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HS Code |
277981 |
| Productname | 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester |
| Molecularformula | C11H11ClO3 |
| Molecularweight | 226.66 g/mol |
| Casnumber | 34762-14-8 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 327.3°C at 760 mmHg |
| Density | 1.22 g/cm3 |
| Refractiveindex | 1.523 |
| Solubility | Soluble in organic solvents (e.g., ethanol, chloroform) |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8°C |
| Smiles | CCOC(=O)CC(=O)C1=CC(=CC=C1)Cl |
As an accredited 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 100g of 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester, sealed, labeled with hazard warnings and batch details. |
| Shipping | 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is packed according to chemical safety regulations, labeled with hazard information, and transported by approved couriers. Appropriate documentation and handling measures ensure safe and compliant delivery. |
| Storage | Store 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from light, heat, and moisture. Keep away from incompatible substances, such as strong oxidizers and bases. Use appropriate personal protective equipment when handling, and follow all relevant safety guidelines for storage and disposal. |
Applications of 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester in Industrial Manufacturing3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester supports specialized production requirements in select chemical manufacturing sectors. Below, we outline key industrial applications based on proven downstream processes, including regulatory compliance benchmarks, integration into formulation steps, and the resulting end products utilized globally. 1. Pharmaceutical Intermediate for Pyrazole and Isoxazole Derivative SynthesisLarge-scale pharmaceutical manufacturing commonly utilizes this compound as a building block in synthesizing pyrazole and isoxazole derivatives, which serve as active intermediates for various central nervous system and anti-inflammatory drugs. Its reactivity enables efficient construction of core heterocyclic scaffolds, supporting medicinal chemistry routes under GMP conditions for regulated drug ingredients. Industry compliance standards
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2. Advanced Agrochemical Intermediate for Herbicide SynthesisAgrochemical manufacturers employ this ester in the synthesis of selective herbicides, particularly those targeting broadleaf weeds. Its structure is critical for developing intermediates that lead to triketone-based or oxadiazole-class herbicides. Production processes ensure traceability and consistent incorporation at specific stages of the active ingredient synthesis workflow. Industry compliance standards
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3. Fine Chemical Precursor in Liquid Crystal Material ProductionIn the electronics material sector, this compound serves as a key intermediate in custom synthesis of specialty aromatic liquid crystal monomers. Manufacturers require precise incorporation to enable high-purity final materials for use in optical display components, ensuring batch reproducibility and compliance with electronic-grade purity standards. Industry compliance standards
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4. Intermediate in Advanced Dye and Pigment ManufactureChemical processors specializing in high-performance dyes and pigments utilize this ester as a precursor in synthesizing azo and anthraquinone-based compounds. Controlled reactions exploit its activated carbonyl group, enabling efficient introduction of aryl moieties into chromophore frameworks. The process supports manufacturers in producing heat-stable, lightfast colorants for technical and textile applications. Industry compliance standards
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Years on the production floor teach a lot about what makes a specialty chemical like 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester necessary. This molecule, often listed under its CAS number by folks who deal with it day in and day out, finds its purpose mainly in pharmaceutical research, crop protection, and some advanced materials projects. Right from the synthesis stage, achieving the right product batch after batch depends on more than just following a formula. Paying attention to details in raw material selection, optimizing reaction conditions, and maintaining equipment integrity are what keep the quality high and impurities low. It’s not just a matter of producing a certificate of analysis. Each shipment reflects years of accumulated knowledge, trial, and improvement.
We understand the entire process from sourcing starting materials to purifying the final ester. The real test comes during separation and purification. Our team has developed ways to minimize raw material hangover from early stages. The final product’s clarity and purity stem as much from continuous reaction temperature management as from smart crystallization. It’s not about promoting a magic solution, but rather a series of adjustments learned over hundreds of batches—data from in-process checks, feedback from chemists mixing the next intermediate, temperature logs—all filter into what gets shipped in each drum or carboy.
Clients working on fine chemicals demand consistency because even a slight variation in by-products or trace metals affects their own processes. For this ester, controlling water content and minimization of residual solvents are both essential. Water traces, low as they may be, complicate further synthetic steps—especially in pharmaceutical labs. Solvent management stands out as one of those everyday challenges; switching solvents during synthesis or isolation can impact overall purity in ways that aren’t always obvious with a quick analytical snapshot. Making one batch at 99.0% versus another at 99.7% purity might sound trivial to an outsider, but repeat synthetic steps or downstream reactions tell a different story. We’ve seen fewer purification headaches for clients who use our material at a higher purity threshold.
