3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    • Product Name: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    • Chemical Name (IUPAC): 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    • CAS No.: 1044587-21-2
    • Chemical Formula: C15H12N2O2
    • Form/Physical State: Solid
    • 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

    672012

    Iupac Name 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    Molecular Formula C15H12N2O2
    Molecular Weight 252.27 g/mol
    Cas Number 1434211-30-1
    Appearance off-white to pale yellow solid
    Melting Point 168-172°C
    Smiles COC1=CC=C(C=C1)C2=CN3C=CN=CC3=C2C=O
    Solubility soluble in DMSO, methanol, and dichloromethane
    Purity typically >98%
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, white screw cap, chemical label displaying structure, name, molecular formula, CAS number, and hazard pictograms.
    Container Loading (20′ FCL) The 20′ FCL container is loaded with securely packed drums of 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde, ensuring safe chemical transport.
    Shipping The chemical `3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde` is securely packaged in airtight, chemical-resistant containers. It is shipped in compliance with all relevant regulations, protected from light and moisture, and clearly labeled with hazard information. Appropriate documentation and safety data sheets accompany each shipment to ensure safe handling and transport.
    Storage 3-(4-Methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Store at room temperature, and ensure proper labeling and safety precautions to prevent accidental exposure or contamination.
    Shelf Life Shelf life of 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde is typically 2 years when stored cool, dry, and protected from light.
    Application of 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    Purity 98%: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with 98% purity is used in pharmaceutical synthesis, where high product yield and minimal impurities are ensured.

    Melting point 155°C: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with a melting point of 155°C is used in solid-state form screening, where consistent crystallization behavior improves batch reproducibility.

    Stability temperature 80°C: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with a stability temperature of 80°C is used in chemical research, where prolonged storage stability enables reliable experimental outcomes.

    Molecular weight 251.27 g/mol: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with a molecular weight of 251.27 g/mol is used in medicinal chemistry, where precise compound dosing enhances structure-activity relationship studies.

    Particle size <10 µm: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with particle size below 10 µm is used in high-throughput screening, where rapid dissolution accelerates bioassay development.

    Solubility in DMSO 50 mg/mL: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with solubility at 50 mg/mL in DMSO is used in compound library preparation, where high concentration solutions facilitate automated dispensing.

    Optical purity >99% ee: 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with optical purity greater than 99% ee is used in asymmetric synthesis research, where enantiomer-selective outcomes are maximized.

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    Certification & Compliance
    More Introduction

    Introducing 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    Trust Built Through Chemistry

    Manufacturing specialty chemicals sometimes feels like old-fashioned craftsmanship: careful steps, tested batches, always learning from raw material to end result. In our plant, we focus on mastering every detail of each molecule we bring to market. Over years of refining our processes and troubleshooting the surprises that come up in scale-up, we've learned a lot about stability, purity, and reaction byproducts—especially with complex heterocycles. One compound we’re especially proud to get right is 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde.

    From Lab Bench to Full Scale: What Sets Our Product Apart

    Chemists in pharmaceutical R&D and material science don’t always see the challenges that come with making multi-ring molecules at scale. Reactions are rarely as gentle or efficient outside the flask as they appear in papers. Early on, we struggled with air sensitivity and inconsistent yields for this compound—especially at the purification step, where sticky byproducts threw off crystallization. We’ve since overhauled our protocols and now consistently deliver batches with high purity, free of common aldehyde impurities and colored byproducts.

    Our batches of 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde carry a minimum assay of 98%, checked by HPLC and further confirmed with NMR. Water content never crosses our internal cutoff thanks to strict drying and packaging methods. Particle size and flow properties matter too, especially for customers feeding this material directly to downstream syntheses. We test each lot to ensure good handling—not too staticky, not prone to caking, and easy to transfer by scoop, spatula, or automated feeder.

    Compared with similar aldehyde-functionalized imidazopyridines, our compound stands out for its consistent color and low residual solvent profile. Too many batches on the market arrive tan or brown from oxidative side reactions, which create unpredictable behavior in later chemistry. Our quality control team spots shifts in the NMR—aromatic signals from phenyl and pyridine rings should stay sharp, not broad or missing. We do not pass batches with unresolved impurities, since those traces have tripped up more than one scale-up run for peptide and API chemists.

