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HS Code |
676722 |
| Iupac Name | 3,5-Dimethoxy-4-pyridinecarboxaldehyde |
| Molecular Formula | C8H9NO3 |
| Molecular Weight | 167.16 g/mol |
| Cas Number | 36052-38-9 |
| Appearance | White to off-white solid |
| Melting Point | 85-89 °C |
| Solubility | Soluble in organic solvents such as DMSO, ethanol, methanol |
| Smiles | COC1=CC(=NC=C1OC)C=O |
| Inchi | InChI=1S/C8H9NO3/c1-11-7-3-8(12-2)9-4-6(7)5-10/h3-5H,1-2H3 |
| Pubchem Cid | 3223783 |
As an accredited 4-pyridinecarboxaldehyde, 3,5-dimethoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled “4-pyridinecarboxaldehyde, 3,5-dimethoxy-” with hazard symbols, tightly sealed for safe storage. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 160 drums (200kg/drum), totaling 32,000kg; securely packed, moisture-protected, for 4-pyridinecarboxaldehyde, 3,5-dimethoxy-. |
| Shipping | 4-Pyridinecarboxaldehyde, 3,5-dimethoxy- is shipped in tightly sealed, chemical-resistant containers under ambient or controlled temperatures, typically via ground or air freight. Packaging adheres to regulatory standards for hazardous materials. Proper labeling, documentation, and handling procedures are followed to ensure safety and compliance during transportation. |
| Storage | **4-Pyridinecarboxaldehyde, 3,5-dimethoxy-** 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. Protect from light and moisture. Store at room temperature, and ensure proper labeling. Use appropriate safety measures, including gloves and eye protection, when handling this chemical. |
| Shelf Life | The shelf life of 4-pyridinecarboxaldehyde, 3,5-dimethoxy- is typically 2–3 years when stored in a cool, dry, and dark place. |
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Purity 98%: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Molecular weight 181.17 g/mol: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- of molecular weight 181.17 g/mol is used in fine chemical manufacturing, where accurate stoichiometric calculations enhance reaction efficiency. Melting point 84°C: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- featuring a melting point of 84°C is applied in organic synthesis processes, where thermal stability improves compound isolation procedures. Solubility in methanol: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- with high solubility in methanol is used in catalyst development, where rapid dissolution promotes homogeneous reaction conditions. Storage stability at room temperature: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- with storage stability at room temperature is used in research laboratories, where prolonged shelf life reduces material degradation. Low water content <0.5%: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- with water content below 0.5% is used in moisture-sensitive coupling reactions, where it prevents unwanted hydrolysis. Reactivity profile: 4-pyridinecarboxaldehyde, 3,5-dimethoxy- with a reactive aldehyde group is used in heterocyclic compound synthesis, where it enables efficient formation of target molecules. |
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On the other end of every flask and drum of 4-pyridinecarboxaldehyde, 3,5-dimethoxy- shipped from our facility sits a real story: a journey from raw material, to precisely-controlled reactions, to the hands of researchers and formulation teams who rely on chemical consistency. This compound, known for its unique structure—where the pyridine ring carries both the active aldehyde group and two methoxy substitutes at the 3 and 5 positions—doesn't only reflect careful synthetic chemistry; it becomes a testament to years of incremental improvements in our manufacturing process.
Our manufacturing process avoids shortcuts. Instead of relying only on tried-and-true routes, our R&D group frequently challenges existing protocols by optimizing each step for both yield and impurity control. In practical terms, that means several steps in our 4-pyridinecarboxaldehyde, 3,5-dimethoxy- production use high-purity feedstocks and lots of real-time analysis, especially at the methoxylation stage. By monitoring both temperature and reagent ratios closely, we help minimize troublesome byproducts like 2-methoxy impurities, a concern that sometimes appears from less controlled manufacturing setups.
For every kilogram that leaves our reactor, our technical team runs a battery of analytical tests, including HPLC, GC-MS, and proton NMR—not just a single sample but random selections from every lot. Labs and formulation chemists who depend on quality pick up on this difference quickly. Our product typically appears as a white to faintly pale powder or crystalline solid, with purity levels topping 99% in most runs and water content kept low enough to not distort sensitive reactions.
Modifying the pyridine ring changes reactivity in striking ways. The two methoxy groups at positions 3 and 5 don’t just dress up the aromatic structure—they tune electron density, modulate solubility, and often shift the balance of selectivity when reacting with nucleophiles or electrophiles. For pharmaceutical intermediates that need precise installation of further functional groups, this difference can decide the fate of an entire process. In our experience, synthetic chemists notice that the 3,5-dimethoxy arrangement stabilizes the ring while activating the aldehyde group enough for delicate condensation reactions. Pure 4-pyridinecarboxaldehyde oxidizes or polymerizes too easily in certain settings, whereas the dimethoxy variant holds up in more aggressive conditions.
