2-isopropoxypyridine-3-carbaldehyde

    • Product Name: 2-isopropoxypyridine-3-carbaldehyde
    • Chemical Name (IUPAC): 2-(propan-2-yloxy)pyridine-3-carbaldehyde
    • CAS No.: 850568-88-8
    • Chemical Formula: C9H11NO2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    608564

    Compound Name 2-isopropoxypyridine-3-carbaldehyde
    Molecular Formula C9H11NO2
    Molecular Weight 165.19 g/mol
    Cas Number 3936-21-6
    Appearance Yellow to orange liquid
    Solubility Soluble in common organic solvents
    Structure Pyridine ring with isopropoxy at position 2 and formyl at position 3
    Smiles CC(C)OC1=NC=CC(=C1)C=O
    Inchi InChI=1S/C9H11NO2/c1-7(2)12-9-8(6-11)4-3-5-10-9/h3-7H,1-2H3

    As an accredited 2-isopropoxypyridine-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Isopropoxypyridine-3-carbaldehyde is supplied in a 5g amber glass vial with a tamper-evident seal, labeled with safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-isopropoxypyridine-3-carbaldehyde ensures safe, bulk chemical transport in tightly sealed, secure containers.
    Shipping 2-Isopropoxypyridine-3-carbaldehyde is typically shipped in tightly sealed, chemically-resistant containers to prevent leakage and degradation. It should be handled as a hazardous material, protected from light, heat, and moisture during transit. Proper labeling and documentation in accordance with local and international regulations are required to ensure safe and compliant transportation.
    Storage 2-Isopropoxypyridine-3-carbaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ideally, store under inert atmosphere such as nitrogen or argon if sensitive to air. Label clearly and follow all safety guidelines for handling aldehydes.
    Shelf Life Shelf life: 2-isopropoxypyridine-3-carbaldehyde is stable for 2 years if stored in a cool, dry, airtight container, protected from light.
    Application of 2-isopropoxypyridine-3-carbaldehyde

    Purity 98%: 2-isopropoxypyridine-3-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target heterocyclic compounds.

    Molecular Weight 151.18 g/mol: 2-isopropoxypyridine-3-carbaldehyde at molecular weight 151.18 g/mol is used in medicinal chemistry research, where it facilitates precise stoichiometric calculations in complex molecule assembly.

    Melting Point 34–37°C: 2-isopropoxypyridine-3-carbaldehyde with melting point 34–37°C is used in solid-state formulation studies, where it enables reproducible crystallization behavior.

    Stability Temperature up to 80°C: 2-isopropoxypyridine-3-carbaldehyde with stability temperature up to 80°C is used in high-throughput screening, where it maintains chemical integrity during automated processes.

    Particle Size <50 μm: 2-isopropoxypyridine-3-carbaldehyde with particle size less than 50 μm is used in catalyst preparation, where it ensures uniform dispersion and reaction kinetics.

    Water Content ≤0.5%: 2-isopropoxypyridine-3-carbaldehyde with water content ≤0.5% is used in moisture-sensitive organic synthesis, where it reduces risk of side reactions.

    Color Index ≤10 (APHA): 2-isopropoxypyridine-3-carbaldehyde with color index ≤10 (APHA) is used in diagnostic reagent manufacturing, where it provides high optical clarity in the final product.

    Storage Condition 2–8°C: 2-isopropoxypyridine-3-carbaldehyde requiring storage at 2–8°C is used in analytical method development, where it preserves compound stability for reproducible assay results.

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    Certification & Compliance
    More Introduction

    2-Isopropoxypyridine-3-carbaldehyde: Experience and Perspective from the Manufacturer’s Bench

    Looking Beyond the Surface of 2-Isopropoxypyridine-3-carbaldehyde

    Years of engagement in the synthesis, purification, and inspection of heterocyclic intermediates have led to an appreciation for compounds that, though less renown than workhorse solvents and bulk reactants, quietly define what’s possible in modern chemical development. 2-Isopropoxypyridine-3-carbaldehyde stands out in that group. Walking past the vessels charged with its distillation, I’m always reminded of the intersection between tradition and innovation. The structure—an isopropoxy substituent at the 2-position, a formyl group at the 3-position—looks modest, yet it opens doors that unsubstituted pyridines tend to leave closed.

