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HS Code |
833052 |
| Compound Name | 1-(2-Chloroethoxy)-4-Nitrobenzene |
| Molecular Formula | C8H8ClNO3 |
| Molecular Weight | 201.61 g/mol |
| Cas Number | 15740-57-5 |
| Appearance | Yellow to orange solid |
| Melting Point | 44-48°C |
| Density | 1.33 g/cm³ (estimated) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=CC=C1OCCCl)[N+](=O)[O-] |
| Inchi | InChI=1S/C8H8ClNO3/c9-4-5-13-7-2-1-6(10(11)12)3-8-7/h1-3,7-8H,4-5H2 |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory system |
As an accredited 1-(2-Chloroethoxy)-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, tightly sealed with a screw cap; labeled with compound name, molecular formula, warnings, and hazard symbols. |
| Shipping | 1-(2-Chloroethoxy)-4-nitrobenzene should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and must be transported according to local, national, and international regulations, with proper labeling and documentation to ensure safe handling and compliance with safety standards. |
| Storage | Store **1-(2-Chloroethoxy)-4-nitrobenzene** in a tightly sealed container in a cool, dry, and well-ventilated area away from heat, flame, and direct sunlight. Keep away from incompatible substances such as strong oxidizing or reducing agents. Use proper chemical storage cabinets, ideally for organics or toxic substances, and ensure clear labeling. Avoid moisture and protect from physical damage. |
Applications of 1-(2-Chloroethoxy)-4-Nitrobenzene in Industrial ManufacturingAs a specialized manufacturer of 1-(2-Chloroethoxy)-4-Nitrobenzene, we focus on delivering consistent quality for established downstream segments. Our product supports advanced synthesis workflows and originates from controlled processes to serve as a key intermediate in select chemical industries. Below we outline real-world application scenarios, covering precise usage specifications, integration points, product segment outputs, and the applicable industry compliance benchmarks for each domain. 1. Agrochemical Active Ingredient SynthesisAgrochemical formulators utilize this compound primarily as an intermediate in the multi-stage synthesis of phenoxy and ether-linked herbicides and fungicides. It enters the production stream during etherification and nitration phases to build specific molecular frameworks required for crop protection agents. These processes require rigorous material consistency and traceability to meet regulatory approval for agro inputs in major markets. Industry compliance standards
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2. Pharmaceutical Intermediate for API SynthesisIn fine chemical and pharmaceutical operations, this material supports the build-up of advanced intermediates positioned in the early-to-mid phase of active pharmaceutical ingredient (API) synthesis, especially in molecules featuring nitro-aromatic ether scaffolds. Controlled input quality at this stage is critical to minimize downstream impurity carryover and to comply with regulatory dossiers for drug master files. Industry compliance standards
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3. Dye and Pigment Intermediate ManufacturingThis compound provides a functional block in the stepwise synthesis of specialty azo, nitro, and ether-substituted dyes and pigments, ensuring color intensity and chemical stability in final formulations. The addition of this intermediate allows formulation technicians to adjust chromophore length and solubility during pigment finishing stages, especially under regulatory scrutiny for use in textiles and plastics. Industry compliance standards
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4. Synthesis of Liquid Crystal IntermediatesProducers of advanced display materials employ this compound as a precursor to build custom ether-nitro linked molecules essential for specialty liquid crystal blends. Its selective reactivity permits the introduction of both halogen and nitro functionalities, key for tuning dielectric and optical properties of final display-grade formulations, while maintaining compliance with electronics component safety and quality standards. Industry compliance standards
Typical usage ratio
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In over two decades of producing specialty intermediates, we have seen a steady demand for 1-(2-chloroethoxy)-4-nitrobenzene among agrochemical and pharmaceutical researchers looking for consistent input materials. Chemists appreciate its stability under a variety of reaction conditions, and we make it a priority to provide consistent purity and crystal form batch after batch. This compound, recognized in many catalogs by its model code CEB-4NB, has been a core material for a handful of major crop protection programs and a candidate for further transformation in several routes to target molecules.
Chemists who spend any time in the plant notice that slight shifts in reagent quality or temperature can affect the final product. We have learned over the years that our best batches come from strict control—keeping water content under 0.2%, watching chloride levels, and confirming the melting range always sits in the expected window. Our quality control uses a combination of HPLC, NMR, and IR. Consistency does not happen by accident. The yellow needles in each drum should have a clean appearance and minimal dusting. Each kilogram we produce matches over 99% purity unless a customer requests a different grade.
