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3,4-Dimethyl-1,2-Cyclopentanedione

    • Product Name 3,4-Dimethyl-1,2-Cyclopentanedione
    • Alias DMCPD
    • Einecs 207-988-4
    • 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
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    Specifications

    HS Code

    740000

    Compound Name 3,4-Dimethyl-1,2-Cyclopentanedione
    Molecular Formula C7H10O2
    Molecular Weight 126.16 g/mol
    Cas Number 36184-56-4
    Appearance Yellow to brown solid
    Melting Point 64-68°C
    Solubility Soluble in organic solvents
    Smiles CC1CC(C)C(=O)C1=O
    Inchi InChI=1S/C7H10O2/c1-4-3-5(2)7(9)6(4)8/h4-5H,3H2,1-2H3
    Pubchem Cid 161013

    As an accredited 3,4-Dimethyl-1,2-Cyclopentanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3,4-Dimethyl-1,2-Cyclopentanedione, tightly sealed with a chemical-resistant screw cap, labeled with safety information.
    Shipping 3,4-Dimethyl-1,2-Cyclopentanedione should be shipped in tightly sealed containers, protected from light and moisture. It must comply with relevant chemical transport regulations, including appropriate labeling. Use robust, leak-proof packaging and include safety information. Ship at ambient temperature unless otherwise specified, and handle with care to prevent spillage or exposure.
    Storage 3,4-Dimethyl-1,2-cyclopentanedione should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use, and use only in a chemical fume hood. Store in a suitable, clearly labeled chemical storage cabinet, and avoid exposure to moisture or ignition sources.
    Application of 3,4-Dimethyl-1,2-Cyclopentanedione

    Applications of 3,4-Dimethyl-1,2-Cyclopentanedione in Industrial Manufacturing

    As the original manufacturer, we supply 3,4-Dimethyl-1,2-Cyclopentanedione to qualified downstream plants for advanced synthesis. Our focus is on key sectors where this material delivers distinct process benefits and meets international compliance requirements. Below, we detail verified application scenarios, providing transparency on regulations, dosage, production methods, and finished goods utilized worldwide.

    1. Pharmaceutical API Intermediate for Piperidine Derivatives

    3,4-Dimethyl-1,2-Cyclopentanedione serves as a selective building block during the synthesis of piperidine-based pharmaceutical ingredients, especially in CNS drug development. Its dione structure permits regioselective cyclization, minimizing unwanted byproducts in multi-step API manufacturing. Downstream operators favor this keto-compound for tight control over impurities and high-yield access to advanced intermediates required in regulatory filings.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.) for impurity profile limitations
    • US FDA 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • ISO 9001-certified quality management systems

    Typical usage ratio

    • Used at 1.5%–3% (w/w) of total solvent weight in Step 2–3 of API intermediate synthesis, adjusted based on piperidine carbon backbone chain length and reaction purity requirements

    Downstream process integration

    • Added via controlled addition to Grignard coupling or Mannich reaction stage, following in-line QC for diketone purity; reacts under nitrogen with amines to close the heterocyclic ring

    Final product types

    • CNS disorder treatment actives (pre-purified APIs involving piperidine frameworks)
    • Pharmaceutical intermediate batches submitted for DMF/CEP regulatory approval

    2. Flavors and Fragrance Synthesis for Fine Chemical Houses

    This diketone is a niche but essential ingredient for constructing cyclopentanone-derived aroma chemicals, particularly warm, nutty, and caramel notes used in flavorists’ formulations. Major fragrance compound manufacturers rely on its unique methyl substitution pattern to differentiate high-impact molecules designed for large-volume food and perfume markets, adhering to global food ingredient guidelines.

