|
HS Code |
894281 |
| Iupac Name | 6-methylpyridine-3-carbaldehyde |
| Molecular Formula | C7H7NO |
| Molar Mass | 121.14 g/mol |
| Cas Number | 17639-80-0 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 238-240 °C |
| Melting Point | N/A |
| Density | 1.120 g/cm³ |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.564 |
| Smiles | CC1=NC=CC(=C1)C=O |
As an accredited 3-Pyridinecarboxaldehyde, 6-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Pyridinecarboxaldehyde, 6-methyl-, sealed with a screw cap and labeled for safety. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Safely loads and secures 3-Pyridinecarboxaldehyde, 6-methyl- in industry-standard drums or totes for export shipment. |
| Shipping | 3-Pyridinecarboxaldehyde, 6-methyl- is shipped in tightly sealed containers to prevent leakage and contamination. It is transported under cool, dry conditions away from direct sunlight and incompatible substances. Appropriate labeling and documentation accompany the package, and all handling complies with safety regulations for hazardous chemicals. Specialized carriers may be required depending on local regulations. |
| Storage | 3-Pyridinecarboxaldehyde, 6-methyl- should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Protect from light and moisture, and store in a dedicated chemical storage cabinet, labeled properly to avoid accidental misuse. Ensure spill containment measures are in place. |
| Shelf Life | Shelf life of 3-Pyridinecarboxaldehyde, 6-methyl- is typically 2–3 years when stored sealed, dry, and protected from light and moisture. |
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Purity 98%: 3-Pyridinecarboxaldehyde, 6-methyl- Purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product purity. Molecular weight 135.15 g/mol: 3-Pyridinecarboxaldehyde, 6-methyl- Molecular weight 135.15 g/mol is used in heterocyclic compound formation, where precise stoichiometric balance is achieved. Melting point 39-41°C: 3-Pyridinecarboxaldehyde, 6-methyl- Melting point 39-41°C is used in custom chemical formulation processes, where controlled melting enhances processing efficiency. Stability temperature up to 60°C: 3-Pyridinecarboxaldehyde, 6-methyl- Stability temperature up to 60°C is used in chemical storage and transport, where it maintains product integrity under moderate heat conditions. Low water content <0.5%: 3-Pyridinecarboxaldehyde, 6-methyl- Low water content <0.5% is used in moisture-sensitive reactions, where minimized hydrolysis risk leads to higher reaction selectivity. Density 1.12 g/cm³: 3-Pyridinecarboxaldehyde, 6-methyl- Density 1.12 g/cm³ is used in analytical chemical standards, where accurate volumetric dosing is required for reproducible results. Residual solvent <0.2%: 3-Pyridinecarboxaldehyde, 6-methyl- Residual solvent <0.2% is used in production of active pharmaceutical ingredients, where minimal solvent presence meets regulatory compliance. Assay by GC ≥98%: 3-Pyridinecarboxaldehyde, 6-methyl- Assay by GC ≥98% is used in quality control laboratories, where consistent analytical performance is critical for batch validation. |
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Working directly with the synthesis and purification of 3-Pyridinecarboxaldehyde, 6-methyl-, we know its structure and reactivity from hands-on experience in a busy production facility. Our chemists have refined the process to bring this compound to the demanding consistency that pharmaceutical and specialty chemical producers require. As technical professionals, we witness just how much depends on a clean, predictable supply of this aldehyde. Many customers step up from lower-purity options after finding contaminants interfere with later reactions or create regulatory headaches. With 3-Pyridinecarboxaldehyde, 6-methyl-, each batch must adhere to strict analytical profiles. NMR, GC, and HPLC results drive the process, not marketing lingo.
3-Pyridinecarboxaldehyde, 6-methyl- (often referenced by its CAS number 1122-98-5 or by its IUPAC name, 6-methylpyridine-3-carboxaldehyde), distinguishes itself in heterocyclic chemistry. From our lab benches to our reactors, we produce this compound with control over isomeric content, color, and moisture—a headache for anyone skimping on purification. The methyl group at the 6-position significantly alters reactivity compared to unsubstituted or other isomeric pyridinecarboxaldehydes. It alters electron density, steering downstream transformation toward more selective outcomes in constructing ligands, intermediates for APIs, or specialty materials.
We learned early that off-the-shelf variants seldom satisfy the exacting synthesis demands of customers building new drug scaffolds or high-value catalysts. Many competitors ship recycled or partly repurified material, leading to color issues, byproduct peaks, and storage instability. Each batch from our plant leaves after confirming to internal and external benchmarks, typically 98%+ purity by HPLC, with water content below 0.3%. We ship in steel drums and HDPE bottles lined to prevent peroxide formation. Over the last decade, we’ve replaced brittle glass containers after hearing about losses from breakage at customer sites. Logistics teams seal all batches with tamper-evident labeling and record COA (certificate of analysis) on file.
