|
HS Code |
655789 |
| Chemicalname | Monochloroacetone |
| Casnumber | 78-94-4 |
| Molecularformula | C3H5ClO |
| Molecularweight | 92.53 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Pungent, irritating odor |
| Boilingpoint | 117-119°C |
| Meltingpoint | -47°C |
| Density | 1.178 g/cm³ at 20°C |
| Flashpoint | 28°C (closed cup) |
| Solubilityinwater | Miscible |
| Refractiveindex | 1.425 at 20°C |
As an accredited Monochloroacetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Monochloroacetone is supplied in a 500 mL amber glass bottle, securely sealed, with hazard labeling and chemical identification markings. |
| Shipping | Monochloroacetone is shipped as a hazardous material due to its toxicity and flammability. It must be transported in tightly sealed, corrosion-resistant containers under ventilated conditions. Proper labeling, documentation, and adherence to international and local regulations (such as DOT, IATA, or IMDG codes) are required to ensure safe handling and transit. |
| Storage | Monochloroacetone should be stored in a tightly sealed container, away from light, heat, and sources of ignition, in a cool, dry, and well-ventilated area. Keep it away from oxidizing agents, bases, and strong acids. Use corrosion-resistant containers and ensure proper labeling. Access should be restricted to trained personnel, and appropriate spill containment measures should be in place. |
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Purity 99%: Monochloroacetone with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproducts. Stability temperature 25°C: Monochloroacetone with a stability temperature of 25°C is used in chemical reagent formulations, where it maintains structural integrity during storage. Low viscosity: Monochloroacetone with low viscosity is used in polymerization reactions, where it enables efficient mixing and uniform reaction rates. Boiling point 119°C: Monochloroacetone with a boiling point of 119°C is used in organic synthesis processes, where it facilitates controlled evaporation and process safety. Molecular weight 92.52 g/mol: Monochloroacetone with molecular weight 92.52 g/mol is used in active ingredient design, where it provides predictable reactivity and consistency in end products. |
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Monochloroacetone stands out in the world of chemical reagents for its sharpness and versatility. Chemists quickly notice its strong, pungent odor—something you never forget after opening a bottle in the lab. With the formula C3H5ClO, it brings a blend of reactivity and selectivity that’s tough to substitute. This compound has a knack for acting as a building block in both academic research and industrial chemistry, especially for those exploring the chemistry of α-halo ketones. You’ll spot it listed under the model 3-chloro-2-propanone in catalogs, but the core of its value goes deeper than a name.
You don’t need to look far to see its practicality. Monochloroacetone comes as a colorless to slightly yellow liquid, boiling around 119°C, which gives it the right volatility for controlled reactions but keeps it manageable under standard lab fume hoods. Handling it always calls for respect—its strong lachrymatory effect clears a room in seconds if you’re not careful with ventilation. Some earlier experiences in academic labs taught me quick lessons about the importance of PPE (personal protective equipment)—we learned fast that even a drop left uncapped could bring an unnecessary break to an experiment.
What makes monochloroacetone more interesting than similar α-halo ketones comes from how cleanly it introduces a chlorine atom next to a carbonyl group. Synthesis work involving it feels like unlocking a side door in molecular design. In pharmaceuticals, you see it appearing in the synthesis of intermediates where precise halogenation is required. I remember an industry project where we needed to prepare a fine-tuned pharmaceutical precursor—monochloroacetone delivered that right balance, reacting quickly with nucleophiles without scrambling the desired structure.
It’s not just about medicine, though. Agrochemical companies prize its ability to build more complex molecules for crop protection agents. The speed and selectivity of its reaction make it useful in small batch settings, where yield and purity matter to downstream processes. In academic settings, you’ll find it in protocols as a key reagent for making heterocycles—students learning nucleophilic substitution often get their first exposure to monochloroacetone in hands-on organic labs, and its reputation precedes it when the bottle comes out.
Many labs use bromoacetone or iodoacetone for similar halogenation routes. Bromoacetone is more reactive, but that extra reactivity tips into unpredictability sometimes. Bromo compounds carry tighter regulation, partly for safety but also for their misuse potential. Monochloroacetone finds a sweet spot: less volatile than its bromo- and iodo- cousins, less likely to cause those run-to-the-eyewash moments. It feels slightly friendlier to manage. Even though chloro- derivatives pack a punch, the narrower regulatory track for monochloroacetone gives research teams less red tape to cut through for approval.