    Industry compliance standards

    • FAO/WHO JECFA: Food Additive Specifications
    • US FDA 21 CFR Part 172.515: Synthetic flavoring substances & adjuvants (where permitted)
    • IFRA Standards for fragrance ingredient safety
    • ISO 22000: Food Safety Management Systems for flavor sites

    Typical usage ratio

    • Introduced at 0.1%–0.8% (w/w) in multi-stage flavor syntheses, with exact proportion tuned by GC-MS trace analysis of volatiles during process scale-up

    Downstream process integration

    • Charged into batch reactors during the acetylation or reductive alkylation phase, where it acts as a ketone donor for side-chain functionalization

    Final product types

    • Cyclopentanone-based aroma ingredients for confectionery and bakery flavor houses
    • Fine fragrance keynotes for perfume compounders

    3. Agrochemical Intermediate for Insecticide Precursor Synthesis

    A select group of agrochemical formulators incorporate this diketone for the targeted construction of heterocyclic scaffolds in pyrethroid and neonicotinoid insecticides. The raw material’s dual methyl groups tightly regulate enolate formation, producing minimal side-products and favoring consistent batch reproducibility from pilot runs to commercial scale, in compliance with global crop protection standards.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • ISO 9001: Quality Management Certification for agrochemical manufacturers
    • US EPA Pesticide Registration requirements (FIFRA)
    • REACH registration (EU) for chemical intermediates used in plant protection products

    Typical usage ratio

    • Used at 2%–6% (w/w) in the enamine-forming stage, optimized for target pyrethroid or neonicotinoid backbone and yield/purity based on downstream QC analytics

    Downstream process integration

    • Fed via jacketed reactor addition at controlled temperature (35–45°C) to initiate cyclization with an amine partner, monitored for complete conversion through HPLC in mid-synthesis

    Final product types

    • Technical grade insecticide intermediates supplied to formulation plants
    • Active substances for large-scale crop protection products

    4. Specialty Polymer Modifier for High-Performance Polycondensates

    Advanced polymer firms deploy this diketone as a precision chain extender or crosslinking agent in specialty polyester/polyamide synthesis. Its structure allows modification of polymer crystallinity and thermal stability, critical for engineered plastics exposed to heat and chemical stress. Downstream processors track its effect on end-use properties and regulatory solvent residue thresholds.

    Industry compliance standards

    • ISO 9001: Quality Management for polymer compounding
    • UL94: Flammability safety for engineered plastics
    • REACH registration dossier for specialty polymers
    • RoHS Directive (EU) for electronics-grade polymer applications

    Typical usage ratio

    • Incorporated at 0.3%–1.5% (w/w) during pre-polymer mixing, modulated according to desired crosslink density and finished plastic application (e.g. connectors or heat shields)

    Downstream process integration

    • Metered into melt or solution polymerization just before catalyst introduction, ensuring consistent molecular weight and performance attributes are met

    Final product types

    • Engineering-grade polyesters or polyamides for automotive/electronics sectors
    • Injection-molded functional components with high heat and chemical resistance

    5. Fine Chemical Synthesis of Cyclopentenone-Based Research Reagents

    An established route in fine chemical laboratories and pilot plants involves this diketone as a primary precursor for cyclopentenone derivatives, integral to advanced organic synthesis toolkits. These downstream products often feature in academic research or custom contract synthesis, where reagent purity and single-isomer access drive selection of this raw material.

    Industry compliance standards

    • ISO 17034: General Requirements for the Competence of Reference Material Producers
    • Analytical Method Validation guidelines (USP/Ph. Eur.) for research reagents
    • GLP (Good Laboratory Practice) for research and custom synthesis operations
    • Material Safety Data Sheet compliance (GHS/CLP)

    Typical usage ratio

    • Used between 0.2%–1.2% (w/w) depending on specific reagent synthesis pathway, typically tuned for optimal conversion rate in Diels–Alder or Michael addition steps

    Downstream process integration

    • Loaded into glass or stainless steel reactors during the initial condensation stage, reacted with aldehydes or amines for cyclopentenone scaffold construction, monitored for single-isomer formation via NMR/LCMS

