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Tetramethyl-1,3-Cyclobutanedione

    • Product Name Tetramethyl-1,3-Cyclobutanedione
    • Alias Tetraacetylethylenediamine
    • Einecs 210-132-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    687599

    Cas Number 5610-67-1
    Molecular Formula C8H12O2
    Molecular Weight 140.18 g/mol
    Iupac Name 2,2,4,4-Tetramethylcyclobutane-1,3-dione
    Appearance White to off-white solid
    Melting Point 104-107 °C
    Density 1.05 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Smiles CC1(C)C(=O)C(C)(C)C1=O

    As an accredited Tetramethyl-1,3-Cyclobutanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of Tetramethyl-1,3-Cyclobutanedione is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping Tetramethyl-1,3-Cyclobutanedione should be shipped in tightly sealed containers to prevent moisture and contamination. Store and transport in a cool, dry, well-ventilated area away from incompatible substances. Follow all pertinent regulations for hazardous materials, including proper labeling, packaging, and documentation. Use chemical-resistant materials and avoid exposure to heat or direct sunlight during transit.
    Storage Tetramethyl-1,3-cyclobutanedione should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protect it from light and moisture. Store in a chemical storage cabinet, clearly labeled, and prevent exposure to heat or open flames. Follow all relevant safety and regulatory guidelines for chemical storage.
    Application of Tetramethyl-1,3-Cyclobutanedione

    Applications of Tetramethyl-1,3-Cyclobutanedione in Industrial Manufacturing

    Tetramethyl-1,3-Cyclobutanedione plays a distinctive role in fine chemical processes due to its unique diketone structure and reactivity profile. Our direct manufacturing expertise ensures supply quality and process-specific consistency for downstream clients across several high-value-added sectors. Below, we outline established industrial applications, with practical details to support your technical and regulatory planning.

    1. Pharmaceutical Intermediate for Piperidine Derivative Synthesis

    Producers in the pharmaceutical sector use Tetramethyl-1,3-Cyclobutanedione as a critical building block for proprietary piperidine and heterocycle APIs. During multistep organic syntheses, the diketone structure enables regiospecific condensation reactions, reducing by-product risk and facilitating high purity API output. Sourcing directly from us allows formulation chemists to tightly control raw input profiles and batch traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) raw material guidelines
    • European Pharmacopoeia (Ph. Eur.) monograph requirements
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Applied at 0.15–0.35 molar equivalents as a core condensation reagent, reflecting the targeted piperidine derivative; stoichiometry adjusted per API process route

    Downstream process integration

    • Stagewise introduction during the first or second condensation step within multi-step synthesis, typically following activation or acylation of amino intermediates

    Final product types

    • Active pharmaceutical ingredients (APIs) for anti-Parkinson and analgesic drugs (e.g., piperidine-based compounds)
    • Small-molecule drug substances relying on cyclobutanedione coupling chemistry

    2. Functional Resin Modifier in High-Performance Coatings

    Tetramethyl-1,3-Cyclobutanedione acts as a molecular crosslinker and backbone modifier in specialty polymer and resin synthesis, specifically for manufacturers of high-performance coating materials. Formulators add the diketone during prepolymerization to achieve improved hardness and solvent resistance in their end products. Our process-quality assurance assists coatings companies in maintaining batch reproducibility at industrial scale.

    Industry compliance standards

    • ISO 16000-9:2015 Indoor Air Part 9—Measurement of emissions for coatings
    • REACH (EC 1907/2006) substance registration and safety data protocols
    • ASTM D5402 Standard Practice for Determining Solvent Resistance of Organic Coatings
    • RoHS Directive (where applicable for electronics coatings)

    Typical usage ratio

    • Generally used at 0.5–2.2% by mass within total monomer or polyol feed; precise ratio determined by solvent content and required performance grade

    Downstream process integration

    • Directly blended into resin reaction vessels before thermal or UV-induced curing, enabling scaffold modification and crosslink density tuning

    Final product types

    • Industrial protective coatings (anti-corrosion, solvent-resistant finishes for metal and plastic parts)
    • UV-cured automotive topcoats
    • Electronics encapsulation varnishes