In trying to decide which reagent to buy, many researchers weigh cost, reactivity, ease of handling, and availability. Bromoacetone isn’t just pricier; it latches onto glassware and leaves an unmistakable odor that lingers for days. Monochloroacetone washes out easier, and its physical behavior gives fewer headaches for storage and shipping. It ships under the standard protocols for chlorinated aldehydes and ketones, and while suppliers still demand a business license and demonstrated lab safety protocols, the hoops are not as frequent as with certain brominated reagents.
Nobody working in a lab overlooks purity. Monochloroacetone usually comes at technical or higher purities, around 98% or better. This level of purity is enough for most synthesis or development work. Overly impure batches set off a domino effect—side reactions, worse yields, wasted time on purification. I’ve watched project timelines slip because someone tried to save a dollar on a reagent grade, only to spend hours tweaking chromatography steps to chase down unknown by-products.
Storage tells a lot about a chemical. Monochloroacetone demands cool, dry conditions, far from bases, oxidizing agents, and sources of ignition. Anyone who has slipped up on capping the bottle or adjusting the fridge temperature has paid by losing an entire stock through evaporation and decomposition. Modern packaging, such as amber glass with PTFE-lined caps, reflects lessons learned the hard way. Old metal cans and thin plastic stoppers just didn't make the cut against this compound’s stubborn volatility.
Beyond single-lab settings, monochloroacetone finds scale-up potential in specialty chemical industries. Its role in producing dyes, intermediates for pesticides, and certain polymers puts it on the order forms for many industrial chemists. Companies looking for ways to trim process steps turn to reagents that offer high selectivity—monochloroacetone rarely disappoints. Its handling cost is lower than many functional equivalents, and its liquid form lets producers meter it into reactors using standard pumps, giving more precise control over the process.
The same qualities that make monochloroacetone useful also spark sharp debate about chemical risk management. The strong odor and acute effects on the eyes and mucous membranes mean only trained personnel should handle it. Labs and plants need engineered controls—fume hoods, air scrubbers, and clearly labeled spill kits at the ready. I’ve worked in places where regular smell checks and air filter replacements became part of the routine, long before regulatory audits caught on.
As more companies focus on accountability, there’s no room for silence on health and environmental impact. Monochloroacetone’s toxic profile asks for respect. Exposure limits are clear, and monitoring indoor air is not just best practice—it’s non-negotiable for a responsible organization. News of an accidental release can damage trust in a heartbeat, not to mention cause harm to workers and nearby communities. Knowing the origins of your chemical lot, understanding batch-to-batch variation, and keeping up-to-date safety data sheets nearby help foster a culture that values both productivity and care for people.
Disposal also deserves more than an afterthought. Monochloroacetone stocks that have spoiled or passed their recommended shelf life get treated as hazardous waste. Proper neutralization and incineration at certified facilities cut risks that linger when chemicals are dumped down the drain or tossed in regular trash. It’s not just about ticking boxes for compliance; it’s a practical issue of keeping workspaces—and the spaces surrounding them—safe and healthy. Anyone who has lost a project to an unplanned exposure or undetected vapor leak knows the real costs aren’t just in lost chemicals or broken glassware.
For research and product development, time is precious. Compounds that speed up synthesis, cut purification steps, or offer more direct routes to target molecules take a premium slot on inventory shelves. Monochloroacetone supports those efficiencies. The clean conversion of reactants, a high selectivity profile, and relatively simple workup routines add up to shorter turnaround times for R&D teams. Researchers reaching for monochloroacetone rarely have to guess about what they might get; the results are consistent, which means more reliable data and faster rework in case of roadblocks.
Education matters here, too. Graduate students and junior scientists benefit from using compounds like monochloroacetone in supervised experiments. They learn to respect the hazards, appreciate the simplicity of certain transformations, and carry those lessons forward to safer lab practices. Training programs that highlight specific risks, such as severe lacrimation or quick evaporation, give a realistic preview of what proper lab technique looks like. For supervisors, having hands-on experience with monochloroacetone means catching mistakes before they turn into incidents.
