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HS Code |
986965 |
| Chemical Name | 2-(4-Chlorophenoxy)aniline |
| Cas Number | 25335-46-2 |
| Molecular Formula | C12H10ClNO |
| Molecular Weight | 219.67 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 79-82°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.27 g/cm³ (estimated) |
| Pubchem Cid | 184502 |
| Smiles | C1=CC=C(C(=C1)N)OC2=CC=C(C=C2)Cl |
| Inchi | InChI=1S/C12H10ClNO/c13-10-4-6-11(7-5-10)15-12-3-1-2-9(8-12)14/h1-8H,14H2 |
As an accredited 2-(4-Chlorophenoxy)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 100-gram amber glass bottle, sealed with a screw cap, labeled “2-(4-Chlorophenoxy)Aniline” and hazard information. |
| Shipping | **Shipping Description for 2-(4-Chlorophenoxy)aniline:** Ship 2-(4-Chlorophenoxy)aniline in tightly sealed containers, protected from light and moisture. Ensure labeling complies with relevant chemical safety regulations. Handle as a potentially hazardous organic compound, using appropriate protective measures. Consult the Safety Data Sheet (SDS) for specific transport classes, and follow all regional and international shipping guidelines for chemicals. |
| Storage | 2-(4-Chlorophenoxy)aniline 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 oxidizing agents. Keep away from sources of ignition and moisture. Clearly label the container and ensure safety measures are in place to prevent spills or accidental exposure. |
Applications of 2-(4-Chlorophenoxy)Aniline in Industrial Manufacturing2-(4-Chlorophenoxy)Aniline performs as an essential intermediate in high-value chemical manufacturing. Its versatile structure and reactivity facilitate integration within key industrial sectors. Below, we detail proven downstream applications with focus on regulatory adherence, accurate dosage guidance, process placement, and end product relevance. 1. Synthesis of Agrochemical Active IngredientsMajor agrochemical producers utilize this aniline derivative for synthesizing herbicide and fungicide actives. The compound enters chlorinated aromatic pathways, supporting targeted molecule construction for selective weed and disease control. Rigorous contaminant control and batch traceability characterize this route due to agricultural and environmental demands. Industry compliance standards
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2. Pharmaceutical Intermediate for API SynthesisPharmaceutical contract manufacturers select this compound to build advanced intermediates for non-steroidal anti-inflammatory drugs and select antihypertensive agents. Its chlorinated phenoxy moiety enables regioselective coupling, minimizing byproducts. Processes must comply with strict GMP protocols, process validation, and impurity control. Industry compliance standards
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3. Dye and Pigment ManufacturingIndustrial dye producers use 2-(4-chlorophenoxy)aniline as a building block for specialty azo and anthraquinone dyes. Its molecular characteristics enable strong chromophore-linker interactions, supporting vivid color strengths and superior fastness. Operations follow chemical management protocols as per textile and printing material requirements. Industry compliance standards
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4. Specialty Polymer Additives and ModifiersProducers of engineering plastics and coatings employ the material for synthesis of custom polymer additives. Its aromatic backbone supports development of antistatic agents and UV stabilizers required in electronics and automotive polymers. Manufacturing involves precise feed and quality monitoring to ensure downstream compatibility and performance. Industry compliance standards
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Drawing from years of hands-on chemical synthesis, our team’s experience with aromatic ether anilines informs everything we do. 2-(4-Chlorophenoxy)Aniline, also known as 4-Chlorophenoxy-2-aniline, occupies an important space in our portfolio. Not just another intermediate, this molecule brings a unique combination of electronic effects and reactivity that serves modern, forward-looking chemistry. Our facility dedicates considerable resources to process controls for this product, taking special care with chlorination stages and ether formation to avoid uncontrolled byproducts—a concern we’ve addressed with intensive monitoring and targeted purification steps.
Achieving tight purity remains our focus, not simply for chemical aesthetics, but for the role purity plays in customer processes. With 2-(4-Chlorophenoxy)Aniline, minor impurities can interrupt downstream synthesis, create purification headaches, and compromise targets in pharmaceutical, crop protection, and materials science projects. We aim for a minimum assay of 99%, with residual solvents well below industry thresholds, a standard established through regular in-house calibration and feedback from customers over a decade. Feedback from customers highlighted specific impurity profiles that confounded analytical metrics before, so our method development includes regular adjustment cycles, aligning with realistic needs instead of speculative ones.
Most users handle 2-(4-Chlorophenoxy)Aniline as an off-white to pale yellow crystalline powder. Temperature and humidity control during packaging influence final texture and bulk density—a factor that arose after our initial batches a few years ago, when some users’ storage conditions affected downstream dissolution times. Based on those lessons, our production shifted towards moisture-reduced final processing and inert atmosphere packaging. We label batch quality with actual inspection values instead of relying on typical ranges, a habit developed from working closely with partners who required tighter process predictability.
