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HS Code |
724597 |
| Productname | 4-Chloro-3-Nitrocinnamic Acid |
| Casnumber | 57398-92-8 |
| Molecularformula | C9H6ClNO4 |
| Molecularweight | 227.60 |
| Appearance | Yellow powder |
| Meltingpoint | 242-245°C |
| Purity | Typically >98% |
| Solubility | Slightly soluble in water, soluble in organic solvents like DMSO |
| Smiles | C1=CC(=C(C=C1C=CC(=O)O)Cl)[N+](=O)[O-] |
| Inchi | InChI=1S/C9H6ClNO4/c10-8-5-7(11(14)15)4-3-6(8)2-1-9(12)13/h1-5H,(H,12,13) |
| Storagetemperature | 2-8°C |
| Synonyms | 4-Chloro-3-nitro-alpha-phenylacrylic acid |
As an accredited 4-Chloro-3-Nitrocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure cap, labeled "4-Chloro-3-Nitrocinnamic Acid, 25g," hazard symbols, and product details clearly displayed. |
| Shipping | **Shipping Description:** 4-Chloro-3-Nitrocinnamic Acid is shipped in tightly sealed containers, protected from moisture, heat, and light. The packaging complies with local and international regulations for chemical transport. Handle with care as an irritant; avoid inhalation and skin contact. Suitable documentation and safety data sheets accompany the shipment for proper handling and emergency procedures. |
| Storage | 4-Chloro-3-Nitrocinnamic Acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and reducing agents. Ensure proper labeling and avoid exposure to moisture. Use appropriate personal protective equipment when handling. Store at room temperature and follow standard chemical storage protocols. |
Applications of 4-Chloro-3-Nitrocinnamic Acid in Industrial ManufacturingAs a specialized manufacturer of 4-Chloro-3-Nitrocinnamic Acid, we support a diverse range of downstream industries. Our expertise covers precise integration of this compound in pharmaceutical intermediates, agrochemical synthesis, specialty polymer modification, and organic electronics. Each application requires unique quality, formulation, and process controls for final product performance and compliance. 1. Synthesis of Pharmaceutical Intermediates4-Chloro-3-Nitrocinnamic Acid serves as a key intermediate for active pharmaceutical ingredient (API) synthesis, particularly for non-steroidal anti-inflammatory agents and antihypertensives. In multi-step processes, its halogen and nitro functional groups facilitate selective coupling, hydrogenation, and condensation reactions. Manufacturers prioritize impurity profiles and reaction yields, optimizing the input according to strict documentation and validation requirements for regulated pharmaceutical workflows. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingDownstream agrochemical producers incorporate 4-Chloro-3-Nitrocinnamic Acid for the synthesis of pre-emergent herbicide actives and certain fungicidal agents. The molecular structure supports the construction of systems with specific activity against hard-to-control weeds and fungal threats. Production fidelity, analytical specification, and environmental release regulations govern manufacturing integration into field-ready formulations. Industry compliance standards
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3. Functionalization in Specialty PolymersChemical processors employ 4-Chloro-3-Nitrocinnamic Acid as a monomer modifier for advanced polymers, especially in applications requiring halogenated or nitro-aromatic side chains. The compound enhances thermal and UV stability in end-use plastics. Strict input tolerances and batch consistency remain critical to meeting customer downstream requirements such as moldability and electrical insulation standards. Industry compliance standards
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4. Fine Chemical Intermediate for OLED MaterialsOrganic electronics manufacturers select 4-Chloro-3-Nitrocinnamic Acid as an intermediate in the design of specific light-emitting and charge-transport molecules for OLED display and lighting solutions. Photoelectronic properties and functional group versatility make it valuable for proprietary molecule synthesis pathways. The electronic grade purity, trace metal control, and solvent compatibility guide batch acceptance for final device integration. Industry compliance standards
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Every chemical tells a story of transformation, utility, and necessity. 4-Chloro-3-Nitrocinnamic Acid does more than fill an order sheet; it anchors research, problem-solving, and production flow in a diverse set of industries. As a manufacturer, witnessing demand patterns and end-use shifts, I've seen how subtle changes in one molecule can unlock new applications or resolve sticking points downstream.
