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HS Code |
228954 |
| Chemical Name | 3-(Ethoxycarbonyl)Phenyl Isocyanate |
| Cas Number | 4461-78-9 |
| Molecular Formula | C10H9NO3 |
| Molecular Weight | 191.18 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 330 °C |
| Melting Point | -16 °C |
| Density | 1.18 g/cm3 |
| Refractive Index | 1.551 |
| Flash Point | 144 °C |
| Solubility | Insoluble in water; soluble in organic solvents |
| Synonyms | m-(Ethoxycarbonyl)phenyl isocyanate |
| Smiles | CCOC(=O)C1=CC(=CC=C1)N=C=O |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Purity | Typically ≥98% |
As an accredited 3-(Ethoxycarbonyl)Phenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle, tightly sealed, with hazard labels, product details, and safety information on the exterior. |
| Shipping | 3-(Ethoxycarbonyl)Phenyl Isocyanate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Packages must be clearly labeled as hazardous and compliant with relevant transport regulations (DOT, IATA, IMDG). Handle with care; use appropriate cushioning and leak-proof secondary containment to prevent spills during transit. Store upright and avoid extreme temperatures. |
| Storage | 3-(Ethoxycarbonyl)phenyl isocyanate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as amines, alcohols, acids, and bases. Protect from light and sources of ignition. Ensure proper labeling and access control to prevent unauthorized handling. Use appropriate personal protective equipment when handling. |
Applications of 3-(Ethoxycarbonyl)Phenyl Isocyanate in Industrial ManufacturingAs a direct manufacturer with global clientele, we supply 3-(Ethoxycarbonyl)Phenyl Isocyanate specifically for advanced chemical synthesis in targeted, quality-driven sectors. Our application focus below details the downstream manufacturing scenarios where our material proves essential, presenting key integration points and regulatory references for industry professionals. 1. Polyurethane Specialty Elastomer ProductionLeading elastomer manufacturers consistently specify this isocyanate as a core building block in precision-cast polyurethane systems, especially where molecular rigidity and tunable thermal properties are required. It enters prepolymer formulations designed to meet exacting physical performance in demanding industrial environments. Industry compliance standards
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2. Synthesis of Polyurethane Coatings for Electronics EncapsulationThis molecule is frequently introduced into two-component electronics-grade polyurethane potting formulations, valued for its ability to deliver chemical and moisture resistance while maintaining controlled flexibility for sensitive device encapsulation. Downstream users leverage the resulting polymers for high-purity coating applications in electronics assembly lines. Industry compliance standards
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3. Synthesis of Aromatic Polyurethane Adhesives for High-Performance LaminatesAdhesive manufacturers apply 3-(Ethoxycarbonyl)Phenyl Isocyanate as a functional crosslinker in aromatic polyurethane adhesives, particularly for the aerospace, automotive, and packaging sectors where bond strength and environmental durability set critical quality thresholds. It enhances specific adhesion to engineering plastics and composite substrates. Industry compliance standards
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4. Intermediate for Agrochemical Active Ingredient SynthesisMajor agrochemical synthesis plants rely on this isocyanate for targeted derivatization steps in small-molecule pesticide and herbicide active ingredient manufacture. Its unique ring-substituted structure enables selective urea and carbamate formation, contributing to product portfolios of global crop protection firms who demand consistent reactivity and narrow impurity footprints. Industry compliance standards
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5. Building Block for Custom Polyurethane Optical MaterialsProducers specializing in advanced optical polymers utilize this raw material for synthesizing highly defined polymers free from color bodies and inclusions. It contributes to index tuning and molecular uniformity critical to optics-grade polyurethane sheets and films used in laser, imaging, and lens fabrication. Industry compliance standards
Typical usage ratio
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Decades in the chemical industry teach practical details that don’t make it into textbooks. When working with compounds like 3-(Ethoxycarbonyl)Phenyl Isocyanate, firsthand experience separates lab theory from scale-up reality. Over years in our own facilities, we’ve seen this specific isocyanate grow from a specialty research material to a vital intermediate in several industrial and discovery-driven settings.
We routinely handle isocyanates with a range of functional modifications, and in daily production, small changes at the molecular level can significantly alter reactivity, safety, and end-use possibilities. The ethoxycarbonyl group, in particular, offers more than a minor tweak: it imparts a unique balance of reactivity and selectivity not present in more common phenyl isocyanates. This means more control for chemists seeking reliable coupling, amidation, or urea/urethane formation under milder conditions or with sensitive substrates.
Unlike basic phenyl isocyanate, the 3-position ethoxycarbonyl substituent acts as a built-in modulator. During our scale-up trials, we’ve measured how this structure shifts solubility profiles and makes separation steps less of a headache. It crystallizes more cleanly from many organic solvents, reducing the risk of persistent impurities. For formulators, these subtle distinctions translate into lower batch rejection rates and tighter downstream specifications.