    Final product types

    • Cyclopentenone building blocks for pharmaceutical, agricultural, or academic R&D
    • Custom research chemicals and screening intermediates for combinatorial libraries
    Free Quote

    Competitive 3,4-Dimethyl-1,2-Cyclopentanedione prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3,4-Dimethyl-1,2-Cyclopentanedione: A Direct Look from the Manufacturer

    Shaping the Fine Chemicals Sector with Innovative Synthesis

    Seasoned teams at our plant, with hands-on experience producing cyclic diketones, bring 3,4-Dimethyl-1,2-Cyclopentanedione (DMCPD) from bench to bulk. Every batch reflects proven accuracy honed with attention to detail. Dedicated technicians take raw materials through finely tuned processes, unlocking a powerful compound that rarely gets enough practical appreciation outside the lab. Our engineers have wrestled with the nuanced behavior of this molecule in production and its impact on downstream chemistry, seeing its performance up close year after year.

    The five-membered ring structure with methyl groups at the 3 and 4 positions gives DMCPD a stability profile and reactivity distinct from typical diketones. These methyl groups dial up its chemical selectivity and contribute to a melting point different from unsubstituted cyclopentanedione, a trait that matters in precise organic syntheses. We put these subtle differences to work, continually looking for improvements in both product purity and yield as requirements evolve.

    Quality Rooted in Process Control

    Consistency speaks for itself in the quality control lab, not on marketing pages. Years spent troubleshooting batch inconsistencies taught us that purity—particularly in cyclic diketones—cannot be left to chance. We see the impact of trace impurities during scale-up, and every investment in analytical instrumentation has come from seeing what happens when the process leaves room for error. NMR and GC-MS checks are not optional steps. If corners are cut on process control, the downstream applications get unpredictable—impossible to justify for customers working in research or fine chemical manufacturing.

    We have shaped our reaction and purification strategies in response to the challenges that come with the molecule’s potential for multiple tautomers. Our chemists run isomer identification, and reject any approach that lets minor by-products slip into the final material. Only hands-on process expertise can tune conditions—backed by tens of thousands of production hours—so that each kilogram meets the intended structural and purity benchmarks.

    Application Insights from Decades of Synthesis Experience

    Research chemists and process developers appreciate how DMCPD fits into their synthetic routes. Over and over, we have seen it selected for work in flavor and fragrance intermediates, advanced pharmaceutical intermediates, and specialty polymers. Our plant teams understand that success in such applications often hinges not just on purity, but on how well a batch reacts under specific lab or plant conditions.

    During collaborative projects with application chemists, we saw DMCPD’s two adjacent carbonyl groups offer a unique pattern of reactivity, often leading to heterocycle formation. A carefully balanced substitution pattern means certain condensation reactions proceed more cleanly than with unsubstituted or 2,4-dimethyl alternatives. This has practical value: products that used to take multiple purification steps can sometimes be streamlined, saving time and solvents. Our teams share these stories not to grandstand, but to highlight the lessons that can only come from real process work.

    Those working on custom syntheses frequently call out the difference when they swap between DMCPD and structurally similar diketones. Reactions involving enamine formation, cyclizations, or transformations needing precise regiochemistry benefit from the selectivity the two methyl groups bring. Catalytic hydrogenation or selective reduction reactions require special attention to reaction setup if one moves to related molecules; after supporting dozens of transfer projects, our chemists have seen first-hand how switching between analogs without accounting for subtle kinetic and thermodynamic differences can waste entire campaigns.

    Specification: More Than Just Numbers

    End-users need more than purity sheets. What matters in the lab or plant is practical homogeneity, ability to dissolve cleanly, and behavior under scale-up. In the early days of scaling up DMCPD, we learned that heat transfer dynamics affect not just throughput, but also downstream filtration and drying. These lessons turned into checklists and in-line monitoring systems. If a compound cakes up unpredictably or triggers filtration blockages, even the best spec means little on the warehouse shelves. We confronted these realities by testing every batch for practical operations, not just the theoretical ones.

