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HS Code |
233290 |
| Chemicalname | 3-Chloropropionyl Chloride |
| Casnumber | 920-46-7 |
| Molecularformula | C3H4Cl2O |
| Molecularweight | 126.97 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 143-145 °C |
| Meltingpoint | -40 °C |
| Density | 1.328 g/mL at 25 °C |
| Flashpoint | 60 °C (closed cup) |
| Solubility | Reacts with water |
| Refractiveindex | 1.446 |
| Synonyms | 3-Chloropropionyl chloride; 3-Chloropropanoic acid chloride |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8 °C |
| Hazardclass | Corrosive, causes burns |
As an accredited 3-Chloropropionyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 3-Chloropropionyl Chloride is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 3-Chloropropionyl Chloride is shipped in tightly sealed containers under a dry, inert atmosphere. It requires cool, well-ventilated storage, away from moisture, heat, and incompatible substances. Classified as a hazardous material, it must be handled and transported following stringent regulatory guidelines, with appropriate labeling and documentation, to ensure safety during transit. |
| Storage | 3-Chloropropionyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible materials such as water, alcohols, and strong bases. Store under inert gas, such as nitrogen, if possible. Protect from light and heat. Use corrosion-resistant containers and clearly label all storage vessels to avoid accidental exposure or reaction. |
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Purity 99%: 3-Chloropropionyl Chloride with purity 99% is used in the synthesis of pharmaceutical intermediates, where high chemical purity ensures minimal by-product formation. Boiling Point 117°C: 3-Chloropropionyl Chloride with a boiling point of 117°C is used in acylation reactions in agrochemical manufacturing, where precise thermal behavior allows controlled process conditions. Moisture Content ≤ 0.5%: 3-Chloropropionyl Chloride with moisture content ≤ 0.5% is used in polymer modification processes, where low moisture prevents unwanted hydrolysis. Stability Temperature up to 40°C: 3-Chloropropionyl Chloride stable up to 40°C is used in storage and transport of chlorinated intermediates, where thermal stability maintains product integrity. Density 1.38 g/cm³: 3-Chloropropionyl Chloride with a density of 1.38 g/cm³ is used in fine chemical synthesis, where consistent density supports accurate dosing and mixing. Melting Point -43°C: 3-Chloropropionyl Chloride with a melting point of -43°C is used in continuous-flow acyl compound production, where low melting aids in efficient liquid handling systems. Molecular Weight 129.95 g/mol: 3-Chloropropionyl Chloride at molecular weight 129.95 g/mol is used in flavor and fragrance synthesis, where precise molecular specification ensures consistent quality of derivatives. Acid Value ≤ 1.0 mg KOH/g: 3-Chloropropionyl Chloride with acid value ≤ 1.0 mg KOH/g is used in surfactant manufacturing, where low acidity enhances product compatibility. Colorless Appearance: 3-Chloropropionyl Chloride with a colorless appearance is used in laboratory reagent formulation, where clear solutions facilitate accurate analytical measurements. Reactivity Index High: 3-Chloropropionyl Chloride with a high reactivity index is used in custom organic synthesis, where fast acyl transfer increases throughput. |
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Every industry leans on specific tools that quietly drive progress, and in fine chemicals, 3-chloropropionyl chloride earns a spot at the table. In my years spent working with intermediates, few substances have stood out like this one for their ability to open doors in specialty synthesis. Its chemical model—C3H4Cl2O—tells a simple story on paper, but its real-world uses highlight the fundamental ways chemistry evolves to suit new demands. The liquid form comes with a pungent odor, recognizable in a lab, setting it apart from more familiar acyl chlorides. This uniqueness matters. A single atom shift—here, the presence of a chlorine atom at the three-position in the propionyl backbone—marks the dividing line between routine utility and strategic advantage in chemical processes.
