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HS Code |
565745 |
| Chemical Name | Dichloropinacolone |
| Iupac Name | 1,1-Dichloro-3,3-dimethyl-2-butanone |
| Cas Number | 759-94-4 |
| Molecular Formula | C6H10Cl2O |
| Molecular Weight | 169.05 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 156-157°C |
| Density | 1.196 g/cm³ |
| Flash Point | 53°C |
| Solubility In Water | Insoluble |
| Smell | Pungent |
| Refractive Index | 1.459 |
As an accredited Dichloropinacolone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dichloropinacolone, 25g, is packaged in a sealed amber glass bottle with a tamper-evident cap and labeled for laboratory use. |
| Shipping | Dichloropinacolone is shipped in secure, tightly sealed containers to prevent leaks or contamination. It must be labeled as hazardous and handled according to regulatory guidelines. Transport typically requires compliance with safety standards, including UN identification, and may involve temperature control and secondary containment to ensure safe delivery and storage. |
| Storage | Dichloropinacolone should be stored in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep the container tightly closed and clearly labeled. Store at room temperature, ideally in a chemical storage cabinet designed for hazardous substances. Always follow safety protocols and local regulations for storing chlorinated compounds. |
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Purity 98%: Dichloropinacolone with purity 98% is used in pharmaceutical intermediate synthesis, where high assay ensures optimal yield and minimal byproduct formation. Melting point 54°C: Dichloropinacolone with a melting point of 54°C is used in agrochemical precursor formulation, where controlled thermal properties improve reaction predictability. Molecular weight 195.04 g/mol: Dichloropinacolone with molecular weight 195.04 g/mol is used in organic synthesis pathways, where precise stoichiometric calculations are required for efficient process control. Stability at 25°C: Dichloropinacolone with stability at 25°C is used in storage for chemical manufacturing, where extended shelf life and consistent reactivity are crucial. Particle size < 100 µm: Dichloropinacolone with particle size less than 100 µm is used in fine chemical production, where enhanced surface area promotes increased reaction rates. Water content ≤ 0.2%: Dichloropinacolone with water content ≤ 0.2% is used in sensitive catalytic reactions, where low moisture prevents undesirable hydrolysis. Chlorine content 36.4%: Dichloropinacolone with chlorine content 36.4% is used in halogenation processes, where defined halogen loading facilitates targeted transformation steps. Refractive index 1.532: Dichloropinacolone with refractive index 1.532 is used in analytical method development, where reliable identification and purity verification are required. Viscosity 2.3 cP: Dichloropinacolone with viscosity 2.3 cP is used in automated dosing systems, where consistent flow properties ensure precise material delivery. Boiling point 130°C (at 10 mmHg): Dichloropinacolone with boiling point 130°C at 10 mmHg is used in vacuum distillation setups, where efficient separation and purification are necessary. |
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Few chemicals step into the spotlight and actually manage to make life noticeably easier for chemists, pharmaceutical engineers, and researchers. Dichloropinacolone is one of those rare compounds that solves real-world problems without forcing users to accept unnecessary compromise. Right off the bat, you find that this colorless liquid brings a level of reliability to workflows that involve complex transformations in organic synthesis. Its streamlined formula puts focus on the exact traits needed for clean, high-yield reactions, and that alone boosts confidence when you’re aiming for efficiency in the lab or production environment.
Dichloropinacolone goes by the molecular formula C6H10Cl2O. At the core sits a ketone backbone, bookended by two chlorine atoms. This structure might seem modest on paper, but it offers a sturdy platform for precision work where each atom counts. Through decades of laboratory use, chemists have recognized that minor molecular tweaks can have outsized impacts on reactivity and stability, and the design here strikes a solid balance. The two chlorines on the pinacolone base elevate its resistance to unwanted side reactions—a clear step up from similar ketones on the market.
Some products carry reputation through flashy marketing or big brand labels. Dichloropinacolone earns its place through stability under a variety of storage and reaction conditions. Temperature swings, moderate humidity, and exposure to light barely budge its performance, and you won’t find it breaking down into unpredictable byproducts unless you push it well outside the envelope of normal chemical handling. That peace of mind means a lot to those who have ever had a synthesis derailed by microscopic changes in the bottle—an experience I personally don’t care to repeat.
Clarity and consistency show up from the moment the bottle is opened. Dichloropinacolone is typically delivered as a clear, nearly odorless liquid, with a boiling point that hovers close to 178°C and a density around 1.24 g/mL at room temperature. These are more than just textbook numbers. When you handle a chemical, every degree of boiling point or decimal of density translates into how it evaporates, how precisely it pours, and how efficiently it distills. Reliable physical properties reduce surprises during critical tasks—acylation, alkylation, or participating in Grignard reactions. You can trust each batch to behave consistently, which beats the guesswork that creeps in when suppliers cut corners on purification or don’t run tight quality checks.
One overlooked detail is the extremely low moisture content you get in high-grade Dichloropinacolone. Traces of water spelled the end of early syntheses in my graduate days, so running modern reactions with a nearly bone-dry reagent feels like a minor luxury. Every chemist can appreciate the time saved by skipping unnecessary drying steps, especially in fast-paced commercial labs.
