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HS Code |
979008 |
| Iupac Name | 2-methylimidazo[1,2-a]pyridine-3-carboxylic acid |
| Molecular Formula | C9H8N2O2 |
| Molecular Weight | 176.17 g/mol |
| Cas Number | 120313-79-3 |
| Smiles | Cc1nc2ccccn2c1C(=O)O |
| Pubchem Cid | 89355 |
| Appearance | Off-white to light yellow solid |
| Synonyms | 2-Methylimidazo[1,2-a]pyridine-3-carboxylic acid |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at room temperature, away from light |
As an accredited imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package is a sealed amber glass bottle with a printed label specifying "imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl-". |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 2-methyl imidazo[1,2-a]pyridine-3-carboxylic acid, compliant with chemical transport regulations. |
| Shipping | Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- is shipped in tightly sealed containers, protected from light and moisture. It is packaged following standard chemical safety regulations and typically transported at ambient temperature, unless specified otherwise. All shipping complies with applicable hazardous material guidelines to ensure safe handling and delivery. |
| Storage | Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- should be stored in a tightly closed container, away from moisture, direct sunlight, and incompatible substances. Store at room temperature in a cool, dry, and well-ventilated area. Ensure proper labeling and restrict access to trained personnel. Avoid exposure to extreme temperatures and keep away from sources of ignition or reactive chemicals. |
| Shelf Life | Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- typically has a shelf life of 2–3 years when stored properly. |
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Purity 98%: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting Point 210°C: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with a melting point of 210°C is used in high-temperature medicinal compound formulation, where it provides thermal stability during processing. Particle Size <10 μm: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with particle size less than 10 μm is used in tablet manufacturing, where it results in improved dissolution rate and uniform drug dispersion. Molecular Weight 173.17 g/mol: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with molecular weight 173.17 g/mol is used in structure-activity relationship studies, where it offers reliable data for lead optimization. Stability Temperature up to 150°C: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with stability temperature up to 150°C is used in solid-state drug storage, where it maintains chemical integrity under accelerated conditions. HPLC Assay ≥99%: imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- with HPLC assay ≥99% is used in reference standard preparation, where it ensures precise quantitation during analytical validation. |
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Manufacturing imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl-, often called 2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid on our floor, offers a window into both the rigor and the real-world considerations of chemical production. In a lab textbook, this molecule might look straightforward, but the challenges and decisions start before the first reaction runs. Sourcing high-purity starting materials with a reliable supply chain supports consistent output, and our synthesis paths must balance cost, reproducibility, and environmental compliance.
Chemists often need products where every batch meets strict analytical criteria. We’ve found that absolute purity, well-defined particle size, and traceability from the raw material to the final drum matter as much as the chemical name on the label. For 2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid, a close eye on HPLC and NMR data tells us more than any certificate sheet. Years of tweaking have shown us how even subtle changes to reaction temperature or solvent quality can impact crystallization, color, and yield. For this compound, avoiding colored impurities in the final product requires more than textbook conditions — it demands attention to real-time data and willingness to adapt processes when results slip out of line.
Real expertise emerges from the details most don’t publish. With our in-house processes, purity for this compound typically meets or exceeds 98 percent by HPLC, a benchmark combining market expectations and the realities of chemistry. Our control of water content through Karl Fischer titration gives us confidence that every kilogram behaves consistently during downstream processing. Most customers rely on this consistency to plan their own syntheses, especially if their downstream chemistry depends on amide bond formation or heterocycle elaboration. Solid samples blend with their reagents, dissolve predictably, and run through columns without unexpected byproducts rearing up midstream.
We found that crystalline product, with a stable melting point and minimal dust, travels better and stores longer than earlier granular forms. Particle size impacts flow rates and compaction in reactors, and it's something our blending and milling operators fine-tune batch by batch. Analytical staff run FT-IR and NMR on every lot, which minimizes the surprises that sometimes crop up with off-the-shelf or resold material. Customers want assurance that nothing extra will creep into their yields, especially where subsequent steps are both high value and high sensitivity.
