4-Methylpyridine-2-carboxaldehyde

    • Product Name: 4-Methylpyridine-2-carboxaldehyde
    • Chemical Name (IUPAC): 4-methylpyridine-2-carbaldehyde
    • CAS No.: 696-30-0
    • Chemical Formula: C7H7NO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    715730

    Cas Number 872-85-5
    Molecular Formula C7H7NO
    Molecular Weight 121.14 g/mol
    Iupac Name 4-methylpyridine-2-carbaldehyde
    Appearance Colorless to pale yellow liquid
    Boiling Point 233-235°C
    Density 1.099 g/cm³
    Flash Point 97°C
    Solubility In Water Slightly soluble
    Refractive Index 1.553
    Synonyms 4-Methyl-2-pyridinecarboxaldehyde

    As an accredited 4-Methylpyridine-2-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 50g of 4-Methylpyridine-2-carboxaldehyde is supplied in a tightly sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 160 drums x 200 kg each, totaling 32,000 kg of 4-Methylpyridine-2-carboxaldehyde, secured safely.
    Shipping 4-Methylpyridine-2-carboxaldehyde is shipped in tightly sealed containers, protected from light, heat, and moisture. It is handled according to hazardous material regulations, with labeling for flammability and toxicity. Ground and air transport comply with local and international rules. Ensure proper documentation accompanies each shipment for safe handling and delivery.
    Storage 4-Methylpyridine-2-carboxaldehyde should be stored tightly sealed in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep the container away from sources of ignition and direct sunlight. It should be properly labeled and stored in a chemical-resistant container, ensuring protection from moisture and air to maintain stability and prevent degradation.
    Shelf Life The shelf life of 4-methylpyridine-2-carboxaldehyde is typically 2-3 years when stored tightly sealed, cool, and protected from light.
    Application of 4-Methylpyridine-2-carboxaldehyde

    Purity 98%: 4-Methylpyridine-2-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity formation.

    Molecular weight 121.14 g/mol: 4-Methylpyridine-2-carboxaldehyde of molecular weight 121.14 g/mol is used in heterocyclic compound manufacturing, where consistent molecular mass guarantees precise stoichiometric calculations.

    Boiling point 217°C: 4-Methylpyridine-2-carboxaldehyde with a boiling point of 217°C is utilized in organic reaction processes, where thermal stability allows for high-temperature conditions without decomposition.

    Stability temperature up to 60°C: 4-Methylpyridine-2-carboxaldehyde stabilized up to 60°C is used in industrial storage and handling, where it minimizes degradation risk during transportation.

    Density 1.14 g/cm³: 4-Methylpyridine-2-carboxaldehyde with density 1.14 g/cm³ is applied in fine chemical formulations, where accurate volumetric dosing enhances formulation accuracy.

    Low water content ≤0.5%: 4-Methylpyridine-2-carboxaldehyde with low water content ≤0.5% is used in moisture-sensitive reactions, where minimized hydrolysis increases product integrity.

    Appearance as clear yellow liquid: 4-Methylpyridine-2-carboxaldehyde in clear yellow liquid form is used in dye precursor synthesis, where visual consistency aids in quality control.

    Melting point -24°C: 4-Methylpyridine-2-carboxaldehyde with melting point -24°C is used in low-temperature catalytic processes, where liquid stability at sub-ambient temperatures facilitates continuous flow operations.

    High solubility in organic solvents: 4-Methylpyridine-2-carboxaldehyde with high solubility in organic solvents is utilized in advanced material research, where rapid dissolution enables uniform reaction mixtures.

    GC assay ≥98.5%: 4-Methylpyridine-2-carboxaldehyde with GC assay ≥98.5% is used in standard analytical calibrations, where precise quantification improves analytical reliability.

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    Certification & Compliance
    More Introduction

    Introducing 4-Methylpyridine-2-carboxaldehyde: A Niche Chemical With Big Possibilities

    Getting to Know 4-Methylpyridine-2-carboxaldehyde

    Chemistry continues to move fields like pharmaceuticals, agrochemicals, and specialty synthesis forward, and a lot of innovation circles around molecules with just the right tweaks. One of those tweaks involves the addition of specific groups to core structures, which shifts chemical reactivity in a way that experts can turn into practical benefits. 4-Methylpyridine-2-carboxaldehyde stands out in this context. Folks who spend time in research labs or custom synthesis work likely know its place among a family of pyridine derivatives, each holding its edge for a reason. The methyl group at the 4 position and the carboxaldehyde at the 2 position together set the tone for what this compound brings to the table.

    Understanding the Structure and Model

    Chemists often look past the name and ask what the structure says. This molecule features the six-membered pyridine ring, with a methyl group at the para spot and an aldehyde function at the ortho position. That setup doesn’t just influence reactivity on paper; it changes how the compound interacts with various reagents, how it behaves as a building block, and what sort of products people can derive from it. Small changes in substitution patterns in pyridine rings tend to mean big shifts in physical and chemical properties, and this is no exception. Its molecular formula sits at C7H7NO, and folks recognize its yellow to pale brown hue, usually packed as a liquid. A boiling point near 220°C helps in certain reaction setups without racing toward evaporation. These features look minor, but to someone in the middle of a synthesis or scale-up, details like that can save the day.