Chemists recognize 4-Chloro-3-Nitrocinnamic Acid by its structure, where a chloro group at the 4-position and a nitro group at the 3-position decorate a cinnamic backbone. This particular arrangement doesn't just define its name; it actively shapes how it interacts in synthesis reactions, whether in pharmaceutical intermediates, specialty polymer precursors, or agrochemical pathways. Some clients bring questions about this structure’s benefits. What sets it apart from plain cinnamic acid derivatives? It’s not just the presence of chlorine and nitro groups. Each group shifts reactivity and solubility, dictating where and how the compound meets real-world needs with fewer processing headaches.
Years of producing 4-Chloro-3-Nitrocinnamic Acid have taught us what matters to repeat buyers. Color deviations or purity drifts can cause bottlenecks in synthetic routes. Our processes emphasize lot-to-lot consistency and impurity profile control because small changes ripple through the chain, delaying timelines and clouding analytical results. Most batches exhibit a well-defined crystalline appearance and the robust yellow color typical for its nitro-substituted backbone. We don’t aim for the highest theoretical purity at unmanageable costs, but instead balance robust isolation and manageable downstream workup for our partners.
During scale-ups, issues such as exothermic nitrations and chlorination side reactions demand careful attention. Not all nitrated cinnamic acids are created equal. Some will frustrate reactors with sticky tars or unpredictable crystallizations. In-house knowledge built over decades lets us produce this acid so practitioners see the clean transformation of educts, minimal byproducts, and a manageable, filterable solid at the end. For us, every shipment reflects not just specification sheets, but a robust process that growers from bench scale to tonnage reliably.
Most commercial requests specify assay values, melting points, and trace residual solvents. We offer 4-Chloro-3-Nitrocinnamic Acid with typical assay above 98%, which reflects more than just a number from a titration curve. Our quality department checks for tight melting range, often observed near 240°C, and keeps a sharp eye on moisture absorption since hygroscopicity determines stability during storage or shipping. Accurate data from spectroscopy and HPLC matter, but batch traceability and communication with client analysts define real-world reliability.
Some buyers ask about heavy metal residue or the possible presence of dimerization products, especially when using this acid in sensitive syntheses for pharma or fine chemicals. We developed additional post-synthesis washes and filtration tweaks to minimize any signal from these secondary compounds. Storage in light-protected, corrosion-resistant drums preserves product integrity and prevents unexpected reactivity. These choices reflect years of running into and then solving, not just listing, minor batch faults.
4-Chloro-3-Nitrocinnamic Acid isn’t a volume-driven commodity like salicylic acid or acetic anhydride. Most years, it plays a specialized role in custom syntheses and short-run manufacturing projects, particularly where electron-withdrawing substituents drive selectivity. Advancements in organic synthesis demand greater performance from every reagent. Chlorine and nitro groups both pull electrons from the aromatic ring, which not only guides reactivity during subsequent transformations but also offers built-in points for further derivatization. This feature attracts researchers designing compounds for targeted biological activity, especially where a more polarized aromatic system elevates the pathway to novel molecules.
From my seat in operations, I’ve seen an uptick in demand from medicinal chemistry teams, working to expand into new series of anti-inflammatory agents or enzyme inhibitors. They aren't seeking “off-the-shelf” building blocks. They need starting points that let their chemistry progress smoothly, cutting back on labor-heavy purification steps. With this acid, the difference between well-controlled batches and questionable purity cascades into project success or revision rounds. Drug development cycles often compress to meet new regulatory or market pressures, so our reputation for hitting tight specs— and notifying quickly should something deviate— means more to teams on tight timetables than any spec sheet ever could.
Comparisons between 4-Chloro-3-Nitrocinnamic Acid and its relatives, such as 4-Chloro-3-Nitrobenzoic Acid or plain cinnamic acid, may seem subtle on paper. The differences leap out in the flask. Standard benzoic acid derivatives lack the vinyl linkage, cutting off routes for conjugation or extension. Unsubstituted cinnamic acid won't engage electrophilic substitutions like a nitro-chloro derivative. For those running multi-step syntheses, the electron distribution and steric profile of 4-Chloro-3-Nitrocinnamic Acid clear more hurdles, especially where regioselective functionalization counts.