Production scale has increased gradually, as we moved from lab-scale syntheses to mid-size batch reactors, adjusting the reaction profiles over time to minimize energy expenditure without sacrificing material consistency. We take extra precaution with the chlorination reaction, which can drift under uncontrolled conditions. A burst of monochloro substitution can cause byproducts that do not come out easily. Feedback from our chemists on the frontline led to improved agitation and quench sequencing, beneficial for the end-user as well. By working on honest process refinement, waste is reduced, staff exposure is minimized, and timeline pressure eases across the board.
Buyers most often use 2-(4-Chlorophenoxy)Aniline in agrochemical discovery and crop protection compound development. The placement of an electron-withdrawing chlorine on the aromatic ring activates the molecule in ways that benefit structure–activity relationships within several engineered pesticides and fungicides. The phenoxy linkage allows medicinal chemists to explore new heterocycle attachments and to fine-tune solubility profiles in advanced chemical libraries. In my own experience collaborating on structure optimization programs, high-purity lots sharply reduced rework cycles, sped up hit confirmation, and gave project teams confidence to scale up reactions. Our strict luminescence and color testing, adjusted after a round of customer complaints in earlier years, practically eliminated troublesome fluorescent-like side compounds.
Some customers come from specialty materials fields, using this compound to open up new block copolymer motifs, dyes, or optoelectronic materials. Specific requests from polymer chemistry firms led us to optimize post-synthesis purification, which can spell the difference between a project that proceeds and one that stalls during upscaling. Through repeated joint process reviews with their technical teams, we discovered potential incompatibilities tied to minor isomer contamination. Our chemical engineers now inspect not just the main component’s purity, but isomer distribution as well, heading off problems before material leaves our plant.
A question arises regularly: why use this molecule over standard anilines or more familiar phenoxy-building blocks? Based on supplier and industry data, most basic anilines or phenol derivatives lack the combined electronic modulation and solubility potential found in 2-(4-Chlorophenoxy)Aniline. Standard p-chloroaniline, for instance, brings aggressive reactivity but creates harsh environmental challenges and demands more aggressive handling measures in place. Phenoxy anilines without the chloro group, though easier to produce, do not offer comparable aryl activation or the same range of downstream reaction options for chemists pursuing difficult syntheses.
From my vantage point, the inclusion of a chlorine substituent at the four-position of the phenoxy group grants subtle but impactful effects. For cyclization, coupling, or even simple N-acetylation steps, customers report more predictable yields and fewer purification surprises, drawing on internal studies as well as open scientific literature. We have tested batches head-to-head with non-chlorinated analogues, observing measurable differences during kinetic assessments and chromatographic profiling. The tighter tolerance of this product for polar and nonpolar solvents widens its utility, letting end users try alternate process solvents and reach higher concentrations without messy solubility issues.
As a chemical manufacturer, facing—and solving—production bottlenecks is a daily job. Early on, our batch yields lagged behind projected targets because of insufficient mixing and solvent management. Staff training highlighted that quick, unchecked solids separation led to dense aggregates that trapped solvents. Months of process tweaks followed, with staff input guiding agitation upgrades and filtration line redesign. Final throughput improved by over 20% after implementation, with less material lost in transfer. Such improvements stem from direct shop-floor input, not from desk-based engineering.
Reaction exotherms posed another concern. The chlorination stage releases heat that, if uncontrolled, risks partial degradation and creates non-target chlorinated phenols. We fitted automated calorimetry alongside high-volume condenser systems, then tailored exotherm controls based on real-time shop experience. Lessons learned in scaling-up feed directly into our process safety plan, covering both routine runs and rare upsets. In a notable example, a multi-shift production run faced unexpected cooling-water pressure outages—quick thinking by the production crew, drawing from regular hands-on drills, kept the batch within safety envelope limits and safeguarded the material.
Waste minimization also ranks high in priority. Standard purification schemes in the past meant large solvent footprints and complicated waste streams. Drawing on direct consultation with downstream users, we updated solvent recycling loops, changed over to greener purification solvents in two key steps, and worked with local environmental auditors. This work paid off with measurable reductions in both solvent use and offsite treatment cost, an outcome that the team achieved without compromising delivered product consistency. Right feedback loops and transparent reporting ensure these process benefits last.
Working direct with our customers, we listen to challenges as they emerge, not months after the fact. For example, last year a pharmaceutical partner struggled with phase separation issues during a late-stage process stemming from trace nonpolar byproducts. A series of collaborative test batches, using iterative tweaks to our post-synthesis wash sequence, eliminated this issue entirely in future runs. Open communication and honest technical sharing brings practical outcomes—lower in-line analytics rejects, cleaner product, fewer headaches later.
