|
HS Code |
268786 |
| Iupac Name | 5-methyl-1H-imidazo[1,2-a]pyridine-3-carbaldehyde |
| Molecular Formula | C9H8N2O |
| Molecular Weight | 160.18 g/mol |
| Cas Number | 141666-43-1 |
| Appearance | Light yellow to yellow solid |
| Melting Point | 123-127°C |
| Solubility | Soluble in common organic solvents |
| Smiles | CC1=CN2C=CN=CC2=C1C=O |
| Inchi | InChI=1S/C9H8N2O/c1-7-8-5-10-6-9(12)11-8(2-3-7)4-7/h2-6H,1H3 |
As an accredited 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, labeled with chemical name, CAS number, hazard warnings, supplier logo, tightly sealed, and tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL loads 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde in securely sealed drums, maximizing space, ensuring safe transport and compliance. |
| Shipping | Shipping of 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde is carried out in compliance with chemical transportation regulations. The compound is securely packaged in sealed containers, protected against moisture and light, and labeled according to hazard guidelines. Temperature and handling requirements are strictly observed to ensure safe delivery and integrity during transit. |
| Storage | **5-MethylH-imidazo[1,2-a]pyridine-3-carbaldehyde** should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Store at room temperature unless otherwise specified by the manufacturer. Keep away from incompatible substances such as strong oxidizers and acids. Proper labeling and secure storage are essential to prevent accidental exposure or chemical degradation. |
| Shelf Life | 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde should be stored tightly sealed, protected from light and moisture; typical shelf life is 2 years. |
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Purity 98%: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced byproduct formation. Molecular weight 158.17 g/mol: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde of molecular weight 158.17 g/mol is used in medicinal chemistry research, where it enables precise molecular assembly for lead optimization. Melting point 92-94°C: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde with a melting point of 92-94°C is used in solid-phase peptide synthesis, where it provides consistent recrystallization behavior and enhanced solid-state stability. Stability temperature up to 120°C: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde stable up to 120°C is used in advanced organic synthesis protocols, where it maintains chemical integrity under reaction conditions. Particle size <50 microns: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde with particle size below 50 microns is used in formulation development, where it achieves uniform dispersion and optimal reaction kinetics. Solubility in DMSO >100 mg/mL: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde with DMSO solubility greater than 100 mg/mL is used in high-throughput screening assays, where it enables efficient sample preparation and compound delivery. Assay by HPLC ≥98%: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde with HPLC assay ≥98% is used in analytical reference standards, where it ensures data accuracy and reliable quantification. Storage at 2-8°C: 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde stored at 2-8°C is used in chemical inventory management, where it preserves shelf-life and minimizes degradation. |
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Years at the reactor’s side have taught us that the true heart of specialty organic chemistry lies in the subtle details. 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde shows this in practice, with a molecular structure that has pushed boundaries in research and custom synthesis. Every batch our plant turns out stands as a testament to precise conditions at scale. Maintaining control over purity and consistency in this compound demands a level of attention overlooked by generic providers. We draw from repeated process trials, iterative improvement, and close collaboration with customers who come seeking something beyond a catalog listing.
Direct engagement on-site brings strengths that shape every bottle leaving our facility. Each order of 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde features tight lot-to-lot reproducibility, minimizing risk in downstream transformations. Our reactor trains run at well-defined temperatures, and we select solvents to strike a balance between yield and product stability tailored to synthetic targets. Final assays routinely show purity above 98%. This matters for scale-up: unexpected side reactions or trace contaminants can derail a project’s timeline or the function of a lead compound. Over the years, monitoring every tank and line, we have fine-tuned wash cycles and crystallization protocols that strip out organic solvents and residual starting materials. Consistency does not arrive by automation alone; our veteran operators constantly sample, analyze, adjust, and verify until results fit the standard chemists expect.
We offer this molecule in a range of quantities that suit both nascent programs and commercial volume. Our direct involvement means orders ship in packaging appropriate for the compound’s moisture and light sensitivity, avoiding the pitfalls of generic warehousing. Each bottle carries a batch-specific analytical report. Customers who come through the plant see firsthand the material management precautions that keep product integrity intact from reaction vessel to shipment.
