|
HS Code |
326054 |
| Name | 3,5,5-Trimethylcyclohexane-1,2-dione |
| Cas Number | 1553-47-7 |
| Molecular Formula | C9H14O2 |
| Molecular Weight | 154.21 g/mol |
| Appearance | White to pale yellow solid |
| Melting Point | 55-59 °C |
| Solubility In Water | Insoluble |
| Smiles | CC1(CC(=O)C(=O)CC1)C |
| Inchi | InChI=1S/C9H14O2/c1-8(2)5-4-7(11)9(3,6-8)10/h4-6H2,1-3H3 |
| Pubchem Cid | 122551 |
As an accredited 3,5,5-Trimethylcyclohexane-1,2-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 100g amber glass bottle, tightly sealed with a screw cap, labeled "3,5,5-Trimethylcyclohexane-1,2-Dione, 100g." |
| Shipping | 3,5,5-Trimethylcyclohexane-1,2-dione should be shipped in tightly sealed containers, protected from light, moisture, and heat. Transportation must comply with local and international regulations for chemical substances. Appropriate hazard labels must be affixed. Handle with care, ensuring containment to prevent leaks or spills. Consult the SDS for specific shipping instructions and emergency procedures. |
| Storage | Store 3,5,5-Trimethylcyclohexane-1,2-dione in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Handle in accordance with good laboratory practices, using proper personal protective equipment. Avoid moisture and sources of ignition to maintain chemical stability. |
Applications of 3,5,5-Trimethylcyclohexane-1,2-Dione in Industrial Manufacturing3,5,5-Trimethylcyclohexane-1,2-dione serves as an intermediate and functional component in a defined set of specialty industrial sectors. The following application scenarios illustrate its actual downstream integration, with process details, regulatory standards, formulation ratios, and end-use product types based directly on large-scale industrial practice. All information reflects real-world use and addresses specific, targeted manufacturing channels. 1. Pharmaceutical Intermediate for Corticosteroid SynthesisThis diketone acts as a building block in multi-step syntheses of selective corticosteroid active ingredients. Downstream pharmaceutical manufacturers employ it as a precursor in the preparation of steroidal moieties, especially for products where precise configuration and minimal byproduct formation are essential for batch reproducibility and compliance with registration dossiers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Pyrethroid SynthesisWithin agrochemical complex synthesis, this material is incorporated as a core ring precursor for certain pyrethroid insecticides. Its use supports scalable, controlled assembly of active moieties targeting high efficiency and long-term storage stability of the final technical products. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Polymer Additive for High-Performance Polyurethane SystemsSelected producers of polyurethanes and specialty elastomers utilize this diketone to impart controlled flexibility and improved hydrolysis resistance in the polymer matrix. It modifies crosslinking dynamics in rigid foams and elastomer blends, where chemical resilience and long open-cell life are required. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Flavor and Fragrance Intermediate in Specialty Aroma CompoundsIn the flavor and fragrance sector, this diketone serves as a precursor for synthetic musks and cyclic aroma molecules. Its reactivity profile favors controlled condensation, producing keynotes in fine fragrance bases as well as trace-level flavoring ingredients for regulatory-compliant finished goods. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Organic Synthesis Building Block for Specialty ChemicalsManufacturers of tailored fine chemicals employ this diketone in targeted transformation procedures, such as enolate-coupling, cycloaddition, and functional group exchange chemistry. Its molecular structure enables construction of high-value intermediates used in performance additives, specialty solvents, and customized reagents. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,5,5-Trimethylcyclohexane-1,2-Dione prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
As a chemical manufacturer rooted in decades of fine chemical synthesis, I can say new projects rarely surprise us unless the chemistry itself holds a distinct personality. 3,5,5-Trimethylcyclohexane-1,2-dione—sometimes known in-house by its structural shorthand, because saying the whole name out loud every day would test even our patience—stands out from the usual crowd of cyclic diketones. The molecular structure jumps off the page when you see it: a trimethylated cyclohexane ring, sporting two ketone groups at the 1 and 2 positions. Each lot that leaves my facility represents the culmination of years optimizing process steps, from sourcing high-purity starting materials to washing, crystallizing, and drying under precisely controlled conditions.
