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HS Code |
691383 |
| Chemical Name | 2,6-dimethylpyridine-4-carbaldehyde |
| Cas Number | 13947-69-8 |
| Molecular Formula | C8H9NO |
| Molecular Weight | 135.17 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 255-257°C |
| Melting Point | N/A |
| Density | 1.083 g/cm³ |
| Flash Point | 111°C |
| Solubility | Soluble in organic solvents (ethanol, ether, etc.) |
| Smiles | CC1=CC(=NC=C1C=O)C |
| Iupac Name | 2,6-dimethylpyridine-4-carbaldehyde |
| Pubchem Cid | 351593 |
| Synonyms | 2,6-Lutidine-4-carboxaldehyde |
| Refractive Index | 1.569 |
As an accredited 2,6-dimethylpyridine-4-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with chemical name, formula, and hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12 metric tons packed in 200 kg HDPE drums, securely palletized for safe international shipping. |
| Shipping | 2,6-Dimethylpyridine-4-carbaldehyde should be shipped in tightly sealed containers under cool, dry conditions. It must be clearly labeled and packaged according to regulations for hazardous organic chemicals, avoiding exposure to heat and direct sunlight. Ensure compliance with local and international shipping regulations, including appropriate documentation and safety data sheets (SDS). |
| Storage | 2,6-Dimethylpyridine-4-carbaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Store under inert atmosphere if possible, and clearly label the container. Follow all local, state, and federal guidelines for safe storage. |
| Shelf Life | 2,6-Dimethylpyridine-4-carbaldehyde should be stored tightly sealed, protected from light and moisture; shelf life is typically 1–2 years. |
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Purity 98%: 2,6-dimethylpyridine-4-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield target compound formation. Melting point 85°C: 2,6-dimethylpyridine-4-carbaldehyde at melting point 85°C is used in solid-phase organic synthesis, where controlled temperature processing improves batch reproducibility. Stability 120°C: 2,6-dimethylpyridine-4-carbaldehyde with stability up to 120°C is used in high-temperature catalytic processes, where structural integrity is maintained under reaction conditions. Moisture content <0.5%: 2,6-dimethylpyridine-4-carbaldehyde with moisture content below 0.5% is used in moisture-sensitive coupling reactions, where it minimizes unwanted hydrolysis. Molecular weight 149.18 g/mol: 2,6-dimethylpyridine-4-carbaldehyde at molecular weight 149.18 g/mol is used in structure-activity studies for agrochemical design, where it enables precise dosage calculations. Color index ≤10 APHA: 2,6-dimethylpyridine-4-carbaldehyde with color index ≤10 APHA is used in fine chemical manufacturing, where low color values ensure product purity. Assay (HPLC) ≥99%: 2,6-dimethylpyridine-4-carbaldehyde with assay by HPLC ≥99% is used in analytical reference standard preparation, where it provides reliable calibration results. Reactivity index: 2,6-dimethylpyridine-4-carbaldehyde with high reactivity index is used in novel heterocycle synthesis, where enhanced electrophilicity accelerates reaction rates. Solubility in methanol >30 g/L: 2,6-dimethylpyridine-4-carbaldehyde with solubility in methanol greater than 30 g/L is used in solution-phase peptide synthesis, where improved precursor dissolution increases yield. Storage stability >12 months: 2,6-dimethylpyridine-4-carbaldehyde with storage stability exceeding 12 months is used in inventory-limited laboratories, where extended shelf-life reduces material loss. |
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Working with 2,6-dimethylpyridine-4-carbaldehyde every day in our own production lines, we have learned plenty about what this material offers and where its real value lies. We bring in knowledge not just from the lab bench, but from scaling up batches, fielding technical questions from process chemists, and troubleshooting at the reactor level. The talk around fine chemicals can get abstract, yet behind the glassware and piping remains a straightforward question: Will this aldehyde do its job the way research and industry actually demand?
Out on the market, specialty aldehydes—especially substituted pyridines—fill a range of niches. 2,6-dimethylpyridine-4-carbaldehyde is a standout in our catalog. Its structure gives it two methyl groups at the 2 and 6 positions of the pyridine ring, with a reactive formyl group at the 4-position. That makes the core properties predictably reliable, even at scale. Some may overlook the significance of these methyl substitutions, but they matter. They introduce electron-donating effects, which change both the chemical behavior and the downstream yield of certain transformations, particularly when the compound moves through catalytic reactions or when it’s coupled into more complex molecules.
For chemists and engineers who need precise reactivity, these small differences change the story a lot. We do not rely on textbook generalizations—we manufacture and analyze every lot to make sure those methyl groups are there, because downstream selectivity and stability depend on it.
