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HS Code |
772123 |
| Cas Number | 34931-88-1 |
| Molecular Formula | C9H6Cl2O |
| Molecular Weight | 201.05 g/mol |
| Iupac Name | 2-chloro-3-phenylprop-2-enoyl chloride |
| Appearance | Pale yellow to light brown solid |
| Melting Point | 56-59°C |
| Boiling Point | 314.6°C at 760 mmHg |
| Density | 1.31 g/cm³ |
| Synonyms | 2-Chloro-3-phenylacryloyl chloride |
| Solubility | Reacts with water; soluble in most organic solvents |
As an accredited 2-Chlorocinnamoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Chlorocinnamoyl Chloride (25g) is packaged in a tightly sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | 2-Chlorocinnamoyl chloride is shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. It must be labeled as a hazardous material (corrosive and lachrymatory), handled by trained personnel, and transported according to local and international regulations to ensure safety and prevent environmental contamination during transit. |
| Storage | 2-Chlorocinnamoyl chloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as water, alcohols, and strong bases. It should be kept under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis or degradation. Protective gloves and safety goggles are recommended when handling this compound. |
Applications of 2-Chlorocinnamoyl Chloride in Industrial ManufacturingAs a direct producer, we supply 2-Chlorocinnamoyl Chloride for advanced synthesis processes across focused sectors. Its unique reactivity and structure support efficient production in fine chemicals, pharmaceuticals, agrochemicals, liquid crystals, and specialty polymers. The following section details proven downstream applications and technical integration. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisLarge-scale pharmaceutical manufacturers adopt this material as a core intermediate in the multi-step synthesis of select anti-infective and anti-inflammatory drug substances. Its acyl chloride function allows precise aromatic acylation under controlled temperatures within enclosed reactors, supporting batch or continuous operations. We supply consistent particle size and purity, streamlining stepwise reactions, improving yield, and meeting strict impurity profiles for regulated final APIs. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisMajor agrochemical firms utilize this building block to introduce chlorinated cinnamoyl moieties into selective herbicide actives. Within dedicated agrochemical synthesis suites, the reaction with amine or phenol functionalities creates precursor molecules with tailored crop selectivity. Process safety demands high-purity material to minimize environmental discharge and off-target toxicity, guided by regional agrochemical approval and environmental limits. Industry compliance standards
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3. Liquid Crystal Material Synthesis for Display TechnologyManufacturers specializing in advanced LCD and OLED technologies use this compound as a precursor in the fine chemical synthesis of key mesogenic molecules. Accurate introduction of the chloroaromatic group influences electro-optic characteristics, molecular alignment, and thermal stability of display fluids. Integration demands analytical-grade purity, complete documentation, and traceable batch records to support electronics quality assurance and trace contaminant specifications. Industry compliance standards
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4. Specialty Polymer and Resin AdditivesChemical processors in the specialty polymer sector employ this intermediate to acylate polymer backbones, imparting chlorinated aromatic properties that enhance chemical resistance, thermal rigidity, and UV stability. The controlled reaction with polyols or aromatic diamines occurs in closed-plant environments using continuous stir reactors, with strict monitoring for endpoint conversion. All operations follow industry emission and workplace safety standards due to the high reactivity of acyl chlorides. Industry compliance standards
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5. Fine Fragrance and Aroma Intermediate ProductionLeading fragrance ingredient producers use this compound to make aldehyde and ketone derivatives with spicy and woody notes for perfumery applications. It reacts with benzene, phenol, or aliphatic compounds in Friedel–Crafts acylation under precisely monitored conditions to prevent off-odors and maintain batch consistency. We provide standardized grades that ensure compliance with international fragrance ingredient guidelines and analytical traceability for high-volume blending operations. Industry compliance standards
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2-Chlorocinnamoyl chloride stands apart in our lineup not just for its molecular construction, but for the manner in which we bring it to market. This compound, with the molecular formula C9H6Cl2O, has a structure that gives it a unique reactivity across several downstream transformations. Strong activity of the acyl chloride group, paired with the chlorinated aromatic ring, helps set the stage for creative synthesis routes. Out on the production floor, we keep a close eye on the moisture content and purity at every step—hydrolysis being the usual adversary for acid chlorides like this. A keen QC team watches the color, from off-white to pale brown, and tests by HPLC or GC to ensure specifications match the demands of our end users.