Working with 3-chloropropionyl chloride invites possibilities. Laboratory teams and process engineers reach for this molecule in pharmaceutical projects or when sculpting agrochemical intermediates. A big driver stems from its dual reactivity: the acyl chloride group quickly engages with alcohols, amines, or water, while the terminal chlorine allows for further substitution. This two-pronged behavior saves time and avoids messy workarounds. Take the case of synthesis in medicine, where time-consuming stepwise routes can grind research to a halt. Here, the molecule’s built-in reactivity reduces the number of reaction steps, cutting down on raw material waste and improving overall efficiency. Chemists tend to remember its potent ‘nose,’ but that profile signals the molecule's readiness to bond, to attach, to transform—essential attributes whenever short, direct reaction pathways make the difference between lab curiosity and viable product.
A seasoned chemist learns quickly that numbers on a page rarely tell the whole story. For 3-chloropropionyl chloride, specifications like purity, acidity, and chlorination are more than checkboxes—they shape every downstream application. High assay values, usually topping 98%, mean fewer byproducts in final formulations. Lower water content translates into safer reactions. Low color index tells you impurities remain under control, which is crucial when preparing ingredients for finely tuned pharmaceuticals. This attention to specification steps up during tightly regulated synthesis, as meeting purity standards influences batch consistency.
What stands out most is how even small breaks from spec can wreak havoc later. In one development project, a minor moisture spike forced a team to halt a weeks-long experiment, resulting in costly delays. Lessons like this underscore a truth: behind every well-working supply chain is a supplier who respects the little things, not just the headline specs. There’s a mutual trust—between provider and user—that each liter carries with it the discipline your next reaction depends on.
Many buyers arrive at 3-chloropropionyl chloride after trying less specialized acyl chlorides. Ask those manufacturers what sets it apart—they’ll point to its reactivity, cost curve, and selectivity. The structure, with a chlorine tacked onto the beta carbon, breaks with the conventions of simple propionyl chloride or even more common benzoyl or acetyl chlorides. This structural twist opens up chemoselective substitutions that just don’t happen in other analogues.
In one agricultural application, having the beta-chloro group meant the molecule provided a reliable anchor for heterocyclic ring formation—a step that dictated not just yield but also regulatory approval timelines. Another distinction crops up in the pharmaceutical world: some drug precursors require strong electron-withdrawing effects for subsequent transformations, and the beta-chlorine on this molecule delivers that without fuss.
Most operators remember their first encounter with 3-chloropropionyl chloride. The fuming, acrid liquid commands attention. Safety isn’t just a procedural box—mistakes leave impressions that stick with you. The compound reacts vigorously with water, so storage and transport revolve around sealed drums and gloves that stand up to corrosives. I recall a facilities manager explaining how one forgotten seal in a transfer line resulted in an unplanned shutdown, reinforcing safety habits every time fresh stock comes in. Engineering controls and rigorous training matter with a chemical this potent. Fast and predictable reactivity has its price; operators learn to treat each drum with respect, which circles back to the tight bond between supplier reliability and user trust.
Some chemical specialties exist solely for basic transformations, but 3-chloropropionyl chloride takes a broader view. Its reach extends into pharmaceutical, agrochemical, and polymer fields. In building blocks for pain management drugs, the molecule shortens synthetic routes, side-stepping intermediate purification headaches. In crop protection chemicals, it acts as both a synthon and a reagent, creating unique scaffolds with reliable yields.
Newer applications piqued my interest lately, especially in high-performance polymer development. Certain research groups use this molecule to introduce tailored functional groups into polyesters, dialing up hydrophobicity or making room for further cross-linking. The story here is adaptability—chemists get a reactive handle that survives challenging conditions and creates products that perform better out in the field, whether a medical device or water-resistant coating. These stories rarely make the news, but inside labs, the molecule’s flexibility gives researchers a leg up when racing to innovate.
