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HS Code |
591032 |
| Product Name | Hexachloroacetone |
| Chemical Formula | C3Cl6O |
| Cas Number | 116-16-5 |
| Molecular Weight | 296.75 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | ≥95% |
| Boiling Point | 165-166°C |
| Melting Point | 1°C |
| Density | 1.68 g/cm³ at 25°C |
| Solubility In Water | Insoluble |
| Vapor Pressure | 1.2 mmHg at 25°C |
| Flash Point | >110°C |
| Refractive Index | 1.527 at 20°C |
As an accredited Hexachloroacetone (≥95%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Hexachloroacetone (≥95%) is packaged in a 100 mL amber glass bottle with a secure screw cap, clearly labeled for laboratory use. |
| Shipping | Hexachloroacetone (≥95%) is shipped as a hazardous chemical, typically in securely sealed containers to prevent leaks. The shipping container must comply with international regulations for toxic substances, featuring appropriate hazard labels, documentation, and secondary containment. It is transported under controlled temperature conditions, often with restricted access, to ensure safety during transit. |
| Storage | Hexachloroacetone (≥95%) should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong bases, strong oxidizers, and moisture. Keep away from direct sunlight and sources of ignition. Store under inert atmosphere if recommended by the manufacturer. Label clearly and ensure secondary containment to prevent leaks or spills. |
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Reagent: Hexachloroacetone (≥95%) is used in organic synthesis reactions, where its high purity enhances yield and selectivity of halogenation processes. Intermediate: Hexachloroacetone (≥95%) is used in agrochemical intermediate preparation, where its molecular stability ensures reliable downstream product formation. Solvent: Hexachloroacetone (≥95%) is used in analytical chemistry as a halogenated solvent, where its controlled volatility aids in precise sample dissolution and extraction. Catalyst: Hexachloroacetone (≥95%) is used in the catalysis of polymerization reactions, where its purity reduces unwanted side-reactions. Photoinitiator: Hexachloroacetone (≥95%) is used in photopolymerization systems, where its absorbance properties enable efficient initiation under UV light. Derivatization Agent: Hexachloroacetone (≥95%) is used in GC sample derivatization, where its chemical reactivity improves analyte detection sensitivity. Stability: Hexachloroacetone (≥95%) is used in high-temperature synthetic operations, where its stability above 100°C minimizes decomposition risks. |
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Hexachloroacetone conjures up images of a complex chemical, the kind a lab coat crowd genuinely appreciates. But real value shines when folks outside synthetic chemistry take a good look at what this compound pulls off. With a purity of 95% or greater, this product leaves behind a shadowy world of vague chemical descriptions and shows up fit for purpose, with a clarity in its makeup that matters when safety, outcome, and predictability count. Instead of being niche, hexachloroacetone carves out its place across multiple industries and university research groups as a crucial intermediate and reagent. Sometimes the stories that unfold in labs, behind thick chemical-resistant glass, quietly shape how pharmaceutical, agricultural, or material innovations reach shelves and change everyday lives.
Take a bottle of hexachloroacetone with at least 95% purity and the first thing that matters is its reliability. You don’t deal with suspicious leftovers or unpredictable reactions—what’s on the label holds up under scrutiny. Hexachloroacetone stacks up as a colorless to pale-yellow liquid, spotting a distinct, heavy chemical scent that reminds any careful handler to keep it capped tight and well-labeled. Its melting point sits at about -21°C, and boiling runs near 192°C—solid enough to let a researcher know how to store and handle it when weather shifts or labs lack top-notch climate control.
Over my career leaning into chemical supply chains, most focus falls on whether a compound stays stable and uncontaminated as it travels between continent-spanning warehouses, postdocs hunched over glassware, or remote tech startups hungry for prototyping materials. Hexachloroacetone at this grade brushes off moisture well enough in sealed containers, but it remains sensitive enough to hydrolysis to matter—get a little careless with humid air, and you risk breakdown, evidence showing up in spectroscopy or a disappointing experiment.
This product matters for its track record in real-world industrial and research chemistry. Once you see how it fits into multi-step syntheses for some of the world’s backbone materials and medications, you appreciate its status as more than just another hazardous liquid.
