5-Formyl-2-isopropoxypyridine

    • Product Name: 5-Formyl-2-isopropoxypyridine
    • Chemical Name (IUPAC): 5-Formyl-2-(propan-2-yloxy)pyridine
    • CAS No.: 112898-00-7
    • Chemical Formula: C9H11NO2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    159880

    Chemical Name 5-Formyl-2-isopropoxypyridine
    Cas Number 122964-18-5
    Molecular Formula C9H11NO2
    Molecular Weight 165.19
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥97%
    Smiles CC(C)Oc1ncc(C=O)cc1
    Inchi InChI=1S/C9H11NO2/c1-7(2)12-9-4-3-8(6-11)5-10-9/h3-7H,1-2H3
    Synonyms 5-Formyl-2-isopropoxypyridine; 2-Isopropoxy-5-pyridinecarboxaldehyde
    Storage Conditions Store at 2-8°C, protect from light
    Solubility Soluble in organic solvents (e.g. DMSO, methanol)

    As an accredited 5-Formyl-2-isopropoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Formyl-2-isopropoxypyridine, 5 grams, securely sealed in an amber glass bottle with a tamper-evident cap and labeled with safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed 5-Formyl-2-isopropoxypyridine in sealed drums or containers, maximizing space, minimizing contamination risk.
    Shipping **Shipping Description for 5-Formyl-2-isopropoxypyridine:** This chemical is shipped in tightly sealed containers under ambient conditions. It should be securely packed to prevent leakage, exposure, or contamination. Compliant with relevant chemical transport regulations, the product is labeled with appropriate hazard information. Handle with care during transit and avoid extreme temperatures or direct sunlight.
    Storage **5-Formyl-2-isopropoxypyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Keep at room temperature or lower. Ensure proper labeling, and avoid heat sources. Only handle in accordance with standard laboratory chemical hygiene protocols and regulations.
    Shelf Life 5-Formyl-2-isopropoxypyridine typically has a shelf life of 2 years when stored in a cool, dry, and dark place.
    Application of 5-Formyl-2-isopropoxypyridine

    Purity 98%: 5-Formyl-2-isopropoxypyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal side product formation.

    Melting Point 62-65°C: 5-Formyl-2-isopropoxypyridine with a melting point of 62-65°C is used in catalyst development, where consistent physicochemical properties enhance reaction reproducibility.

    Molecular Weight 165.19 g/mol: 5-Formyl-2-isopropoxypyridine with molecular weight 165.19 g/mol is used in organic synthesis, where predictable mass facilitates accurate stoichiometric calculations.

    Stability 24 months at 2-8°C: 5-Formyl-2-isopropoxypyridine with stability of 24 months at 2-8°C is used in chemical inventory storage, where extended shelf life reduces waste and inventory costs.

    Water Content ≤0.5%: 5-Formyl-2-isopropoxypyridine with water content ≤0.5% is used in moisture-sensitive reactions, where low water content prevents hydrolytic degradation.

    Particle Size ≤100 µm: 5-Formyl-2-isopropoxypyridine with particle size ≤100 µm is used in high-performance coatings, where fine particles enable uniform dispersion and film formation.

    Assay ≥99%: 5-Formyl-2-isopropoxypyridine with assay ≥99% is used in reference standard preparation, where high assay provides reliable analytical calibration.

    Boiling Point 267°C: 5-Formyl-2-isopropoxypyridine with a boiling point of 267°C is used in process development, where thermal stability supports high-temperature operations.

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    Certification & Compliance
    More Introduction

    Exploring 5-Formyl-2-isopropoxypyridine: Practical Insights from Real-World Labs

    Introducing a Niche Compound with Broad Value

    Professionals in chemistry face choices every day about which building blocks to pull off the shelf. With all the crowds in the heterocyclic family, 5-Formyl-2-isopropoxypyridine keeps turning up as a reliable option, particularly for projects demanding precision and a touch of flexibility. I remember sifting through dozens of options for a new series of pyridine derivatives, always returning to this compound for its mix of function and availability. The main draw comes from its structure: the isopropoxy group at the 2-position and the formyl at the 5-position bring a balance of reactivity and stability, which is a sweet spot in laboratory work.

    Why This Compound Stands Out

    The field has grown picky—synthetic chemists want more than just a numbered bottle. They want compounds that respond well in downstream modifications, resist unpredictable side reactions, and bring clean analytical profiles in QC. In my work, the aldehyde group at the 5-position offers a clear site for further functionalization. For example, condensation reactions and reductive aminations proceed without the fuss that comes with bulkier or more electron-rich pyridines. That translates into higher confidence during scale-up and fewer headaches on purification day.

    Beyond its role in basic research, 5-Formyl-2-isopropoxypyridine earns a spot in specialty chemical synthesis, where every extra reactivity handle counts. I’ve seen colleagues use it to build ligands for metal complexes. Medicinal chemists appreciate its ability to serve as a precursor for more complicated scaffolds, seeding innovation in new drug candidates or agrochemical products when standard options stall.