    3. Heterocycle Synthesis Agent in Agrochemical Production

    In agrochemical manufacturing, Tetramethyl-1,3-Cyclobutanedione provides a reactive scaffold for constructing nitrogenous heterocycles, which are common in crop protection and herbicide molecules. Process engineers utilize its diketone reactivity for step-growth transformations, aiming to minimize hazardous waste and maximize intermediate yield during scale-up in continuous or batch reactors.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Environment, Health and Safety Publications: Testing and Assessment guidelines
    • ISO 9001:2015 Quality Management for chemical production control
    • Directive 2009/128/EC (Sustainable Use of Pesticides in the EU)

    Typical usage ratio

    • Dosage set at 0.08–0.25 molar equivalents per heterocyclic target molecule; process engineers optimize ratio to balance cost with reactivity in stepwise synthesis

    Downstream process integration

    • Dosed in the early cyclization step, after primary amine derivatization, under controlled temperature and catalytic conditions for heterocycle ring closure

    Final product types

    • Precursor molecules for selective herbicides and fungicides
    • Nitrogenous pesticide active components

    4. Active Monomer Component in Advanced Polymer Synthesis

    Manufacturers specializing in advanced performance polymers use Tetramethyl-1,3-Cyclobutanedione as a reactive co-monomer for synthesizing specialty cyclic polyesters or diketone-based macromolecules. Incorporating this diketone enables engineers to modulate crystallinity, thermal resistance, and chemical inertness in the resulting polymers, supporting the development of engineered plastics for electronics and aerospace.

    Industry compliance standards

    • UL 94 (Flammability rating for plastic materials in devices and appliances)
    • ISO 9001:2015 for quality management in polymer production
    • IEC 60216 (Thermal endurance for insulating materials)
    • REACH (EC 1907/2006) registration for new polymers

    Typical usage ratio

    • Commonly applied at 1–4% by weight as a co-monomer; adjustments based on molecular weight target and performance requirements for end-use sector

    Downstream process integration

    • Introduced at the monomer feed stage during melt polycondensation or solution polymerization, allowing chain structure modification as polymerization proceeds

    Final product types

    • Cyclic polyesters with high dielectric strength
    • Electronics-grade insulating films
    • Dimensionally stable molded plastic parts for automotive and aerospace

    5. Specialized Intermediate for Fragrance Ingredient Synthesis

    In the fine fragrance and aroma chemical sector, Tetramethyl-1,3-Cyclobutanedione serves as a starting intermediate for constructing specific macrocyclic musk and scent molecules. Our clients use its diketone moiety to facilitate high-yield cyclization reactions under mild conditions. The analytical consistency of our batches ensures predictable reactivity, minimizing purification steps during macrocycle formation.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • ISO 9001:2015 for manufacturing and process traceability
    • EU Regulation (EC) No 1223/2009 on cosmetic products (for fragrance safety)
    • RIFM Guidelines for safety and purity in synthetic musks

    Typical usage ratio

    • Introduced at 0.18–0.45 molar equivalents per macrocyclic musk target; refinements based on ring size and desired olfactory profile

    Downstream process integration

    • Added to cyclization reaction vessels as the primary carbon backbone precursor for macrocyclic musks and related aroma compounds

    Final product types

    • Synthetic musks for perfumes, body care, and consumer cleaners
    • Macrocyclic fragrance ingredients for fine and functional fragrances
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    Certification & Compliance
    More Introduction

    Tetramethyl-1,3-Cyclobutanedione: A Practical Introduction from the Factory Floor

    Tetramethyl-1,3-Cyclobutanedione shows its worth every day inside our production lines and research benches. Since our team started producing this compound, we’ve seen growing interest across specialty chemical fields, especially in pharmaceutical synthesis and advanced material development. We don’t just ship barrels and hope for the best—we work side by side with customers to understand why a material with a name as long as Tetramethyl-1,3-Cyclobutanedione earns its place in high-value and technical uses.

