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5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione

    • Product Name 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione
    • Alias Dimedone isovalerate
    • Einecs 249-275-0
    • 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
    Specifications

    HS Code

    285491

    Chemical Name 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione
    Molecular Formula C13H20O3
    Molecular Weight 224.30 g/mol
    Cas Number 79983-71-4
    Appearance White to off-white solid
    Melting Point 105-110°C
    Solubility Soluble in organic solvents such as ethanol, acetone
    Purity Typically ≥98%
    Storage Condition Store at 2-8°C, keep container tightly closed
    Iupac Name 5,5-Dimethyl-2-(3-methylbutanoyl)cyclohexane-1,3-dione

    As an accredited 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione 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 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione, sealed with tamper-evident cap and labeled for laboratory use.
    Shipping **Shipping Description:** 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione should be shipped in tightly sealed containers, protected from moisture and light. It must be packaged according to local and international chemical transport regulations, with appropriate hazard labeling. Ensure temperature control if required, and include safety documentation with each shipment. Handle with standard laboratory precautions.
    Storage **Storage:** Store 5,5-Dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed when not in use. Store in an appropriate, labeled chemical storage cabinet. Avoid sources of ignition and excessive heat. Handle under inert atmosphere if sensitive to moisture or air.
    Application of 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione

    Purity 98%: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 125°C: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione with a melting point of 125°C is used in industrial solid-formulation processes, where thermal stability during processing is critical.

    Molecular Weight 226.3 g/mol: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione with a molecular weight of 226.3 g/mol is used in agrochemical development, where it enables precise dosage control in formulation.

    Particle Size < 50 µm: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione with a particle size of less than 50 µm is used in catalyst preparation, where enhanced dispersion and reactivity are achieved.

    Stability Temperature up to 180°C: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione stable up to 180°C is used in high-temperature polymerization, where it maintains chemical integrity under processing conditions.

    Solubility in Ethanol: 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione with high solubility in ethanol is used in liquid formulation synthesis, where homogeneous distribution and rapid dissolution are required.

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    Certification & Compliance
    More Introduction

    Exploring 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione: Innovation Meets Precision

    Introduction to the Molecule

    Inside chemical research and synthesis labs, practical solutions matter more than buzzwords or shiny marketing. Operators and scientists look for real, tangible benefits in the compounds they choose to work with. 5,5-Dimethyl-2-(3-Methylbutyryl)-1,3-Cyclohexanedione, with its straightforward cyclohexane backbone, aims to offer a dependable performance profile in a range of industries. This molecule brings reliability to research projects thanks to its consistent structure. Drawing on years of hands-on lab work, one thing I know is that consistency cuts through frustration when you’re chasing reproducible yields or mapping out new routes in synthesis. The value here is found in real-world experience, not just charts or bullet points.

    Structural Precision and Model Features

    Compounds don’t earn attention by standing still; they earn it by delivering results. Structural integrity matters, since functional groups and steric configuration set the tone for how a molecule behaves in the field. The 5,5-dimethyl substitution on the cyclohexanedione core, together with the 3-methylbutyryl addition, gives this compound a fine balance between reactivity and stability. In my own experiments, substitutions at these positions often change how molecules interact with nucleophiles, solvents, and catalysts during synthesis. This structural nuance helps chemists anticipate and control reaction outcomes more reliably. In practice, this means operators can cut down on guesswork—and anyone who’s ever chased a rogue side reaction knows just how much time that can save.

    Purity checks and quality control always sit near the top of the list when working with such specialized molecules. The product’s tight specification range for melting point, often hovering near the 100–120 °C region, provides reassurance for those running multi-stage syntheses. Consistent melting behavior often correlates with low impurity content, a point that’s been reinforced again and again during chromatography runs over the years. Customers with stringent purity demands, especially those in pharmaceutical or advanced materials sectors, likely appreciate the attention to these details. Reliable batches mean less troubleshooting, a smaller headache for analytical teams, and smoother progress during scale-up.

    Real-World Usage: What Makes It Useful?

    Products like this serve more than the needs of one small corner of the industry. The reactive diketone functionality makes it a sound building block for a range of advanced syntheses. In organic chemistry, versatility gets rewarded. My own experience has shown that these diketone products often serve at crossroads—forming ligands, templates, or even acting as intermediates during C–C bond constructions. With 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione, the hydrophobic side chains mean you can coax out unique solubility profiles that can benefit isolation procedures after a reaction. Chemists who wrestle with mixed-phase separations or with high-boiling solvents know that the right hydrophobic tweak can make the difference between a nightmare workup and a ten-minute filtration.