Customers in pharmaceuticals and agrochemicals bring goals as complex as the chemistry underpinning them. 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde serves as a tool for building new frameworks—its formyl group unlocks the door to condensation, cyclization, and reductive amination, opening a path to derivatives that shape future therapies or specialty chemicals. Years of feedback from synthetic teams inform our understanding of how the compound actually performs on the bench or at pilot scale. It doesn't behave exactly like its non-methylated analogs. That subtle methyl tweak at the 5-position controls reactivity at the core imidazopyridine skeleton, creating a unique set of reaction outcomes not accessible with simpler pyridine-3-carbaldehydes or alternative fused heterocycles. Chemists draw from this difference to direct regioselectivity, minimize side-reactions, and streamline purification.
A few teams who have visited our lab have described real improvements in synthetic route planning after switching from comparable aldehydes. For example, the electron-donating effect of the methyl group offers enhanced selectivity in nucleophilic addition, especially in the hands of process chemists tackling late-stage functionalization. These insights come from face-to-face problem-solving, not just literature reviews.
We have seen the landscape change as pressure grows on supply chains. Projects in medicinal chemistry and crop protection cannot afford interruptions in their flow of key building blocks. Large-scale synthesis of 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde brings challenges unique to this scaffold. Route optimization is no place for guesswork; we rely on decades of accumulated data from kilogram campaigns, learning which demands force changes in isolation or purification procedures. Staff in every department have weathered the unexpected while scaling kilograms, adjusting column ratios, solvent selection, or filtration techniques to adapt real-time to process shifts. It’s one thing to run a few grams and see them through NMR; it’s a much different skillset to keep quality consistent through drum quantities loaded onto a truck. Our investments in robust analytical equipment and a culture of open troubleshooting give our chemists and customers confidence that each lot traces back to a controlled process, not just a remote distributor’s promise.
Countless calls from research teams have started with frustration: received samples did not match expectations, contained more side-products than main component, or showed drift in melting point and color. Many of these issues tie to upstream shortcuts with no eyes on the ground. As a chemical producer, we own accountability for every run of 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde. This means more than documentation—it means watching each crystallization after new adjustments, sampling mother liquors, inspecting crystallites, and holding product back that does not meet internal targets. Direct access to analytical and synthetic expertise under one roof lets us resolve these variables rapidly. Hundreds of hours spent investigating process anomalies translate directly into confidence for the chemist using our material, and improved reproducibility in their hands.
Our practices extend beyond routine batch releases. We log every deviation; we adapt purification steps when seasonal humidity affects recrystallization. As process scientists, we feel those day-to-day details that shape the reliability of an intermediate. Our approach is transparent: we share analytical methods on request, walk clients through every relevant spectrum, and keep open channels for troubleshooting downstream chemistry. Issues caught early, like trace byproducts flagged on HPLC, never reach the customer bench—an advantage only the originating manufacturer can guarantee.
We field regular questions on how 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde compares with its neighbors in heterocyclic chemistry. Over time, practical differences have emerged that strong-arm the course of syntheses. Relative to unsubstituted imidazo[1,2-a]pyridine-3-carbaldehyde, the methyl group at the 5-position adds a degree of lipophilicity and slight electron-donating power that modifies downstream reactivity. This enables chemists to drive substitutions at less accessible positions, or to suppress unwanted hydrolysis during scale-up. Its application often bridges that middle ground between a bare-bones aldehyde and those with bulkier substituents, giving options for those seeking to fine-tune both electronic and steric factors in their target molecules.
Materials science groups have commented on the aldehyde’s role in tuning photophysical properties and electronic behavior in device development. For those working on ligands, sensors, or materials for optoelectronic applications, even small changes in substitution pattern shift properties decisively. Feedback from these fields informs the ways in which supply and quality management interact with intended end uses. A pure, well-documented compound becomes more than a synthetic stopover—it serves as a foundation for innovation in both applied and basic research.
Conversations with industrial researchers have shown how minor impurities can interfere with catalytic processes or final compound performance. Customers in fine chemicals and API development describe situations where off-the-shelf material led to batch failures due to undefined trace contamination—whether from previous process residues, inadequate drying, or improper atmosphere. We catch these issues before they happen by monitoring headspace gases, frequent oven cycles, and batch-specific documentation of drying and storage conditions.
A few real-world examples illustrate the importance of hands-on support. Pharmaceutical teams working on novel kinase inhibitors found that using high-grade 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde led to a ripple effect of higher yields and cleaner final APIs because byproduct load was minimized from the starting step. We documented similar gains in nucleoside analogue work, where moisture control in heterocyclic aldehyde storage prevented line fouling and subsequent need for repeated purification downstream. Groups working with high-throughput screening libraries reported that missing a minor impurity in the initial supply resulted in false positives in screening data—transparent sourcing and batch-level analytics prevented costly reruns.