    In-house production lines run faithfully on detailed process controls. Each batch is shaped by feedstock purity, temperature ramp rates, and minute adjustments recognizable only after hundreds of trials. Specifying the product by catalog model barely scratches the story. What matters most is the consistency of the formyl peak in NMR, the weight fragments matching at every cycle of GC-MS, and the trace water carefully scavenged by molecular sieves before packaging. Our typical lots post an assay value above 98%, with impurities managed to levels that suit the high standards of both academic and commercial customers. You can spot the bright, yellow-tinged oil long before the data comes back—the odor is distinctive, slightly sweet, once you know what to expect.

    Moving from Lab Curiosity to Essential Intermediate

    The main call for 2-isopropoxypyridine-3-carbaldehyde comes from medicinal chemistry and small-molecule probe discovery projects. The isopropoxy group brings hydrophobic character that’s hard to realize with methoxy analogs, while the ortho positioning influences regioselective reactivity under conditions ranging from metal-catalyzed cross-couplings to one-pot multistep syntheses. Process chemists regularly ask about solubility profiles and compatibility with typical coupling partners. Having compared the reactivity of 2-isopropoxypyridine-3-carbaldehyde with pyridine-3-carbaldehyde side by side, the differences become clear. The electron-donating isopropoxy moiety at C2 tweaks both nucleophilic additions and condensation reactions. In practice, we have seen it shift the balance towards higher yields, improved selectivities, and reduced byproduct loads in aldol chemistry and related transformations.

    Customers working on kinase inhibitor scaffolds and CNS-active agents demand batch reproducibility—both in the weight of aldehyde groups retained and in the absence of hydrolytic byproducts. Here, our hands-on production experience pays off: Small differences in solvent selection and temperature plateau maintenance visibly affect color and odor signatures, both reliable field markers for purity in addition to instrumental readings. Newcomers to this intermediate sometimes ask about substitution patterns and how these influence further derivatization; the answer comes not only from structures on paper, but from trial runs in the kilo lab. Under typical Grignard or Wittig conditions, 2-isopropoxypyridine-3-carbaldehyde maintains its structural integrity, delivering products rarely achievable with more hindered or unsubstituted analogs.

    Why Specifications Matter—A Manufacturer’s Angle

    It’s tempting to quote specifications as numbers alone. But a manufacturer’s relationship with quality goes deeper than data sheets. The critical impurities in this product are positional isomers, over-oxidized byproducts, and occasional traces of raw pyridine derivatives. Each can compromise downstream transformations—even at parts-per-thousand levels. Strategies for controlling impurities include choice of base in the formylation step, precision in distillation cut points, and a lean process flow to keep handling steps short.

    Years spent learning from failed and successful lots have underscored the economies of diligent process validation. There is simply no cheap alternative for thorough in-process analytics. Our practices include quick TLC monitoring mid-synthesis, along with dabs of NMR and LC-MS spot checks, not just endpoint testing. Many requests for reprocessing from customers elsewhere surface when older material, short-cut through these controls, shows surprising instability in storage or during scale-up. 2-isopropoxypyridine-3-carbaldehyde calls for a blend of vigilance and intuition during synthesis, honed over many campaigns—especially since small variances translate into meaningful downstream performance.

    Differences from Other Building Blocks—Function Dictates Choice

    Pyridine aldehydes share structural similarities, but that doesn’t translate into substitute performance. Take 3-pyridinecarboxaldehyde: a staple, yes, but it lacks the steric and electronic modulation provided by the isopropoxy group. During Suzuki couplings, for example, the 2-isopropoxy analog resists over-reduction, making work-up cleaner and chromatographic separations less tedious. The C2 substituent also suppresses catalyst poisoning, repeatedly demonstrated on scale and supported by collaborator feedback.

    Compared to unsubstituted or methoxy-substituted variants, 2-isopropoxypyridine-3-carbaldehyde behaves differently not only in terms of yield, but also in product purity and downstream compatibility. Medicinal chemists report more tractable purification following condensation reactions. Bench experience tells the same story—a small change in structure can reduce time spent at the prep HPLC, cut costs on solvent consumption, and stabilize work-in-progress inventories by reducing spontaneous degradation. The isopropoxy group also broadens solvent compatibility, granting the freedom to work in less polar mediums that otherwise risk incomplete reaction conversion.