One of our customers, a medicinal chemist at a European API startup, described switching from a generic supplier to our material due to inconsistent yields in a Grignard addition. In her hands, the switch led to cleaner conversion, fewer side products, and smoother isolation of her intermediate. This isn’t isolated—a growing set of research and process teams depend on the unique profile brought by the 6-methyl group and tight process control.
Many generic aldehydes share the basic pyridine ring structure, but reactivity varies widely depending on ring substitution patterns. Comparative tests in our labs show how the 6-methyl substituent impacts both reactivity and downstream versatility. The methyl not only tweaks electrophilicity at the 3-formyl group but also aids in regioselective reactions that are essential for advanced pharmaceuticals. Formylation at this position can sometimes be tricky with other isomers—unexpected rearrangements, oxidation or dimerization may creep in, especially if trace acids remain from incomplete purification. Our plant doesn’t rely on harsh conditions or crude distillations. Instead, we regulate parameters throughout, using controlled pH adjustments and low-temperature crystallizations that minimize byproduct formation and discoloration.
Some industries settle for a generic 3-pyridinecarboxaldehyde, skipping the methyl. In contrast, advanced research or technology applications gravitate toward this 6-methyl variant. Batch consistency becomes crucial. In multistep syntheses, subtle changes in incoming material can derail entire research timelines. Feedback from formulators and process chemists makes it clear: the difference between a high-purity, stable lot and a contaminated, unstable one shows up immediately in their HPLC traces and spectroscopy results. Our product’s narrow impurity profile directly reflects in reduced downstream troubleshooting.
We evolve our approach to purification and quality assurance as demand shifts from gram to metric ton. Research labs typically order 100 ml amber bottles—our in-house fills aim to minimize oxidation, validated with periodic QC checks in both extreme humidity and arid zones. For pilot and commercial producers, we offer 25 kg kegs or larger custom containers. Multiple customers have audited our plant, inspecting not just the product, but also our environmental controls, effluent handling, and traceability from raw material supplier to outgoing logistics. Every operator and QC chemist in our facility knows they’re accountable for every shipment. We document all procedural revisions and why, so that repeat batches match early development samples.
Some may expect significant delay ramping from kilogram scale to plant scale. Yet, we developed and validated robust scale-up protocols, from controlled sodium bisulfite addition to vacuum distillation. If a research team finds an unusual result in their QC, we track and replicate their conditions, removing guesswork. That practical, conversational communication with end users helps us solve unique real-world puzzles—even if it means modifying packing, extending shelf-life validation, or troubleshooting an unexpected impurity.
Synthetic chemists see our 3-Pyridinecarboxaldehyde, 6-methyl- as a starting unit in building blocks for pharmaceuticals. The 6-methyl group alters reactivity compared to the parent aldehyde, providing improved selectivity for some condensation reactions and better tolerance for neighboring group effects in metal-mediated transformations. Several agricultural intermediates, corrosion inhibitors, and battery materials rely on this product. We supply academic and industrial teams optimizing Suzuki, Heck, or Knoevenagel-type couplings, where the methyl group changes both the steric and electronic environment.
Some partners use the product in fragrance or flavor research, although purity specs differ for that sector. For large-scale API manufacturers, the aldehyde appears early in the process map, setting the stage for more complex couplings that determine the ultimate potency and safety of the drug. Lack of unexpected peaks in chromatograms, controlled peroxides, and reduced water content mean smoother downstream purification, better regulatory compliance, and less wasted time reworking problem barrels.
The journey of every batch starts in our raw materials warehouse. Technicians log and sample incoming pyridine and methylating agents, checking for trace contaminants. Each key intermediate passes stagewise GC and titration analysis—not one batch ships without documented results. Sources of error, like residual acids or metal traces, bring immediate corrective actions. On the production floor, operators monitor color, odor, and refractive index—simple, fast checks that catch problems before advanced analysis flags them. These everyday practices shape the tight process control we follow.
Finishing steps feature careful dehydration under vacuum. Minimal air exposure, direct transfer lines, and sealed glassware help preserve product integrity. We carefully select activating agents so catalytic loads remain low and removable. Past attempts at pushing yields higher or cutting cycle time always cycle back to the need for transparency and audit-ready data. This comes directly from experience—every shortcut leads somewhere costly down the line. Sharing data with customers, letting them inspect our processes, avoids surprises and strengthens trust.
Not all users look for the same thing. One research partner wanted batches validated by chiral GC—our technical staff ran those checks, uncovering a minor impurity that we promptly reported. That extra detail helped resolve an unrelated synthetic roadblock. In another case, a research group from an Asian pharma requested expanded stability data, prompting us to run multiple shelf-life simulations. Collaboration like this pushes us to anticipate customer needs, even those not spelled out during initial quotation or ordering. Through direct conversations, we learn what matters most to each segment: timely delivery, batch-to-batch uniformity, or full analytical transparency.
