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HS Code |
753062 |
| Chemical Name | 2-Chlorocyclopentanone |
| Cas Number | 4477-50-1 |
| Molecular Formula | C5H7ClO |
| Molecular Weight | 118.56 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 185-187°C |
| Melting Point | -38°C |
| Density | 1.198 g/cm³ at 25°C |
| Refractive Index | 1.478-1.482 |
| Flash Point | 73°C |
| Solubility In Water | Slightly soluble |
| Synonyms | 2-Chloro-1-cyclopentanone |
| Smiles | ClC1CCCC(=O)1 |
| Inchi | InChI=1S/C5H7ClO/c6-4-2-1-3-5(4)7/h4H,1-3H2 |
As an accredited 2-Chlorocyclopentanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with airtight screw cap, hazard labels, and white chemical-resistant label marked "2-Chlorocyclopentanone, 250g, CAS 4477-57-2." |
| Shipping | 2-Chlorocyclopentanone is shipped in tightly sealed containers, protected from moisture and incompatible materials. It should be transported following hazardous material regulations, with proper labeling and documentation. Storage and handling must ensure good ventilation, avoidance of ignition sources, and use of PPE. Comply with international and local shipping regulations for hazardous chemicals. |
| Storage | 2-Chlorocyclopentanone should be stored in a tightly sealed container, away from sources of ignition, heat, and direct sunlight. Store it in a cool, dry, well-ventilated chemical storage area, separated from incompatible materials such as strong oxidizers and bases. Use appropriate chemical-resistant containers and ensure clear labeling. Access should be restricted to trained personnel wearing suitable protective equipment. |
Applications of 2-Chlorocyclopentanone in Industrial Manufacturing2-Chlorocyclopentanone serves as a valuable intermediate in several specialized chemical manufacturing sectors, particularly where precise molecular transformation and stringent regulatory adherence are critical. The following application segments highlight where our manufacturing expertise enables customers to integrate high-purity batches of this compound into demanding industrial processes, supporting innovation across complex downstream uses. 1. Pharmaceutical Intermediate: Synthesis of Antiviral AgentsPharmaceutical companies rely on 2-Chlorocyclopentanone as a core building block in the multistep synthesis of select antiviral drug candidates, specifically as an electrophilic cyclopentanone scaffold for constructing chiral centers pivotal to biological activity. The compound undergoes controlled condensation and nucleophilic substitution steps as part of the protected intermediate phase, contributing to the yield and chirality of final APIs. Strict in-process controls mitigate trace impurity carryover, maintaining compliance with international regulations during scale-up for commercial batches. Industry compliance standards
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2. Agrochemical Synthesis: Crop Protection Agent ProductionManufacturers in the agrochemical sector incorporate 2-Chlorocyclopentanone during the structural assembly of certain selective herbicide and insecticide molecules. Utilizing its reactivity, formulation chemists design substituted cyclopentanone motifs that underpin the biological selectivity of these active ingredients, achieving high purity through multiple crystallizations. The compound features primarily in prefinal steps, where structural integrity and residual profile critically affect toxicology assessments for market authorization. Industry compliance standards
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3. Fragrance and Flavor Intermediate ManufacturingSpecialty fragrance compound producers value 2-Chlorocyclopentanone for its efficacy in creating highly functionalized cyclopentanones and lactones, serving as signature building blocks for musk-type and green note aromas. Expert formulators perform selective reductions and ring transformations, precisely tuning the molecule for optimal threshold properties in trace-level dosing. Integration into closed-loop flavor and fragrance plants ensures alignment with food and consumer safety requirements in high-scrutiny end markets. Industry compliance standards
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4. Fine Chemical Resin and Polymer Modifier SynthesisProducers of advanced resins and specialty polymers employ 2-Chlorocyclopentanone as a reactive modifier to confer unique performance behavior in cationic-curable resin systems and ladder polymers. By introducing controlled amounts of this reagent, formulators can tailor backbone halogenation and modulate crosslinking density, directly influencing final product mechanical and resistance characteristics. Entry occurs at the monomer or oligomer functionalization stage with process monitoring for material balance and downstream QA. Industry compliance standards
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Daily work at our plant has taught us that even a single functional group on a molecule can make all the difference, and nowhere is that more evident than in 2-Chlorocyclopentanone. This compound shows up each month on our production schedules and gets people talking, because its presence in a project signals demanding chemistry and precise results. Over the years, we’ve watched as its reputation grows among chemists who need robust, consistent building blocks with very specific reactivity. Manufacturing 2-Chlorocyclopentanone is a story of exact control over every stage: the starting material selection, chlorination, careful purification, and unwavering attention to operational safety.