    What Drives Chemists to Tetramethyl-1,3-Cyclobutanedione?

    You’ll rarely find Tetramethyl-1,3-Cyclobutanedione in catalogs aimed at hobbyists or entry-level labs. This compound walks a fine line between stability and reactivity, and that’s precisely why synthetic chemists turn to it. A four-membered ring structure already creates its own unique rules, but the decoration with four methyl groups at the right positions brings new reactivity. We prepare this crystalline solid to exceed 99% purity to ensure it performs as expected. Subtle differences in impurity profiles—minute traces of tri-methyl derivatives or unreacted precursors—can spell disaster for critical downstream applications, so we've invested in closed-system crystallization and in-line analytics.

    Researchers and process chemists demand more than a product that simply fits a catalog number. They’re looking for repeatability, batch-to-batch transparency, and a line to the actual people who made the compound. We serve a customer set that already understands why a tight melting range can mean the difference between meeting a drug development milestone and losing a week’s work. After years engineering these processes, our staff knows which steps in the ketone formation pathway can encourage unwanted ring opening or lead to oxidized byproducts. We’ve worked closely on customer projects that needed kilo-scale lots without sacrificing the impurity thresholds established during early research phases.

    How the Production Line Shapes Reliability

    Tetramethyl-1,3-Cyclobutanedione’s production draws on both classical organic chemistry know-how and a readiness to tweak parameters by hand, sometimes for days at a stretch. We avoid large-batch approaches that mask variability—small reactors backed by constant GC and HPLC checks keep us honest about quality. This hands-on monitoring picks up on solvent effects or subtle shifts in the base-catalyzed cyclization that mark the difference between a workable product and lots that don’t meet a customer’s critical path. Our operators have no illusions about the risks of relying on scale-up tricks that sacrifice reliability. We’ve learned—sometimes the hard way—that there’s no substitute for direct oversight and the kind of pride that comes from running a line yourself.

    Every kilogram we ship comes with a batch record written by real hands. The team that weighs, purifies, and tests Tetramethyl-1,3-Cyclobutanedione signs off on the final results. Customers don’t get factory-line blandness: they see the melting range, the residual solvent profile, and reactivity check runs, plus a short summary of any deviations in that batch. One R&D partner told us he can trace every project milestone back to details seen in these batch notes—and we take that responsibility hard.

    The Model and Specifications: What Makes Ours a Trusted Benchmark

    Within our factory, chemical manufacturing isn’t about detachment or anonymity. Each time we fill a request for our TMK-490 model of Tetramethyl-1,3-Cyclobutanedione, it travels through a controlled chain built for both purity and transparency. We prepare our product to strict parameters: white to off-white crystals, moisture measured to below 0.15%, and retention samples frozen for future spot checks. Lab teams in universities and process plants have put it through infra-red, NMR, and elemental analysis, and we keep every data file for internal review if a question arises months or years down the road.

    End-users describe requesting spectral data post-shipment, sometimes pushing us for microanalytical repeat testing. We answer these requests as directly as possible, because we’ve seen the difference it can make when someone needs confirmation before launching a scale-up run or patent filing. Meticulous recordkeeping, from the type of nitrogen sweep to vacuum oven pull-downs, catches little things—tiny impurities or slight changes in isomeric ratio—that wouldn’t raise alarms in a lower-touch process. We learned that the most demanding customers aren’t trying to nitpick—they’re building medicines, polymers, or specialty catalysts with one shot at getting it right.

    Usage: Where Tetramethyl-1,3-Cyclobutanedione Goes to Work

    Compound design sits at the core of most breakthroughs. Drug development teams use Tetramethyl-1,3-Cyclobutanedione as a building block for complex heterocycles and substituted aromatics. New ligand architectures in catalysis rely on strained ring intermediates, where methyl substitution blocks undesired pathways and gives shelf stability. We’ve worked with academic labs and major pharmaceutical firms exploring syntheses that need a clean, high-purity source at every trial stage—from single-gram metrics up to dozens of kilograms for preclinical runs.