Product models for this aldehyde generally reflect high purity, low water content, and tightly managed trace metals. In the early days at our plant, the formyl group sometimes changed color or exhibited trace instability, and that led us to invest in continuous drying, argon sealed storage, and better final distillation steps. In the push to exceed 98% purity, we discovered that trace methylpyridine isomers and byproduct aldehydes cause big challenges for our customers in drug discovery and agrochemical pilot runs. It’s not just about hitting a GC area percentage—these extras may interfere with coupling reactions or add noise to analytical screens in scale-up.
We ship this compound as a pale-yellow liquid or sometimes in stabilized crystalline form, typically in amber glass to keep it from degrading under light or atmospheric oxygen. Lab customers have told us off-record that other vendors’ aldehydes turned dark too quickly, so we focus on keeping our product consistent from shipment to its first use, whether that’s in a startup’s fume hood or a multinational’s kilo lab. Seeing containers that still look right six months after packing tells us we did the job right.
Many research teams hunting for new pharmaceuticals or crop protection agents use this compound in their earliest reactions. We see orders coming from medicinal chemists trying to build pyridine-linked scaffolds—structures where controlling substitution is not just a nice detail but a regulatory necessity. The formyl group at the 4-position opens the door for condensations, reductive aminations, or more nuanced construction via Grignard reactions. Industrial intermediates, including specialty ligands for homogeneous catalysis and functional materials, rely on the predictable electron environment 2,6-dimethylpyridine-based starting blocks deliver.
In fragrance and advanced pigment synthesis, this aldehyde acts as a critical precursor. Sometimes we help partners in flavor and fragrance labs, who want aldehydes that avoid unwanted by-notes and provide good conversion without forming mystery side products. An aldehyde with the right ring substitution can keep odor or color development sharp and reproducible.
It’s not just bench chemists who benefit. Large-scale users watch batch times, waste stream costs, and purification logistics. Cleaner, more stable aldehyde cuts down on chromatographic headaches and supports sustainable process goals, since less off-specification material winds up in waste. We have visited plants who switched to our material and shaved hours off their workup sequence—jobs like these are satisfying to hear about.
Within the family of pyridinecarboxaldehydes, each variant holds its own place. 2,6-dimethylpyridine-4-carbaldehyde doesn’t behave like unsubstituted pyridine-4-carbaldehyde, nor does it simply mimic the 2-methyl or 3-methyl analogues. The steric hindrance from two methyl groups can temper over-reactivity, which matters in condensed-phase chemistry and multistep synthesis. We’ve watched customers try to substitute with a cheaper non-dimethyl pyridine aldehyde, only to run into yield or selectivity problems—sometimes subtle, sometimes painfully obvious.
There are economic reasons behind subbing one pyridine aldehyde for another, but as a manufacturer, we see the price-per-mole calculation change once a failed batch or extra purification step enters the mix. Seeing the completed API or pigment with high purity at the end of the line is what builds trust; nobody wants recalls or regulatory flags because of an avoidable isomeric impurity. This compound carves out a unique position—a precision tool in a toolbox which can otherwise seem commoditized.
Experience has taught us that consistency matters more than headline numbers. Sourcing agents and procurement teams often want benchmarks: purity, color, shipment timelines. We meet those, but we watch for what happens at the interface with the world’s real chemistry. Over the years, we learned that impurities in this aldehyde often come from leftover pyridine derivatives in the feedstock, insufficient water scavenging, or sluggish crystallization conditions. Continuous feedback loops with customers help us prioritize which parameters impact the work downstream most—yield, stability, solvent compatibility, or even the handling profile.
There’s a balance between pushing throughput and protecting quality. We changed our column packing and drying routines more than once after conversations with large molecule innovators who traced problems back to invisible moisture or ambiguous storage conditions. We also dedicated batches to custom specs, running longer or with alternate solvents, so researchers who needed precise profiles didn’t have to compromise. Direct engagement has shaped our sense of pride and responsibility in keeping the chemistry honest.
The demand for well-characterized pyridine aldehydes shows no sign of ebbing. Over the last five years, as bioconjugation and advanced materials research matured, we saw an uptick in requests for higher grades, larger volumes, and even tighter impurity profiles. Analytical teams with decades of domain knowledge have told us that the best products are transparent about baseline aldehyde content, water ppm, and exact spectral profile. Early in our manufacturing journey, we fielded more generic requests, but now each run may support a new patent application or an FDA submission. That responsibility shapes how we talk to our partners and prioritize what gets made next.
It’s common for R&D-scale users to screen this aldehyde across several parallel couplings. Speed of delivery and supply assurance have entered the conversation, since nobody wants to run short in the middle of a critical series. Some projects can wait, but a medicinal chemist or new materials engineer often has to deal with one supplier’s out-of-stock message at the worst time. We pay close attention to inventory coordination, backup batch scheduling, and same-week shipping wherever feasible, because delays on our end can stall progress globally.
