3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    • Product Name: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    • Chemical Name (IUPAC): 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    • CAS No.: 219905-87-6
    • Chemical Formula: C14H9ClN2O
    • 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

    441420

    Iupac Name 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde
    Molecular Formula C14H9ClN2O
    Molecular Weight 256.69 g/mol
    Cas Number 2229127-73-9
    Appearance Off-white to light yellow solid
    Solubility Soluble in DMSO, DMF
    Smiles C1=CC=CC=C1C2=CN3C=CC=NC3=C2C=O
    Inchi InChI=1S/C14H9ClN2O/c15-12-6-2-1-5-11(12)13-8-17-10-4-3-7-16-14(10)18-13/h1-8H
    Synonyms 2-chlorophenyl imidazo[1,5-a]pyridine-1-carboxaldehyde
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 3-(2-chlorophenyl)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 with screw cap, labeled “3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde, 5 grams, for laboratory use.”
    Container Loading (20′ FCL) Container Loading (20′ FCL): The product is securely packed in sealed drums, loaded efficiently to maximize space, ensuring safe international transport.
    Shipping The chemical 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde is shipped in sealed, chemical-resistant containers under ambient or specified temperature conditions. Packaging complies with international regulations for hazardous materials, ensuring protection against leakage and contamination. Appropriate labeling and documentation accompany the shipment for safe handling, transport, and delivery in accordance with regulatory requirements.
    Storage **Storage of 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde:** Store the compound in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Refrigeration (2–8°C) is recommended unless otherwise specified. Properly label the container and ensure access is restricted to trained personnel wearing appropriate personal protective equipment (PPE).
    Shelf Life Shelf life: Store 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde in a cool, dry place; stable for at least two years.
    Application of 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    Purity 98%: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and product yield.

    Melting point 182°C: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with melting point 182°C is used in solid-state formulation development, where it enables reproducible crystallization and enhanced stability.

    Stability temperature 60°C: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with stability temperature 60°C is used in storage and transport of chemical stocks, where it maintains compound integrity under ambient and elevated temperatures.

    Particle size <50 μm: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with particle size less than 50 μm is used in high-throughput screening assays, where it facilitates rapid dissolution and uniform sample dispersion.

    Molecular weight 255.7 g/mol: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with molecular weight 255.7 g/mol is used in analytical method calibration, where it provides accurate mass spectrometric quantification.

    Assay ≥99%: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with assay ≥99% is used in reference standard preparation, where it delivers consistent analytical results for quality control.

    Solubility in DMSO >10 mg/mL: 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde with solubility in DMSO greater than 10 mg/mL is used in compound library generation, where it supports high-concentration stock solutions for bioassays.

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    Certification & Compliance
    More Introduction

    3-(2-Chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde: Direct from Manufacturer Bench

    Understanding the Molecule from the Manufacturing Floor

    Every run in our facility demands focus. We constantly evaluate the behavior and properties of our products as we scale batches of specialty intermediates for clients around the world. 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde occupies a unique position among our imidazopyridine line. This compound brings structure, selectivity, and reactivity that play a pivotal role in advanced pharmaceutical research and fine chemical synthesis.

    Our own operators learned early that maintaining precise conditions during synthesis determines the fate of this molecule. The intermediate, formed by fusing a 2-chlorophenyl group with the imidazo[1,5-a]pyridine skeleton and topped by the carbaldehyde moiety, holds together only when temperatures are tightly regulated, solvents handled with care, and timing never slackens. Our chemists meet these thresholds by pairing hands-on experience with advanced instrumentation—HPLC, NMR, and mass spectrometry stand ready not just to check boxes for quality, but to guide us through the texture and purity of each batch, run after run.

    Specifications in Action

    We produce 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde to exceed 98% assay by HPLC. Residual solvents and water content get monitored batch by batch. The color—pale yellow, sometimes edging toward white—reflects not just raw material quality but the way we control each synthetic step, each rinse, each dry-down. Powder flow and crystallinity make all the difference on a large scale, and our team works in direct communication between quality and production so nothing falls off spec between lab and drum.

    A task that stands out is particle size control. This isn’t a cosmetic detail. Downstream processes—from further chemical coupling to formulation—benefit when the material moves smoothly and disperses reliably. Particle morphology affects solubility, which can swing yield and reproducibility. Our team constantly investigates milling options, solvent systems, and filtration protocols to prevent hang-ups and deliver genuine improvements to end-users.

