consistent reactivity. Density 0.92 g/cm³: 3,5-Dimethylpyridine with a density of 0.92 g/cm³ is used in liquid chromatography, where it enables accurate calibration and separation efficiency. Acidity (pKa 6.91): 3,5-Dimethylpyridine with pKa 6.91 is used in buffer solution preparation, where it delivers reliable pH control. UV Absorbance 0.01 AU (at 254 nm): 3,5-Dimethylpyridine with UV absorbance 0.01 AU at 254 nm is used in spectroscopic assays, where it ensures minimal background interference. Colorless Appearance: 3,5-Dimethylpyridine of colorless appearance is used in laboratory reagent mixes, where it eliminates visual contamination and enhances assay reproducibility. Melting Point -25°C: 3,5-Dimethylpyridine with a melting point of -25°C is used in low-temperature reaction media, where it prevents crystallization and maintains homogeneous solutions. |
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In the world of specialty chemicals, finding a compound that hits the right balance between versatility, stability, and performance can make a real difference in lab work and larger-scale processes. 3,5-Dimethylpyridine, sometimes called 3,5-lutidine, steps into this role with a certain confidence earned over years of practical use. The model most people look for comes with high purity, often tested at levels above 99%, ensuring reliable behavior in research and industry settings. Its chemical identity carries the formula C7H9N, and it weighs in on the conscious side for those keeping track of precise stoichiometry.
The simple act of opening a bottle brings to mind a pungent, often fishy smell—a trait common to many pyridine compounds, and one worth noting for those working in closed environments. This isn’t just a curiosity; it’s a sign of its robust volatility, something practical chemists either love or plan around. In terms of appearance, clarity and absence of color speak volumes about quality. People working with analytical-scale synthesis tend to notice if the sample turns yellow or develops sediment, often a tip-off that impurities have crept in. I’ve seen projects derailed by ignoring something as basic as visual cues.
Handling 3,5-dimethylpyridine feels routine, but its boiling point—right around 172°C—signals that it holds its form well under most lab conditions. Solubility stands out, too. It blends smoothly with most common organic solvents, especially those like ethanol, ether, or acetone. Water solubility matters less for pyridine derivatives, which tend to drift into the realm of nonpolar or slightly basic. Anyone running extractions or crystallizations will appreciate this predictable behavior, reducing the need for trial and error.
Navigating through options for methylpyridines, it may surprise some to learn just how much location matters. The methyl groups on the 3 and 5 positions keep this compound from acting just like its cousins (such as 2,6-lutidine). Even though these molecules look related, the way they handle electron distribution across the ring structure turns out to be distinctive, and I’ve seen this impact basicity, reactivity, and interactions with acids or catalysts. Real-world processes, like selective alkylations or dehydrogenations, often hinge on these small differences. This is not splitting hairs for the sake of it; it’s the difference between a smooth reaction and a headache.
3,5-Dimethylpyridine finds its way onto the bench in several ways. In my own experience, as well as in the published literature, it acts as a reliable base in organic synthesis. People lean into it for reactions where a non-nucleophilic base makes life easier. The steric hindrance from the two methyl groups means it’s less likely to get involved in side reactions, and this helps when the goal is subtle manipulation of sensitive molecules. I’ve seen chemists reach for this compound to steer tricky alkylations or to mop up acids generated during reactions. Sometimes, it’s the only base that calms down an unpredictable mechanism.
Beyond the lab, some manufacturers use it to build other chemicals that end up in everyday products. Its ring structure can serve as a starting point for pharmaceuticals or agrochemicals. This isn’t just a footnote—compounds based on pyridine rings show up across drug discovery, crop protection, and even the dye industry. Those inside R&D pipelines come across 3,5-dimethylpyridine more often than you’d expect. It helps to remember that this is one small piece in a much larger, often invisible, puzzle that affects global industries.
No chemical slips through the cracks when it comes to health and environmental scrutiny. 3,5-Dimethylpyridine stands no exception. The vapor isn’t just unpleasant; it can irritate mucous membranes and, with prolonged contact, may affect liver or kidney function. Good ventilation, proper gloves, and respect for fume hoods aren’t just box-checking; they’re about looking out for your own well-being and those who work nearby.