Supply reliability sits right at the intersection of chemistry and commerce. I’ve seen buyers push for alternate sourcing when price fluctuations or import barriers threaten production schedules. In global chemicals, even two weeks’ delay ripples downstream—especially for products with volatile reactivity like 3-chloropropionyl chloride. That vulnerability means businesses favor suppliers with robust checkpoints, documented batch history, and transparent logistics. Quality assurance stretches beyond the factory, right through the last mile until the drum passes inspection on-site.
Packaging design also steps up. The choice of container—often lined, vented steel drums—reflects a careful balance between safety needs and cost realities. The industry’s gradual drift toward smaller pack sizes reflects rising demand at the pilot plant scale, not just bulk. For those new to chemical procurement, the learning curve on identifying reputable supply partners climbs fast. Reputation matters, but so does proactive technical support. I’ve heard more than one research manager credit their best runs to having direct access to knowledgeable reps who knew their product firsthand, not just via spec sheets.
Working with halogenated acyl chlorides means threading a needle between tight regulatory controls and the need for fast-moving innovation. Many regions classify chlorinated intermediates as hazardous, tracking each shipment with more paperwork than most buyers care to acknowledge. Over time, regulations shape the way companies handle, store, and move these substances. As safety standards evolve, producers have adopted on-site recovery systems and real-time monitoring to bring emissions lower, reducing risks to people and the planet.
Not every regulation triggers headaches. Some requirements force better practices—spurring users to rethink process design, minimize emissions, or add an extra purification step. In one case, a regulation on airborne hydrogen chloride emissions nudged a company to install new scrubbers, dropping exposure levels and yielding stronger community relations. The lesson here: The right mix of compliance and practical savvy doesn’t stifle progress. Producers and users grow more resilient by building safer, cleaner, and more efficient ways to keep chemistry moving forward.
Environmental interests grow year by year, both from public concern and internal company goals. Halogenated chemicals have a reputation that keeps some buyers wary, but efforts at greener synthesis have started to bear fruit. Producers reduce waste by reclaiming solvent and recycling byproducts; more and more facilities install closed-loop systems to contain both fumes and liquid leaks.
There’s ongoing research into using milder chlorinating agents or renewable feedstocks for producing chloropropionyl derivatives. While broad adoption remains slow, pioneers prove that alternative routes can work at commercial scale, albeit at a price premium today. In one pilot process, a team used in situ generation of the acyl chloride to cut down waste streams, finding a way to recover over 85% of process solvents as part of a circular model. These innovations don’t just answer environmentalists’ demands—they also drive efficiency, cut long-term costs, and insulate companies from regulatory shocks down the road.
In practical use, chemists look closely at performance, not just label claims. Purity matters most to those working on multi-step synthesis, and a single failed batch—traced back to a contaminant in the starting material—can unravel months of planning. Here’s where experienced teams make a difference, running incoming QC on every delivery, logging batch details, and sharing notes internally if anomalies crop up.
Consistent reactivity gives researchers confidence. They know roughly how each batch will perform in their own setups, relying on that predictability to troubleshoot product yields or optimize reaction times. The tale repeats: robust supply chains, not just high assay numbers, shape customer loyalty and downstream success.
Global demand throws pricing swings into sharp relief. Since the pandemic, raw material costs and shipping snarls have put a premium on reliability. Buyers willing to roll with small price adjustments often sleep better at night, knowing their process will stay on track. Still, cost-pressured industries—especially in bulk agrochemical segments—push hard for value, not lowest sticker price.
Some companies offset price volatility by signing longer-term supply agreements or diversifying supplier networks. That strategy comes with upfront negotiation but lowers exposure to market shocks. Distributors and traders operate in the middle, buffering shocks for smaller buyers, but direct-from-producer deals often unlock customization that big projects crave. In every model, value rides on trust and technical support, not just spot market rates.
Plenty of acyl chlorides fight for space in commercial catalogs. Acetyl chloride and propionyl chloride land most frequently in entry-level reactions for their generality, but neither offers the directed reactivity of 3-chloropropionyl chloride. In my experience, projects needing beta substitution run cleaner and yield fewer side products with this molecule, especially where selectivity and functional group compatibility matter.