    Real-World Applications, Not Just on Paper

    Clients come to us for this compound because it connects high-value research projects and commercial syntheses. It fits into a growing toolkit for medicinal chemists looking at kinase inhibitors, antivirals, and more—it’s often a building block for advanced heterocyclic scaffolds. Several partners rely on our batches to serve as starting points for SAR (structure–activity relationship) work, and when we visit labs at client sites, the bottles from our warehouse sit right alongside their in-house stock for daily use.

    The molecule’s aldehyde group brings it to life at the bench. Aromatic carbaldehyde chemistry provides cross-coupling opportunities, opening doors for Suzuki, Sonogashira, and Wittig transformations. Unlike some simpler analogs, the 2-chlorophenyl ring introduces both electronic and steric control, steering reaction pathways and product selectivity in a way plain imidazoles won’t. Several of our customers have fed back that switching from non-chlorinated analogs altered their lead trajectory, giving them new hits in screens or sharper profiles in ADME studies.

    Our R&D input often goes beyond toll synthesis. When production started, some researchers asked if we could support alternative functionalities or expand the range of available purities. This dialogue sharpened our own process and helped us blend experience—both our own and that of the most exacting clients—into every lot sent out. We track all feedback and rapidly resolve any challenges with real root cause analysis, never just patchwork fixes.

    Side-by-Side versus Other Products: Why This Matters

    It’s easy to lose sight of how two molecules compare until scale or complexity ramps up. 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde stands apart from typical imidazopyridine aldehydes, especially those without a chlorinated phenyl group. This single substitution affects reactivity at multiple sites. For example, the presence of the 2-chloro group shields parts of the aromatic ring, protecting it during harsh conditions and reducing byproduct formation during Grignard or arylation steps. Competing unsubstituted analogs risk side reactions or require extra protection–deprotection cycles, which inflate overall project costs.

    Clients who have switched to our molecule typically shorten reaction times in their downstream work. Isolation improves and chromatography workloads shrink. Each batch we supply gets used more efficiently, which turns up not in a chart, but in worked hours saved and cleaner final products down the pipeline. Having spent years troubleshooting with customers, we’ve found that even subtle changes in the starting material structure can cut hours off a project—real dollars, real turnaround times, not just incremental lab gains.

    The Reality Inside the Manufacturing Plant

    We see new molecules in journals all the time, but their journey from a fresh printout to a bulk drum is thorny. 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde joined our pipeline after persistent requests from medicinal chemists who struggled sourcing consistent batches from non-manufacturing intermediaries. Before our own scale-up, customers shared headaches over variable quality and unreliable delivery. The difference comes from manufacturing the compound ourselves—from raw materials procurement, through all reaction and purification stages, to final packaging. Each step leaves a fingerprint. Our operators track yields and impurity profiles not just by end-point testing, but by process control methods developed in-house.

    One engineering adjustment stands out. Several years ago, a sticking point with filtration delayed one scale-up run. Product solubility in common quench solvents made fine crystal recovery inefficient. Rather than blame the raw materials, we reevaluated solvent systems and installed a new centrifuge stage. Recoveries went up, and what we learned there still shapes how we approach downstream separation for current and novel products. The lesson: only direct manufacturing experience allows swift adaptation—and this readiness passes directly to end users in the form of higher consistency.

    Safe Handling and Day-to-Day Lab Realities

    Our teams train on robust chemical safety, especially on a molecule like this, where the aldehyde group responds to air and moisture. Carefully managed containment, fast workup, and minimized transfer steps form daily protocols. We label each lot with precise shelf-life and transport guidelines, and conduct internal audits to spot cycle slips or storage issues before they can reach a site. Each drum or bottle gets packed with real handling in mind—nothing leaves until we can vouch for stability through transit and into longer-term bench storage.

    The product’s physical form—fine, free-flowing powder with low tendency to cake—has been refined over batch iterations. This attribute, while often overlooked by others, came directly from early user feedback. Researchers working with cumbersome or clumped solids lose valuable time in repulping and accurate weighing. Several months into initial production, we rebuilt our drying regimen, which led to a notable improvement in ease of use and minimization of waste.

    Learning from Each Batch: From Chemist’s Notes to Production Notes

    Every year brings subtle tweaks. As demand for 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde grew, our chemists started logging micro-observations—subtle color shifts, smell differences under varying humidity, solubility data under fresh and aged conditions. These notes, pooled into a rolling batch history, guide improvements as directly as any formal process review. We keep an eye on the unexpected, knowing firsthand how tricky it is for researchers to reconcile small changes in materials across a long-term project.

    We also experiment regularly with new process monitoring options. Recent years saw us trialing online spectroscopic checks in concert with chemical sampling. This dual approach proved that with large runs, spot checks never catch everything. Real-time data lets us intervene before deviations balloon, and that means our delivered product hasn’t just been tested at the end of the line, but continually managed for quality throughout the entire batch cycle.