Manufacturing and storing 2,6-dimethylpyridine-4-carbaldehyde introduces real-world hazards—fewer when handled right, but always present at scale. The aldehyde is prone to oxidation, and over-exposure to air or moisture gives rise to polymerization or brown coloration, hurting purity and downstream usefulness. Lessons from experience taught us to train our teams on minimizing atmospheric contact, whether in drum-filling or reactor charge. Every operator in our shop knows the distinctive almond-like odor and how to spot off-spec color shifts. Factory routines now include rapid analytics to catch quality issues early.
We follow strict containment for liquid and solid phases—mostly with sealed lines, nitrogen or argon overlays, and temperature controls. We never had a major spill in recent years, but minor releases do prompt fast environmental monitoring and cleanup drills, especially because pyridine derivatives bring both flammability and strong odors. Employees and partners can walk through our plant and see the difference between dedicated handling for sensitive aldehydes and generic solvent transfer areas. We carry this knowledge directly into advising customers on lab- and plant-scale handling protocols.
Not every batch is a glory story. We have chased raw material supply issues, adjusted for bad weather affecting upstream precursors, and wrestled with batch-to-batch variation due to subtle changes in temperature ramp profiles. Each day on the line, our team confronts real-world limitations—not just theoretical purity, but shelf life, bottle compatibility, and risk of unintended condensation. We have worked with R&D teams troubleshooting low-yield couplings or odd-tasting flavor compounds that traced back to hidden traces of an isomeric side product. Listening to these challenges, we introduced extra in-process controls and now run deeper NMR checks on uncertain lots.
Where partners confronted issues using less stable aldehydes for key precursor syntheses, we shared methods to improve isolation and purification. One pharmaceutical team battled low conversion after condensation, and we worked through protocols—adding extra drying cycles, leveling up argon blanketing, and reducing exposure to light. Product support for us is not just a polite email; it is our own technical team on the phone or video call, reviewing line-by-line with colleagues a world away, finding fixes that keep projects moving.
In the early years, little thought went into waste management for specialty aldehyde synthesis. As regulatory focus sharpened, and as environmental goals shaped global supply chains, we shifted our process toward less hazardous reagent streams, fewer organics in effluent, and improved yield-per-reactor hour. The flavor and fragrance sector especially flagged the need for clean, responsible production without persistent pollutants. By developing closed-loop solvent recovery and reusing mother liquors from crystallization, our team achieved tangible progress—not slogans, but reduced waste drums and fewer complaints from local water authorities.
Customers increasingly ask not just for a data sheet, but a sustainability profile. How much energy, how many GHG emissions, what is the expected impact from mismanaged waste? We took these questions seriously, not just for branding, but because our operators live and work near these facilities. When fielding a chemist’s technical support call, now we can share both product data and responsible production stories—with nothing hidden, and nothing spun.
Direct relationships with innovation labs, process chemists, and industrial engineers have fueled continuous improvement. Instead of waiting for formal complaints or anonymous survey results, we visit customers, join their technical meetings, and walk through what success and failure look like in their world. If one batch of 2,6-dimethylpyridine-4-carbaldehyde drifts high on moisture or delivers less-than-expected coupling yields, we own that problem up front. These conversations not only guide adjustments in synthesis and QC, they also open new eyes to demand trends—alternative forms, custom packaging sizes, or blends with added stabilizers.
A standout example: we learned from a polymer synthesis startup that latent acidity in aldehyde stock caused unwanted polymer chain breakdowns, something our analytical suite had never caught. The fix meant zeroing in on neutralization at the final synthetic quench stage, creating a better product across the board. Trust builds batch by batch, sometimes from the simplest shared observation on a morning call.
The world of heterocyclic chemistry and the use of 2,6-dimethylpyridine-4-carbaldehyde is anything but static. We track not only published research but also direct requests for new uses—like cross-coupling into photoactive materials, or as a linker for emerging bioconjugation platforms. Rather than just producing and shipping, we stay alert for where standards are rising, whether that means screening down to lower ppt impurity levels or refining supply chain transparency for pharmaceutical compliance. Our take as manufacturers: agility and honesty outperform superficial guarantees.
We have watched this compound move from a narrowly traded intermediate to an essential part of next-generation platforms—always tracked by regulators and end-users, always under scrutiny from spectroscopic methods that only grow sharper. As producers, that challenge motivates careful attention, creativity, and respect for every chemist who depends on the aldehyde being what the label says, every time.
People ask: what makes a good batch of 2,6-dimethylpyridine-4-carbaldehyde? It’s clean starting material, no corners cut in workup, real-time monitoring, quick shipping, and a readiness to answer tough questions if anything goes wrong. Our own history has been shaped by mistakes and successes both; today, we hold onto every lesson. As chemical production shifts and regulatory standards evolve, attention to authentic feedback and the actual needs of working chemists will drive the next improvements. We don’t promise miracles—just the kind of steady, honest delivery that lets others keep building and innovating off a dependable foundation.
That’s our approach. We welcome questions, tough feedback, and real-world problem-solving. It’s how this aldehyde has earned its place in so many toolkits, and how we intend to keep improving.