Synthetic chemists keep hexachloroacetone around because it does things that aren’t easily replaced by safer or cheaper compounds. For example, it’s a go-to chlorinating agent, driving transformations in organic syntheses by delivering chlorine atoms predictably. Its chemical formula, C3Cl6O, sits at the core of reactivity—a dense, halogen-laden molecule that paves the way to making other fine chemicals, specialty polymers, and even crop protection products. In practice, it helps labs build cyclic ketones, glyoxals, and intermediates for pesticide development.
On a personal level, after observing a team pull off a synthesis of certain pyrethroid insecticides, the chain reaction all hinged on hexachloroacetone as the pivotal chlorinating force. You could see the respect the process earned; few reagents get that starring role in routes where efficiency, selectivity, and predictability govern success or failure. Even with the shadow of toxicity, teams came back to it because alternatives failed to keep yields up or introduced unwanted by-products.
Comparison in chemistry isn’t just about purity or price. The differences step out clearly when you look at what other chlorinated acetones or standard chlorinating agents offer. Take something like trichloroacetone. While less hazardous by reputation, it lacks the same dense chlorine content, forcing you to use more of it or accept less effective conversions. Hexachloroacetone’s heavy halogen substitution makes it especially potent at tasks where efficient activation is non-negotiable.
Phosgene and thionyl chloride enter the conversation, too. They’ve been mainstays for adding chloro groups or activating carboxylic acids. Yet, phosgene brings a whole new level of risk—not just for users but for everything around the facility. Workers need specialty equipment and rigorous procedures. Hexachloroacetone, by contrast, comes with serious hazards, but its liquid nature and lower volatility help mitigate some uncontrolled exposures especially when handled in smaller batches. Many facility managers favor it for onsite work where strict environmental or safety controls are harder to guarantee.
As for physical properties, the relatively high boiling point compared to some gaseous reagents offers more manageable handling. Volatility matters less, and accidental releases risk spreading less rapidly. I’ve seen personnel take comfort in knowing a spill, bad as it might be, will hang around as a slow-clean option rather than a catastrophic cloud.
Every product faces scrutiny now to prove it stands up both in performance and health or environmental stewardship. Hexachloroacetone is not exempt. Its halogenated nature means trace disposal can create real headaches. Over the last couple of decades, industrial users have pushed suppliers to hone their purification, minimizing contaminants that can gum up downstream processes or boost side reaction rates. In the pharmaceutical sector, regulatory pressure shows up in batch documentation and strict impurity profiles, so the 95% benchmark isn’t just pride—it reflects a minimum to keep FDA or EMA auditors satisfied.
On the environmental side, hexachloroacetone makes nobody’s green chemistry wish-list. Most research focuses on working around it when possible or improving waste capture. Yet, for some applications—the last steps in a novel pesticide’s synthesis; a specific transformation in advanced materials—no cleaner alternative works as well. The focus has shifted to minimizing use, controlling emissions, and ensuring trained staff understand short- and long-term risks.
The chemical doesn’t show up at neighborhood hardware stores or agricultural supply chains, nor should it. Much of the safeguard comes from limiting availability to buyers with proper credentials, engineering controls, and disposal systems.
Reagent grade matters—especially when scaling up production or striving for regulatory approval. In my days assisting researchers troubleshooting failing syntheses, impurities in hexachloroacetone explained plenty of headaches: side reactions that created colored tars, batch inconsistencies revealed by NMR, or mysterious dips in reaction yield after changing suppliers. The standard 95% mark serves as a buffer, aiming to keep those unpredictabilities out of high-stakes work.
Modern markets have given rise to a new tier of expectations. Pharmaceutical and agrochemical companies often specify even tighter standards, asking for certificates of analysis and batch traceability. Companies willing to document the nitty-gritty of their production processes win contracts—those skipping steps or offering vague assurances lose out. This dynamic nudges suppliers to invest in equipment and quality systems, which ultimately benefits not just one plant, but the integrity of the whole end-use supply chain.