Compared to the parent compound cyclopentanone, 2-Chlorocyclopentanone introduces a chlorine atom onto the ring, and if you’re looking for effects that matter, this is a big move. That one change brings a level of chemical reactivity that any downstream application can exploit. Over the years, chemists have reported its use as a key step in the synthesis of flavors, fragrances, agrochemicals, and especially pharmaceutical intermediates. We have seen customers seek it out when they need that extra electrophilicity at the 2-position, opening doors to further modifications that simple cyclopentanone just can’t deliver.
From our operators’ perspective, the manufacturing run for 2-Chlorocyclopentanone is never a plug-and-play effort. Compared to halogenation at other positions, the chlorination at the 2-position demands controlled conditions—temperature, time, solvent, and choice of chlorinating agent—every parameter affects the outcome. Residual monochloro byproducts can be stubborn, so we monitor for these with close care and batch documentation. Our approach is hands-on: we track every cylinder, every reaction profile, and keep batch samples archived for comparison years down the line.
While many are familiar with the molecular formula (C5H7ClO) and its modest molecular weight, the reality on the floor insists on more relevant numbers. Each production campaign delivers 2-Chlorocyclopentanone as a clear, colorless to pale yellow liquid, with a boiling point falling reliably in the expected range. The chemical purity target is never less than 98 percent, and by the time it leaves our QA lab, we verify the composition by multiple analytical methods. Slight shifts in impurity profiles can impact downstream steps; we make it our job to listen carefully when customers call us with results from their own labs so we can adjust procedures, not just once, but batch after batch.
Every specification line on our COA traces back to lab notebooks, not just digital files. Our GC traces must show clean baselines, and water content gets tested by both Karl Fischer and by infrared spectroscopy to catch even low levels. Even if the aldehyde levels seem minor, small differences can affect storability and reaction reliability. In our business, close isn’t good enough; we've seen how the difference between 97.5 and 99 percent purity shapes the work of medicinal chemists and industrial process designers alike.
Through years of work, 2-Chlorocyclopentanone has found a niche in several chemical syntheses that demand high selectivity and reactivity at the 2-position. In the pharmaceutical sector, our partners use it to generate spirocyclic compounds, heterocyclic scaffolds, and chiral auxiliaries. The cyclopentanone scaffold is deceptively simple, but the introduction of a chlorine atom has enabled reactions like nucleophilic substitution and further elaboration through cross-coupling. In crop science and flavor chemistry, the same reactivity brings value-added building blocks for products that ultimately land on supermarket shelves or in home gardens.
We don’t just take orders; we work with customer R&D teams running new syntheses or troubleshooting difficult steps. The difference between a successful or unsuccessful library of compounds sometimes tracks back to the lot of 2-Chlorocyclopentanone they used. Through these collaborations, we’ve developed proprietary purification and stabilization methods to meet non-standard requests, often cutting out steps in our customer’s own work by delivering clean, high-purity product with low residual solvent.
Some customers ask why not just use cyclopentanone or 3-chlorocyclopentanone instead. The answer, from a synthetic perspective, lies in how much reactivity is dictated by the chlorine atom’s position. The 2-chloro substitution sets off different reaction pathways than a 3-chloro isomer or a non-chlorinated version. This comes into play in selectivity during further functionalizations, helping improve yield and limit byproducts. For years, process chemists have told us their cross-coupling and alkylation steps work more cleanly when starting from 2-Chlorocyclopentanone due to its reactive carbon-chlorine bond. In practice, compounds with chlorine at the 2-position can open entirely new synthetic sequences. This saves time and streamlines steps in the route—a real win in both pilot and full-scale manufacturing.
We’ve compared isomeric products, and the differences go beyond the bench. 3-Chlorocyclopentanone, for example, behaves differently under Lewis acid catalysis, sometimes producing more side products and lower yields. In every comparison run in our pilot lab, our operators found that 2-Chlorocyclopentanone’s reactivity, ease of purification, and stability at ambient storage conditions offered a noticeably better experience for the end user, saving hours of post-synthesis cleanup and product isolation.
Chlorinated ketones demand attention to details that sometimes don’t show up until you’re handling multi-kilo quantities. Vapors generated during distillation require specialized containment. We’ve implemented closed-system distillation and fractional condensation to minimize exposure and reduce environmental footprint. Each waste stream gets monitored with updated analytical methods; if the process can be tightened, we do it, and we edit our batch instructions after every significant incident or observation, learning alongside the changing industry landscape.