Users balancing performance and safety may switch between candidates during early process development. Each has its quirks—different boiling points, reaction kinetics, and toxicity. 3-chloropropionyl chloride’s relative stability allows control over addition rates and temperature, but demands careful isolation and ventilation. The upshot: you pick this tool when the extra chlorine anchors value no other off-the-shelf option brings.
Chemical progress accelerates as new applications reveal themselves. In the past decade alone, makers of advanced materials and specialty compounds started harnessing 3-chloropropionyl chloride for roles no one pictured a decade ago. This flexibility cements its place among specialty substrates. Market watchers predict further demand growth in pharmaceutical intermediates and high-performance polymers as new drug scaffolds and materials crop up.
Yet challenges persist. Choked transportation routes, tightening environmental norms, and workforce shortages all loom on the horizon. Some companies lead by investing in digital logistics tracking or building regional supply hubs that cut down border delays. Others bank on R&D, aiming to broaden the substance’s range of derivatives or streamline its integration into one-pot synthesis. Collaboration with academic partners sometimes shakes loose smarter routes—greener, more stable, or less hazardous—helping to push boundaries without undercutting safety.
In my time supporting both new labs and large plants, I saw the best results where teams directly engaged with their suppliers, learning the specifics of batch-to-batch variations and sharing lessons learned from failed runs. Cross-functional meetings—engineers, safety officers, and chemists at one table—often dug out bottlenecks nobody spotted on paper. These conversations steered purchasing, waste handling procedures, and even research directions, tying technical expertise directly to daily practice.
To developers facing tight project timelines or navigating regulatory hurdles, the lesson is clear: prioritize communication, share real-world feedback, and choose partners who will adjust on the fly to urgent needs. A molecule like 3-chloropropionyl chloride isn’t just a commodity—it’s a strategic asset shaped by the human networks that understand and deploy it well.
Meeting tomorrow's needs means blending deep chemistry knowledge with process adaptability. Investments in cleaner production tackle both public expectations and regulatory requirements. Process engineers continue to refine recovery techniques, catching emissions before they leave the plant and making internal recycling for solvents and byproducts standard practice.
Education plays a big role, too. Many universities now include real-world acyl chloride handling and synthesis in their curriculum, ensuring that newcomers to the field grasp best practice from the start. Mentorship—seasoned practitioners guiding new workers—transfers not just theoretical safety but the all-important, experience-informed caution that keeps work safe and productive.
One promising area lies in collaborative innovation. Partnerships between producers, users, and academic researchers accelerate adoption of greener synthesis. By testing process tweaks on small scales and quickly rolling out what works, these teams carve out better production models—leaner, less wasteful, and more sustainable. The trend points toward local production clusters, which reduce transportation risk and site-specific pollution, all while maintaining high-quality output.
As regulatory landscapes evolve and buyers grow better informed, the emphasis shifts from basic reliability to proactive support and continual improvement. For teams building tomorrow’s medicines, materials, and agricultural tools, access to a reliable, responsive supplier network for specialized reagents like 3-chloropropionyl chloride can mean the difference between a stalled project and a breakthrough launch.
A reputation for quality, safety, and environmental responsibility matters more each year. Successful users foster a culture of accountability, tracking product lots, maintaining transparent incident reporting, and prioritizing upgrades to safety infrastructure. People watch how their partners respond to setbacks, seeing those moments as accurate indicators of long-term reliability.
Ultimately, the story of 3-chloropropionyl chloride mirrors the broader tale of chemical progress: innovation matched with rigor, and efficiency balanced by responsibility. No one molecule speaks for the entire field, but this one, with its unique reactivity and broad potential, captures the way a single change on the molecular level can ripple outward, shaping everything from workflow to marketplace. The best results go to those who respect those ripples, adapt to challenge, and push for solutions that run deeper than the spec sheet.