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HS Code |
163464 |
| Cas Number | 673-40-5 |
| Molecular Formula | C12H11NO |
| Molecular Weight | 185.22 |
| Iupac Name | 2-phenoxyaniline |
| Appearance | Pale yellow to brown solid |
| Melting Point | 56-58°C |
| Boiling Point | 337°C |
| Density | 1.186 g/cm3 |
| Solubility In Water | Insoluble |
| Smiles | c1ccc(cc1)Oc2ccccc2N |
As an accredited 2-Phenoxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a tightly sealed cap, clearly labeled "2-Phenoxyaniline", including hazard warnings and handling instructions. |
| Shipping | 2-Phenoxyaniline is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous chemical and should be transported following relevant regulatory guidelines, including appropriate labeling and documentation. Handle with care, avoiding contact with skin and eyes. Store in a cool, well-ventilated area during transit. |
| Storage | 2-Phenoxyaniline should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Protect from direct sunlight and moisture. Use appropriate labeling and ensure access is restricted to trained personnel. Follow all applicable safety and chemical storage regulations. |
Applications of 2-Phenoxyaniline in Industrial ManufacturingAs a direct manufacturer of 2-Phenoxyaniline, we support key process industries with this specialty intermediate. Our focus is on actual commercial use cases proven by regulatory demand, production efficiency, and downstream technical requirements. Below, we outline proven application fields where 2-Phenoxyaniline is an essential building block, detailing compliance frameworks, formulation ratios, integration points, and end-market product types recognized in global markets. 1. Synthesis of Benzophenoxazine Dyes for Textile and Paper Colorants2-Phenoxyaniline plays a critical role in the benzophenoxazine dye sector, especially for high-performance coloring of cellulose-based fibers and high-purity paper substrates. Its aromatic structure enables dye manufacturers to achieve colorfast, heat-resistant pigments vital for textile and specialty paper printing where durability, lightfastness, and precise hue control are priorities. We consistently support dye producers who require batch-to-batch traceability and conformance to stringent regulatory colorant purity minimums. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Phenoxy Substituted Herbicide ActivesMajor crop protection manufacturers use 2-Phenoxyaniline as a primary intermediate in the synthesis of select phenoxy-substituted heterocyclic herbicide actives. Its chemical profile supports coupling reactions that introduce stability and target-specific crop selectivity, especially in non-selective and selective pre-emergence herbicides. The accuracy of dosing and raw material handling aligns with tight regulatory controls incumbent in agrochemical active production workflows. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Precursor in Advanced Polymer Manufacturing for Heat-Resistant ResinsPolymer manufacturers incorporate 2-Phenoxyaniline as a specialized amine monomer in the formation of high-performance polyamide and polyimide resins. This precursor enhances the thermal and oxidative stability profile of resins destined for use in electronics, automotive, and aerospace parts where traditional aromatic monomers fall short in meeting operational temperature ranges. Our consistent QC ensures downstream users meet international product reliability expectations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Pharmaceutical Impurity Profiling in API SynthesisChemical and pharmaceutical process manufacturers utilize 2-Phenoxyaniline in specific synthetic routes for regulated API intermediates where controlled aromatic ring substitution is required. The molecule serves both as a critical building block and a reference standard for impurity profiling in analytical method development. Precise control over raw material specification ensures downstream compliance with global pharmacopoeia requirements and minimization of process impurities. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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In a world steadily prioritizing precision and dependability, 2-Phenoxyaniline stands out in our line-up, not just for its chemical identity, but for how it fits into the daily challenges and long-term needs of manufacturers. Here on the production line, there’s no substitute for familiarity—not just with synthetic routes, but with the quirks that come from creating this particular aniline ether consistently batch after batch. Our years spent refining every step have shaped how we think about, handle, and talk about 2-Phenoxyaniline, far beyond what a datasheet ever reveals.