We’ve heard from polymer chemists working on specialty films and resins who saw improved reactivity with this acid compared to simpler cinnamates. They noted increased compatibility with modified epoxy resins, as well as more defined crosslinking points during curing. Every new application is a collaboration: clients bring project-specific hurdles, and we offer not just the material, but insight born from making thousands of kilograms under variable conditions. Questions arise about how modifications in the chloro or nitro positions— or swapping one for an alkoxy or alkyl— change both the safety profile and process window. We don’t just send certificates of analysis; we engage through years of shared improvement and troubleshooting.
A recurring conversation concerns shelf life and safe handling. The nitro group in 4-Chloro-3-Nitrocinnamic Acid, while less reactive than in some high-energy compounds, still demands respect in storage and transit. Fumes and dust control remain a priority. Many of our institutional clients have implemented air-tight, labeled storage using inert liners. This approach avoids both oxidative and moisture-induced degradation, protecting not only the product but also preventing accidental low-level contamination of other stockroom materials.
I've seen poorly labeled or mismatched containers lead to confusion or safety reviews in customer labs. Detailed secondary containment, robust lot marking, and ongoing technical guidance from our site prevent these lapses. Packing methods influence stability more than customers often realize. We’ve made the shift away from metal drums with loose caps toward modern, high-density plastics with integrated seals after watching too many batches degrade through casual humidity exposure. These lessons took years, and plenty of feedback from partners, to cement into protocol.
Researchers typically use 4-Chloro-3-Nitrocinnamic Acid as a precursor in multi-functional synthetic projects. We’ve shipped to facilities building enzyme inhibitors, UV stabilizers for advanced coatings, as well as developing bioconjugation tools. The nitro function allows straightforward reduction to an amine, opening up further rings, side-chain elaborations, or crosslinked scaffolds. Meanwhile, the chloro substituent serves as a persistent point of differentiation, allowing fine-tuned modifications under mild catalytic conditions, without risking unwanted overreactions.
One notable project involved a team tackling selective herbicide design. Their route called for high-purity, single-lot material to avoid misattributed biological activity. They needed lower than 0.2% total unknown impurities and absolute confidence about absence of isomeric co-products from incomplete syntheses. We orchestrated a dual-column chromatography purification, sacrificing some throughput for the reproducibility that field trials required. The result— no false positives in their screening and clear, interpretable metabolic breakdown profiles. This kind of collaboration highlights the value of real chemical manufacturing expertise. It's not enough to “supply” material; solving with clients separates routine batch makers from strategic partners in discovery.
Regulatory expectations consistently increase. Traceability and impurity identification, even for non-pharmaceuticals, now reflect levels that a decade ago existed only for GMP APIs. As a manufacturer, this drives constant review and upgrades, not just in the quality lab but in every operator’s workflow. Digital batch records, automated environmental controls, and negative pressure workstations guard against cross-contamination. End users see it in the reliable, documented composition of every outgoing container.
More regions look for REACH, TSCA, or similar registration status. Often, that requires toxicology profiles, exposure models, and validated analytical methods. We have adapted to run regular third-party audits for both lab results and inventory flows. Testing for nitrosamine formation, even where not required by statute, fills an important role. Our responsibility as upstream process guardians forms the backbone of our customer relationships. Every new client brings its own standards, requiring adaptation from us by internalizing not only global regs but local safety, transit, and disclosure rules.
We maintain a robust archive of all testing, including NMR, IR, and HPLC runs for each production campaign. This ensures that our records are not just a compliance measure but a resource for troubleshooting, product development, and retrospective analysis. Clients often call with one-time issues— a gel observed in a reaction, a spot on a TLC where none was expected— and the depth of our data helps resolve these uncertainties without repeated delays.