Transporting hexachloroacetone demands a careful touch and the right paperwork. From my years helping with logistics for hazardous chemicals, I’ve come to respect the work put in at every stage: sealed containers, tightly controlled inventories, and regular audits. Chemical-grade materials cannot be handled like bulk commodities. Temperature swings, air exchange, and secure packaging turn into daily talking points when dealing with containerized shipments across state or international lines.
Some stories stick with me. One time, a delayed rail shipment led to storage in a less-than-ideal, humid warehouse corner. A couple of container seals failed, and the resulting breakdown products cost the customer tens of thousands, set back their research, and forced a closer look at warehousing contracts. Experiences like these highlight the need for vigilance, sound supply chain partners, and, always, respect for chemistry’s unforgiving nature.
Hexachloroacetone’s use draws oversight from multiple directions. In the United States and Europe, agencies like OSHA and REACH keep tabs on safe exposure limits and restrict sales to unqualified buyers. Facilities need robust ventilation, spill containment, and access to eyewash stations before a single drop is unpacked. Proper labeling plays a role too. Safety data standards push suppliers to invest in training for downstream workers, even if the product ships in bulk to large formulators.
Health-wise, direct exposure risks irritation, respiratory distress, and organ injury at higher doses. Protective clothing, solvent-resistant gloves, and safety goggles stand as everyday barriers. Waste streams containing hexachloroacetone head off to professional disposal facilities, sometimes spiking costs for research projects but reflecting society’s broader concern about halocarbons in groundwater and air.
Industry groups sometimes push back, arguing that overregulation could send production offshore—where controls lag—without actually reducing risk. The balance comes by learning from accidents and tightening up best practices, not by shutting down whole classes of chemistry.
Every chemical carries stories—usually not publicized. In university labs, a bottle of hexachloroacetone serves as a shared tool, and an unspoken trust builds up among users. Mistakes stay fresh in people’s minds: the sting of a missed glove, the relief at having proper fume hoods, the end-of-shift stories traded over coffee. Graduate students, technicians, and their supervisors know that keeping records, reviewing labels, and double-checking protocols isn’t just bureaucracy; it keeps everyone healthy.
For every industrial breakthrough pinned to hexachloroacetone, there are also learning moments—a batch run outside spec, raw material shortages, or news of an overseas incident that reminds you to never cut corners. These connections, built on personal experience, push whole teams to stay alert and keep growing in their respect for what specialty chemicals really require.
Some chemists search for drop-in substitutes, but most see little direct replacement for hexachloroacetone’s chemical role in high-end synthesis. Where alternatives fall short, progress shifts toward new containment technologies, improved chemical sensors, and waste minimization systems. Automation, for example, lets companies keep workers farther from risks without sacrificing quality or speed.
Biotechnology and green chemistry research race to invent less hazardous routes for key intermediates, sometimes skipping the need for heavy halogenation. For clients willing to shift methods and invest in pilot trials, these approaches reduce environmental impact and boost workplace morale. Success doesn’t show up overnight, and not every project transitions out of using halogenated reagents. But attention to greener alternatives ensures the field doesn’t stand still.
Industry-wide, supply chain transparency and third-party audits support responsible handling across borders. Some companies partner with academic groups to take on ‘end-of-life’ treatment and recycling, pushing to keep persistent chemicals out of landfills and the broader environment.
Hexachloroacetone isn’t just a tool of the past. Its track record, strong performance, and relative manageability in the right hands mean it keeps a steady spot in chemistry’s toolkit. Yet, it’s never just about the molecule. The emphasis turns toward how it’s handled, who gets to work with it, and what steps tie its use to modern standards of environmental care and worker safety.
Smart labs and factories invest in training and tech not out of paranoia, but from watching small mishaps turn into big setbacks. They document every shipment, keep materials fresh, and support innovation toward greener chemicals—not because regulators tell them to, but because it’s proven way to protect people and keep science moving forward.
Long after most people forget the precise name or formula of what made a certain process tick, the habits formed around chemicals like hexachloroacetone leave their mark. Beyond labels, specs, or certificates of analysis, it’s that underlying respect for risk—and for progress—that lifts specialized chemicals from toxic curiosities to essentials in pharmaceutical, agricultural, and polymer breakthroughs.