Disposal brings its own challenges, as with many nitrogen-containing organics. From an environmental standpoint, dumping it down the drain doesn’t square with good stewardship or regulatory law. Waste collection protocols exist for a reason, and having spent time on both sides of chemical procurement and waste management, it’s clear this extends beyond just ticking forms. The risk of groundwater contamination, bioaccumulation, or spreading noxious odors into wider communities creates headaches not just for workers but also for facility managers and neighboring residents. I know research teams who have shifted protocols to cut back on usage, both to avoid regulatory headaches and to reduce the load on waste-processing units.
At a glance, it’s easy to lump all methylpyridines together. The truth is, position matters, not just in theory but in practice. Take 2,6-dimethylpyridine for example—sometimes called 2,6-lutidine—it comes with higher electron density on the nitrogen, shifting its basicity. I’ve watched reactions go sideways because someone used the wrong isomer. Even the melting and boiling points take a hit, showing up in purification protocols and storage requirements.
3,5-Dimethylpyridine fits into those reactions where minimal nucleophilicity and moderate basicity are a must. It holds its own against stronger bases like triethylamine or DBU, carving out a place where balance is needed over brute strength. Against regular pyridine, it stands less reactive toward electrophilic substitution because of those methyl groups, lending more predictability where reaction control beats raw activity.
I remember back in graduate school, working with a team focused on heterocyclic synthesis. Many late nights narrowed in on getting just the right base for a critical reaction step. 3,5-Dimethylpyridine provided just enough suppression of side products without turning the medium too basic. It makes a big difference when purification time drops—columns run faster, chromatograms look cleaner, and less time gets wasted tracking down impurities.
Beyond the academic setting, commercial syntheses benefit from this reliability. People scaling up know that minor shifts in reagent purity or solvent choice can wreak havoc on yields or product quality. Products like 3,5-dimethylpyridine become quiet workhorses, holding the production line steady across thousands of liters. Making quality structures isn’t always glamorous, but consistency and predictability matter when deadlines and budgets loom.
Reliable sourcing counts for more than most realize. Supply chain hiccups create bi-weekly crises for R&D teams and purchasing departments. In the last few years, global disruptions have made sourcing chemicals a day-to-day concern. 3,5-Dimethylpyridine has faced delays due to raw material shortages and shipping snarls. When it’s missing from inventory, entire projects come to a halt, so alternate suppliers or backup stocks keep stress levels down. Trust builds over time, and teams develop sixth senses about which products arrive as advertised and which demand extra QC.
Sustainability grows in importance each year. Questions land on the table about greener synthetic routes or reducing waste. At one point, we started looking into catalytic processes using more benign conditions—reactions that would make less waste or avoid harsh oxidants. Some startups and established firms have developed process improvements that cut emissions or energy use. For academic groups or startups, even small savings in cost or disposal fees add up. The real prize comes when safer or more efficient options enter the market—sometimes through biocatalysis or continuous-flow systems. The push for cleaner chemistry is constant; people talk about green chemistry, but in practice, it’s about solving bottlenecks while protecting health and budgets.
In chemical supply, purity levels predict consistency. I’ve seen the consequences of cutting corners, usually in the form of inconsistent reaction yields or mystery byproducts. 3,5-Dimethylpyridine products rated above 99% purity cost a bit more, but deliver peace of mind when things go right. Laboratories usually pay attention to evidence like GC-MS or NMR analysis as proof of composition. Practical chemists trust but verify, and deviations in these tests cause delays or reruns. This matters for applications where error margins run tight—like pharmaceuticals or fine chemicals—where regulatory compliance checks every detail.
Storage comes with its own quirks. Keeping bottles out of sunlight and away from moisture prevents degradation, so shelving and climate control matter in long-term stockpiles. Caps should seal tightly and bottles labeled clearly; more than once, a misread label or open bottle sent an otherwise orderly project off course. Even in digital inventory systems, human oversight saves chemical stockrooms from costly errors.
Years working in various labs show that the little details often matter most. 3,5-Dimethylpyridine doesn’t usually make headlines, but it finds its way into dozens of processes behind the scenes. Whether it’s catalyzing a reaction, tweaking the acidity, or locking in a key structural change, its supporting role makes the lives of product engineers and chemists easier.