Packing this compound in airtight, lined drums or HDPE containers preserves the nitro group integrity and prevents the faint chlorine odor from building up during transit. Exposure to sunlight can cause slight changes in color after months on the shelf, which we note from experience rather than speculation. We store the material in cool, dry rooms, not only for compliance reasons but because we have seen firsthand what happens to batches left in humid environments—caking, off-odors, and hydrolysis, which create headaches for downstream users.
Most inquiries we receive come from development teams pursuing new or next-generation herbicides, pesticide actives, and in several cases, antiviral intermediates. This compound features an electron-withdrawing nitro group and a substituted chloroethoxy chain, which offers flexibility for further derivatization. Among all nitro-substituted intermediates we produce, this one stands out for the balance it offers between reactivity and process safety. Downstream reactions—especially nucleophilic substitutions or reduction to an aniline—proceed smoothly, giving chemists more control during scale-up.
Synthetic teams use 1-(2-chloroethoxy)-4-nitrobenzene as a stepping stone to more complex molecules, especially when building ether linkages or modified anilines. Its use expands beyond just conceptual research; several multinational partners scale this intermediate at a tonne-level for continuous production plants. We have provided samples for formulation studies and over time scaled several hundred-kilogram batches to full metric-tonne streams. Looking back at development notes from the past ten years, we see its biggest adoption tied from fungicide innovation, where its presence in the route delivers consistent yields and greater cost predictability.
Compared to simple nitrobenzenes or unsubstituted chloroethoxy benzenes, 1-(2-chloroethoxy)-4-nitrobenzene handles differently in both small glassware and stainless steel reactors. The electron-withdrawing power of the nitro group tends to temper the rate of nucleophilic attack on the chloroethyl side, reducing by-product formation during halide displacement steps. Experienced operators recognize that batch time can stay shorter and filter press operations run cleaner with less sticky by-product compared to chlorinated toluene analogues, especially under basic conditions.
We have observed that competitive products with substitutions at the 2- or 3-position do not perform as well in side-chain modification reactions. Yields often drop by up to 15% in pilot trials, and dechlorination seems to occur more frequently. For customers working toward pharmaceuticals, the meta position nitro analogues tend to create more color impurities after catalytic hydrogenation; our para arrangement minimizes side products and keeps assay results steadier. This is not speculation—it shows up each year as unambiguous process data, especially as the compound moves from the R&D bench to kilo lab and finally to plant scale reactors.
Batches that fail to meet the required melting range almost always trace back to uncontrolled moisture or sluggish reaction times during synthesis. In our plant operations, we run routine checks every two hours to ensure reaction completion, as incomplete conversion leads to persistent contamination with di-substituted by-products. Our maintenance crew has developed a set of checks for vapor-phase leaks in quenching lines to keep exposure risk low. Importantly, we never rely on third-party blends or off-the-shelf reagents in production—every batch of raw materials undergoes full requalification before use.
On a few occasions, customers contacted us after noticing changes in downstream crystallization when trying alternative suppliers. We have stepped in and found that the minor residual solvent trapped during spray drying—often less than 0.05%—can dramatically influence the next hydrogenation step. Making this minor adjustment brought the project back on track. Lessons like this escape textbook statistics; they only come from making, testing, storing, and shipping thousands of kilograms over years of steady production.
Working daily with 1-(2-chloroethoxy)-4-nitrobenzene means addressing the real-world impacts of nitroaromatic intermediates. While not among the most toxic of our handled materials, all nitro compounds demand solid housekeeping and well-maintained ventilation. We avoid heating above 150°C and store away from reducing agents. Regular cleaning routines leave little waste behind, but we still run spent mother liquors through solvent recovery units to cut down on incineration. Unlike the simpler halobenzenes, this compound does not volatilize heavily at ambient temperature, making container breach events less likely to threaten worker safety.
Spills on concrete absorb readily with bentonite or kaolin clay. Our safety team drills on this response quarterly, building on the hard lessons of past near-misses. We keep our staff equipped with nitrile gloves and acid gas respirators, especially when cleaning jackets or patching insulation in enclosed pump houses. Fume hoods vent at the right velocity, confirmed during each major maintenance shutdown. Over the last decade, process changes have reduced our lost-time incident rate by half, partly due to refinements in handling materials like 1-(2-chloroethoxy)-4-nitrobenzene.
In the late 2000s, average order sizes were only a fraction of what we fill now. Market shifts toward high-selectivity pesticides and lower-dose active ingredients pushed many organizations to demand higher-purity intermediates. 1-(2-chloroethoxy)-4-nitrobenzene saw its demand climb as manufacturing routes pivoted away from older, less environmentally friendly coupling steps. Our production engineers adapted synthesis equipment, exchanging older packed-bed assets for jacketed glass-lined reactors. This investment lets us hold internal temperatures to tighter tolerances and hit narrower impurity profiles for regulated markets.