Our customers approach this intermediate for a few major purposes. A significant portion heads toward medicinal chemistry, especially library screening and small molecule API projects. In those programs, the 3,5-dimethoxy substitution profile allows for robust divergent synthesis. Research teams often highlight how the product’s aldehyde group enabling various C–C bond-forming routes—like Knoevenagel and Wittig reactions—streamlines new lead structures.
Other projects land the compound into fine chemical syntheses where the tuneable reactivity is central to constructing complex heterocycles. We frequently supply kilo quantities for agrochemical research, where it serves as a building block for products requiring intense regulatory scrutiny. Process chemists have told us of their frustrations with variable reactivity in batches from less-controlled producers, especially in scale-up work; our consistent impurity profile—especially low levels of starting pyridine, methylated byproducts, and acid residues—means their process development cycles stay on track.
The landscape of pyridinecarboxaldehydes includes simple, unsubstituted versions and variously positioned alkoxy or halogen derivatives. Many of these, while synthetically useful, don’t match the performance of 3,5-dimethoxy-substituted compounds in certain scenarios. Through countless pilot batches, we’ve charted some consistent themes:
We’ve received detailed testimonials from trusted customers praising the product’s low tendency to form dark decomposition products in storage—a direct reflection of less autoxidation, thanks to careful exclusion of transition metals during final workup.
Inside chemical manufacturing, stories of “batch drift” and mysterious colorations are all too familiar, especially among specialty fine chemicals sourced from non-specialist suppliers. Some labs have faced repeated headaches where commercially sourced 4-pyridinecarboxaldehyde, 3,5-dimethoxy- arrives yellow or tan, not white, due to uncontrolled reaction temperatures during methoxylation or improper isolation techniques.
Because we understand these pitfalls, our QA and QC teams dig into the fundamental causes behind batch-to-batch variability. Close relationships between process engineers and analysts help pinpoint root problems: unreacted starting material, traces of metal contamination, or incomplete removal of side products after cyclization. Solving these issues sometimes demands months of experiment—tweaking purification sequences, testing new filtration aids, evaluating inert atmosphere protocols at every stage. Only after we see sustained improvements do we scale updates to full production.
Chemists downstream have asked about alternatives or fixes for off-color batches. Our answer stays straightforward: trace the source, not just blame odds or “process noise.” Over time, repairing upstream processes—like refining raw material grading or investing in better reactor design—delivers more lasting quality improvements than just adding more steps to purification. We’ve seen how these investments come through for customers: retention of white color, higher solution clarity, and—with the right packaging—longer shelf life.
Manufacturing isn’t only about making grams or kilos—it involves building trust. Our lab books track each batch, linking raw material codes, operators, and detailed parameters, including reaction temperatures and vacuum levels. No step slips through the cracks. All traceable to original source lots, so any anomaly traces quickly from shipment back to originating reactor or handler.
This breed of meticulous traceability builds confidence with clients, some of whom require near-pharmaceutical-grade documentation. For academic groups, the data set acts as a foundation for reproducible synthesis, while industrial partners tap into transparency as support during regulatory audits or tech transfers.
We’ve learned the hard way that “black box” manufacturing and incomplete paperwork fuel suspicion and delays. Opening process logs and providing full COA data—rather than only summary test results—shortens questions and builds clearer expectations. Information is shared not because it’s required by regulation, but because real science unfolds faster when uncertainty shrinks.
Everyone in our team—from shift operators to warehouse workers—recognizes that the journey of 4-pyridinecarboxaldehyde, 3,5-dimethoxy- does not finish at the plant gate. Packaging forms a critical line of defense. We favor high-barrier triple-lined polyethylene bags, hermetically sealed, and stored in shaded, cool environments. Cardboard drum packaging has been reinforced over the years to resist both breakage and accidental humidity ingress. We encountered rare cases where mishandling during transport or storage allowed atmospheric moisture to enter—resulting in clumped, discolored material. That led us to rebuild our logistics chain to reduce risk at transit breakpoints.
Customers benefit from this relentless focus: materials arrive in usable, laboratory-ready form, without the need to dry or reprocess. A simple scoop, weigh, and measure is all that separates our product from the reaction flask, which is especially important when working against tight development timelines or urgent production windows.