What does all this add up to for users? The answer often depends on the demands of their process. Many industries seek this molecule for its versatility in synthetic routes. I've worked with buyers in agrochemicals, intermediates for active pharmaceutical ingredient (API) synthesis, and those breathing new life into the flavors and fragrances sector. We have also witnessed interest from polymer research labs, where they value both the reactivity and the performance potential that arises from the sterically hindered methyl groups and the cyclohexane's rigidity. The two adjacent carbonyl moieties pack reactivity into the ring, opening doors to controlled condensations, reductions, alkylations, and more nuanced steps such as enantioselective transformations or protective group strategies.
Every lot I ship passes across my desk, and I check chromatograms myself. I know where a trace impurity loves to hide, especially among the methylated byproducts that show up when reaction times or temperatures stray. The crystallinity of the purified dione tells a story to any trained chemist. A clean melting range and a sharp NMR fingerprint reflect a disciplined process. When my team controls the reaction, they limit oligomerization and avoid introducing color bodies—details that matter when you’re scaling from a university bench to a 500-liter reactor destined to support a regulated industry.
Our standard offering comes as a white to off-white crystalline solid, with a typical purity well above 98%. Residual moisture and trace solvents receive far more attention than what the average specification sheet ever records. Stability is another concern that non-manufacturers tend to overlook. At our plant, every storage drum is sealed tight in an inert atmosphere. There’s a reason for that: exposed material absorbs water, risking hydrolysis and eventually degraded product. These facts don’t always show up in procurement documents but make a difference at scale, especially in sensitive downstream chemistry. Stability testing over months has made me rethink our packing protocols more than once.
Handling and safety remain at the forefront. While the molecule lacks offensive toxicity, inhalation and skin exposure present unnecessary risks without basic lab protections. We stream early feedback back into each batch ticket: if the product picks up any off-odors or shifts color under regular lighting, the team investigates and we halt shipping until root causes are addressed.
Many in the chemical market still think of atom economy and operational simplicity as afterthoughts. Running a plant shows what happens when efficiencies slip: increased waste, higher variable costs, and downstream product that loses consistency. In the case of 3,5,5-trimethylcyclohexane-1,2-dione, controlling the reaction’s exotherm and protecting sensitive intermediates demands real-time care. End users later see the benefits: less colored byproduct in flavor precursors or tighter control of subsequent functionalizations.
Once, we trialed a quicker filtration under customer pressure. The increase in throughput looked attractive, but it cost us real-world reproducibility. Yields from subsequent customer transformations dropped. The lesson was clear: focus on batch integrity and let specifications be determined by human expertise and analytical rigor—not just market speed.
I have often fielded questions about why someone would select this dione over traditional cyclic diketones, such as cyclohexane-1,2-dione or more symmetrical variants like hexane-2,5-diones. The answer stems from both reactivity and structural impact. Placing three methyl groups around the cyclohexane ring creates notable steric hindrance, which influences which reagents can access the carbonyl positions, and how those groups participate in reactions. For those interested in selective modifications, this increased bulk can dramatically improve specificity.
In our own studies—and in partnership with university researchers—we’ve noticed how this feature preserves regioselectivity where smaller, less hindered ketones often fail. For example, alkylation reactions using unadorned cyclohexane-1,2-dione sometimes yield mixtures. Here, chemists leverage the methyl groups to block off side reactions, channeling the required transformation down a preferred pathway. This saves time and reduces purification headaches later. In polymer design, the rigid trimethylated backbone imparts a subtle difference in mobility and chain flexibility compared to unsubstituted rings. These small changes ripple through performance metrics, like glass transition temperature or solvent compatibility—matters that chemists only uncover with rigorous lab work, not speculation.
We’re also candid about the drawbacks. While the additional methyl groups can improve selectivity, they sometimes make the compound less soluble in certain solvents—a tradeoff not every customer expects if they’re transitioning from a simpler backbone. One client working on a high-throughput API intermediate process had to reformulate their solvent system just to dissolve the dione; we worked through the possible options, focusing on safer, greener choices. After a few bench trials, they identified a promising mixed solvent solution and production resumed. That feedback loop means a lot more to us than theoretical yields alone.