    Supply Chain Reality: Not “Just-in-Case”, but “Always-Ready”

    Some in the industry treat imidazopyridine intermediates as commodities—they pick from any available stock, wary of slowdowns or price jumps. The cost comes later, when off-quality material slows down vital synthesis or fouls up pilot studies. Because our compound is made in-house, clients face fewer surprises. During pandemic supply chain crunches, we doubled down on local sourcing for key reagents and expanded on-site storage. Our team spent weekends not pushing paper but standing over inventory, drawing up practical contingency plans for every link in the production chain.

    We never see demand as “static.” Project pipelines swell; new clinical leads spring up. To keep pace, we hold buffer stocks and rotate material not just for inventory efficiency, but for real freshness and project reliability. Storage conditions—sealed drums under dry nitrogen, labeled with accurate “packed-on” dates—matter as much as the synthetic steps themselves. Our experience tells us that overlooked storage details can sour even the best-planned project downstream.

    Addressing the Tough Stuff: Byproducts and Environmental Stewardship

    Production scales up, and byproducts follow. We capture, treat, and document all streams as part of responsible operations. For 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde, chlorinated waste and spent solvents present ongoing attention points. Over the years, we’ve invested in solvent recovery—distilling and reclaiming usable fractions for internal use reflects real cost savings but also cuts environmental load. Building in excess recovery capacity lets us buffer against ups and downs in run size and yield changes.

    Most developers only see the end product. We see the tanks, filtration columns, and waste lines. Each process improvement gets reviewed for impact—both on process safety and on reducing end-of-pipe load. Recently, trials with alternate, greener solvents cut hazardous contributions significantly without compromising purity. The process tweaks came straight from our shop floor teams—those who work the equipment and clean the reactors. Accountable environmental stewardship runs through the veins of all chemical manufacturing, not just as a “compliance” checkbox, but as a set of ongoing, real-world decisions at every batch scale.

    Supporting Discovery: Bridging the Lab and Plant Worlds

    As direct manufacturers, our link to R&D doesn’t end after delivery. We field regular requests from researchers exploring new heterocyclic frameworks or optimizing old standby reactions. Sometimes, a chemist stumbles upon an unexpected side reaction or solvent effect using our aldehyde. We encourage and log every report, testing ideas on our pilot line—close enough to the plant for real-world results, fast enough to support fast-moving development teams. What emerges is a loop—experimental ideas from the field spark in-house application trials, which feed back out to all users. Clients value not just a product, but a source of manufacturing know-how honed by hard-won learning and failure alike.

    Several long-term partners now request special lot documentation or batch code histories for reference in regulatory filings. Having all synthesis data, impurity profiles, and chain-of-custody records assembled on the producer’s side takes enormous burden off researchers aiming to submit for clinical trials. We maintain complete transparency from raw material to packed bottle, both for quality assurance and for regulatory traceability.

    How We Adapt with Industry Needs

    We track the trends—novel drug discovery, sustainability mandates, ever-stringent quality rules. Flexibility only matters if built on deep familiarity—knowing exactly how 3-(2-chlorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde crystallizes, how it responds to temperature and humidity, how it acts in the hands of the chemist at 2 a.m. or the pilot plant engineer at the end of a long shift. Every batch we release is a reflection of the manufacturing talent beneath the roof; no anonymous lot leaves our site without this stamp.

    New ways to fulfill demand—smaller bespoke lots for medchem teams or monthly delivery for large-scale pilot lines—grew directly out of client dialogue. Our production crew stays ready to tweak scale, adjust packaging, or refine QC standards to match unexpected R&D routes and regulatory shifts. As rules on residual solvents or nitrosamine content tighten across jurisdictions, our QC protocols stretch to new limits, and we pride ourselves on never simply “meeting minimums.” We aim to outperform both regulatory guidelines and the best standards we encounter among clients.

    Direct From Source: Why That Matters

    Manufacturing at source brings control. Traceability is immediate. Troubleshooting becomes fast and honest. The value comes through every time a project stays on schedule because material performs as expected, or every time a downstream issue gets traced directly to a known process event—never a guess between middlemen. The person responsible for the run, the bottle, and the report line up on this side of the fence.

    For customers, the end user feedback never just sits in a suggestion box. Every point circulates into our operational and R&D cycles. Real expertise never crystallizes from a manual alone—it takes batch failures and process victories alike to teach what product really works for a medicinal chemist, a regulatory auditor, or a high-volume synthesis team. That experience keeps us focused, not only on the molecule but on the researchers who count on it for their daily work.