In larger chemical plants, throughput and reproducibility matter. Staff rely on robust materials that don’t bring surprises during upscaling. Conversations with process engineers highlight how trusted compounds like 3,5-dimethylpyridine make transitions from bench to pilot plant smoother. There’s less hand-wringing over reaction times, and safety protocols build on a known track record.
Many facilities take their lead from the experience of teams who have dealt with every possible mishap—ranging from spills to instrument failures. These “walked the walk” stories become folklore in companies, but they shape day-to-day operating procedures. One learns quickly that products with reliable documentation and clear storage guidelines save headaches down the line, whether running a kilo-scale synthesis or troubleshooting batch failures.
Practical chemistry comes down to trust built on results. Stories circulate about bad batches but also about high-quality materials that made development cycles smoother. Decision-makers use a mosaic of data—supplier transparency, batch history, analytical test results, and peer experience—to guide purchasing and handling of 3,5-dimethylpyridine. Strong relationships between lab managers, procurement officers, and technical sales support mean hiccups get addressed with minimal drama.
Regulators play a part by setting guidelines for purity, storage, and transport. Following these rules isn’t about red tape—it’s about ensuring that the same reagent delivers the same outcome, batch after batch. In fields like pharmaceuticals or environmental analysis, consistent results can mean the difference between compliance and setbacks. Product recalls or regulatory penalties leave lasting marks on team morale and company reputation.
The push for improved process safety keeps evolving. In some labs, automation has crept in, meaning chemicals must behave within tighter process parameters. 3,5-Dimethylpyridine’s narrow range of reactivity and stable profile help these systems run with fewer shutdowns or unpredictable incidents. For manual operations, having protocols based on decades of shared knowledge makes for smoother training and better outcomes.
Some current projects focus on using less hazardous surrogates or bulkier bases, but the sweet spot for 3,5-dimethylpyridine persists in balancing reactivity with predictability. Teams continue to re-evaluate procedures to minimize evaporation losses, cross-contact, and worker exposure. Industry moves in sync with new findings—spill-response kits, better glassware, and real-time air monitoring all play their part in safer use.
People in chemical manufacturing live with constant reminders that no process stays static for long. With cost pressures and sustainability mandates, interest grows in finding ways to recycle spent pyridine derivatives or recover solvents from waste streams. Some partners share ideas in symposia and industry working groups; others invest in pilot programs to test new approaches.
Not all solutions arrive overnight. Yet, there are small wins—like switching to renewable raw materials, bolstering green chemistry credentials, or trimming waste disposal costs—each adding up. At universities, collaborations with industry sometimes spark new synthetic routes that eventually reach commercial application. These projects serve as proving grounds, demonstrating that safer, cleaner, and more efficient practices make sense for both business and the environment.
Change sticks best when teams bring everyone up to speed. Repetitive training drills and sharing best practices pay back each year in accident reduction and cost savings. Safety circles back not as empty ritual, but as embedded culture—one where open dialogue about product hazards and handling translates into fewer injuries.
Involvement from every stakeholder—lab techs, R&D scientists, logistics staff—raises the bar. Chemists who understand the nuances of 3,5-dimethylpyridine pass their lessons on to new hires, making for a more capable and confident workforce. Written protocols turn effective when backed by real stories and practical insights from those who’ve weathered past mistakes.
3,5-Dimethylpyridine stands as more than a point on a data sheet. Day in and day out, it’s a tool that helps bridge gaps between bench research and industrial output. Its modest profile belies a presence in a spectrum of industries, from pharma to agriculture to fine chemicals. Users care about what goes in their reactors because tiny differences add up, influencing bottom lines, safety records, and environmental footprints.
Those who source, use, and manage 3,5-dimethylpyridine know the value of reputation—earned by safe, predictable results and guided by practical wisdom. Improvements in supply, safety, and sustainability reflect a broader commitment to smarter science and responsible manufacturing. Through shared experience, improved training, and incremental process improvements, the value of reliable products like this one only grows, shaping both the daily grind and the future direction of the entire chemical field.