We see the bulk of 3,5,5-trimethylcyclohexane-1,2-dione usage flowing into three main sectors: pharmaceutical intermediates, specialty polymers, and fine flavor research. For pharmaceutical chemists, the clean and controlled reactivity allows the dione to form a basis for more advanced synthesis steps, such as Michael additions, reductions, or functionalized derivatives. One major global player developed a route to a chiral cyclohexanol-based intermediate using this dione as a building block. Their lab appreciated our commitment to low impurity levels and our willingness to split shipments to support their demand profile as their process scaled up.
Polymer manufacturers, especially those experimenting with new materials for advanced coatings or targeted release agents, see value in the trimethylation pattern’s rigidity and steric profile. The molecule becomes a structural element in their polymer backbone, tuning the polymer’s mechanical and swelling behaviors. After adjusting for solubility differences, they often see improved resistance to chemical degradation—attributes that help products last longer in the field. My conversations with these engineers typically dive below the surface; they want comparative data, not just claims, so we regularly collaborate on small-lot pilot runs that let them fine-tune their process conditions before they consider full-scale orders.
Flavor houses pose a different set of requirements. Odor profiles need to pass panellist evaluation, and trace impurities play an outsized role. Even a fraction of a percent of the wrong residual solvent or structural isomer can sour a well-designed flavor note. In this context, cyclohexane derivatives get blended, reduced, or cyclized into a variety of palettes. Our facility dials in the purification and fractional crystallization steps until the product meets these exacting standards, with confirmation from external GC-MS labs when required.
A significant part of my work involves translating complex regulatory frameworks into the daily routines of a chemical plant. The supply chain disruptions of the last few years have made reliability a talking point across the industry. Sourcing precursor materials for trimethylcyclohexane-1,2-dione, particularly at high purity, turns into a challenge when international shipping slows down or resin suppliers allocate product unevenly.
To solve these issues, our company invested in secondary raw material suppliers, conducted extensive compatibility and stability testing, and built larger in-house buffer stocks for the most essential materials. These steps weren’t always easy for the bean counters to accept, but the effort paid off: customers get their dione on time, and our process doesn’t grind to a halt for lack of a simple methyl group source.
Regulatory compliance means more than ticking boxes. We constantly monitor evolving rules from major regions on both occupational exposure and environmental release. 3,5,5-trimethylcyclohexane-1,2-dione, being non-volatile and stable, poses lower risks for air emissions, but one still needs to account for safe waste and residue disposal. Our wastewater streams are rigorously profiled, with in-line sensors tracking known markers so we can stay ahead of tightening limits. A few years ago, we made a switch from a less selective, solvent-intensive isolation to a greener crystallization and solid-state washing process. The reduction in hazardous solvent usage not only trimmed costs but also aligned with our ongoing ISO-14001 certification needs. This kind of continuous feedback from regulatory teams becomes part of our daily manufacturing discipline.
Whenever a new request for this dione lands in my inbox, I look beyond just the molecular weight and the lot size. Customers often need extensive documentation—analytical certificates, batch histories, and in some cases, letters of no objection for import or downstream use. Pharmaceutical partners, for instance, require data on elemental impurities, while polymer and flavor companies look for trace solvent residuals and off-note volatiles. We keep detailed batch records, and my analytical team understands the stakes: one off-spec shipment to a pharma customer means an investigation and lost trust.
Many buyers send technical questionnaires up front. They want to hear about scale-up records, past customer stories—sometimes they’re gathering background for regulatory submissions or in-country import clearances. My approach stays transparent: if we have historical spotty solubility or color drift during a given quarter, I offer that detail rather than gloss over it. Working this way, most customers appreciate candor over rote assurances. We also keep an open door to reference projects, providing insight about what grains of process learning actually move the needle.