    What It’s Used For in Real Labs

    4-Methylpyridine-2-carboxaldehyde grabs attention mostly in organic and medicinal chemistry. The aldehyde group brings options for forming imines, hydrazones, oximes, and plenty of other derivatives that serve as keys or intermediates in building much larger and more complex molecules. Medicinal chemists sometimes choose it to craft new heterocycles, since pyridines often crop up in molecule libraries and drug candidates. I remember discussions with peers where a single functional group like this changed a project’s direction. The methyl group adds some subtle influences: it helps tweak lipophilicity, metabolic stability, as well as basicity. Such shifts prove valuable when you’re racing against patents or trying to beat solubility roadblocks in a synthesis project.

    Practical Details That Matter

    Materials like 4-methylpyridine-2-carboxaldehyde do more than sit on a shelf; bench chemists and engineers want to know about its temperament in the real world. This compound usually acts as a liquid at room temperature, making it easy to handle in lot sizes ranging from a few grams to kilograms. Its odor leans into that typical pyridine sharpness, something that old hands in the lab recognize instantly. Storage in tightly sealed amber bottles keeps its aldehyde group from picking up water or decomposing over months. These are little realities that affect whether a project hits a snag or not, especially if regular supply chains stumble or if a side reaction builds up from neglecting storage quirks.

    Comparing Similar Tools in the Chemist’s Toolbox

    Not all aldehydes or pyridine compounds behave the same way, and sometimes swapping just one group flips a whole research program. Comparing 4-methylpyridine-2-carboxaldehyde to its close relatives – maybe 2-pyridinecarboxaldehyde with no methyl, or 4-methylpyridine without any aldehyde – shows how one functional group sets the stage for different routes. The added methyl group can steer the course of a reaction, providing extra steric bulk or nudging electronic density around the ring. These effects ripple through to outcomes in reactions like the Knoevenagel condensation or Mannich-type processes. Chemists also notice changes in how easy it is to purify intermediates, extract products, or even comply with regulatory checks, if certain analogues trigger a flag due to toxicity or volatility.

    Why the Specifics Matter—And Why They Don’t Always Get the Spotlight

    It’s easy in daily science to overlook how critical small industries and mid-tier suppliers are in keeping these chemicals available. Specialty compounds like this don’t hit the same headline as massive-volume solvents, but they make a big difference down-chain. Those running a startup, a pilot plant, or a small-scale drug screen often build progress on the backs of access to molecules like this. Companies that maintain consistent quality, low levels of impurity, and batch-to-batch consistency give researchers confidence. I’ve seen entire project timelines hinge on whether a source delivers reasonable certificate of analysis, or whether a batch passes gas chromatography or not. Even tiny variations in purity or impurity levels can create analytical confusion or torpedo a clinical lead.

    Challenges in Handling and Safety Considerations

    Pyridine derivatives bring their own occupational safety stories. 4-Methylpyridine-2-carboxaldehyde shouldn’t get brushed off as just another aromatic aldehyde; seasoned chemists recognize the mix of solubility, reactivity, and odor as points to watch. Wearing gloves, using a fume hood, and ensuring spill procedures rest just a reach away help. This isn’t just about policy—it’s about practical lab culture. One forgotten open bottle, and you’re cleaning up sharp odors or, worse, facing headaches and more.

    Industry Context and Sourcing Insights

    Not every supplier on the market maintains the standards needed for specialty intermediates. In my work with both academic and small industry teams, sourcing sometimes reveals major variations in reliability, especially with chemicals used less frequently or at smaller scale. Intermediates such as 4-methylpyridine-2-carboxaldehyde don’t have global commodity production chains behind them. This means supply uncertainty comes up, especially if a single facility faces regulatory, environmental, or logistical problems. Sourcing strategies sometimes involve keeping relationships with several distributors, not just for cost but for security of supply.

    Regulatory and Environmental Concerns

    The world pays more attention to the environmental impact of chemical manufacturing each year, especially after news stories highlighting industrial accidents or toxic exposures. Pyridine derivatives sometimes carry environmental persistence, bioaccumulation, or workplace safety challenges. Companies handling larger quantities often monitor waste streams, vapors, and disposal practices. Staying ahead of scrutiny not only prevents fines and shutdowns but can also become a badge of diligence for companies hoping to build a stable client base in the pharma and tech sectors.

    Why Some Research Sectors Lean on This Compound

    Medicinal chemistry and agrochemical innovation often depend on rapid creation and screening of new molecules, many built around heterocyclic cores like pyridine. The aldehyde group held at the 2-position unlocks entry into new ligand scaffolds, enzyme inhibitors, coordination compounds, and electronic materials. These advantages feed into growing areas, such as green chemistry, nanotechnology, or diagnostics. I’ve seen grad students carve out a thesis project starting with this one compound, following transformation after transformation to reach a final product published as a lead in a patent.