We work with the model known by its CAS number, 2113-58-8. Each run in the reactor shapes a product that’s more than a molecule. There’s the faint earthy nuance at the tail end of the distillation, the slight color shift if there’s any trace oxygen. These details don’t show in pure percentage or melting point tables. If there’s ever been a test of patience for anyone on the process team, it’s hitting the right balance, keeping phenol-related byproducts away—the difference between a yellow cast and the off-white that customers expect. Form and function both depend on painstaking steps: that means closed glass reactors, sharp nitrogen purges, and a hands-on approach with every sample drawn.
The specification for our standard product runs at a purity of not less than 99%. This isn’t just a box to tick. End-users in dyes, organic synthesis, and pharmaceuticals make decisions based on those last decimal points. No one wants to troubleshoot a failed coupling reaction only to find trace impurities in the raw aniline ether. When we talk about meeting this purity, it reflects hours in QC, method tweaks, and the constant push to beat signal-noise in HPLC results by just a fraction more. The average product shows water content below 0.1%. Every trace of moisture gets chased out with the same vigilance as the tiniest batch impurity. There’s nothing routine about this step—moisture, after all, means potential side reactions, wasted catalyst, or unexpected haze in a colorant batch.
As simple as aniline ethers may seem on paper, every lot of 2-Phenoxyaniline runs the gauntlet: melting point range checked right out of the filter, GC-MS fingerprints compared to reference standards, and, for more demanding customers, custom packaging and detailed certificate documentation. The difference is visible right at the microcrystal scale. Well-controlled production lays the foundation, but follow-through in packing and logistics closes the loop. Small details—desiccant changes, double-lined bags—can decide whether a consignment survives humid shipping ports or arrives clumped and useless.
From the factory floor, 2-Phenoxyaniline is more than another reagent in a catalog. Our experience traces through its main role as an intermediate. Its chemical structure brings a subtle but vital reactivity, bridging the gap between phenolic ethers and anilines. That unique oxygen linkage gives it a spot in the synthesis of specialty dyes, advanced materials, and several pharmaceutical candidates. Sometimes, customers ask why not use a simple aniline or plain phenol derivative? The reason lies in subtle but crucial reaction pathways. The phenoxy group offers electronic influence, steering nucleophilic substitution or cross-coupling into clean, efficient transformations—especially in dye molecule frameworks where colors, fastness, and shade stability all hinge on small structural tweaks.
Working with dye customers means seeing their formulas evolve over time. Some years, we see demand spike for 2-Phenoxyaniline when pigment grades shift for automotive or synthetic fibers. The compound’s position in azo dye construction comes from its ability to stabilize the azo linkage, pushing shades toward deeper reds or lasting yellows. A shift in textile color trends or a new regulatory bar against certain precursors can turn what feels like a “routine” intermediate into a critical supply chain material almost overnight.
There’s pride in mastering this synthesis. In today’s market, customers don’t just expect a technical product—they expect the same product, every time, without surprises. That doesn’t happen by chance. We’ve learned to avoid batch-to-batch drift, not just through automated dosing or standardized batch records, but through old-school attention to weather, raw phenol lot variation, even seasonal humidity shifts. In summer, reaction kinetics stretch. In cold months, precipitation slows. The process crew calls for extra temperature control, and sometimes, manual agitation tweaks keep things on track.
From all these, we’ve found ways to fine-tune final product handling, packaging for both bulk and laboratory users. An extra filtration run can mean the difference between a sparkling white solid and a marginal off-color, especially when customers use it in applications sensitive to trace chromophores.
In our field, a comparison often crops up between 2-Phenoxyaniline and its isomers, as well as with less substituted analogues. Where competitors might offer simple aniline ethers or just plain diphenyl ether, true specificity comes with the ortho orientation of the phenoxy group on the aniline ring. The reactivity profile changes—not dramatically, but enough to drive certain couplings, substitutions, or cyclization reactions more efficiently. Synthetic chemists, especially in fine chemical houses, appreciate how this can cut down on byproduct formation and make downstream purification steps less of a headache.