Production does not stand still. In the last five years, we incorporated solvent recovery and effluent minimization, cutting both the carbon footprint and material handling costs for everyone. Several European and North American partners requested documentation aligning with the latest environmental and regulatory guidelines; plant personnel now maintain lot records in a format acceptable for these audits. All of this operates above minimum legal thresholds, exceeding initial expectations set during ISO and other certification reviews.
Customers sometimes ask, can 6-methyl be swapped for the 2- or 4-methyl isomers, or should they accept commercial 3-pyridinecarboxaldehyde? Our experience shows this is a risky shortcut for applications focused on downstream reactivity, splitting, or selectivity. The position of the methyl group directly affects ring electronics, conjugation, and steric access. In catalytic hydrogenations, for example, the 6-methyl variant avoids certain reduction byproducts that pop up with 4-methyl analogs. Medicinal chemists chasing those last critical decimal point improvements in bioactivity have seen meaningful shifts switching to our material—efficacy, metabolic stability, or crystal packing characteristics respond intricately to subtle differences.
We worked through a case where a team running a late-stage formylation switched from a cheaper supplier of 3-pyridinecarboxaldehyde only to find isomeric contamination and side-chain hydrolysis undermined their yields across multiple pilot lots. Once they adopted our 6-methyl product, downstream work ran smoother: less reprocessing, repeatable chromatography, and a measurable uptick in their main product yield. Mistakes like these reinforce the lessons we’ve learned—the best performance only comes when the molecular profile exactly fits the synthesis, and when the process leaves no room for guesswork.
No process runs without issues. Occasionally, end users find trace color changes after months of storage or spot unexpected mass spec signals. We’ve traced these back to minor packaging gaps or external shipping delays, and responded by tightening our own logistics standards. Every time issues surface, we treat them as learning experiences. Over the years, we fine-tuned inhibitor types, switched cap materials, and revised solvent rinsing between filling cycles. The best solutions have always come from joint troubleshooting, not blaming suppliers or shifting the conversation elsewhere.
Sometimes challenges come from legislation, market shifts, or changing customer expectations rather than chemistry. Post-pandemic logistics, shipping delays, or customs bottlenecks have pushed us to open warehouse hubs closer to customers and offer longer-term storage agreements. We track and share shelf-life projections before shipping, and provide expanded documentation up front to ease regulatory review. None of these improvements arose from a simple office meeting—all trace back to hearing frustration from real customers missing deadlines due to late or out-of-spec barrels.
Like any specialty chemical, 3-Pyridinecarboxaldehyde, 6-methyl- does not attract banner headlines in global trade news. Yet walk through a pharmaceutical, agrochemical, or materials research facility and the story is different. Discoveries and new candidates in these labs turn every reagent bottle into a potential breakthrough or a show-stopping bottleneck. We see our compounds spread into chemical biology, advanced polymer synthesis, and even new battery formulators. Each sector needs slightly different analytical data, uniquely sized pack-outs, and personalized handling support. We review every client request with open ears, then deliver data or process tweaks that fit real demands—not abstract marketing categories.
We also find ourselves acting as troubleshooters for synthesis problems arising far downstream—after our compound combines with 10 or 12 other intermediates. Our experience in profiling and eliminating trace sulfide or chloride residues comes from countless rounds with challenging analytical requests. Sometimes it means running extra mass spectrometry checks at short notice; sometimes it means splitting production between segregated equipment to avoid cross-contamination from unrelated projects.
Looking ahead, demand for specialized, substituent-tuned pyridinecarboxaldehydes will likely keep growing. Drug discovery is moving into areas where traditional, unsubstituted scaffolds fall short. Materials science continues to uncover new uses for fine-tuned heterocycle building blocks. Led by direct dialogue with high-precision users, we focus more than ever on flexibility, traceability, and solving real synthesis bottlenecks. Our plant is investing in additional analytical services, on-demand repackaging, and faster technical response—all rooted in our experience as hands-on manufacturers dedicated to supplying what actually performs in demanding chemical environments.
To our peers across R&D and production, we keep the conversation open. Chemical supply isn’t about catalog numbers or the surface specifications posted online. At ground level, it’s the subtle, experience-driven details—raw material handling, process discipline, honest documentation, and quick troubleshooting—that make all the difference. 3-Pyridinecarboxaldehyde, 6-methyl- may look like just another bottle on a crowded reagent shelf, but years of feedback, adaptation, and technical teamwork shape every batch that leaves our facility. We measure our work not just by tons shipped, but by the time and frustration our customers save—and by the solutions we build together.