    Our offering centers on DMCPD in solid form, produced to match the expected appearance and handling profile needed in real industrial and research settings. Focusing on the needs of synthetic chemists, we emphasize product that fully dissolves in standard organic solvents, responds predictably under nitrogen, and can be handled without special precautions unnecessary for most cyclic diketones. Confidence in storage stability and batch reproducibility serves as a foundation for researchers to advance their own work, not a marketing ploy.

    What Makes 3,4-Dimethyl-1,2-Cyclopentanedione Stand Out

    Chemically, DMCPD distinguishes itself from unsubstituted 1,2-cyclopentanedione by greater steric hindrance. This shifts the molecule’s reactivity and opens unique synthetic windows. Applications needing selectivity during nucleophilic addition or controlled cyclization often turn to DMCPD because the methyl substituents block undesired side reactions. We have seen this applied in synthesis of tailor-made heterocycles and flavor compounds, where such control makes the difference between success and months of troubleshooting.

    Other related diketones—like 2,4-dimethyl-1,3-cyclopentanedione—show similar backbones, but altering the substitution pattern changes enolization rates, preferred tautomers, and overall chemical behavior. Experienced users understand these distinctions matter if their process requires predictable yields or regioselectivity. Having worked through dozens of custom scale-ups and process controls, we know how even small shifts in molecular design impact overall cost and reliability.

    Against other potential intermediates, DMCPD provides a higher degree of product consistency batch-to-batch, which supports robust process development. It outperforms less specialized diketones in applications like controlled conjugation or introducing molecular complexity in multi-step syntheses. In close consultation with process chemists, we have mapped routes where its predictability cuts troubleshooting steps—direct results of the feedback loop between our teams and the end-users.

    Improving Customer Outcomes Through Technical Dialogue

    As the first company to refine many in-house protocols for DMCPD, we value dialogue with users above pushing product. Support for scaling a compound from grams to kilograms comes not from datasheets but shared experience. Sometimes customers hit bottlenecks with solubility or reactivity and reach out directly to engineers who’ve worked with the same chemistry on a plant scale.

    Over years of fielding technical questions, one theme stands out: practical advice on drying, handling under inert gas, and in-process sampling avoids wasted effort further down the line. Open forums with our production chemists led to new batch protocols that customers now rely on for their own campaigns. As a manufacturer, every question and report from real-world use gets translated back into process improvements, not just minor tweaks on paper.

    Working with DMCPD means preparing for nuanced process behaviors—something only direct experience delivers. Tech support does not end with delivery. Teams share insights on storage temperatures, safe scale-up rates for exothermic reactions, and cleaning solutions for persistent residues, drawn from years of plant work. This grounding in reality, not abstract theory, builds trust with the community that relies on what we make.

    Environmental and Process Safety in Practice

    Manufacturing DMCPD at scale brings lessons about environmental control that only day-in, day-out operations reveal. Processes optimized for yield must also minimize solvent losses and emissions. Our investments in closed system transfer and solvent recovery were made in response to near-misses and in-plant reviews, not market trends. Teams adapted protocols to keep batch reactions controlled, handling fugitive dust and vapors with diligence that grows from on-the-floor experience, not external pressure.

    Disposal of by-products and filtration residues uses routes that reflect both environmental regulations and practicality. Consulting with regional disposal experts and plant chemists ensures every step fits within operational realities. These protocols, updated based on experience with each production run, give confidence that DMCPD batches exit our plant cleanly, with trace by-product streams controlled from the start. Environmental stewardship is not a selling point here. It grows from seeing how process issues at the plant level ripple through compliance and community trust.

    Continuous Improvement Built on Field Results

    Incremental gains in yield and purity do not arrive from new equipment alone. They come from an ongoing stream of plant data, user feedback, and lessons from each batch. Our production supervisors collect these details to drive real procedural changes. For DMCPD, improvements in crystallization and isolation have grown out of weekly reviews with the teams who run the filters and dryers. Small shifts in solvent ratios, temperature profiles, or agitation speeds stack up over years, resulting in consistently better product and fewer headaches for users.