Over time, we’ve seen R&D requests to tailor the material: slightly different grades for those developing advanced polymers, resins, or organic electronic materials. The feedback loop from these customers helps us spot trends in reactivity, uncovering which minute impurity profiles might create issues in ultrafast instrumentation applications, for example. No amount of catalog description ever matches the details worked out across dozens of pilot lots and scaled campaigns.
One of the most telling moments from shipping 2-Phenoxyaniline comes from a pharmaceutical project. A formulation specialist contacted us after runs with “generic” material from various sources led to batch failures in a late-stage drug intermediate. We ended up walking through their NMR and HPLC data, matching it against our internal QC on archived batches. It turned out that a trace by-product—completely invisible in routine IR screens—accounted for their lost yields. We tightened our own fractionation, stripped out a potential source in the upstream coupling, and, on the customer’s next trial, their synthesis clocked the highest yield yet recorded.
That’s the difference between mass-produced base chemicals and a vendor who tracks lot contribution from raw phenol drums, manages internal standards across every analyzer, and maintains pilot batch reserve samples for years. Those real-life stories, the push-and-pull between operator and R&D chemist, filter right back into our process discipline and inform our advice to customers looking to swap in 2-Phenoxyaniline as a drop-in alternative in complex syntheses.
Shipping stable shipments of 2-Phenoxyaniline remains a chemistry lesson. While the compound avoids the volatility of lighter anilines, it still responds to long-term exposure to light, heat, and moisture. Our packing line uses not just high-barrier plastics but also selected multilayer liners—anything less and the product can discolor or lose flow characteristic, particularly during extended sea journeys. Warehouse teams watch for seasonal swings, rotating stock, and maintaining tight FIFO protocols, since old product, even if technically “within spec,” begins to lose its crisp, free-flowing property.
End users have shared stories of opening shipments after long transit and finding the material unchanged, thanks to reinforced drum seals and humidity sensors. These stories reinforce our belief: quality doesn’t end with HPLC numbers, but with the product’s condition at your site. Problems caught upstream—such as post-reaction washing solutions, filter press timing, even anti-static bag additions in especially dry conditions—all make the small but repeated difference.
Handling 2-Phenoxyaniline involves a real-world appreciation for its chemical hazards. On a lab bench, a chemist thinks in terms of gloves and good ventilation. On our plant scale, the story grows: closed transfer pipelines, local exhausts, and well-drilled handling teams. Even tiny spills can carry lasting odors, which means tight discipline and regular air monitoring, not just heroic engineering controls.
The toxicology profile doesn’t leave room for shortcuts. Everyone—from process operator to warehouse loader—must follow personal protective steps developed from years of incident logs, not just safety manual checklists. Over time, we’ve made practical improvements: double loading valves, integrated emergency shower monitoring, and process worksheets colored for “high alert” operations days. These aren’t marketing measures—they stem from on-the-floor lessons and direct experience with what happens when even a single batch deviates from plan.
We’ve faced more scrutiny each year over discharge, solvent recovery, and byproduct minimization. The phenol and aniline origin of this compound forces every producer to re-examine not only end-of-pipe emissions but upstream supply chain practices and the fate of spent process water. We’ve invested in fractionation for spent solvents, higher-efficiency scrubbers, and downstream biological treatment. Success is measurable: environmental unit reports in the plant have shown steady drops in key organics for four years running.
What isn’t always obvious from outside is the impact of better process discipline—not just environmental numbers, but reduced flare shutdowns, less operator exposure, and markedly lower scrap rates. We practice internal audits, not because auditors demand them, but because every unaccounted kilogram affects our long-standing relationships with both users and the wider community. Byproduct management, for us, means more than regulated treatment thresholds—it shapes production choices, warehousing layouts, and the technical criteria we relay to customers looking for sustainable-sourced product.