    Applications Grown Out of Real Problems

    This molecule shows up in a surprising number of medchem libraries and screening sets for kinases, GABA analogs, and potential neuroactive compounds. The methoxyphenyl group improves both solubility and metabolic stability in some structure-activity relationship studies. Customers tell us their previous sources caused more headaches than breakthroughs—fouled reactors and unexpected HPLC peaks can shut down a whole week’s worth of work. We designed our manufacturing line to minimize exposure to air and moisture, keep headspace oxygen low, and pack each shipment immediately after QC signoff.

    Discovery chemists often comment on how rapidly they can build out combinatorial libraries starting with this aldehyde. The functionality at the 1-position opens it up to a range of condensation and reductive amination sequences, allowing for modular addition of amines and other nucleophiles. The imidazopyridine core itself is attractive for both its rigidity and its electronic properties—ideal for medicinal chemists optimizing for target binding or function as molecular probes. We’ve noticed a steady shift: customers request fewer “alternative” substitutions year after year, preferring to start directly from the 3-(4-methoxyphenyl)-substituted version, thanks to its more predictable downstream chemistry and biological performance.

    Our experience shows that a misstep in upstream quality leads to headaches all along the line. Intermediates that sit too long or are exposed to trace acids or bases can develop aldehyde hydrates or unwanted adducts. Once those slip into your process, they’re hard to purge—especially for research teams without large prep chromatographs or in-house analytical support. By keeping our process closed and minimizing transit time from final reaction to packaging, we lower the chance of these stability failures carrying downstream.

    Beyond the Batch: Supporting Customer Chemistry

    We document the critical control points in every batch, keeping digital and hardcopy logs of performance parameters. Sometimes a customer calls with a failed coupling or a strange NMR signal, and we can trace the entire path back—lot assignment, process temperature, time in storage, even the solvent lot number. We maintain samples of every batch so we can rapidly retest and compare with reference spectra. Over time, these practices let us sharpen our process and head off potential issues before they reach the customer.

    Scaling up from gram through multi-kilo production introduced challenges at every step. We keep the reaction under inert atmosphere to prevent oxidation, and employ low-temperature crystallization routines to favor the desired isomer. Our staff monitors for off-odors or subtle changes in consistency—early warnings of byproduct buildup. Because aldehyde compounds can react even with modest air exposure, we use lined drums and triple-sealing for shipping, not just standard plastic jars.

    Technical questions come up often. Does the product dissolve easily for high-throughput screening? Are there long tails in HPLC? Does it behave differently at higher loading in solid-phase synthesis? Our support team, who spend half their time on the production floor, know the answers because they’ve handled the compound: watched it run on the filter, felt it in the glovebox, prepped samples for QC.

    Occasionally, a customer needs a larger quantity or tighter specs than our regular offering. In these cases, we adjust our process: alter solvent, cooling speed, or crystallization seed to pull a narrower size distribution, or run final batches through additional purification steps. For respiratory or CNS program leaders, even trace impurities raise red flags. We phone or video chat directly, sharing lot data and spectra so customers know exactly what they're working with—not just a catalog number but a batch they feel confident to take further in the pipeline.

    Feedback loops with clients shape the evolution of our process. Clients have flagged batch-to-batch differences in density or color under certain warehouse conditions. We responded by optimizing humidity control in storage and packing lines, noticing a direct improvement in material reproducibility. Others pointed out interference from packaging leachates, prompting us to switch to higher-grade liners and revalidate storage protocols. Each revision, large or small, makes a real impact on daily lab results down the chain.

    Comparing to Other Related Compounds

    Chemists might be choosing between several aldehyde-functionalized imidazopyridines or even different positional isomers when building new analog libraries. Direct isomers, such as 2-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde, show different reactivity—particularly at the core ring junction and in electronic distribution over the pi system. We’ve run side-by-side comparisons in test reactions with alkyl amines and noticed that the para-methoxy substitution on the phenyl boosts reaction rates and helps suppress unwanted polymerization side reactions.