Having filled drums of this material personally, I’ve watched how a shift in room humidity can trigger a heavier, more acrid odor, telling us the lot needs to move directly to final packaging. This sense for the compound’s handling nuances has helped our customers avoid cross-contamination in multi-purpose reactors, whether they’re building APIs or functional polymers.
The majority of requests we get for 2-Chlorocinnamoyl chloride fall around a purity of 98% and above. That figure isn’t chosen by accident—most reactions only tolerate minor levels of byproducts before yields start to suffer. As a manufacturer, we’ve learned control begins with the choice of raw material. Cinnamic acid derivatives, carefully sourced to avoid trace aldehydes and phenols, then enter a chlorination step using phosphorus oxychloride. Over the years, we’ve adjusted reaction profiles to cut down on side product formation—keeping the color and reactivity uniform from drum to drum.
Our standard packaging for this product uses fluorinated liners to resist attack from HCl, which inevitably forms during storage and transport. It only takes one leaky barrel to see the cost of cutting corners. Proper handling and packaging don’t just protect our workers and our customer’s operators, but also keep material loss at a minimum, which for any acid chloride, isn’t just a financial concern, it carries safety implications up and down the supply chain.
2-Chlorocinnamoyl chloride isn’t the sort of chemical you find on an open market shelf or tossed in with generic reagents. Most often, its acyl chloride group ends up as a key intermediate for pharmaceuticals, especially when medicinal chemists demand unique substitution patterns for the aromatic ring. That extra chlorine at the ortho or para position can drive selectivity or modulate biological activity in the finished API.
In one project, a customer from the pharmaceutical sector needed to selectively acylate an amine group without touching a nearby alcohol. 2-Chlorocinnamoyl chloride made that possible by letting them adjust solvent and temperature until the selectivity matched their needs. Compared to ordinary cinnamoyl chloride, the presence of an additional chlorine holds back the reactivity just enough to give a window for careful control. That’s not something you can dial in after the fact; it comes from a deep familiarity with how acid chlorides behave, and with the quirks of each batch run.
Beyond pharma, we’ve seen this product head to specialty polymer synthesis. Its reactivity with amines produces amides that can be coaxed into high-performance materials, sometimes with enhanced resistance to UV or oxidative damage. The added chlorine often means the final polymer can survive harsher processing conditions, or resist hydrolysis longer in the field. For research chemists, this opens the door to new monomers or crosslinkers—the kinds that don’t just incrementally improve properties, but truly redefine performance in a finished material.
I’ve heard chemists mention frustration with unpredictable reactivity in seemingly similar acid chlorides. In my experience, the smallest impurity in the batch—whether a dimer or a trace of hydrochloric acid—skews the outcome, especially if moisture plays a role. That’s part of why our technical team works alongside customers, not just as a vendor, but as fellow problem-solvers, dissecting each failure and tracing it back to root causes in production or handling.
Most manufacturers, including ourselves, offer several related compounds: cinnamoyl chloride, 3-chlorocinnamoyl chloride, and 4-chlorocinnamoyl chloride among others. Each comes with its own quirks. The position and number of chlorine atoms don’t just affect reactivity, but also handling and storage. 2-Chlorocinnamoyl chloride’s ortho-chloro configuration sits just close enough to the carbonyl group to influence electron flow, changing how it reacts compared to its 4-chloro cousin.
For example, 4-chlorocinnamoyl chloride tends to offer smoother reactions with soft nucleophiles, since the para-chloro exerts a weaker electronic effect on the carbonyl. On the other hand, the 2-chloro positional isomer demands cleaner conditions and sometimes different solvents to achieve the same functionalization without side reactions or over-acylation. Our chemists often recommend a head-to-head test in your synthetic route to decide which works best, especially at larger scale where yields and cost sensitivity matter.
