|
HS Code |
103037 |
| Iupac Name | 1,3-Dimethylpiperidin-4-one |
| Molecular Formula | C7H13NO |
| Molecular Weight | 127.18 g/mol |
| Cas Number | 1193-02-8 |
| Appearance | Colorless to pale yellow liquid or solid |
| Boiling Point | 226-229°C (estimated) |
| Melting Point | 37-40°C |
| Density | 0.96 g/cm³ (approximate) |
| Smiles | CC1CN(C)CCC1=O |
| Inchi | InChI=1S/C7H13NO/c1-6-5-7(9)3-4-8(6)2/h6H,3-5H2,1-2H3 |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.479 (approximate) |
As an accredited 1,3-Dimethylpiperidin-4-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a tamper-evident cap, labeled “1,3-Dimethylpiperidin-4-One,” includes hazard and handling information. |
| Shipping | **Shipping Description:** 1,3-Dimethylpiperidin-4-one is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packages are clearly labeled, handled according to relevant safety regulations, and accompanied by proper documentation. Transport occurs via licensed carriers following applicable hazardous material guidelines, ensuring safe and compliant delivery. |
| Storage | **1,3-Dimethylpiperidin-4-one** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Protect it from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature or as recommended by the manufacturer. Clearly label the storage container and restrict access to trained personnel only. |
Applications of 1,3-Dimethylpiperidin-4-One in Industrial Manufacturing1,3-Dimethylpiperidin-4-One serves as a key intermediate in several specialized industrial sectors. Our material integrates within controlled synthesis environments, supporting strict compliance and high-quality standards for downstream users. Below are typical application fields and the associated specific manufacturing scenarios. 1. Pharmaceutical Intermediate for CNS-Active Molecule SynthesisAs a building block in central nervous system (CNS) drug synthesis, 1,3-Dimethylpiperidin-4-One enters the core framework assembly of active molecules, especially for antipsychotic and analgesic APIs. Process chemists employ it within multi-step routes, utilizing its piperidinone core to construct motifs present in several established pharmaceuticals. Strict documentation and traceable raw material identity remain essential throughout all stages. Material quality and purity directly impact reaction yields and downstream purification burdens. We provide extended CoAs to meet global customer QA requests. Industry compliance standards
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2. Agrochemical Synthesis IntermediateProducers of advanced crop protection agents use 1,3-Dimethylpiperidin-4-One to synthesize heterocycle-enriched actives. The intermediate supports the development of insecticides and herbicides requiring nitrogen-functionalized scaffolds. Close analytical QC and clear batch identification are required by agrochemical auditors. Formulators depend on consistent purity and moisture control to prevent by-product formation during condensation or cyclization procedures. Industry compliance standards
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3. Specialty Polymer Synthesis ComponentIndustrial polymerization facilities use the compound as a chain control agent when designing advanced polyamides and functionalized plastics that benefit from nitrogen incorporation at specified sites. Its role includes modifying polymer flexibility and adjusting solubility for technical applications. Accuracy in material addition and storage under inert conditions is key for avoiding side reactions, while batch QC checks for amine value and residual solvent ensure quality. Downstream plastic compounding firms rely on documented supply chain integrity. Industry compliance standards
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4. Fine Chemical Intermediate for Flavor and Aroma SynthesisManufacturers of flavor and aroma compounds select 1,3-Dimethylpiperidin-4-One to build nitrogen-containing cyclic aroma constituents. Experienced formulators adjust charge levels to meet both safety and functional requirements for downstream use in fragrances. Automated batch logs document material addition, and trace impurities must meet strict regulatory thresholds before blending into finished essences. Sensory specialists routinely analyze for unreacted piperidinone to protect consumer safety. Industry compliance standards
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Every day in our plant, the sound of reactors humming and the sharp scent from the latest batch remind us why intermediates like 1,3-Dimethylpiperidin-4-One matter to so many laboratories and production lines. We have spent years perfecting this compound’s synthesis, and that hands-on familiarity has shaped a solid understanding of what makes it stand out in real-world applications.