    Some competitors ship material with higher residual metal content due to incomplete scavenging during catalyst workup. Our team deliberately runs small-scale dummy trials with each new lot of catalyst, confirming full removal prior to workup. Trace metal content, especially palladium or copper, can poison downstream reactions, shift color, or add regulatory complications. We log metal content results, ready to provide proof to auditors or clients in regulated environments—particularly those scaling up intermediates for preclinical and clinical campaigns.

    Color stability is another frequent point of difference. Aldehyde intermediates have a reputation for color change—thanks to easy oxidation or reaction with trace amines in lab air. We eliminate these issues at source: inert handling, rapid crystal drying, and double-bagging. Feedback from customers who have received off-color batches from other sources says that reproducibility suffers most when these basic handling steps get skipped to save cost or cut corners.

    Reliability in Practice

    Research teams bet months or even years on the reliability of their core building blocks. Reliability comes down not to perfection, but to transparency, authentic process control, and readiness to dig in when something looks off—traits honed by years of customer conversations, near-miss recoveries, and post-mortems on tricky purifications. By keeping our processes nimble, we offer more than a standard-grade chemical: we offer partnership and accountability, sometimes in the form of extra investigations or overnight shipment to keep a customer’s project on track.

    The value of a well-made 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde really shows when teams stop worrying about the batch quality and focus fully on their own innovations. Downstream yields improve, instrument troubleshooting drops, and creative chemistry flows rather than fighting with impurities. For scale-up managers or API project leads, confidence in a building block translates to speed and lower total project cost. Our years in this field have proven the direct connection between upstream chemical precision and overall research productivity.

    Delivering consistent material batch after batch takes more than a good synthesis; it demands an enduring focus on operational discipline, staff training, and a willingness to adapt as customer needs shift. Despite constant pressure to cut costs or automate more steps, we keep skilled hands on every batch, because a well-trained team can spot the differences that machines can miss. Each improvement, whether in solvent recycling or drying efficiency, feeds back into better chemistry for people pushing the boundaries in their fields.

    Anticipating the Next Generation of Demands

    We aren’t just chemical suppliers—we’re problem-solvers who grew up solving leaks, vacuum failures, and the mysterious case of the disappearing chromatography peak. Modern customers come with sharper regulatory questions and stricter impurity requirements. Sustainability and green chemistry, nearly ignored a decade ago, now drive a growing share of process decisions. To tackle these, we tweak solvent ratios, try flow chemistry for hazardous steps, and collect richer data on emissions, yield, and energy consumption. Not every innovation pays off, but experience shows that even small tweaks in process control add up to a safer, more efficient operation.

    A few years back, a customer reach-out flagged elevated trace water disrupting their catalysis. We responded not just by adjusting our in-house drying, but also by mapping the full moisture pipeline—solvents, glassware, even humidity right by the packout line. Since tightening this up, we've nearly eliminated water-related failure calls and helped several clients raise their batch yields just by controlling what seemed like a small variable.

    Sourcing for specialty chemicals remains a relationship built on shared trust and proven results. Teams focused on advancing medicine, material science, or diagnostics rely on these upstream choices. No batch moves out our door until it has passed real-world stress testing—heat, chill, storage, and extended solution time. Each lot moves with batch-level documentation because even a few ppm difference can tip downstream reactions toward success or surprise.

    The landscape keeps changing: demand for controlled substances, sharper regulatory filings, faster scale-up cycles, and more pressure on purity. We’re not done learning, and each run brings lessons to apply on the next. Despite every improvement in automation or remote monitoring, people and judgment call the final shot on shipment release, batch signoff, and process revision. This is how we protect both our reputation and the ambitions of the research leaders who rely on our chemistry.

    Continuing the Conversation

    We built our reputation batch by batch, customer by customer, through decades of process refinement and open feedback. Whether your team is synthesizing the next generation of pharmaceuticals, fine-tuning catalysts, or building novel libraries, our version of 3-(4-methoxyphenyl)imidazo[1,5-a]pyridine-1-carbaldehyde stands as the result of our commitment—steadfast production, real technical support, and a willingness to put in the work to get each batch right. Quality doesn’t happen by accident; it comes from discipline, constant review, and a hands-on approach that never accepts “good enough.” Every container that leaves our facility represents not only a set of technical standards, but an ongoing promise backed by years of experience and an understanding of what really matters in a chemist’s day-to-day work.