2-Phenoxyaniline’s usage profile ebbs and flows with industry. The churn in dye chemistry pushes the limits of what one can expect in colorfastness, pollutant trace, and customer rules. On the pharma side, regulatory shocks (such as EU changes in precursor approval) can surge demand unpredictably—and sometimes, customers need answers overnight. We’ve geared up to keep inventory strategies flexible, aiming to buffer spikes without holding wasteful excess. Oddly enough, these supply dynamics feed directly into our process improvement cycle. Anticipating a demand rush led us to rethink raw material sourcing, improving upstream supply guarantees with detailed drying protocols and second-supplier agreements.
We’ve learned from experience that offering technical support—sharing not just product batches but insight into how the compound performs in real-world systems—rewards patience with long-term partners. Sometimes, end-users report not just on obvious purchase metrics, but on days saved in lab validation, or successful scale-ups that count just as much as price per pallet. This body of knowledge can’t be faked and doesn’t arrive from simply brokering bulk stock. Our technical team sits with production and logistics, reviews lab-scale syntheses with actual users, and collects stories of what worked and what proved tricky.
Every plant run offers a fresh test. Minor tweaks in the protocol—reaction rate, filtration time, heating cycle—may deliver small, hard-won improvements to yield or to finished product quality, yet these details become cumulative over hundreds of cycles. We record them, share with the team, and sometimes, they end up rewriting the “standard” process—especially as market and regulatory pressure grows. Open feedback with users, a pragmatic tolerance for process surprises, and disciplined record-keeping give an edge that’s more robust than any untested innovation.
Looking back, every success with 2-Phenoxyaniline comes down to the synthesis journey. Consistent outcomes rely less on theoretical optimums and more on real-world tuning—knowing the synergy between batch controls, worker experience, and field feedback. The compound’s journey from reactor to user includes every fingerprint of the plant’s daily rhythm, every course correction, and each shared lesson between plant and customer.
If the last few years have made anything clear, it’s that dependable chemical supply starts with groundwork at the factory. There’s no shortcut to knowing each raw material source, backup plan, and shipping route. We navigate customs changes, trade delays, and rising scrutiny over hazardous shipments with the same thoroughness we bring to synthesis. Supply isn't a numbers game—it's a function of daily diligence. Drums arriving dented or with broken seals get flagged, not shipped onward. Inventories match up week to week, and nothing leaves without an experienced eye checking off against the booking schedule.
Shipping stability matters: lined container trucks for winter months, monitored rail tanks for bulk movement. As it turns out, those technical problems—humidity control, vibration resistance, degradation risk—become the core of quality when that shipment crosses continents.
Over all these years, our approach with 2-Phenoxyaniline has centered on more than producing or selling a molecule. From the earliest stage of process development to routine large-scale campaigns, every stage connects us to the real work shaping specialty chemicals in today’s industries. The best advances grow from conversations with customers working through their own synthesis or formulation challenges. We listen, adapt, and occasionally return with a tweak or an idea that began years earlier in another sector.
In chemical manufacturing, every compound has its quirks. 2-Phenoxyaniline reinforces the lesson that experience—real, accumulated, and shared—matters most. Quality persists because teams care, habits run deep, and every improvement survived the scrutiny of application, not just analysis. This makes the compound more than a raw material. It becomes a record of problem-solving, cooperation, and iterative improvement carried forward.
Selecting a supplier for a compound like 2-Phenoxyaniline is about more than a spec sheet and price. From our vantage point, reliability is built directly into the production and delivery routine. Years of refining every step, tracking every shipment, and welcoming feedback from the field give substance to our offering. The details shape not just the finished product but its role in every customer's workflow.
Wherever innovation, consistency, and direct technical knowledge make a difference, our teams strive to provide the foundation needed for confident, successful application. The lesson is clear on our factory floor: real quality comes from hard-earned expertise and a willingness to keep learning, improving, and helping partners do the same.