On the plant floor, this all plays out in the precise control of reflux conditions, temperature ramps, and quench sequences. Because 2-chloro-substitution can prompt faster hydrolysis under ambient humidity, even the rate of nitrogen blanketing or cooling must be tweaked accordingly. These aren’t hypothetical choices but day-to-day realities—the difference between a barrel of usable intermediate and a failed batch.
Every batch tells a bit of a story. From the sourcing arm keeping tabs on upstream producers, through the technical team vetting raw acid stock, down to the people who operate the reactors, everyone brings a different set of eyes to the process. We never push intermediates out the door before running a full battery of tests. While it’s tempting to rely only on purity checks, our QC lab measures not just assay, but checks the acid value, residual phosphorus, and visual appearance. Acid chlorides, especially the more volatile ones, react fast with ambient moisture—sometimes the difference between clean product and a semi-solid mass comes down to how quickly we can transfer between vessels.
We’ve experimented with both glass-lined and Hastelloy reactors and found that trace metal catalysis can spell trouble for post-reaction cleanup. Although our main line leans toward glass-lined, some specialized runs exploit the extra temperature stability of Hastelloy, especially during exothermic chlorinations. These decisions aren’t made in isolation—they reflect feedback from process engineers and production crew who spot issues through routine cleaning or flashpoint testing.
Customers rely on us for full traceability, and we keep detailed batch records down to the supplier and date of each key raw. Any fluctuation—whether a supplier switched packaging or a delivery sat too long—shows up in the minutiae of our test sheets. Everyone along the chain knows one off-spec drum can spoil a full campaign of downstream chemistry.
Few industries reward care in handling like fine chemicals. Acid chlorides, with their keen sensitivity to water and air, demand not just the right packaging but the right timing. We’ve learned this through direct experience, from watching HCl plume out as a drum head is cracked to seeing labels delaminate if the outgassing isn’t controlled with the right vented inserts.
For 2-Chlorocinnamoyl chloride, our preferred approach involves tight-sealing HDPE containers, fluorinated inside, always inerted with a dry nitrogen blanket. The moment an operator loads a drum for shipment, timing becomes crucial—shipping delays in hot summers lead to higher levels of decomposition, discoloration, or even overpressure if residual acid picks up moisture on the road. Over the years, we’ve adjusted our logistics partners, truck routing, and even added remote monitoring tags to keep temperature spikes from turning a valuable batch into a loss.
End users benefit most when they receive material in predictable, stable condition. We’ve shortened lead times for most shipments so that feedstock spends less time on the road or at dockside, and offer small-lot packaging for R&D teams who don’t want the risk of opening large drums multiple times. These practical choices grew out of hard lessons learned by watching real customers encounter real-world setbacks, then working backward to solve the gaps in the supply chain.
It’s easy to think of quality as a checklist, but for complex intermediates like this, reality is far messier. Early in our scaling process, we saw one of our pharma customers report odd peaks by GC: suspected dimerization. Our technical team went back, checked the reactor logs, and found a temperature spike during the final distillation. The solution wasn’t just adjusting the heat—switching to an incremental vacuum ramp and staged addition made all the difference, cutting impurities by nearly half in subsequent batches.
Over and over, we’ve seen how each customer application comes with its own unexpected demands. Whether a team is building combinatorial libraries for drug discovery or bulk monomer for high-performance plastics, no two batches act exactly the same. One plant needed to tweak their solvents when moving from bench to pilot scale, because the reaction time ballooned by hours—later traced to slight changes in our color index that correlated with altered moisture control during post-chlorination filtration.
For each troubleshooting ticket, we keep direct lines open, not just for shipment status but for application advice. Our chemists handle everything from batch failure autopsies to pre-shipment sample discussions. No distributor, no matter how attentive, can offer the sort of root-cause analysis that comes from living and breathing the chemistry day-to-day, hands-on, from raw to finished product.
Our long-term partners trust us precisely because we speak plainly about batch risks, variation, and required precautions. If a customer’s process needs higher purity or a particular crystal habit, our technical staff walks through every modification, sometimes adjusting our drying protocols or recommending alternate solvent mixtures. No document or technical data sheet can substitute for the back-and-forth that comes from close collaboration between manufacturer and end user.