Packaging has required just as much ingenuity. We field requests ranging from 500-gram jars to industrial drums. After losses were observed due to minor leaks in plastic containers, we switched to fluorinated steel drums for bulk shipments, logged those outcomes, and tracked recipient feedback. Now, our standard approach matches the chemical’s actual volatility and reactivity, so the product reaches every user in the same condition as the day it left our plant.
Years of direct handling have sharpened our insight on storage. 2-Chlorocyclopentanone holds up best under cool, dry, and inert-gas-purged conditions, away from strong bases and oxidants. Laboratories can sometimes miss this, especially when working at the benchtop. Each time we get a call about unexpected discoloration or decreased reactivity, our support team traces the history and shares advice based on what’s worked — or not worked — in production runs.
Producing and shipping chlorinated compounds taught us that regulatory expectations keep evolving. Our QC analysts and safety engineers follow guidance updates, and every batch record ties back to traceable sources. If an issue gets flagged, we dig in, often re-examining retained samples from production lots shipped years ago. Auditors from major partners walk our floor and always find us with documentation stacked high, scribbled with engineer notes, and annotated by operators who noticed “something different” about a reaction.
Cost of compliance isn’t something we just absorb; it becomes part of each batch’s value. We’ve retrofitted areas of our plant to improve air handling near the chlorination recirculator. Solvent recovery was a footnote once; now, it’s routine, and solvent purity checks are standard with every mix. Beyond the walls, we have learned to coordinate with shipping partners, clinics, and local officials to log transport details and guarantee every delivery meets international safety codes.
Feedback from research chemists brings changes to our process almost every year. Small shifts in impurity profile prompt tweaks in our washing and phase separation steps. Our R&D team once discovered that using a particular grade of solvent made a positive impact on product stability over months of storage, and this finding was integrated directly into our SOP. Each tweak typically starts with a call from a lab facing problems on the bench, and ends with a new batch instruction in our manuals. This continual learning process separates a true manufacturer from a commodity supplier or reshuffler.
Peer-reviewed journals sometimes feature new ways to synthesize cyclic ketones. We run side-by-side trials and, in the rare event a new method truly improves yield or reduces waste, we consider updating our processes. These steps take time, but we never chase trends just for the sake of novelty. Trial runs, full documentation, and a focus on real-world reliability guide every improvement.
Starting from single grams produced for a university lab, we’ve scaled up to metric ton quantities delivered for industrial production lines. This progression brought plenty of hard-earned lessons about process control and batch-to-batch consistency. As demand for advanced intermediates in pharmaceuticals and agrochemicals grows, so does the expectation for transparent, traceable, and sustainable manufacture. Clients expect more than a certificate of analysis; they want to know about our emissions controls, waste disposal, and ability to offer custom lots tailored to their exacting targets.
We view each inquiry as an investment in mutual progress. When a customer proposes a new transformation using 2-Chlorocyclopentanone, we share historic process data, likely impurity outcomes, and stability profiles from storage trials. Feedback from these collaborations is carved back into the plant’s routine. Over the last decade, this willingness to listen has helped us cut down on off-spec batches, reduce process downtime, and increase overall production capacity.
We have faced pressures for “greener” process chemistry. 2-Chlorocyclopentanone’s synthesis produces halogenated waste and requires responsible management, so each production run reflects our commitment to sustainability. We select greener solvents where possible and continually test alternatives to legacy chlorination agents. Process engineers monitor mass balances and pursue ways to reclaim and repurpose byproduct streams. If a new method enables us to recover more starting material or reduce waste, we adopt it, no matter the adjustment required to existing plant equipment.
Customers want proof, not promises, and we welcome audits from partners securing their own supply chains. With open doors and transparent records, we keep learning how to balance economic and environmental sustainability in a field where change is slow but constant.
Every batch of 2-Chlorocyclopentanone carries the story of hundreds of process improvements, customer conversations, and plant-floor innovations. The people who run the reactors, stand over the distillation columns, and verify purity in the lab know this product as more than a bottle on a shelf. Whether used to build the next pharmaceutical hit, support a new crop-protection strategy, or speed up a research project, it remains a testament to careful work, experienced judgment, and respect for the capabilities of a simple but versatile intermediate.
From the inside, the journey from raw material to finished, bottled product means constant engagement with science, safety, and the requirements of modern industry. By focusing on real customer needs, operational transparency, and the realities of working with reactive chlorinated ketones, we keep advancing our own standards—and, hopefully, supporting chemistry that makes a difference for years to come.