Manufacturing specialty chemicals like 4-Chloro-3-Nitrocinnamic Acid isn’t a static routine. Seasonality in raw material supply, supply chain disruptions, and evolving environmental requirements add variable pressures. For example, the route to install the nitro group on an aromatic ring often requires careful modulation of nitrating agents and reaction heat release. Small miscalculations in cooling or reagent addition timing during scale-up lead to runaway conditions or unwelcome by-products. Here, the value of decades-deep process knowledge surfaces— we know hidden danger points and design around them with interlocks, staged addition, and experienced supervision.
Solvent selection also plays a major role in finished product performance. Traditional systems used mixed acids and chlorinated solvents, but ongoing efforts target safer alternatives and reduced waste generation. We test greener alternatives whenever possible, balancing their environmental and safety benefits against any compromise in yield or impurity carryover. Engineers, chemists, and operators meet frequently to share run logs, review batch data trends, and implement improvements suggested by both field feedback and internal studies.
One persistent challenge is variation in starting material quality. We vet every new supplier, audit their operations, and run multiple pilot syntheses before scaling up. We’ve joined industry-wide consortia to standardize upstream sourcing and create early warning systems for contamination risks. These steps keep our process stable, but also offer external assurance to customers who require transparent audits from feedstock to finished acid.
Different projects require tailored solutions. Some buyers request micronized material for rapid dissolution, others want bulk crystalline form for continuous reactors. That flexibility stems from listening to client chemists in both R&D and production settings. In several cases, a process tweak— longer cooling or a finer final filtration— produced cleaner end product for a bioassay lab. Resting on old protocols rarely works in a field as dynamic as specialty organics.
Our role bridges large-scale industrial experience with the experimental needs of academic teams. Responding to a sudden spike in requests for analytical standards, we quadrupled sub-kilo packaging runs and distributed stability data gained from real, not hypothetical, stress testing. This approach has prompted productive discussions on novel applications, stretching the boundaries of what this acid can do in synthesis, labeling, and formulation.
Manufacturing 4-Chloro-3-Nitrocinnamic Acid extends beyond reaction vessels and drying ovens. It depends on hard-won experience adjusting to pressures both in the plant and in global demand. Regular engagement with client chemists, project leads, and engineers gives us direct insight into what works—and what could still improve. The feedback loop shapes our batch records, shipping protocols, and even the technical content on our documentation.
Many in the industry chase lowest-cost supply. We focus on reliability— knowing that a project’s success can hinge on whether a single batch performs as expected. By keeping tight controls and an open channel for client feedback, we maintain confidence not only in the product itself but in the backbone of support that brings it consistently from our site to yours.
Ongoing R&D in our facility ensures we stay ahead of both regulatory demands and application trends. Every year, new demands emerge for higher purity versions, reduced environmental footprint in manufacture, and faster, more flexible delivery systems. From tweaking drying cycles for better powder flow to automating pH and temperature ramp-ups during synthesis, we embed improvements rooted in real data and production experience. This continual process of learning, unlearning, and relearning projects forward-looking energy into both legacy and new product lines.
Some customers push for custom derivatives, exploring not just 4-chloro or 3-nitro variations but compounds with alternate halogenation or further ring substitutions. These requests showcase the value of active collaboration: sharing early-stage syntheses data, discussing reaction bottlenecks, and diverting process R&D toward emergent fields such as advanced agrochemicals or photonic applications. Our technical team enjoys working side-by-side with partners, knowing each cycle of process development extends the reach and impact of our collective expertise.
What truly distinguishes a trusted manufacturer in the specialty chemical market is not just consistent purity or strong documentation. It is a willingness to invest in clients’ real challenges, troubleshoot complex syntheses, and provide rare insight when unexpected issues arise. That’s why we continue to devote resources toward rigorous analytical validation, transparency in process improvements, and honest, regular dialogue with every partner— from small university groups to global manufacturers.
4-Chloro-3-Nitrocinnamic Acid represents one specialty within a broad catalog, but the principles behind its manufacture— reliability, customization, continuous improvement, informed support— reflect the foundation of our work across every offering. Years of experience, and the lessons learned from both our successes and challenges, shape how we see both the immediate utility and the broader potential held by these carefully crafted chemical building blocks.