For any reader not living in the world of organic chemistry, context helps. Dichloropinacolone is famously known as an anchor building block for the synthesis of specialty compounds, with direct roles in pharmaceutical development and the production of certain crop protection agents. These aren’t just speculative uses, either. Production teams in pharmaceuticals reach for this compound when reproducibility and purity demand the best starting material. When targets such as pesticides need a tough but versatile intermediate, Dichloropinacolone becomes part of the standard toolkit.
I’ve spoken with colleagues in scale-up chemistry who prize this material for the way it bridges lab work and plant-scale production. Bench chemists might run a pilot reaction to test a route; on the factory floor, engineers push those conditions to hundreds or thousands of times the scale. Dichloropinacolone moves between both worlds without incident. It isn’t going to throw off unwanted side reactions or force extra clean-up steps, which means lower waste and higher yields—you notice the savings in both time and resources.
For those in the early discovery stages, the compound’s reactivity profile allows researchers to explore creative modifications of existing molecules or design entirely new scaffolds. Medicinal chemistry teams leverage it to build and screen molecular libraries, probing new chemical space for promising drug candidates. Agricultural chemists employ its underlying structure to tailor new pest control agents. The tight control over halogenation and ketone functionality makes it valuable for introducing diversity into a molecular series, which expands the project’s creative options.
Every buyer wonders what sets apart one reagent from another. In practice, not every product labeled as a ketone or halogenated compound plays as well with sensitive reaction partners as Dichloropinacolone. Many competitive options lack both the steric accessibility and documented stability you get here. I remember early research projects bogged down by unwanted byproducts, which forced endless column chromatography and ultimately drove up production costs. Standard pinacolone or basic dichloroacetone just didn’t offer the right blend of selectivity and shelf-life. Dichloropinacolone’s thoughtful balance of volatility and resistance to hydrolysis has saved more projects than I can count.
Another edge comes from its safety profile. Handling large volumes of volatile chemicals can turn even basic lab work into a headache. Dichloropinacolone’s moderate vapor pressure cuts down on loss through evaporation, lending a practical sense of control to large-scale operations and routine handling. That beats spending half an afternoon scrubbing chemical fumes from the air and worrying about exposure or environmental impact.
On the analytical side, Dichloropinacolone responds clearly to established identification techniques. Nuclear magnetic resonance (NMR) and infrared (IR) readings are crisp, with diagnostic peaks that confirm its identity with little need for detective work. Compare that to certain off-the-shelf chemicals, which present with fuzzy or ambiguous spectra, and the advantage grows obvious.
Purity means more than just a marketing promise; it shows up as fewer complications and smoother downstream operations. I’ve witnessed pilot campaigns where questionable batches of reagents hinted at purity on paper, only for reactions to grind to a halt midway. With Dichloropinacolone sourced from reputable suppliers, the measured purity consistently hovers above 98%, often reaching analytical grade without heroic purification steps on the user’s part. The payoff is tangible—less troubleshooting, faster process development, and a smoother handoff to scale-up chemists down the line.
Anecdotes matter. In one project, my team needed to generate a custom intermediate with strict requirements for chlorine placement. Even mild impurities in the starting material cratered our yields, forcing a costly reordering cycle and setting timelines back almost a month. Dichloropinacolone arrived with a batch certificate and measured to spec—no last-minute curveballs. By streamlining the sourcing and verification process, its dependable quality stands out in an industry where even small missteps carry heavy consequences.
Navigating regulatory scrutiny gets easier with well-characterized chemicals. Dichloropinacolone boasts clear documentation—Safety Data Sheets, Certificates of Analysis, and full traceability. This record-keeping speeds up audits and batch reviews. Watching supply chain failures hamper whole projects, I’ve come to appreciate any chemical whose provenance can be defended at every turn. Environmental responsibility also matters more as regulations tighten industry-wide. The relatively contained handling risks and moderate volatility reduce environmental and workplace exposures. Combined with a low impurity rate, this helps companies keep closer tabs on emissions and waste streams. Responsible storage and disposal protocols also go hand in hand with its demonstrated stability, making routine compliance less of a hurdle.
No product solves every problem out of the box. Dichloropinacolone isn’t immune to limitations—notably, aggressiveness in reactions with strong bases or long-term exposure outside inert environments. Handling protocols usually recommend limiting unnecessary exposure to moisture and adopting proper secondary containment during transfer. In the field, labs sometimes grapple with the costs of sourcing and transporting tightly regulated ketones. Bulk purchasing agreements with trusted suppliers become essential, and digital tracking platforms can help labs avoid delays in reordering or mismatched inventory records. Translating lab success to factory-scale production means constant review of procedures and frequent recertification, and Dichloropinacolone’s consistent behavior keeps that process on schedule.
As with any potent synthetic tool, the stakes attached to mismanagement stay high. Improper disposal or uncontrolled spills could add unwanted chlorine load to effluent streams. For every research director tasked with hitting sustainability targets, that means updating training modules and investing in well-maintained containment and neutralization gear. Experience says cutting corners here always backfires. Straightforward procedures, spelled out clearly and reinforced often, keep things moving in a compliant direction.