Labs often debate why they choose 2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid over other imidazo[1,2-a]pyridine derivatives. The straightforward answer ties to the methyl group at the 2-position — it influences both chemical reactivity and physical characteristics. We see this difference in melting point, HPLC retention, and solubility. Some structurally similar compounds, lacking the methyl, can show more variability in handling or offer less site-selectivity in synthesis. Colleagues in medicinal chemistry emphasize the utility of this substitution pattern in designing kinase inhibitors or other small-molecule leads, where minor changes in structure can alter biological outcomes dramatically.
From a production viewpoint, the 2-methyl group imposes extra care during synthesis to avoid over-alkylation or unwanted positional isomers. The downstream benefit is twofold: chemists can build new motifs on the imidazo[1,2-a]pyridine core with higher predictability, and the molecule offers just enough hydrophobicity to support a range of applications in pharmaceutical discovery or agrochemical research. Stability against hydrolysis and oxidation adds a clear advantage over some close analogues, where shelf-life and batch-to-batch consistency prove trickier to guarantee.
Chemistry textbooks rarely capture the reality of industrial workflows, but working on the manufacturer’s side grants exposure to countless project types. Most orders for this material come from R&D labs eyeing heterocyclic intermediates for complex synthetic targets. The core ring and carboxylic acid group provide handles for functionalization, which often means amide coupling, esterification, or heteroannulation in the early steps of drug discovery. Even where our customers don’t disclose their end-use, conversations reveal the material showing up in fragment-based screens, early-stage lead generation, or library expansions in medicinal and process chemistry units.
A few customers push toward material science, capitalizing on the aromatic character and nitrogen-rich core of the structure. In applications where electronic properties matter, these chemists prize purity and reproducibility to support downstream characterization by mass spectrometry, NMR, and even single-crystal X-ray diffraction. Each batch that ships represents weeks of collaboration between production and analytical teams to ensure compliance with both internal standards and external expectations for quality.
Every new batch offers a learning opportunity. Early runs gave us valuable insight into controlling reaction exotherms and minimizing unwanted N-alkylation. The unique odor of intermediates and the stubborn foaming during workup required process changes. Testing cooling rates helped balance yield with the ease of filtration, and careful attention to solvent ratios made the difference between free-flowing product and sticky residue. Analytical controls developed in response to occasional darkening of product taught us the importance of rigorous process validation before any change is fully adopted.
Safety factors extend beyond compliance paperwork. Handling nitrogen-based heterocycles requires a culture of diligence and respect for the consequences of scale-up mistakes. Experienced operators run trials with scaled-down glassware before introducing new methods to production vessels. Waste streams receive as much scrutiny as final product, especially in anticipation of growing regulatory expectations for responsible manufacturing in the chemical sector. By sticking close to the chemistry and maintaining open communication between lab, plant, and quality staff, we minimize delays and avoid costly or wasteful rework.
Many clients compare our batches with those of other producers, and the feedback flows both ways. There are instances where small impurities in off-the-shelf products will derail a scale-up or leave a residue that no one expects until the chromatogram shows up with a mystery peak. In the best cases, our close attention to trace contaminants and physical characteristics delivers confidence, freeing chemists to focus on what matters in their development process. We often hear about failed reactions or headaches avoided due to reliable quality at this foundational stage.
Our analytical team tracks every batch from synthesis through storage, matching production records with quality data. Where others may blend lots or source from multiple origins, producing material from the same facility under consistent conditions drives better predictability. Tracking purity and water content lets us flag issues early, and this proactive approach helps avoid expensive surprises downstream for anyone who relies on our molecule for key steps.
Markets and applications shift each year. More synthetic chemists need larger volumes as project timelines shrink, and specifications for impurities tighten as analytical methods advance. We have adapted by expanding reactor volume and optimizing downstream crystallization. Our shift from batch to semi-continuous processing for certain steps responds to both cost pressure and rising demand. Customers looking for multi-kilogram scale-out find that our scalable approach keeps lead times reasonable and pricing stable.
We gather feedback from both routine orders and the tough, one-off requests — adapting specifications or packaging on demand. The flexibility built into our operation isn’t just a cost equation; it reinforces trust with long-term partners, including those developing new APIs or evaluating advanced materials. We never claim perfection, but our steady review of each lot forms the backbone of risk management and long-term reliability for both us and our customers.