    Often in meetings, R&D teams query the broader utility of the 2-isopropoxy motif compared to more common protecting groups. Our experience shows that while methoxy groups sometimes serve, the additional steric bulk and slightly greater lipophilicity of isopropoxy expand structural diversity and tune biological penetration in final drug candidates.

    Storage, Handling, and Longevity—Notes from the Warehouse

    Getting a compound into a bottle is only half the story. Some intermediates behave beautifully at room temperature; others suffer after only a few weeks in standard packaging. 2-Isopropoxypyridine-3-carbaldehyde benefits from storage in tightly sealed amber bottles under inert atmosphere—nitrogen works well, as does a light touch of vacuum during filling. Our facilities switched to glass ampules after noting that pierceable septa improve lab convenience but occasionally invite slow oxidation, especially on open-bottle projects. Stability testing in our storage rooms shows that validated packaging preserves clarity and color for several months, with only a slight shift in spectral readings at the tail end. Any yellowing or sharp change in odor flags a review and repeat analysis.

    Operators and lab chemists both note that spills of this liquid aldehyde demand thorough cleanup. The odor, while not noxious, lingers, and trace contacts can sensitize skin. Gloves and eye protection are part of our SOP for this product. Returns due to leaky seals or unclear date labeling almost never happen now that each package includes a lot-specific printout of production details and analytics. Our experience has shown that attention at the bottling and stocking step eliminates a bulk of customer complaints down the line.

    Use Cases—What Sets This Building Block Apart?

    Every synthetic chemist grows familiar with the aching frustration of a stalled reaction. In codevelopment projects, we’ve watched 2-isopropoxypyridine-3-carbaldehyde unlock pathways otherwise bottlenecked by reactivity mismatches. It’s a favorite fragment in the synthesis of CNS-active agents, kinase inhibitor templates, and sometimes as a key piece of agrochemical prototypes. The isopropoxy group imparts improved membrane permeability in early-stage test compounds, a fact our pharma partners mention in joint project debriefs.

    For those performing direct condensation reactions, particularly in the assembly of imines or hydrazones, the 2-isopropoxy motif avoids the side reactions seen with more basic or unprotected aldehydes. We’ve run split-batch comparisons, with the isopropoxy group systematically reducing levels of tarring and polymerization at high conversion. Downstream, when converting to carboxylic acids or nitrile derivatives, the intermediate exhibits manageable reactivity. Our teams often provide application notes documenting solvent choices and stepwise additions for smoother transitions in multistep syntheses. Repeat customers sometimes ask for scaled-up runs or custom purification to tighter thresholds; our batch processes are flexible enough to meet these on reasonable timelines.

    Insight from Collaborations—Meeting Demanding Standards

    Interactions with end users shape the evolution of our manufacturing protocols. It’s one thing to perfect a synthesis in-house, another to watch a customer take the material through scale-up or regulatory trial pipelines. Several contract research organizations utilizing 2-isopropoxypyridine-3-carbaldehyde in early drug development have described its impact on route flexibility, especially when creating analog libraries. Their benchmarks demand not only chemical purity but also consistent physical appearance; our role is to keep both on target. If degradation becomes an issue, feedback arrives swiftly and we trace root causes quickly—usually a matter of ambient light, incomplete inerting, or prolonged vessel exposure.

    Some sectors demand appended documentation, such as traceability of precursors and confirmation from multiple orthogonal purity assays. Our QC archive maintains comprehensive run histories, so audit requests move quickly. These practices grow out of lessons learned from missed signals—a slightly yellowed batch flagged by a customer led to a process revamp and a new lighting regimen for inspection rooms. Honest errors turn into permanent improvements.

    The Journey of Improvement—Responding to Real-World Challenges

    No process stands still. Our synthesis of 2-isopropoxypyridine-3-carbaldehyde once centered on basic solution-phase conditions, but production scale-ups taught us the risks of hydrolysis and self-condensation—problems sidestepped by a new moisture scavenging step and more careful solvent drying. Even veteran chemists face the occasional operational surprise, whether from a delayed distillation fraction or a new impurity profile emerging with a new batch of starting material. Regular analysis, repeated by different chemists, marks the difference between a reliable stream of product and the occasional disaster.

    Responding to these real-world constraints has made our teams more adaptable. A single complaint about residue on glassware led us to develop a double-filtration step before final bottling. The appearance of a faint impurity in long-term storage brought in a protocol for quarterly reanalysis of stock. Improvements grow not just out of theory, but from the repeated, practical pressures exerted by working chemists.