A reliable supply chain shapes the success of research and manufacturing projects. Access to monochloroacetone depends on producers who know what quality means, distributors who recognize the importance of safe packaging, and regulators who set clear but realistic rules for transport. In recent years, disruptions have reminded teams not to take basic chemical supplies for granted. Lockdowns, changes in import law, and surging demand for certain classes of reagents all play their part. Some researchers have started to diversify suppliers, stockpile essential reagents, or look for alternatives that won’t leave them stranded mid-project.
Choosing a supplier for monochloroacetone isn’t just about price per kilogram. It asks for checking the credentials of a distributor—making sure they understand UN transport rules for hazardous materials, and that chain-of-custody records will stand up to scrutiny. Poor packaging or mishandling can result in leaks, spoilage, or regulatory fines. In the worst cases, unsafe supply chains have put entire university programs or mid-size companies on hold after a single shipment goes wrong. I’ve seen research directors pivot funding in response to a shipment that arrived in corroded containers—with air-tight discipline following every order since.
Interest in greener chemistry invites questions about whether traditional reagents should give way to safer, less toxic substitutes. Monochloroacetone, once introduced, often stays on the shelf for specific high-value reactions, but some research groups push for less hazardous chlorination methods. Ionic liquids, milder chlorinating agents, or even enzymatic approaches offer alternatives, but few approach the blend of efficiency and reliability monochloroacetone brings for certain transformations. Balancing efficiency, cost, and safety is a challenge every lab and production manager grapples with.
Industry experts push for closed reactors, microfluidic-scale syngas setups, or catalytic strategies that limit venting and exposure. Investments in better ventilation and automation have already paid off by reducing the risk of mishandling during sample prep. For small-scale users without full industrial controls, clear written procedures and regular refresher training help keep accidents rare. Many chemists, myself included, look forward to the day when synthetic goals can be met with compounds that are safer without losing the specificity that monochloroacetone offers today.
For all its risks, monochloroacetone holds a unique place on the chemist’s shelf. Seldom does a reagent deliver such utility in carbon-carbon bond formation, α-halogenation, and nucleophilic substitution pathways. The hands-on experience of handling it teaches lessons about chemical safety, respect for volatility, and the importance of controlled environments. Famed for its effectiveness, monochloroacetone often turns up in “tried and true” protocols—where alternatives either take more steps or result in lost selectivity.
Chemists share stories about memorable moments—reaction flasks that changed color faster than expected, or the unmistakable onset of eye-watering vapors after a missed glove change. Over time, these stories underline why protocols matter and why respect for chemicals never goes out of style. It’s not nostalgia that keeps monochloroacetone in play—it's results, reliability, and the accumulated experience of generations of chemists who balance practical needs against everyday risks.
The next chapter for monochloroacetone will likely blend new technology and old-school discipline. Digital inventory systems now flag expiring stock and track hazardous materials with more accuracy, making unplanned exposures less common. Predictive maintenance for storage and reaction vessels helps teams keep tabs on conditions, preventing spoilage or dangerous leaks. Adapting to this digital infrastructure asks for more training—not just in using the platforms, but in understanding the underlying reasons for such detailed monitoring.
Calls for higher transparency don’t just come from regulatory agencies; they come from workers and communities who want to know what chemicals enter their neighborhoods. Companies that share data on accident rates, emissions, and supply chain integrity foster trust with the public. This trend pushes the entire chemical industry to raise the bar, not only for monochloroacetone, but for all high-impact reagents.
Monochloroacetone’s continuing popularity rests on its well-established utility and the expertise of those who handle it. For organizations focused on innovation, having compounds that work as intended, arrive on time, and can be used with confidence makes a huge difference in productivity. Responsible stewardship of this reagent, from purchasing to final waste disposal, demonstrates a commitment to safety, transparency, and scientific rigor.
Anyone who has worked with monochloroacetone knows the mix of challenge and promise it brings. Its story is a reminder that good science always balances progress with care. Whether developing the next pharmaceutical intermediate, training the next generation of chemists, or streamlining a chemical process, trusted reagents like monochloroacetone support smarter, safer, and more ethical research and industry.