Decision-making starts in the lab. Each input is checked with our own instruments before it hits the reactors. Production chemists log real-time yields, color, and byproduct levels, which lets us adjust conditions mid-batch if required. NMR and HPLC remain fundamental — allowing for both quantification and detailed impurity profiling. FT-IR, melting point, and optical rotation round out the process, preventing chronic issues from appearing batch after batch.
We have invested heavily in maintaining our analytical equipment. Regular calibration and training of staff result in faster, more accurate verification, meaning less waiting and greater confidence with each shipment. This hands-on approach stems from a simple observation: the most reliable material comes from sites where the same people who run the reactions walk into the lab and analyze the results themselves.
Experience shows that maintaining material quality depends as much on handling as on synthesis. Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- may look robust on paper, but moisture control in storage and transit matters. Keeping humidity below certain thresholds ensures product doesn’t cake or oxidize, factors that affect not just shelf-life but also performance in sensitive syntheses.
Packaging development never stops. Simple bags can pose contamination or static risks, so we moved to lined, sealed containers that minimize transfer losses and water uptake during warehousing and overseas transport. Routinely, our staff inspects stored drums, looking for changes in mass or appearance. Combined with clear labeling and digital tracking, these steps help customers know that decades of experience back each shipment.
Modern chemical manufacturing cannot ignore its footprint. Process developments over the last decade allowed us to cut solvent use and minimize waste streams. We recycle mother liquors wherever practical and find outside partners for byproduct reclaiming, striving for both cost and environmental benefit. Compliance with regulatory standards guides these improvements, but the bigger motivator is the long-term health of our staff and the communities we work in.
We field regular questions on biodegradability and disposal guidance. Sincere answers require both data and transparency. While our product does not present special handling challenges under normal circumstances, our team provides as much detail as permissible about upstream and downstream consequences. Hazard assessments factor into every step, and we work to stay ahead of both local and international requirements.
Ordering from a manufacturer means direct access to expertise behind each shipment. Troubleshooting, customization, and problem-solving come faster when both sides speak the same technical language and share stakes in getting the chemistry right. Our team interacts daily with end-users, translating their evolving needs into process adjustments or analytical improvements.
We know that for chemists, predictable performance, clear communication, and reliable delivery justify long-term loyalty. Feedback loops achieved over decades let us refine both product and service. Sharing production realities — from setbacks and process breaks to small advances — makes the relationship more than transactional. No spreadsheet or product list matches the real-time knowledge transfer that comes from talking to people accountable for every molecule that leaves the plant.
No process remains static. We evaluate every batch for missed opportunities to streamline the workflow or further purify the product. Collaborating with synthetic chemists, both in academic labs and startups, exposes us to problems demanding tailored adjustments. For example, fine-tuning the crystal habit or modifying drying protocols sometimes results in a product better suited for difficult downstream transformations.
Process data accumulates, informing both troubleshooting and future scale-ups. Adjusting reaction conditions based on subtle cues — gas evolution rates, slight color shifts — draws on a collective memory spanning hundreds of cycles. These observations, written into batch records and discussed in shift handovers, keep us honest and drive the incremental improvements that set reliable manufacturers apart.
Imidazo[1,2-a]pyridine-3-carboxylic acid, 2-methyl- presents challenges that push both our chemistry and teamwork forward. Consistency stems from hard-won experience: knowing which raw material lot demands extra filtration, which batch needed a temperature adjustment mid-run, which drums need closer inspection before release. We believe the compound offers chemists and formulators a reliable foundation for invention, made possible by transparent manufacturing and responsive quality systems.
From raw ingredient selection to final packaging, the process reflects decades of mistakes, improvements, and teamwork. Each order delivers not just a chemical, but the trust built on follow-through and openness to feedback. This pragmatic perspective, shaped by producing 2-methyl-imidazo[1,2-a]pyridine-3-carboxylic acid batch after batch, grounds our work and guides our response to customers who depend on both the product and the people behind it.