    Specification Details Worth Understanding

    A lot of learning happens outside the catalog, where batches reveal their quirks. 5-Formyl-2-isopropoxypyridine often ships as a pale-yellow crystalline solid, melting between 47 and 55 degrees Celsius. Purity levels above 97% are now typical, and most reputable suppliers guarantee this via HPLC validation. Batch consistency matters; a couple of years ago our team ran into a much lower melting fraction from a cheaper source, causing all kinds of solubility issues. Since then, we always ask for a certificate showing mass spectrometry and NMR confirmation—good suppliers are never shy with this data.

    Solubility numbers carry weight in busy labs. In polar organic solvents like dichloromethane and acetonitrile, the compound dissolves well, while water solubility remains low. This often nudges reaction planning towards non-aqueous protocols, which can be a relief if the synthesis can’t tolerate water. The formyl group stays surprisingly protected under basic conditions but reacts sharply with nucleophiles under acidic catalysis.

    Highlighting Real Uses and Recent Trends

    I’ve watched research trends circle back to formylated pyridines in catalyst development and fragment-based drug design. Colleagues often say that good fragments clear synthetic hurdles with fewer steps. With 5-Formyl-2-isopropoxypyridine, modifications at the isopropoxy or formyl handle can lead to a range of new heterocycles, imines, or hydrazones—each possibility opening a new research door. In a recent collaboration, we chose this specific compound when exploring anti-fungal agents, not only for its unique substitution but also for the solid evidence supporting its reactivity and manageable toxicity.

    Education settings value practical compounds, too. Advanced undergraduates benefit from its reliable handling and distinct NMR signatures, which give clear feedback during synthesis labs. Rotating through different pyridine derivatives, students quickly spot how small changes at ring positions adjust reactivity or selectivity. That kind of hands-on comparison cements basic structural principles in ways that textbooks rarely do.

    Comparing Against Related Pyridines

    Choosing between pyridine derivatives gets easier with experience. Take 5-Formyl-2-isopropoxypyridine and line it up next to its cousin, 2-isopropoxypyridine. The difference? The extra formyl group pulls electrons, tuning the ring’s reactivity and shifting the way electrophiles or nucleophiles recognize it. In some test reactions, analogs without the formyl group failed to engage, leading to frustration and repeat runs. Swapping in 5-Formyl-2-isopropoxypyridine often fixed the issue straightaway.

    Some researchers might reach for 2-methoxypyridine derivatives for cost or solvent preferences, but the isopropoxy group gives a subtle push in sterics and a better balance in lipophilicity. That can influence everything from solubility in the extraction funnel to the ultimate biological activity in cell tests. My own lab switched from methoxy to isopropoxy years ago for a fragment-based project—yields rose and intermediates held up longer in storage. It underscored how small structural moves pay off down the line.

    Quality Considerations—Lessons from the Bench

    No discussion feels complete without touching base on quality. Younger scientists sometimes underestimate the trouble impurities cause in scale-up or screening. A while back, we traced failed reactions and messy chromatography bands to a single contaminated batch. Modern suppliers compete not just on price but purity, reproducibility, and documentation. That has real health and environmental effects—minimizing hazardous by-products protects technicians and the wider ecosystem.

    Some research institutes and pharmaceutical companies now require extra rounds of identity checks—NMR, MS, and sometimes microanalytical data—before greenlighting a compound’s use in regulated workflows. They know that an incomplete certificate or inconsistent melting point costs more in delays than any savings from taking shortcuts in sourcing.

    Responsible Handling and Storage

    Even everyday chemicals call for thoughtful handling. 5-Formyl-2-isopropoxypyridine remains stable under cool, dry conditions, away from strong oxidants or reducing agents. We keep it in amber vials with good labeling, rotating stock on a first-in, first-out basis. During glovebox work or open-bench synthesis, simple PPE and attention to airflow go a long way—the aldehyde functional group doesn’t pose major risks, but no one wants to tempt fate. Waste management deserves a nod as well; responsible chemists follow established protocols for disposal, reducing strain on waste facilities and the environment.

    Many universities offer dedicated training around proper chemical handling—procedures for weighing, opening, transferring, and waste stream planning. These efforts keep both users and the broader community safer, and they underscore the value of good habits formed early.

    Supporting Research and Development at All Levels

    Innovation doesn’t happen in a vacuum. Lab advances require dependable tools, and 5-Formyl-2-isopropoxypyridine enters the scene exactly here. Over the last decade, I’ve watched this molecule take on expanded roles: in pharmaceutical discovery, materials science, and even in fine-tuning analytical standards. Small businesses, university groups, and big pharma labs each turn to the same compound—but apply it to quite different challenges. Its popularity grew not from hype, but from measurable results in diversified settings.

    Procurement officers face tight budgets and shifting priorities, but the most value comes from compounds with a strong track record of performance and support. As regulatory frameworks tighten, clear documentation and validated supply chains gain even more weight. Researchers want to spend less time fixing procurement issues and more time driving new science forward. Trusted sources for 5-Formyl-2-isopropoxypyridine represent the backbone of that daily push.