Making 1,3-Dimethylpiperidin-4-One starts with a precise recipe and constant monitoring. Our teams know the quirks of each raw material lot and the subtle tweaks that safeguard every run’s purity. It’s not enough to follow a reaction chart; experience teaches where temperature spikes affect yields and where additional distillation cycles bring real improvements to the product.
The final product comes out crisp and white—rarely tinted—because control over side reactions means we waste far less material, and customers see fewer unwanted contaminants. Quality always brings its own set of challenges, and sharper analytical tools, such as gas chromatography and NMR, have guided us through unexpected issues far more thoroughly than basic melting point checks ever could.
For chemists hunting for building blocks in specialty synthesis, 1,3-Dimethylpiperidin-4-One delivers more than a label or a simple CAS number. In practice, its methylation at the 1 and 3 positions reduces unwanted side reactions compared to standard piperidin-4-ones. Many five- and six-membered ring intermediates can bog down a reaction sequence with extra steps for protection, deprotection, and purification. Here, you avoid some route headaches thanks to the molecule’s built-in selectivity.
When we ship product out of the warehouse, our teams check typical assay values—customers count on minimums over 98%. Water content often hovers on the low side, well under 0.2%, thanks to vacuum drying before packing. These benchmarks come directly from years working with major process chemists who hammer out real performance demands, not just theoretical ones. You quickly learn from the feedback loop: a little deviation causes a lot of frustration downstream, so our QA teams hold tight to robust protocols.
We’ve had years to compare this compound with close relatives. Standard piperidin-4-one offers greater reactivity at the ring’s secondary positions, which opens other chemistry options but at a cost—more N-alkylation side products or impurities that linger. Unsubstituted versions call for extra purification, especially in pharma routes, where even spots of impurity in late-stage synthesis can ruin entire lots. Choosing the 1,3-dimethyl structure avoids several headaches related to unwanted ring modifications, helping process teams shave off both time and expense.
It pairs particularly well in nitrogen heterocycle expansions, reductive aminations, and as a precursor for advanced ligands in catalysis. In the benches of pharmaceutical R&D, we’ve seen this molecule favored because it unlocks cleaner access to analogues—especially those where alternative N-protecting groups break down prematurely or where deprotection conditions put sensitive substituents at risk. Compared with methylation at only a single ring position, the 1,3-dimethyl’s balance lets teams keep more routes open and pivot during troubleshooting. That sort of flexibility shows its value under real-world deadlines, not just in theoretical retrosyntheses.
Scaling up a molecule like 1,3-Dimethylpiperidin-4-One goes beyond selecting a batch size and running the numbers. Process safety and waste minimization are front of mind for any operation producing at metric ton scale. We have upgraded glass-lined vessels and accurate dosing pumps in our reactor bays for this reason. Each modification grew out of a direct challenge—one year, too much buildup in a filter cost us yield; another, variable impurity profiles told us to invest in tighter in-line monitoring.
This molecule particularly benefits from clean, dry handling. Our staff package every lot in air-tight drums, flushed with inert gas. Freshness is a guarantee—we date all outgoing drums and track storage time closely because even the best-sealed piperidinones will slowly pick up moisture if neglected. Whether it ships to a high-volume generics plant in India or to a small pilot facility in Europe, consistent moisture control means fewer batch reworks and higher trust from customers.
The relationship with our customers shapes how we approach this product. More than once, synthetic chemists have called to discuss issues not apparent from certificate of analysis numbers alone. Some mention crystalline quality—certain polymorphs can make for easier handling and dosing on automated systems. Others want assurance the resin packing the material won’t leach anything unexpected, especially for highly regulated active pharmaceutical ingredient intermediates.