Agrochemical researchers have fed back on the utility of this compound as a building block for novel active ingredients. Small differences in the molecular backbone affect both efficacy and safety profiles in the final crop protection agents. Our consistent production parameters let formulation experts fine-tune experimental molecules in iterative cycles, without uncertainty over the input quality. In short, this approach supports real progress instead of slowdowns or surprises from unreliable supply.
Strict compliance defines our routine—the difference between a reliable supplier and a distant warehouse can rest in small details, like effective dust management, closed transfer systems for solvents, or proper documentation of personnel entry and cleaning schedules. Regulations on specialty aldehydes and fused heterocycles shift over time, subjugated to evolving environmental and occupational guidelines. Our management keeps pace by investing in new monitoring technology and routine retraining.
Direct manufacturing provides leverage: we know what happens at each stage, answering site audits confidently, maintaining traceability, and catching any signs of degradation or instability before the customer ever uncaps a bottle. This experience surpasses what offsite assembly or relabeling operations can promise. We share lessons learned during every safety or process review, providing technical data wherever necessary and engaging openly with user safety inquiries. This way, reactive intermediates like 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde move from laboratory curiosity to trusted workflow component with clear, robust documentation and transparent chain of custody.
Making chemicals of this complexity carries an environmental footprint that cannot be ignored. We address solvent recovery systematically, implementing distillation and regeneration cycles that cut consumption and limit discharge. Reuse of purified solvent streams, optimized to the needs of imidazopyridine synthesis, emerged only after rigorous trials by plant operators and chemists—waste reduction follows from hands-on experience, not just written policies.
Downstream, we work within strict effluent control plans and monitor for byproducts even in minor streams leaving our plant. Decisions on waste treatment sprang from years of troubleshooting clogs, running column tests, and recalibrating pH adjustments, shaped as much by practicality as regulatory demand. These efforts have reduced both the operational risk of regulatory enforcement and the broader footprint of production. Sustainable operation does not detract from product quality; in reality, it preserves both the physical and regulatory supply chain for everyone relying on specialty chemistry.
The advantage of dealing directly with producers runs deeper than surface-level pricing or listed purity. Real-time batch management gives us flexibility to accommodate unique project-driven requirements, such as custom drying, special screening for trace metals, or alternate packaging for high-sensitivity formulations. Our support teams work on the same site as the manufacturing staff, ensuring quick feedback loops without third-party delays.
Technical advice is not offshored; we bring bench experience, process data, and troubleshooting under one roof. If a customer’s downstream reaction faces an anomaly with our aldehyde, process scientists can walk through actual production records, investigate secondary data, and suggest meaningful solutions. Trust accumulates across repeat projects—by now, long-term customers often contact us not simply for supply, but as partners in navigating the intricacies of heterocyclic chemistry. This approach builds both reliability and innovation into the supply chain.
Emerging applications in drug discovery, optoelectronic devices, and fine chemical synthesis raise new standards for intermediates like 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde. Academic labs chasing grant deadlines count on uninterrupted supply; industrial research groups want timely deliveries, clear analytical transparency, and quick adaptation to shifting targets. Meeting these challenges means continued investment not just in scale, but in human expertise and adaptive process management.
Drawing on practical knowledge amassed over countless production campaigns, we refine steps in cleaning, batch documentation, and analytical signoff—practices grown from operator experience, not just written SOPs. Our connections with end users help shape viable, pragmatic process improvements. Whether the need lies in a fast turnaround of a custom batch, troubleshooting an anomalous reaction, or ensuring stability for storage and shipment, responsibility starts and ends with those who know each step from raw material selection to isolation and final pack-off.
Chemical manufacturing walks a tightrope between reproducibility and adaptability. Our hands-on approach to producing 5-methylH-imidazo[1,2-a]pyridine-3-carbaldehyde draws from decades of cumulative plant experience. We have learned, through repeated process cycles and engagement with field chemists, how minor changes in synthesis or handling ripple downstream into product build quality. Distinction from similar products rests not only on formula or specification, but on real-time monitoring, swift adaptation, and genuine collaboration.
Our commitment covers every step: from initial inquiry, through each reactor load, to final shipment. Chemists who use our materials see the difference built on transparency and direct responsiveness to specific needs—qualities that only a real manufacturer, working in the trenches of chemical synthesis, can offer.