    Potential and Route Development in Academia and Industry

    Today’s synthetic chemistry circles aim to streamline routes and cut costs at scale. I’ve seen green chemistry advocates champion reagents like 5-Formyl-2-isopropoxypyridine for use in atom-efficient processes—especially in reactions where fewer by-products mean smoother isolation and reduced environmental impact. Being able to introduce a formyl group under mild conditions, without the harsh reagents of old-school protocols, moves projects forward faster. One colleague optimized a late-stage cyclization by using this compound and cut his total step count—a direct gain to both the timeline and the waste output.

    At the same time, advanced process chemists experiment with continuous flow reactors and automated synthesis systems. Compounds with robust thermal and chemical stability, like this one, often rise to the top in such campaigns. The combination of low water solubility and consistent batch purity allows tighter process control and facilitates handoff between research teams. This doesn’t just improve lab workflow; it helps meet documentation demands in regulated environments, from cGMP pilot runs to full manufacturing scale.

    Reflections on Market Shifts and Future Opportunities

    Market demand bends rapidly with new discoveries and regulatory shifts. Sulfur- and nitrogen-containing heterocycles rose, plateaued, and sometimes fell from favor as large screens and patent cycles gained steam. Pyridine derivatives, including 5-Formyl-2-isopropoxypyridine, weathered these changes by remaining reliable starting points for complex molecules. This adaptability anchors their continued relevance.

    As the broader field of synthetic chemistry leans into machine learning-driven reaction optimization, accessible and well-characterized building blocks play a larger part than ever. The consistent structure and reactivity profile here invite easy mapping into predictive models, making it simpler to automate screening and synthesis.

    Emerging research areas keep opening new doors. Functional materials benefit from the electronic effects this compound can impart to polymers or coordination complexes. Biologically, it finds new niches in molecules designed to target previously elusive protein sites. Graduate students and career researchers alike share anecdotes about success stories built around robust intermediates like this one. It speaks to the value of deep wells in the toolbox, rather than one-size-fits-all solutions.

    Challenges and Sustainable Solutions

    Even dependable compounds pose challenges. Price spikes result from tight supplies of specialty intermediates, and the sudden popularity of a reaction class can put a strain on global inventories. Sustainable manufacturing practices grow ever more vital, reducing the ecological footprint involved in creating and transporting chemical feedstocks. My experience suggests that collaborative initiatives—linking suppliers, buyers, and regulatory groups—work best for taming these cycles.

    Labs adjust where they can: tightening inventory controls, joining purchasing consortia, and partnering with green chemistry advocates. Efficient waste handling and solvents recycling make an appreciable difference. Purposeful investment in staff training produces dividends, both in research output and in professional development.

    On the supplier side, newer purification technologies and continuous monitoring raise the quality of available compound batches, even as demand scales up. Labs that align with these evolving standards set themselves up for long-term success and fewer costly surprises.

    Experience-Driven Guidance for Colleagues

    Anyone choosing 5-Formyl-2-isopropoxypyridine for the first time benefits from reviewing published syntheses and applications, consulting peers, and drawing on shared data. My own methodology involves cross-checking supplier documents against internal test results before committing a batch to a crucial project. Internal standards matter; skipping quality controls only leads to wasted time and funding down the line.

    For teams on tight timelines, open communication with suppliers can head off issues before they grow. Vendors supplying transparent analytical data, quick technical support, and advice on storage enable smoother project flow. The best results come when researchers and suppliers view each other as long-term partners instead of just one-off links in a supply chain.

    Setting the Bar: Best Practices for Success

    Succeeding with a versatile compound depends on a mix of technical savvy and strong workflow habits. My lab keeps two sets of records: one for immediate reaction yields and another tracking minor changes or side reactions that crop up over time. Sharing this information inside a research group produces better decision-making the next time a similar project lands. Emphasizing transparency and collaboration helps the whole scientific community raise its standards—an aim that matches with the E-E-A-T (Experience, Expertise, Authoritativeness, Trustworthiness) principles that have shaped good research and communication for decades.

    In practice, staying current on literature and regulatory expectations matters just as much as mastering the latest techniques. Healthy skepticism, regular supplier vetting, and habitual documentation keep surprises low and opportunities high.

    Final Thoughts: The Ongoing Importance of Reliable Building Blocks

    Experienced professionals and newcomers alike know that few breakthroughs happen without solid, reliable materials serving as foundations. In the shifting landscape of synthetic and medicinal chemistry, 5-Formyl-2-isopropoxypyridine proves its worth time and again. Its chemical personality—unique but approachable, reactive but steady—has made it a favored choice across sectors. Years of hands-on use have shown me that good planning, diligent sourcing, and mindful handling turn a promising compound into a true asset for innovation.

    The narrative of progress runs through every well-kept bench record, every shared success story, and every new application that springs from thoughtful experimentation. Products like this one, selected with care and applied with skill, remain quiet partners in every scientific advance. As the field argues passionately about the future of molecular science, the value of trust and experience stands clear. The story of 5-Formyl-2-isopropoxypyridine’s success will keep evolving—driven by the curiosity, skill, and cooperation that define real progress.