Direct customer connection defines how we approach technical service. Route development chemists regularly share real-time feedback about their problems—maybe a specific reaction sticks at an unexpected intermediate or throws a side product—and our technical support responds by consulting with our synthesis team and laboratory analysts. We don’t believe in off-the-shelf answers; every troubleshooting session deepens collective knowledge on both sides.
One memorable experience: a pharma customer struggled with unexpected peaks in their in-process HPLC report. Their own internal investigation stopped at “trace aldehyde impurity,” and fingers pointed vaguely at raw material. We invited their chemist to walk our plant and test side-by-side. By running split-lot side-by-side reactions using multiple manufacturers’ products—including our competitor’s—they pinpointed the culprit as a storage-induced byproduct, not a manufacturing residue as first suspected. This kind of collaboration dissolves distrust and speeds development, saving weeks otherwise lost chasing false leads.
Years of manufacturing have taught us that chemicals do not just impact the bench—they ripple into the environment and surrounding communities. Waste handling from the 3,5-dimethoxy methoxylation reaction isn’t trivial. The process creates methyl halide byproducts and spent acid streams. Our facility reclaims solvents in closed-cycle systems, reducing air emissions and minimizing off-site incineration. Hazardous residues are neutralized on-site under strict control. Our compliance team reviews all reaction modifications against evolving environmental regulations, using both external audits and internal spot checks, to assure that process changes don’t create unexpected new hazards.
Worker safety matches these priorities. Each reaction step, especially involving aldehydes and strong acids, follows clear protocols. Operators wear chemical arcsuits and work in fully vented hood spaces—an approach learned after early incidents when minor leaks or dosing errors led to strong odors or skin irritation. Safety culture is built through monthly reviews, open-door reporting (even for “near misses”), and routine fire and containment drills. Although these routines don’t grab headlines, our injury-free record for several years running means less downtime and more consistent output.
The customers for 4-pyridinecarboxaldehyde, 3,5-dimethoxy- span academic, CRO, fine chemical, and pharmaceutical fields. We’ve witnessed researchers customizing reaction conditions far beyond original literature protocols: solvent swaps, greener bases, in situ derivatization—all chasing the next formulation breakthrough. Feedback shared with us often turns into R&D projects, eventually leading to shifts in how we produce or purify material. For example, one major agrochemical developer needed consistent lots with tighter control on a specific impurity that showed no biological impact but affected their downstream analytical readout. By re-optimizing our isolation sequence, we trimmed levels of this impurity by 40%, winning not just their repeat business but also new insight into process-chemical relationships.
Broader collaboration extends to industry associations and standards-setting bodies. We send technical leads to working groups focused on sustainable chemistry and best practices in pyridine synthetic workflow. Ideas that spring out of these discussions, such as alternative, lower-toxicity methyl source trials, often make their way back into our development projects.
Producing specialty chemicals such as 4-pyridinecarboxaldehyde, 3,5-dimethoxy- always reveals new challenges, even after decades in the business. Global supply chain shocks, energy price swings, and shifting regulatory landscapes all influence raw material availability and pricing. Sometimes, sourcing high-purity methoxy reagents or specialized catalysts means looking well outside ordinary supplier lists. Delays trace all the way back to mines or petrochemical plants halfway around the world.
To buffer this uncertainty, we maintain both diversified supplier files and in-house purification reserves for critical materials. We invest in long-term contracts and alliances with trusted partners, coupled with an emphasis on strategic stockpiling. Flexibility—reactor scheduling, expedited shipping, dedicated QA hold tanks—keeps disruptions away from regular customers.
Continued process improvement stays at the core of our outlook. Our R&D team tests more selective catalysts, solvent alternatives with a lower environmental footprint, and in-line monitoring tools designed to spot problems before they snowball into failed batches. Process intensification trials, where multiple reaction stages combine, consistently show potential for reduced waste and lower costs—although each advance requires careful validation.
Users working with specialty pyridine intermediates know the difference between buying direct from a maker versus from a general trader. Immediate technical answers, faster troubleshooting, and real process improvement discussions are only possible when consumers and manufacturers maintain a two-way communication line. The demand isn’t just for purity or competitive cost; it’s for predictable support, deep expertise, and supply continuity.
Our plant’s track record is built on this philosophy. From raw material sourcing to final shipment, we stand behind every batch, not just because market competition requires it, but because real advances in chemistry depend on trust between laboratory and manufacturer. As regulations, chemistry, and customer needs evolve, we’ll keep putting process improvements, open information, and hands-on support at the center of what we do.