    On the advanced materials side, the rigid cyclobutanedione motif imparts mechanical stability to polymer frameworks and novel functional coatings. Our customers uncovered new uses for the methylated ring in OLED and solar cell precursor work. In these settings, even faint discoloration from trace amines or residual alkali leads to inconsistent device yields. We test for these impurities on every lot. For those scaling up, we supply full compliance documentation—RoHS, REACH—where needed. Every inquiry about shelf life carries hard-earned answers, as our own team watches for changes in color, melting point, or GC peaks under various storage scenarios.

    We know from working directly alongside the chemists designing new processes that sometimes the difference between success and repeated trial runs comes down to reliable access to specialty building blocks like Tetramethyl-1,3-Cyclobutanedione. During slower times, several of our staff kept up research literature alerts, so anything new gets matched with our latest in-process control results to anticipate shifts in demand or spec requests. Our in-house application chemists collaborated with external partners, tracking new mechanisms in carbon-carbon coupling or enolate chemistry—sometimes these studies open new doors for Tetramethyl-1,3-Cyclobutanedione use.

    Why Experience Matters: Our Factory’s Lessons in Handling and Delivery

    Over years of production, we’ve tackled challenges with storage, shipping, and end-user transfer. Handling a material as sensitive as Tetramethyl-1,3-Cyclobutanedione teaches respect for temperature and humidity controls. Our packaging team double-seals every lot, using moisture-locking drums and oxygen barrier liners; warehouse staff check for physical integrity before loading. Shipping isn’t a formality—we try to catch issues before they ever reach a customer, running temperature stress tests and trial runs through the supply chain. Each mishap and improvement story spreads across our teams quickly—these shared field notes shape routines, update labeling, and shift supplier partnerships.

    We don’t farm out responsibility for after-sales support either. When customers ask why a lot seems less free-flowing than before, or why a portion clumped in shipping, we run comparative tests in our quality lab—moisture regain, particle size, and time-to-dissolve checks. These “extra mile” responses come not from a service script, but because defect logs and customer feedback files shape our training and our upgrades. Field engineers who help resolve customer incidents report right back to the line manager and R&D, tuning both production and future risk management.

    How Tetramethyl-1,3-Cyclobutanedione Sets Itself Apart from Other Ketones

    Related compounds like dimedone or 1,3-cyclobutanedione offer straightforward reactivity, but the extra methyl groups at the four positions transform the utility of our product. Tetramethyl-1,3-Cyclobutanedione holds onto its ring shape well during synthetic steps where other diketones open or over-oxidize. This extra rigidity and methyl shielding let chemists steer selectivity in complex multi-step processes—clustering around strong bases, heat, or moisture won’t topple every batch. Early on, technicians noticed that using unmethylated analogs left too much risk for decomposition; the upgraded methylated variant pushed performance higher for research and pilot-scale production alike.

    We stop short of calling it a universal building block—no real specialty chemical earns that title—but repeat customers stick with Tetramethyl-1,3-Cyclobutanedione after hands-on comparisons. Where others see increased side reactions, ring contraction, or loss of desired isomer proportions, our samples keep to their designed purpose. NMR and GC analysis from partner labs confirms minor impurities drop off when handled and purified using the regimes our own team developed through years of head-to-head testing.

    Why not use a more common or less methylated ketone? Some project teams tried, only to circle back after batches failed to hit key targets for stability or downstream derivatization. The methylation pattern built into this molecule means less fussing over byproducts and lower risk for unexpected spectral spikes or unplanned polymerizations. Our process owes plenty of its reliability to experienced plant chemists repeating and fine-tuning classic reactions, always flagging new sources of risk when scaling up from the glass reactor to the pilot tanks. Every new spec request routes right through this accumulated knowledge, shaped by both the literature and the hundreds of controlled runs we track every year.

    Supporting Quality from Order to Application

    Chemists recognize real experience behind product claims. A trader or middleman can quote specs, but the people who synthesize Tetramethyl-1,3-Cyclobutanedione day in and day out know every quirk and risk, hard-won after dozens of cycles through every season and shipment. Many end users tell us they value the ability to double-check any concern directly with a line chemist or operations manager, bypassing phone queues or language games. Direct access to expertise—real operators who can pull archived samples or explain a shift in TLC profile—means projects advance without guesswork.