Manufacturing and shipping reactive materials like 2-Chlorocinnamoyl chloride brings heavy scrutiny from regulatory bodies. We track our environmental emissions closely—not just because regulations demand it, but because leaks and waste translate into real hazards for both the plant and the wider community.
Incineration of chloride-rich byproducts generates dioxins if not properly managed, so our plant routes waste through closed-loop treatment systems. HCl scrubbing and condensation can reclaim materials safely, minimizing the risk of accidental release. We don’t flinch from investing in better abatement—not just because the law says so, but because experience has shown that cutting corners on compliance nearly always leads to greater cost and reputational damage later.
Safety protocols around acid chlorides require more than just standard gloves and glasses in the production hall. When vapors escape, exposures rise fast, and plant operators know the “smell test” means an engineering review comes next. In our facility, we drill regularly on leak containment, ventilation system upgrades, and remote monitoring for early detection. These aren’t hypothetical risks but everyday facts of manufacturing life.
Working on a manufacturing site has given us a respect for how much chemistry relies on trust. Each batch of 2-Chlorocinnamoyl chloride carries with it a promise—not just to meet a number on a COA, but to show up consistently so downstream processes don’t grind to a halt. We’ve found that most of our long-term customers don’t stick with us for price, but for the ability to talk straight when something goes wrong. Those relationships only grow by tackling problems directly, from polymer chemists who want oddball lots for exploratory work, to pharma process engineers scaling up for regulatory submissions.
We’ve fielded urgent requests for rush shipments, late-night troubleshooting on batch reactivity, and custom runs where the buyer wants just enough extra stability in the shipment to cover an extended transit. Each of those cases triggered a factory huddle—adjustment to process, packaging, or transport—rooted in our direct experience making and handling the product, rather than a distant catalog entry or template reply.
No factory is perfect, and no chemical line runs free of incident. The value comes from how manufacturers respond amid the everyday chaos—watching for the warning signs, sharing hard-won lessons, and leaning in on the technical side when downstream users hit a snag. Our commitment to 2-Chlorocinnamoyl chloride is that every drum carries not just a chemical, but the benefit of our years of hands-on learning, passed on to partners who, in their own right, add value in the most demanding of fields.
Standing still means falling behind in this business. As customer demands grow more stringent, and as regulations tighten, we’ve put more resources into upgrading our analytical tools and process controls. Introduction of in-line NIR sensors, real-time HPLC monitoring, and feedback loops for water content have enabled us to catch process drift before it impacts a final batch.
For high-value intermediates like 2-Chlorocinnamoyl chloride, automation helps maintain better batch-to-batch consistency, but it doesn’t eliminate the judgment needed where technology ends. Operators who know the “feel” of a reaction—the look and thickness of a mixture, the sound of a condenser under stress—continue to play a vital role in delivering top-tier product. Blending old-school craft with new-school analytics gives us an edge that belongs on the factory floor, not just in sales brochures.
We keep in touch with customers to spot shifting needs, whether toward greener chemistry, altered impurity profiles, or compatibility with newer downstream steps. Feedback from the field guides every next step on our side: if someone in development struggles to get clean conversions, we don’t just log a complaint, we pull samples, run repeat tests, and tweak where needed. This direct connection creates a cycle of improvement, visible in trimmed variability indexes and ever-higher success rates in what users actually make from our goods.
Describing 2-Chlorocinnamoyl chloride means more than citing numbers or ticking off features. Sitting at our plant, surrounded by reaction vessels and the steady hum of process chatter, you gain an appreciation for how the right material—made with care, delivered with speed, and backed by hard-earned know-how—serves as a foundation for new ideas in chemistry.
Our experience as a manufacturer shows up not just in the product’s specs, but in the way we handle every unforeseen issue, every frantic call, and every finished batch tucked deep into the supply chain. For innovators in pharma and advanced materials, that difference shows—batch to batch, project to project, year after year.