Research partners occasionally request lots tailored for regulatory submission, with extra trace analysis for metals, solvent residues, and specific aromatic impurities. We draw on our in-house analytical laboratory to expand data packages as needed. Customer roundtables and feedback from full-scale manufacturing managers lead us to tweak our quality agreements, especially as new environmental regulations touch raw material selection and final product handling. We do not see this as bureaucracy—it reflects real expectations from buyers and end-users.
Nitroaromatics manufacturing generates spent acids, high-boiling tars, and trace polychloro impurities. Over the last five years, our plant installed a closed-loop solvent recovery and phase separator. Waste acid streams now feed a neutralization unit, removing load from municipal treatment. We also route spent organic layers through fractionating stills, recycling 80% back to the process, which minimizes fresh solvent demand and lowers cost for each production run. These steps came from practical necessity as well as growing client focus on Life Cycle Analysis scores and reduced greenhouse gas footprints.
Lowering trace color bodies and off-odor in the finished product now starts well before final filtration. Operators realized that batch agitation rates and hold-up times influence the amount of sulfur-trapping—in turn, reducing post-processing treatments and final wastewater color. Since adopting real-time in-line monitoring, we observe a 12% reduction in filter cake mass and lower overall chemical oxygen demand in plant effluent. Environmental stewardship in our plant does not stop at compliance—it shapes how we make decisions at each stage of the process.
Distributors and downstream processors both expect that each container of 1-(2-chloroethoxy)-4-nitrobenzene arrives sealed, labeled, and free of cross-contamination. We run dedicated filling lines for this intermediate, as we have seen firsthand how flavor cross-contact issues can affect sensitive applications. Standing up the correct internal controls both in filling and in labeling prevents unwanted customer callbacks. For long-distance shipments, supply chain interruptions can create temperature swings beyond usual warehouse conditions. We insulate and overpack shipments for sea freight, as unrefrigerated containers can reach over 35°C at port. This step, over time, virtually eliminated customer complaints about clumping.
We monitor monthly batch yields and downtime. Years when we did not invest enough in preventive maintenance led directly to shipment delays. This experience drives current practices—constant checks of pump seals, agitation speeds, and monitoring of batch record accuracy. As a direct producer, we shoulder the responsibility for delivering on contract, and missed deliveries do not help anyone's reputation. We have signed multi-year supply agreements with a number of regular partners, supported by our track record in on-time and in-spec shipments.
Formulators pushing toward greener solvents or cleaner product profiles often approach us to explore alternate processing aids or tweaks to reaction stoichiometry. Our technical staff regularly trials modified feeds and reports on impact, so projects requiring low sodium content or non-standard residual profiles see real-world process data and not just theoretical support. Some partners use 1-(2-chloroethoxy)-4-nitrobenzene for pilot-scale process validation, which demands tightly defined limits on residual impurities. We work in step with their analytical teams, exchanging control samples, comparing chromatograms, and solving challenges that surface in continuous manufacturing.
Over multiple projects, we have edited process flows and control limits based on partner feedback. This trust comes not from marketing language but from hard-earned reliability and transparency in operations. We understand that our partners depend on intermediates that perform the same way every time, and our long-running production lines provide the data and the records to back that up.
From our vantage point, manufacturers who rest on old process know-how without evolving get left behind. We have committed resources to continuous improvement teams who audit older equipment, revisit standard operating procedures, and model new reaction pathways for efficiency and lower waste. Last year, team efforts in raw material screening identified alternate suppliers who deliver starting 4-nitrophenol with a higher initial purity, which helped raise final yields and reduced by-product formation. These practices matter to our team and to our customers, who count on a supply chain partner prepared to stretch ahead of market needs.
Adapting does not mean chasing every industry trend. As more partners pursue low-emission chemistry and solvent alternatives, we start with pilot trials, bench testing, and a clear track record before rolling out changes plant-wide. Each success builds the confidence to move forward, especially when made in partnership with formulators, analysts, and supply chain managers who share the same standards for reliability and compliance.
The history of 1-(2-chloroethoxy)-4-nitrobenzene in our facility is one of adaptation to the evolving needs of the chemical industry. We approach each new batch and each inquiry with the recognition that even small improvements in consistency, safety, or supply reliability ultimately deliver better outcomes for all stakeholders. Our continuous investment in people, analytical tools, and production technology reflects this commitment.
Looking ahead, we believe that the utility of 1-(2-chloroethoxy)-4-nitrobenzene will grow as new synthetic methods and end-use applications develop. Strengthening our capabilities in environmentally conscious manufacturing, analytical support, and agile supply positions us well for the demands of tomorrow’s chemical landscape. Our experience informs every shipment, every improvement, and every partnership.