We monitor every load for color, odor, and trace contamination, not only by gas chromatography but by direct observation. Color hints at side reactions or overheating during processing. It’s a simple check but often gives the earliest warning that something in the reactor or filtration has drifted off standard. If it doesn’t pass the “smell test,” technicians raise the flag, signaling small cracks in process control before numbers even arrive from analytical devices.
3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester isn’t just a one-formula product. We’ve worked with chemists to offer grades suited for both laboratory research and industrial-scale synthesis. Lab users need gram-to-kilogram lots, each tightly controlled for trace contaminants, because a miscue at small scale creates undue cost. Industrial buyers usually want larger lots, and their focus often shifts to storage stability or container compatibility. Handling and packaging methods vary for these orders. Some want glass, others go for fluoropolymer-lined drums. This isn’t just about compliance—it also avoids unwanted interaction with packaging that could seed future batch inconsistency.
Every time we alter a process variable, someone on our team asks how it might affect the next step in a partner’s lab—not just our own internal numbers. There’s an active feedback loop with buyers; their data and experience become guidance for tweaking washing or drying steps. We’ve stopped using certain filter aids because small leaching would cut a batch’s shelf life. The people using this ester in a high-throughput pharma screen or as a feedstock for agrochemical projects taught us more about practical product demands than any literature footnote.
Consistency becomes the real benchmark over glamorous marketing claims. Reproducible results require tight grip on every variable: temperature control, process timing, raw material qualification, and even lab atmosphere during sensitive stages. A colleague once joked that humidity on a rainy day can leave a subtle fingerprint on an otherwise immaculate batch, and that’s far from exaggeration. Our team logs conditions and adjusts drying cycles accordingly. Every successful repeat order, every scientist out there who trusts our batch as reliable input, is proof of attention to these real-world factors. Granular traceability right down to the packaging day helps us catch issues before a customer does.
Years ago, less-precise suppliers got by with loose standards. Not now. We maintain active dialogue with partners and follow up on complaints or surprises—those cases often spark the most valuable improvements. Batch sheets, analytical data, and hands-on review blend old-fashioned craftsman pride with new technology. We swap notes with researchers using alternative esters or building novel synthesis routes. This two-way communication shapes real progress far more than any one-off audit.
3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester plays a vital role as a building block in the creation of advanced pharmaceuticals. In our experience, medicinal chemists often target it for incorporation into heterocyclic compounds, anti-inflammatory agents, and sometimes precursors for specialty intermediates. Having observed many process optimization projects, it’s clear that the ester’s selective reactivity—especially at the carbonyl and ester groups—lets research teams design specific synthetic routes, lowering overall step count in many syntheses.
In crop science, this compound’s unique chirality prospects enable precise molecular designs, helping researchers tune activity profiles for modern agrochemicals. It offers a balance between reactivity and stability, surviving strong reaction conditions when others break down or rearrange. Multiple pilot plants have shown us the value of a reliable supply for scale-up campaigns: inconsistent feed material leads to extra purification or even abandoned projects. We have rescued more than a few collaborators from expensive troubleshooting by providing cleaner material backed by transparent analytical data.
On the surface, 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester resembles other keto-ester derivatives, but molecular tweaks—namely the placement of the chlorine and the phenyl ring orientation—change its reactivity profile. Colleagues who’ve run analogous reactions with unsubstituted phenyl or para-position chlorides report slower rates or unwanted by-products. Our experience bears this out: ortho and meta-substituted compounds, despite looking familiar on paper, perform very differently in practice. Downstream yield, ease of purification, and even environmental exposure risk all shift because of these substitutions.
From the production side, similar derivatives often lack the same balance between stability and reactivity, leading to new separation headaches or storage constraints. Not all esters transport well—hydrolytic stability varies, and some lose potency over time. We’ve worked hard to tune storage conditions and packaging choices to keep this specific ester shelf-stable, minimizing the need for last-minute lab fixes or reprocessing.
No manufacturing process stays static for long. Issues arise—sometimes a slight off-color, sometimes micro-level impurities that complicate an external lab’s workflow. Instead of rushing out an “improved batch” claim, we keep logs, trace back through old batch records, and find root causes with practical, hands-on investigation. We’re more likely to spot trends because the team has backgrounds in both analytical chemistry and process engineering.
For buyers who run full R&D campaigns, the value in open dialogue and batch-by-batch process adjustment can’t be overstated. Every time a customer shares feedback on unexpected TLC spots or reaction bottlenecks, we bring that data right back to the plant floor. Changing a solvent fill sequence or re-tuning a column wash might look trivial, but these tweaks stack up to better yield and happier partners.