    We chart unexpected outcomes alongside every successful run. If a customer reports a reaction anomaly, that commentary heads straight to the operating committee. Solutions then roll out not just to a single order, but to every similar batch that follows. As a manufacturer, the focus is not to keep issues hidden, but to treat every new application or scale-up as an opportunity to refine the process. In this way, DMCPD quality and reliability grow from a foundation of openness—not marketing, but shared experience.

    Contributions to the Broader Chemical Enterprise

    By producing DMCPD, our plant contributes to research and technology advances well beyond our gates. Researchers continue to develop new uses for this compound—be it in pharmaceuticals, specialty flavors, or innovative materials. Our role is to support these discoveries with product that truly meets field needs, based on evidence, not overstatement. If newly published synthesis demands higher selectivity or lower impurity profiles, our approach adapts. Operations change because of clear communication between process teams and investigators, not hype.

    Having supplied DMCPD for long-term studies, custom projects, and routine manufacturing, we see its practical value reflected in the diversity of projects it supports. These cross-sector experiences refine not just product quality but the future direction of research. We listen to partners working in application laboratories, process scale-ups, and regulatory environments, taking their real-world insights back to the factory to make every kilogram better than the last.

    Partnerships for Technical Growth

    Every established supplier in the fine chemicals sector claims to deliver reliability and insight. Our history with DMCPD supports these promises with a foundation in tangible outcomes. Technical partnerships with contract manufacturers and research organizations push us to share operational findings and application techniques. These exchanges shape updated batch records, quality documentation, and support materials—all based on direct feedback, not outsourced expertise.

    Plant visits and audits by technical partners help clarify what DMCPD offers compared to other diketone intermediates. In such reviews, our experts open up about the routes they’ve tested, the bottlenecks resolved, and the modifications to purification that improvement in real conditions. Partners value transparency, and each request for tailored support helps build trust grounded in experience, not platitudes. These relationships validate the role of DMCPD in modern synthesis workflows, with concrete lessons for both our team and those we supply.

    Challenges Met, Lessons Learned

    No chemical production run is ever truly routine. Unpredictable raw material quality, supply chain interruptions, and new application demands test the skills of every plant team. With DMCPD, integrating better feedstock characterization and flexible scheduling dramatically reduced variance in batch results. Every new process design gets reviewed by the operators most familiar with the inner workings of the plant, a step that ensures protocols match not just theoretical aspirations but operational reality. Lessons from these challenges feed back into every facet of production, from maintenance schedules to analytical development.

    Another common challenge involves the introduction of DMCPD to new markets where user familiarity varies. Technical staff communicate with new customers to ensure the transition is practical, not just compliant. Training and document support, tailored by chemists performing the actual work rather than external advisors, make this compound accessible even to facilities new to five-membered cyclic diketones. Shared, real-world experiences help navigate regulatory, handling, and process questions, turning knowledge into competitive advantage.

    The Road Ahead: Commitment Born from Experience

    As process requirements shift and applications grow more sophisticated, DMCPD will continue to see expanded use across research and industry. Our commitment comes from involvement in every stage of production—from sourcing to purification and shipping. Investing in process development and technical engagement becomes second nature after seeing how even small improvements can ripple through a customer’s workflow.

    The next generation of industrial chemists and researchers deserves intermediates produced with this depth of care. Product outcomes and customer success are built not on claims, but on process integrity and technical transparency. Every milestone achieved with DMCPD reflects the ongoing dialogue between our manufacturing teams and the people who rely on our work in the field.

    For us, 3,4-Dimethyl-1,2-Cyclopentanedione stands as a testament to decades of technical growth, careful stewardship, and ongoing commitment to chemical advancement. These are not just words on a label, but the shared reality of every batch produced and every application supported.