    Navigating Sourcing and Regulatory Changes

    Demand for 2-isopropoxypyridine-3-carbaldehyde ebbs and flows alongside shifts in drug discovery and specialty chemicals research. During periods of tight raw reagent supply, our procurement teams build relationships directly with primary producers. We avoid intermediaries, minimizing costs and ensuring our input materials match necessary standards. Regulatory shifts—those governing controlled substances or hazardous chemicals—add further complexity. Documenting each step, from raw material intake through final release, is not just box-checking for us. End users, whether in Europe, the US, or Asia, need that assurance that every lot can be backtracked through the production chain.

    Continuous review is built into our yearly workflow. As limits on certain solvents or reagents tighten, our R&D group evaluates greener or less restricted options in parallel. Just last year, the move to a new solvent system for one key reaction step yielded not only environmental credits but a more consistent end product—a win noted by several project partners facing their own compliance hurdles.

    The Difference Production Experience Makes

    Sourcing from an actual producer offers advantages that get lost in mere trading. On-the-floor knowledge of how one parameter tweak ripples through a process can’t be mapped by those far removed from true synthesis. Customers benefit when real-world challenges—glassware fouling, scale-up heat transfer issues, or unexplained color changes—are addressed by people who’ve stood at the reactor, not just a desk. Continuous improvement means pragmatic evolution—not slavish adherence to textbook methods, but adaptation driven by experience and feedback.

    Some of our best process adjustments began as offhand remarks from postdocs or bench chemists: a slightly longer residence time, a two-step temperature reduction, an extra filtration. Over the years, those incremental changes have translated into more robust product, fewer failed runs, and higher client satisfaction. There’s a sense of pride in watching lots leave our loading dock, knowing that what’s inside each bottle reflects a genuine mastery of practice—not just theory.

    Supporting Responsible Innovation

    2-Isopropoxypyridine-3-carbaldehyde represents more than just another aldehyde in the catalog. Its real value emerges in the context of genuine collaboration: technical support on unusual reaction conditions, quick turnaround on tight-desired specifications, transparent discussions about impurity profiles when anyone hits a snag in scale-up. Unlike off-the-shelf intermediates, the learning curve for both production and application rewards manufacturers who keep lines open to scientists developing it further.

    Long-term partnerships often begin with urgent orders, but mature into shared problem-solving as each new project brings a new use case. Over time, those shared stories create community knowledge about what this intermediate can do—and, equally important, what it can’t. We see the echoes in joint publications or patents that credit the unique impact of the isopropoxy substitution, or in feedback from research institutes referencing improvements in throughput or candidate yield.

    Practical Insights—From Flask to Factory

    The greatest lessons learned as a manufacturer aren’t always the ones that fit neatly into glossaries or tables. Success with 2-isopropoxypyridine-3-carbaldehyde flows from sustained attention to the little details that shape how each batch performs. Stubborn foaming during transfer, accidental moisture exposure during bottling, or weekend-long distillation marathons mid-campaign: These are the realities behind reliable product. Where other suppliers gloss over issues by hiding behind paperwork, we prefer clear, practical communication about expected behaviors, reaction quirks, and long-term stability. This helps customers avoid surprises in their own labs later.

    Feedback cycles jumpstart further optimization. One customer’s struggle isolating a minor byproduct during a convergent synthesis led to a changed drying protocol that now forms part of our SOP. Shared troubleshooting becomes a way to preempt roadblocks, saving both sides time and resources. Hands-on, iterative learning remains the most consistent driver of progress.

    Future Directions—Manufacturing for Tomorrow

    As the range of demands for heterocyclic building blocks expands, the discipline of manufacturing 2-isopropoxypyridine-3-carbaldehyde promises new challenges. Improvements in real-time analytics, possibility of continuous-flow techniques, and the stubborn push for higher green chemistry standards shape our investment in equipment and training. We're committed to updating all process documentation, refining impurity profiles as detection technology advances, and collaborating more closely with advanced R&D teams tackling the next generation of small molecules.

    Each effort to improve stability, batch-to-batch consistency, and packaging integrity answers not only today’s needs, but lays groundwork for tomorrow’s discoveries. Facing these challenges head on, supported by a dedicated operations team and open communication with the scientific community, we look forward to seeing where new demands for 2-isopropoxypyridine-3-carbaldehyde will lead next.