Years ago, we responded to a partner who traced a troublesome interference in their analysis to a particular solvent carryover. Our team spent weeks testing alternatives, rerunning purification, and ultimately narrowed the source to a single upstream step. Since then, we’ve fine-tuned our entire line to cut out that solvent, lowering detectable residues to far below ICH limits. It’s an investment, but it pays off with fewer troubleshooting emails and stronger repeat orders.
Within pharmaceutical research, 1,3-Dimethylpiperidin-4-One plays a distinct role as a versatile intermediate, often showing up where selective substitution is needed without opening the risk of N-dealkylation. Its electron-rich ring stabilizes various transition states, which brings down activation barriers in several C–N and C–C bond-forming routes. We’ve also heard from chemists using it for synthons in CNS-active scaffolds, where other piperidinones falter or require harsh conditions.
In recent years, it turned up as a core intermediate in new candidate drugs targeting neuroreceptor pathways and as part of ligand design for metal-catalyzed reactions in the fine chemical sector. The relatively low boiling point means labs set up careful distillation lines, and we confirm each lot’s trace residue profile before sign-off. Unlike simpler ring compounds, its higher steric demand helps block off-site functionalization, an advantage during process optimization or scale-up.
Specialty coating manufacturers have started to tap into this compound’s characteristics for modification of crosslinking systems, too. Its nitrogen component and twin methyl groups allow fine adjustment in polymer chemistry. While we don’t produce finished coatings ourselves, the feedback from clients has nudged us to improve stability under shipment—so no product leaves the plant before it’s vacuum-sealed and tested for shelf-life consistency.
One of the common hurdles during production comes from batch-to-batch consistency. Even subtle variations in starting amines cause yield fluctuations or impurity spikes. Overcoming this means the procurement team frequently verifies the supply at the source and tracks physical parameters—such as melting points, odor, and even color hints—right to the reactor operators. This hands-on style crosses over into other steps: careful adjustment of pH, precise catalyst dosage, and controlled heating rates. Small gains rapidly add up, especially in high-throughput cycles.
Handling waste and emissions tightly in regulated markets matters for us. Our plants treat mother liquors and vent gases with on-site scrubbers and solvent recovery units. By recycling and using state-of-the-art separation, we reduce waste output and pass recurring local inspections with flying colors. In one recent investment, an in-line spectrometer flags off-spec runs for immediate diversion—cutting down reprocessing cycles and helping us focus resources where they’re needed. Every improvement trickles downstream, lowering overall cost and boosting environmental compliance, which isn’t just about passing an audit but about staying trusted in the neighborhood where our workers live.
Quality isn’t a distant target for us; it’s something we check with every lot, often multiple times a day. Suppliers occasionally send in outside spec material, and experience tells us to never skip a single QC checkpoint. Our facility runs round-the-clock analysis—high-performance liquid chromatography, Karl Fischer titration for water, and trace element checks. Material that doesn’t clear every hurdle doesn’t leave the warehouse.
The more regulated environments, like pharmaceutical active ingredient synthesis, require documentation with full traceability back to the batch and even the drum. Our records stretch back years, and auditors visit regularly to ensure consistency on everything from analytical method validation to temperature monitoring in the storage bays. Each improvement begun because of an audit winds up benefiting every buyer; protocols never regress, and older equipment gets retired well ahead of failure.
Certification is not a paper exercise for us. We host client audits several times a year and join in joint troubleshooting calls over Zoom or in person. These practical visits keep us honest and highlight production bottlenecks we sometimes miss in daily routines. Our best manufacturing changes almost always come from these outside eyes, not just internal reviews.
Personnel safety and environmental controls underpin every production cycle. Our team stands watch over every knob and valve. It’s easy for outside observers to focus only on isolated safety incidents. For us, safety boils down to habit and culture. Workers train on the exact standard operating procedures repeatedly, and every incident, no matter how small, prompts a review and retraining session. Our plant’s strong record with local OHS authorities reflects both the stepped-up investments and a mindset where shortcuts have no place on the production floor.