    In fields such as agrochemical research or medicinal chemistry, intermediate-quality compounds often slow a project’s momentum. This product’s robust synthesis profile allows researchers to spend less time on source validation or impurity tracking and more time on actual target screening or yield optimization. As someone who has sat on both sides of early-stage discovery and scale-up, I know firsthand that the hours lost to purifying “messy” intermediates add up. Clean, well-characterized materials mean the focus stays on finding new leads, not wrestling with old impurities.

    Comparing With Other Diketones and Related Compounds

    Other diketones with less deliberate substitution patterns often swing toward unpredictable side reactions or sluggish yields. My own work has shown that small structural differences can lead to big shifts in chemical reactivity—methyl or ethyl groups placed just so end up shielding sites from unwanted reactions. Here, bulky dimethyl substitutions at carbon-5 and the 3-methylbutyryl side chain help prevent undesired dimerizations, sometimes a notorious problem in less protected cyclohexanedione architectures. Products built without this level of design sometimes need extra purification steps just to meet the same quality benchmarks.

    Some related products feature aromatic substitutions or extended carbon chains, aiming for particular solubility or reactivity profiles in specialized applications. These analogues tend to cost more, limit versatility, or create handling difficulties due to volatility. Experience with both hydrophobic and hydrophilic diketones leads me to prefer balanced options like this one for mid-scale synthesis: it resists both premature degradation and awkward crystallization behaviors during isolation. Customers gain more control, and that’s a return on investment you can measure directly in cleaner products and fewer analytical surprises.

    Applications Across Sectors

    Chemists working on the front lines of chemical research keep an eagle eye out for intermediates that fit more than one use case. In the pharmaceutical sector, 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione steps in as both an intermediate for heterocycle, enone, or pyrazole frameworks, and as a reference standard in analytical method development. My background in pharmaceuticals underscores just how important it is to have reliable standards; trying to develop a method around an intermediate that drifts from batch to batch is a recipe for stalled timelines.

    In exploration of new agrochemical pathways, diketones like this one play a vital role in shaping both backbone structures and the physicochemical profiles of emerging herbicides and fungicides. A stable platform lets researchers explore subtle changes in activity without fighting structural instability in the core template. Colleagues in agricultural chemistry have often leaned on tightly defined diketone intermediates to screen for both selectivity and effectiveness, a method that shortens time-to-market for promising leads.

    Materials science isn’t left out of the conversation. Writing from experience running polymerization trials, cyclohexanedione derivatives like this one provide controlled insertion points for cross-linking or chain-termination. Polymers that need specific flexibility or thermal resistance gain from the controlled introduction of these diketone motifs, sidestepping the brittleness or reactivity loss caused by less stable intermediates. In all these sectors, confidence in both supply and quality opens doors for more aggressive innovation; it’s hard to push boundaries while double-checking your core chemistry every other step.

    Digging Deeper: Sourcing and Quality Challenges

    Behind each successful experiment lies an invisible web of supply-chain decisions. Reliable access to high-quality 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione hinges on rigorous synthesis protocols and robust partnerships with suppliers. Speaking as someone who has tracked down dozens of hard-to-get intermediates late on a Friday evening, the strain of dealing with inconsistent batches haunts research calendars. Delays in shipping, unnoticed shifts in impurity profiles, or documentation gaps play havoc with reproducibility.

    Transparent supply chains make a difference. Trusted suppliers routinely deliver certificates of analysis with full spectra and impurity breakdowns, giving users a clear window into what arrives at their dock. Analytical teams can spot minor variations before they snowball into bigger issues downstream—an ounce of prevention I’ve seen pay off in both cash and confidence. The emerging role of green chemistry also nudges suppliers to adopt cleaner synthesis methods, reducing both environmental impact and unwanted trace byproducts. With growing pressure from regulators and sustainability-minded organizations, product lifecycle accountability means more than just ticking boxes; it speaks to a company’s ability to invest in lasting relationships over short-term profits.

    Lab Experience: Handling, Storage, and Safety

    Working daily with reactive intermediates, best practice doesn’t just live in procedures; it becomes second nature. 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione tends to behave as a stable solid under room temperature, a welcome relief compared to perishable or volatile analogues. Still, as with any diketone, proper containment remains essential. Storing in a dry, well-sealed container shields the compound from moisture-induced degradation; even brief exposure to ambient humidity can nudge outcomes off course in demanding reactions. The few times I’ve cut corners with less-protected diketone intermediates, reactivity suffered, and projects dragged out days longer.

    Regular training in chemical hygiene and hazard recognition makes a measurable difference. Handling with nitrile gloves, eye protection, and well-maintained fume hoods minimizes risk without bogging down workflow. Safety does not mean sacrificing throughput; it means protecting both research and researchers. Industry best practices encourage labeled secondary containments for storage and prompt clean-up of spills, simple steps I’ve seen avert lab mishaps and waste. Monitoring local disposal regulations for diketone-containing waste protects not only the immediate workspace, but also a company’s reputation and license to operate.