This hands-on feedback loop extends to packaging and logistics as well. Some customers need lots that match highly-specific packaging sizes for automated dosing, with full chain-of-custody tracking from tank to testing bench. We built customized packaging stations with full batch validation, led by our production staff who advocated for real-world fixes, not just office-driven solutions. Two years into the current system, error rates connected to packing and barcode mismatch dropped below one incident per thousand units shipped.
Maintaining reliable quality takes more than batch records and routine sign-offs. Every production run involves the entire team—line operators, lab technicians, and plant engineers. Each step, from handling the start materials to setting exact reaction timing, reflects a commitment to doing things the right way, even when the process occasionally means working late or taking extra sample cuts. Our facility rejects the notion that compliance alone brings success; knowledge-sharing and a willingness to learn from experience brings the best results.
We invest in regular internal audits led by experienced staff, drawing from patterns observed during active manufacturing, not just academic procedure. These audits often turn up opportunities invisible to outsiders: a valve adjustment, a tweak to storage room airflow, a chance to improve lighting for better inspection. Progress comes from participation, not just policy. Our analytical approach builds on the real-world situations confronting production teams—actual instrument drift during summer humidity, lighter-shaded powder in winter batches, or gradual deviations in throughput as equipment ages.
Logistics present their own challenges. 2-(4-Chlorophenoxy)Aniline can be sensitive to prolonged light or heat, so our material flows include climate-controlled holding and direct-to-user shipping in sealed units. More than once, customers have asked for just-in-time delivery when pilot plant bottlenecks struck their operations; through an ongoing dialog, our shipping and warehousing team planned adaptive shipments, minimizing the need for stockpiling at either end and reducing batch aging risk. Building such supply routines depends on honest conversation and a willingness to adjust practices on both sides.
We screen all incoming materials for cross-contamination risk and maintain clear separation between product lines. From loading docks to dedicated crystallization tanks, flow control protects both material and staff safety. Training new hires always includes direct participation in material transfers—under supervision—so that hands-on judgment supplements written protocol. This approach gives staff the confidence to spot potential issues before they become problems, and encourages a sense of shared responsibility throughout the operation.
Shipping documentation reflects real-time batch conditions, with clear notations if weather, transit time, or transport conditions diverged from planned values. While it might sound mundane, accurate documentation helps receiving labs troubleshoot anything unexpected, and also builds long-term trust. More than once, this approach has uncovered upstream installation issues on the customer side, allowing fast fixes and avoiding time-consuming finger-pointing.
Industry needs never stand still. Our customers push for both improved material specs and more sustainable practices. Through joint R&D with selected users, we explore new process catalysts to reduce temperature swings during synthesis and trial alternative purification chemistries to cut overall solvent needs. A recent effort investigated a continuous-flow alternative to traditional batch chlorination, and the early experiments hinted at not just better control over byproduct formation, but substantial energy savings and fewer exposure risks for staff. Once these methods prove themselves at pilot scale, we share success metrics and practical findings in technical briefings, inviting further comment from those who rely most on our output.
Regulatory requirements evolve, as do downstream customer specs. Regular direct review of global proposals for ingredient traceability, impurity thresholds, and emerging impurity testing protocols keeps our team one step ahead. We extend our own internal standards to meet—often surpass—external benchmarks. Ongoing dialogue with partners in Europe, North America, and Asia brings early notice of changing legal requirements, helping us to make process adjustments before rules become mandates.
Consistent internal training and open-access technical libraries mean everyone in the plant improves their skillset over time. New processes or synthetic methods never arrive fully formed; shop-floor reporting and cross-unit benchmarking inform adoption, sidestepping the pitfalls of hasty implementation. We see value in letting the people closest to the process shape its evolution—a perspective built through hands-on production, not just engineering theory.
The journey with 2-(4-Chlorophenoxy)Aniline teaches that nuanced, hands-on chemical manufacturing delivers value far beyond baseline compliance or specification sheets. Each batch brings real challenges, shaped by equipment limits, environmental conditions, and the unique needs of the chemists, engineers, and researchers who rely on us. Open feedback and a willingness to do the extra work—whether gathering one more purity metric, updating process steps after customer trials, or simply checking every drum before shipping—create an environment where reliability becomes a habit, not a hope.
Having worked for years in chemical plants and directly with the folks who depend on this product, I’ve learned that success comes from partnership and practical honesty. Putting the customer's process at the center of decisions promotes trust, repeatability, and growth on all sides. The story of 2-(4-Chlorophenoxy)Aniline is not about just another item in a catalogue: it’s about meeting demanding real-world applications, overcoming technical challenges with knowledge, and backing up every shipment with on-the-ground experience.