    Supply chains gave everyone hard lessons over the past years. Our plant wrestled with raw material shortages, sorting out backup suppliers and running comparability studies on each new input. That means we can quantify—and correct for—any tiny changes in precursor quality that influence final batch performance. Every specification slip or unexpected peak on a GC gets tracked, discussed, and, if needed, triggers a deeper route-cause dive. Customers have come to expect this, not as a favor but as a factory standard.

    Documenting each batch outcome with spectra and analysis reports gives science teams certainty for regulatory documentation, patent filings, and internal handoffs. If a pharmaceutical firm or advanced materials lab needs further details, we scan and send historical records, never filtering out “less-than-best” runs, because accuracy matters more than image-polishing. Regular audits and requests for in-process details—the pH at each step, the lot numbers for each solvent shipment—come as part of the routine.

    What We’re Still Learning on the Line

    Research keeps pushing our expectations and our standards for Tetramethyl-1,3-Cyclobutanedione. As customers aim for more ambitious targets—tighter impurity controls, greener synthesis, larger scale output—our teams shift right with them. Ongoing pilot projects target recovery of spent reagents, minimized waste, and improved energy efficiency in ring closure steps. Worker safety programs track air and surface contaminants constantly, because there’s no shortcut to safe, repeatable output when dealing with reactive intermediates.

    We share findings, both good and bad, with customers and sometimes in industry consortia, because private wins mean little if lessons can’t be scaled or transferred. As competition tightens, the people behind manufacturing Tetramethyl-1,3-Cyclobutanedione know sharing new process tricks can lift quality across the sector. Several of our lab staff participate in technical working groups or present updates at regional conferences, helping connect field needs to bench improvements.

    The Human Side of Reliable Chemical Supply

    Supplying Tetramethyl-1,3-Cyclobutanedione means embracing the needs and hurdles shared by end users. Answering difficult questions—about long-term stability, about why a trace impurity evaporated or didn’t, about better packaging for long storage—brings real improvement. We understand each request can mark the difference between project strains and on-time delivery. This respect for uncertainty, and openness to problem-solving, shapes every handoff from our shop floor to our customers’ facilities.

    Chemistry happens at the frontier between the known and the experimental. On this edge, a specialty compound can either unlock new discoveries or drag down lab progress with unexpected hurdles. The staff who make, analyze, and support Tetramethyl-1,3-Cyclobutanedione don’t sit apart from these real-world pressures. Each quality control pass, each adjustment in drying or filtration, each tweak in packing protocol feeds back into the cycle, closing the loop between factory and final application. The satisfaction, or sometimes frustration, shared by customer and supplier, means growth for both sides.

    Looking Forward: Building Trust Through Co-Development

    Manufacturing Tetramethyl-1,3-Cyclobutanedione has never been a static process. Technical demands keep shifting—regulatory frameworks ask for traceability, sustainability, and consistent purity in every drum or jar. Our line meets these expectations because the entire team keeps learning and experimenting, adapting each method or analysis step in light of new findings. We look out for both product performance and the longer arc of purposeful chemical development, so researchers can rely on both our integrity and our technical accuracy.

    Some relationships have lasted years, moving from grams to multi-kilo scale as innovations progress. We continue to update our process documentation, experimental protocols, and risk management so everyone from a start-up drug discovery group to a mature industrial chemistry department knows what to expect. By trading on clear evidence, open dialogue, and respect for the intricacies that an unusual compound brings, we keep Tetramethyl-1,3-Cyclobutanedione a reliable backbone for demanding synthetic and industrial applications.

    Every kilogram we make contains thousands of small decisions by real people. Bringing Tetramethyl-1,3-Cyclobutanedione from the lab to the loading dock, we carry both our technical skills and our commitment to partnership—because, after years on the line, we've seen what true collaboration will build. If a new need arises or a project demands an answer past midnight, our line always stands ready to meet the challenge.