    Potential Hurdles and Ongoing Developments

    No compound is perfect. Sourcing can stumble when key raw materials for synthesis tighten or geopolitical events disrupt distribution routes; cycles of demand within the agricultural or pharmaceutical sectors sometimes spark shortages or price spikes. Shrinking lead times become a balancing act: stockpiling large quantities locks up capital and invites spoilage, but just-in-time delivery can leave projects dangling if supply hits a snag. From my own experience piecing together project timelines and reordering supplies, open communication with distributors and strategic buffer stocks often make or break a lab’s resilience.

    Analytical standards represent another challenge. Pure standards with precise certificates are crucial, since even minor lot-to-lot shifts can mask subtle findings in LC/MS or NMR data. Routine use of internal standards, third-party validation, and cross-checks with reference samples help tamp down variability. Working across international labs, I’ve learned to keep a small but essential library of backup standards to cross-confirm results—insurance not just for the day, but for the years of retrospection that follow.

    Waste management for diketone intermediates keeps climbing up priority lists, both for environmental responsibility and cost control. Developing catalytic processes, solvent-recycling workflows, and even direct recovery of spent diketones can recycle value from what would otherwise become a disposal headache. Teams who embrace this circular philosophy often report not just reduced overhead but also enhanced regulatory standing and public trust. As chemists, the temptation to handle waste “later” runs strong—but speaking candidly from my own lessons learned, early planning always beats crisis-mode logistics.

    Shaping the Future: Opportunities and Solutions

    Looking ahead, opportunities for 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione stretch further than traditional applications. Improved synthetic methodologies continue to drive yields higher, lower energy input, and shrink waste—all qualities welcomed by organizations balancing tightening margins with greater regulatory scrutiny. In research portfolios I’ve managed, collaborating directly with manufacturers to adjust reaction conditions often unlocked new levels of process efficiency or product purity, setting new standards across teams.

    Automation offers another growth vector—streamlining both synthesis and downstream purification minimizes human error, boosts throughput, and reallocates skilled labor to more value-add pursuits. Labs making full use of automated fraction collection and in-line chromatography spend less time on routine tasks and more on hypothesis-driven research. Having worked on both sides of the bench, the relief that comes with a robust, automated workflow cannot be overstated, especially when tight project deadlines loom.

    Open knowledge sharing across companies and academic groups speeds development of new derivatives and analogues. With access to transparent batch histories, validated methods, and honest feedback from the field, progress snowballs. Chemists entering the field today often bring a sense of collaboration matched by respect for hard-earned, time-tested protocols. This shared learning ecosystem, rooted in both trust and transparency, answers tough questions faster, clears roadblocks, and lifts everyone’s results.

    Building Trust: Why Experience Matters

    Trust shapes every decision in chemical manufacturing and R&D. Reliable supply, well-characterized batches, and direct lines of communication between supplier and researcher all make a real difference. Over the years, I’ve learned to value those suppliers who respond with data instead of marketing—ones who don’t just fill an order, but help troubleshoot, adapt, and optimize as needs shift. Relationship matters when it comes to new syntheses or sudden project pivots.

    Risk management forms the backbone of every scale-up plan. Batch failures, unplanned downtime, and recall risks shrink when core materials like 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione consistently meet specifications and arrive with comprehensive data packets. Transparent dialogue with partners who understand the tempo and stakes of real research help align the supply chain with evolving goals—especially as regulatory pressures increase and the lines between fine, specialty, and bulk chemicals continue to blur.

    The compound’s consistent performance continues to reinforce trust with both seasoned professionals and those just starting out. Every new project brings a different set of challenges, but starting from a base of quality material provides a kind of reassurance not easily measured on a spreadsheet. That assurance frees up mental space, allowing focus to shift away from routine troubleshooting toward big-picture advancement.

    Closing Thoughts on Value and Impact

    Over the years, as projects have grown more complex, the need for trustworthy intermediates has done the same. 5,5-dimethyl-2-(3-methylbutyryl)-1,3-cyclohexanedione shows that thoughtful molecular design and strict quality management can support both innovation and reliability. Researchers find new ways to stretch the utility of such compounds—whether crafting novel targets in pharmaceuticals, building out new agrochemical scaffolds, or driving forward material science breakthroughs.

    Value doesn’t just rest in the product or the process, but in the relationships built around shared pursuit of reliable results and informed progress. For anyone committed to pushing their projects further, this compound stands as a testament to what’s possible when excellence, experience, and transparency come together at every stage.