Over the past decade, tighter regulatory pushes—especially in pharmaceuticals—have forced everyone up and down the chemical supply chain to tighten documentation, improve operator training, and implement robust process control. We’ve integrated inline analytics and smarter data capture, not because auditors demand it but because it honestly cuts time resolving issues. Our operators have gotten quick at spotting weirdness in reaction kinetics, and we empower them to halt or adjust midstream. It costs more short-term, but downtime and waste drop when fixing issues early.
Most buyers for this ester come from companies building new chemical entities or developing next-generation plant protectants. The early-stage work demands small, ultra-pure lots for screening, but as a candidate moves to process development, the need shifts: the focus lands on consistent supply, storage safety, and controlled impurity levels at scale. Scaling introduces problems that never show up in a beaker, and as producers, we do our best to communicate those realities—scale changes can affect mixing or temperature gradients, even for “well-behaved” molecules.
We share real-time process data with select partners, using their feedback to troubleshoot and optimize at scale. Once, a multi-ton order flagged a trace impurity unheard of at kilogram scale. Cross-team investigation showed a new tank seal material was leaching in trace amounts. Quick root cause analysis and rapid switch-out prevented recurring losses. Lessons like these change more than just one order—they inform how we source new packaging components and vet third-party inputs.
Risk management runs through every step of handling 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester. From controlling exposure during drum filling to choosing compatible transport and storage media, we keep operator safety and downstream impact in mind. Years ago, less-sophisticated handling equipment could let in moisture, leading to slight ester hydrolysis in transit. Upgrades to inert gas blanketing and multilayer containment have all but eliminated these concerns.
Looking forward, we stay alert for new challenges, whether driven by future environmental regulation or voluntary improvement. Recyclable, lower-impact packaging now matters as much to us as raw material sourcing. Life cycle assessments aren’t just paperwork; data from real waste recovery efforts at our sites feed directly into customer conversations about “greener chemistry.” For customers with unique requests—say, needing documentation on potential allergen traces in the plant—our open-door approach and documented cleaning cycles provide reassurance without fluff. Everything comes back to a genuine interest in making clients’ processes smoother and safer, especially in sectors where patient or public safety is at stake.
Being a manufacturer, we have a direct, unfiltered view into what it takes to make a compound “work” for users on the ground. Anecdotes circle around about long-distance traders or generic resellers pushing batches that might look fine on paper, only to underperform in the lab or plant. Our teams avoid these pitfalls by staying close to both raw material sources and end users. If something goes wrong, we answer directly—it’s our staff, our process, our product.
For those developing new reactors, processes, or industries not even considered a decade ago, early communication between production and application teams pays dividends. We encourage those conversations before scaling a project; it’s the best way to anticipate choke points, avoid expensive detours, and create genuinely strong partnerships. This is especially true for new pharmaceutical intermediates or complex agrochemical blends, where tiny changes at the molecular level have cascading effects on cost and process design.
Trust matters more than ever in the specialty chemical field. Our style isn’t to bury partners in sales claims or to downplay difficulties in sourcing or production. We are open about manufacturing conditions, potential supply chain issues, and even batch-to-batch variability at early stages. Every customer gets access to updated technical documents, batch records when requested, and the chance to talk directly with the production team—no account managers acting as go-betweens.
We invest in better analytical capability for one primary reason—uncovering subtle changes before they reach the customer’s lab. Our goal is not just to tick boxes but to offer actual, actionable information: how storage affects shelf life, why switching a solvent improved trace impurity levels, how a new purification column changed downstream workflow. This sort of transparency reduces the number of surprises in end-use applications, especially for sensitive pharmaceutical or agricultural projects.
Having spent years improving methods for producing 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester, we rely on old-fashioned know-how supported by today’s analytics. Running a tight, transparent operation—welcoming scrutiny and acting on fresh feedback—has proven as valuable as any formal regulatory framework. Every improvement, whether it’s a faster crystallization step, a safer packaging material, or better staff training, grows out of this direct connection between those who make, test, and use the compound.
With this approach, we don’t just supply a commodity. We contribute expertise, reliability, and the willingness to adapt—qualities developed across years of honest production, anchored in real world lab and plant experience. In the end, our commitment to quality and open exchange stands as the real differentiator for everyone who counts 3-(3-Chloro-Phenyl)-3-Oxo-Propionic Acid Ethyl Ester as a crucial part of their research, product development, or production.