Working with piperidinones creates specific hazards—vapors, splashes, dust. Everyone on shift wears full PPE, from chemical goggles to filtered respirators, and routine monitoring’s in place to confirm that exposure remains far below any occupational limit values. Even visitors to our plant see the culture at work: no entrance to sensitive bays without proper gear, and each chemical movement documented and double-checked at shift changes. We believe our employees’ health is inseparable from the consistent quality and reliability customers expect from each drum that leaves our site.
We don’t work in isolation. Customer feedback and market shifts drive our projects. When regulations update to include stricter thresholds on residual solvents or elemental impurities, our lab makes it a top priority to phase out offending sources across every batch run. This keeps our clients’ regulatory teams satisfied and helps their own filings succeed faster. Some project partners bring us early insight into new synthetic needs—for example, an emerging drug candidate may demand even tighter isomer purity, and we work back from their requirements to update our purification trains.
As synthesis strategies in pharmaceuticals, fine chemicals, and polymers evolve, we keep revisiting our own processes. Teamwork between R&D, engineering, and floor operators brings new equipment on faster—like automated crystallization setups or updated solvent recovery systems. Each improvement gets phased in only after daily-use testing, so the changes don’t just work in theory but solve the problems operators face on the ground.
Raw material swings, geopolitical events, and logistics bottlenecks all factor into the real price point of 1,3-Dimethylpiperidin-4-One. As a primary manufacturer, we navigate supplier contracts and freight arrangements directly, absorbing shocks where possible to avoid passing every increase to the end user. Keeping close relationships with upstream suppliers means we get alerted early about delays or out-of-spec incoming shipments, and longstanding deals allow us to tie down predictable allotments needed for regular contracts.
Seasonal fluctuations in demand—especially from the pharmaceutical sector—sometimes force changes in production volumes. Instead of simply scaling back, we rotate staff through cross-training and preventive maintenance projects. This approach keeps our team ready for the next uptick and prevents quality dips when full volume resumes. Price quotes from us reflect these production realities, so buyers see fewer surprises and clearer explanations for cost movements.
Sustainability increasingly guides our investment and product decisions. We’ve adopted solvent recycling and energy-saving reactor designs, shrinking our manufacturing footprint. Projects underway with chemical engineers focus on alternative routes that reduce reliance on less sustainable starting materials. Each success here not only brings down production costs but also keeps us and our partners ahead of future regulatory tightening, both local and global.
We’ve seen growing interest from clients in full chain-of-custody documentation and carbon accounting tied to each batch of 1,3-Dimethylpiperidin-4-One. Our systems now track relevant data at production, packaging, and shipping stages, helping clients with their own ESG goals and disclosure requirements. Far from being just a box-ticking exercise, these efforts strengthen our trust bonds and set the stage for long-term supply partnerships.
Every shipment of 1,3-Dimethylpiperidin-4-One that leaves our warehouse carries not just molecular precision but also the warehouse crew’s tracking, the lab analyst’s finetuning, and our operator’s care for detail. The molecule’s unique structure and reactivity profile open doors for synthetic chemists looking to save effort and sidestep dead ends. What truly sets it apart isn’t visible in a data sheet: it’s the day-in, day-out effort by chemists, engineers, and operators who answer every call for consistency, purity, and safety.
We may never know every synthesis in which our product ends up, but the trust built from years of delivering on these values keeps clients coming back. Engineers and synthetic teams rest easier knowing real people stand behind their supply, working daily to dot every ‘i’ and chase every improvement. On the plant floor, progress isn’t abstract; it’s in every small fix, every audit passed, and every batch signed off. That’s what it means to be a manufacturer in today’s chemical industry—and why 1,3-Dimethylpiperidin-4-One will remain a staple in labs and factories that demand more than basic intermediates.