With synthetic chemistry’s rapid evolution, tools that remain versatile have a ticket to long-term relevance. Dichloropinacolone keeps pace—not just for routine transformations, but also as a starting point for emerging applications. Academic research groups are already exploring its use in developing next-generation pharmaceutical scaffolds, such as oxazoles or modified pyridines. Similar advances are happening in materials science, where researchers re-tool the base structure for unique polymers or specialty coatings. I’ve noticed that open-source literature highlights a growing number of synthetic pathways referencing Dichloropinacolone, a trend that mirrors its acceptance beyond niche applications.
Community-driven forums and peer-reviewed publications increasingly advocate for sharing reaction troubleshooting, innovative uses, and sourcing tips. Collegial sharing of best practices works wonders in saving others from known pitfalls. As knowledge collection grows more distributed, recurring recommendations for Dichloropinacolone in multi-step syntheses point not just to tradition, but to a reputation for dependable function under diverse sets of conditions. The fact that it keeps showing up in both submitted patents and open-access articles speaks volumes about both its foundational role and adaptability.
Career chemists know that every reliable compound is an opportunity to innovate further. Dichloropinacolone’s unique arrangement of chlorine atoms and a sturdy ketone chain opens up countless derivatization strategies. Teams developing libraries of potential drug leads use that as a springboard for quick generation and screening of analogs. Synthetic pathways seeking selective activation or blocking group strategies see consistent gains from the compound’s balance of reactivity and durability.
Educational settings also draw benefits. Students gain a window into practical reaction mechanisms by studying Dichloropinacolone’s behavior, seeing first-hand how subtle structural changes translate into marked differences in reaction paths. Instructors report that demonstration reactions with this compound prompt lively discussions on the effects of halogens in organic systems, pegging curiosity that often leads to senior research projects or creative thesis work.
Industry veterans often measure products by how often they reappear in successful project retrospectives. Dichloropinacolone enjoys repeat business not because it flashes novelty, but because it does its job consistently. On-the-ground stories—whether in pharma process optimization or crop chemical design—point to reliability as a central selling point. Regular dialogue between production chemists and their suppliers helps flag early warnings of batch variation or supply disruptions, which in turn drive greater investment in quality assurance. The upshot is accelerated feedback between the user community and manufacturers, a loop that favors continuous improvement.
With tighter budgets and more demanding project timelines, process engineers and chemists hunt for small advantages. Every high-yield batch, every reduction in post-reaction purification, and every uptick in final product purity translates into bottom-line gains. Dichloropinacolone keeps delivering on these fronts, which builds loyalty among those who value data over hearsay.
Too many products on chemical catalog shelves promise more than they deliver. By contrast, Dichloropinacolone’s reputation grows from field experience and hard-earned trust. Purveyors who try to pass off substitutes or less refined variants seldom win repeat business once teams have used the genuine article. Lab managers and purchasing departments recognize that a modest initial outlay for a verified batch avoids time-sapping remediation downstream. In pharmaceutical trials, where regulatory bodies scrutinize impurities and batch history with a magnifying glass, knowing you’re running with a trusted source can mean the difference between stalled progress and a cleared path to scaling up production.
Direct testimonies from project chemists, not just marketing brochures, fill in the story here. I’ve watched teams map out entire synthetic trees around this reliable compound because it lowers the risk profile of novel reaction designs. That risk mitigation is a quiet driver behind many industry successes, even when credits roll in the direction of more glamorous catalysts or branded intermediates.
Individual responsibility carries more weight than ever. Students, lab techs, and senior researchers all share a role in using Dichloropinacolone with care and transparency. Industry organizations now offer best-practice guidelines, reinforcing safety protocols and promoting sustainable disposal routes. In settings I’ve worked in, routine audits are less about checking boxes and more about troubleshooting real processes using firsthand data. Recommendations drawn from on-the-ground experience—double-checking storage temperatures, confirming label integrity, tracking shelf lives—add up to a smooth shared workflow.
Emerging solutions for waste minimization and solvent recycling align well with the profile of Dichloropinacolone. Companies look for partners whose reputations are built on both product consistency and a record of cooperation with environmental standards. In research settings, open communication around challenges—alongside candid sharing of missteps—raises the bar for best practice and helps the broader community avoid preventable hazards.
While it has carved out a quiet, indispensable role in established processes, Dichloropinacolone still opens doors for tomorrow’s breakthroughs. Research funding continues to prioritize innovative reaction strategies, new pharmaceutical targets, and precision agrochemicals. This compound sits in the toolkit for many such pushes, trusted because of its proven performance more so than any clever hype.
Researchers new and old continue to share success stories where it made the difference between success and a project dead end. For those stepping up to direct their own labs, choosing reliable building blocks like Dichloropinacolone isn’t just about convenience—it’s about giving every team member the best shot at advancing science safely, sustainably, and with genuine confidence in the tools they rely on every day.