    Differences That Shape Downstream Outcomes

    It’s tempting to see chemical intermediates as interchangeable. The reality in a working lab proves different. The methyl group does more than add a carbon and a handful of hydrogens—it changes steric access, changes the electron cloud’s distribution, and sometimes creates or blocks specific reactivity pathways entirely. For example, someone working on a metal-catalyzed transformation might find that the methyl group blocks undesired side products, or that it makes product isolation a bit easier. These subtle differences aren’t always in the textbooks, but they matter to people running reactions at scale or pushing to publish.

    Supporting Claims with Facts and Experience

    Academic and commercial literature shows that substitution on heterocyclic rings, including methyl and carboxaldehyde groups, provides control over both reactivity and selectivity in a wide pool of reactions. For example, in classic Suzuki or Heck coupling reactions, addition of a methyl can push electron density, influencing yields or rates. Analytical chemists note that the presence of a methyl group often sharpens signals in NMR or alters MS fragmentation patterns, making identification clearer. Across pharmaceutical pipelines, small differences in starting building blocks like these often cascade forward, affecting everything from tractability of downstream chemistry to the ultimate bioactivity or process cost.

    The Role of Quality and Trace Impurities

    I can recall times when a major reaction failure boiled down to something unglamorous: trace impurities hiding in a lot of intermediate. 4-Methylpyridine-2-carboxaldehyde offers lessons here, since the aldehyde group loves to pick up water or react with trace amines. People in synthesis and analysis circles build reputations on knowing where contaminants lurk and how to clean up or pre-treat batches. Tools like gas chromatography, NMR, and mass spec help, but vendors that provide solid documentation and clear supply chains win more business in the long run, even if their price tags sit a bit higher. It’s not just a paperwork game—clear supply records can spell the difference between a quick fix and an ongoing compliance headache.

    Potential Solutions to Common Issues

    Keeping quality up in limited-scale and mid-scale synthesis starts with good communication with suppliers. Developing protocols for quick in-house testing, even before the main chemistry project gets rolling, stops most disasters before they start. It helps to set up in-house storage with moisture control in mind, maybe adding molecular sieves to storage bottles or checking periodically for decomposition. In the broader supply chain, people working in sourcing and procurement could do more to share quality trends, like updating colleagues on shifts in supplier performance or new sources. It’s worked in my own teams before—accidental breakthroughs came from side conversations about obscure impurities showing up in incoming batches.

    Supporting Sustainable and Safe Use

    The conversation around specialty chemicals now routinely brings up green chemistry, sustainability, and responsible sourcing. Responsible practices in handling and waste disposal matter not just for compliance but for long-term viability in the industry. Researchers and labs that support greener approaches—like using less hazardous solvents, small-scale reactions, or recovery and treatment of waste streams—stand out when grant deadlines and regulation updates hit. Realistically, smaller specialty chemicals outfits don’t always have the same infrastructure as global giants, but creative workarounds and collaborative disposal agreements serve as practical steps. Educational efforts, like routine team training, reduce both environmental impact and the odds of mishandling chemicals like this.

    Real Differences from Other Pyridine Compounds

    4-Methylpyridine-2-carboxaldehyde differs from peers not just in structure, but in the sort of chemistry it unlocks. The methyl group at the 4-position creates options that straight pyridine-2-carboxaldehyde can't match—for example, by shifting product distribution in side reactions, or by making certain functionalizations more selective. Downstream, you can see differences in yields, purification ease, or even how the compound behaves under light or temperature changes. Process chemists often benefit by evaluating a family of related intermediates, but eventually land on one like this because it ticks more boxes for lab performance and process economics.

    Looking Ahead—Opportunities and Room for Improvement

    The world of specialty chemicals remains fast-moving. Those who work in synthesis, drug discovery, or advanced materials always keep an eye out for building blocks that let them both push scientific boundaries and maintain reliable sourcing. As more industries look to differentiate their pipelines—with fresh heterocycles, novel ligands, and unique active ingredients—compounds like 4-methylpyridine-2-carboxaldehyde unlock new routes. Addressing sustainability and cost means not just making smarter choices in the chemistry, but forging stronger partnerships with suppliers, regulators, and peer labs. If more stories circulate about the real-world hurdles and best practices in handling, storing, and sourcing, then others can build on those lessons.

    Conclusion: The Interconnected World of Specialty Organic Intermediates

    Walking the line between routine chemical commerce and frontier research, 4-methylpyridine-2-carboxaldehyde reminds people in the field how deep expertise trickles into many corners that shape scientific and business outcomes. Little choices in molecule design, sourcing, and handling create ripple effects, deciding whether a batch ends up as another shelf item or goes on to anchor a patent, a paper, or a new product line. Those who pay attention to the details—structure, functionality, supply, and safety—find opportunities hidden in plain sight, whether the endgame sits in a pharmaceutical compound, a crop protection molecule, or a diagnostic tool. The story of this compound stands as a kind of case study for both the promise and the practicalities of specialty chemical use, shaping outcomes far beyond its modest bottle and label.