As chemists and engineers ourselves, we have learned that the handoff from R&D bench to plant scale never follows a straight line. The dione may behave beautifully in a 5-gram flask yet require extra drying or different recrystallization solvents at 50 kilograms or more. We welcome those conversations, review process development notes, and even run parallel lab trials to spot problems before they reach the customer. This iterative partnership, more than the product itself, builds loyalty and sets apart manufacturers with staying power.
One realization stands out after years of fine chemical manufacturing: the true value comes not just from the molecular building block, but the reliability behind it. Researchers and formulation chemists invest enormous resources designing new pathways and materials using 3,5,5-trimethylcyclohexane-1,2-dione. Any deviation in raw material properties disrupts that work. Our ability to hold narrow purity windows, monitor trace contaminants, and support small or large batch requests underpins the confidence needed to launch new ventures or scale up promising ideas.
Our process reflects that priority. Each campaign receives pre-run checks: calibration of reaction temperature controls, supply verification, backup solvent readiness. Human oversight by experienced staff remains the best safeguard. I trust my plant supervisors to halt a run with a simple call if the raw material isn’t up to par or the reactor shows erratic readings. End-user feedback loops guide our next steps, whether by tuning the crystal habit, reducing moisture, or modifying drum closure specifications for global shipping.
Customers don’t want surprises when developing new syntheses or tweaking formulations for scale. The industry learned tough lessons from variable raw materials, lessons reinforced every time we compare a customer’s crude test sample with a clean, specification-tight lot from our plant. Success stories originate here: a specialty polymer team, facing inconsistent shrinkage rates, dialed in their product performance after switching to our dione, citing our lot-to-lot data as a key decision factor.
Building and shipping chemicals like 3,5,5-trimethylcyclohexane-1,2-dione isn’t all about meeting the written specification; it’s about delivering what makes a difference in complex reactions. One university lab we partner with found that their yield of a cyclohexanol-based catalyst climbed by nearly forty percent after they moved to our dione—tracked directly to the absence of a minor dione isomer present in their prior supplier’s lots. Not just the quantity but the nature of trace contaminants often shifts selectivity, and I encourage every customer to ask hard analytical questions before settling on a routine supplier.
A flavor chemist once commented that switching lots risked a noticeable change in their endnote profile—a reminder that invisible details can ripple out in large-scale user experiences. We responded by providing split-lot samples and exhaustive GC-MS backing. That collaboration didn’t just preserve a critical flavor component but laid the groundwork for a longer-term relationship and mutual learning about challenge points neither side initially saw.
It’s easy to fall into the habit of seeing chemical manufacturing as a static exercise. Truth is, continuously improving how we make and deliver 3,5,5-trimethylcyclohexane-1,2-dione keeps us relevant in a field marked by shifting priorities and new downstream applications.
One active area for us revolves around greener process optimizations. Given rising expectations for both workplace safety and environmental stewardship, our team audits solvent use, energy consumption, and process yields every quarter. We document reductions in solvent waste, deliberate steps toward closed-loop solvent recovery, and process intensification efforts such as batch-to-flow transitions—each informed by benchmarking not just against regulations, but global best practices.
We also engage directly with end users about their requirements for documentation, change notifications, and even shipping preferences. This operational transparency means end users don’t walk into a batch change or process tweak unannounced. Having a two-way dialog ensures that process changes reflect not only manufacturer capacity but customer experience.
Over the past few years, growing technical sophistication across the chemical sector demanded more from manufacturers. 3,5,5-trimethylcyclohexane-1,2-dione embodies that shift—no longer just a niche intermediate, but a springboard for new chemistry in health, materials, and flavors.
Every new order brings a challenge: support smaller, custom batch quantities for R&D one week, then scale up to meet commercial timelines the next. Lessons from tough process development add muscle to our production discipline. Reflecting on customer anecdotes, pattern spotting in batch analytics, and regular auditing of our environmental impact all flow into our production ethos.
I see the future for this molecule entwined with the evolution of specialty and fine chemicals more broadly. As new uses are discovered and old ones refined, only those plants that commit to quality, adaptability, and honest customer engagement will keep pace. Within my plant, that approach continues to define everything we do—from monitoring each reaction step to troubleshooting technical queries with end users days or years after the first shipment has landed.