Through continuous process improvement, our current production lot—labeled as Model EQCPI-3—maintains purity above 98% by HPLC, with residual solvents below 0.1%. This isn’t just a laboratory achievement—it reflects adjustments to our distillation cut points and handling protocols, designed to avoid contamination often seen in third-party resold material. Over time, trending data from repeated syntheses allowed us to fine-tune every step—charging order, reaction temperature, and even agitation speed—so that every drum and kilogram we ship matches our commitment to reliable sourcing.
Packing is deliberately non-standard: rather than one-size-fits-all drums, we offer both 25 kg UN-approved containers for bulk customers and smaller 1 kg glass options for research-scale users. We’ve learned the hard way that minimizing exposure during transfer preserves the freshness of even reactive isocyanates, especially for high-stakes pharmaceutical or agrochemical R&D.
This compound lands on our packing bench for one major reason: its ability to react with nucleophiles under conditions where unmodified phenyl isocyanates would either be too sluggish or too harsh. We see consistent demand from companies aiming to develop new heterocyclic compounds for medicinal chemistry. The ethoxycarbonyl group offers new vectors for further derivatization after the initial isocyanate step, allowing for sequential transformations that would stall out or give unwanted by-products using less functionalized analogs.
In agrochemical discovery, 3-(Ethoxycarbonyl)Phenyl Isocyanate offers an extra margin of flexibility in building libraries of urea or carbamate-based candidates. Several collaborators in crop-protection research have confirmed that the improved solubility and the diminished volatility of this molecule simplify both their synthesis and their downstream purification. When staff on our quality team visit client pilot plants, subtle shifts in product isolation methods often trace back to structural tweaks that began at the isocyanate-building stage.
Demand also comes from specialty polymer research groups. The presence of the ethoxycarbonyl group allows for post-polymerization functionalization, which opens the door for target-specific coatings and films—something less practical with simple phenyl isocyanate substrates.
Running a dedicated isocyanate plant means confronting challenges unfamiliar to those who only resell pre-packed bottles. Humidity control, for instance, matters far more for 3-(Ethoxycarbonyl)Phenyl Isocyanate due to subtle hydrolysis risks. We learned early that both the reaction environment and downstream warehousing need desiccant scrubs and positive-pressure rooms—a lesson written in avoidable product loss.
Safety deserves careful conversation. The isocyanate functional group, reactive and potentially hazardous, brings specific handling needs. Our plant trains staff thoroughly on spill protocols and PPE requirements. We modified our reactor charging sequence after an exotherm incident years ago—these real-world adjustments define responsible and efficient operation, not just labels and certificates.
Waste streams from this compound also require thoughtful treatment. We convert drizzle streams into less reactive carbamates before final disposal, an extra step that reduces environmental risk. In practice, closed-loop solvent recovery saves costs and reduces emissions, and years of practice have made these processes second nature in our facility routines.
We’ve always believed the best improvements start at the customer lab bench. Users in both academic and private labs report that our 3-(Ethoxycarbonyl)Phenyl Isocyanate’s batch-to-batch consistency streamlines their synthetic workups. Medicinal chemists have remarked on the clear melting range and absence of persistent side-products. Those details would sound minor to outsiders, but after scaling up kilo-lots for structure-activity-relationship studies, confidence in raw material specs saves real time and expense.
Every modified isocyanate brings quirks; we log customer results and feed those back into both process and purification tweaks. Where one synthetic route can tolerate slightly higher acidity, another wants a more basic environment. Interactions with both sides mean our QC staff learn by direct feedback, not abstract targets.
Chemists with hands-on synthesis series will appreciate the difference that a single ethoxycarbonyl group can bring. 3-(Ethoxycarbonyl)Phenyl Isocyanate stands apart from unsubstituted phenyl isocyanate not by marketing rhetoric, but by practical outcomes: improved handling, fewer off-odors, and less risk in open-lab settings. Trials in our own application lab showed lower rates of unwanted dimerization during storage—a real issue with less substituted analogs.
Price sometimes draws attention, but our manufacturing philosophy aims for value over cost-cutting. Certain high-volume phenyl isocyanates lure buyers by unit price, yet consistently show variable impurity profiles and stability issues when handled outside strictly controlled storage. Drawing on years of shipping and storage data, we see fewer returns and complaints with our ethoxycarbonyl-substituted variant, which hasn't just outperformed competitors on spec, but on tangible user satisfaction.
Fragmented sourcing introduces risks the spec sheet won’t reveal. Reports from new users sometimes highlight “smells off” or “recrystallized prematurely”—signs of micro-impurities or storage abuses common when the supply chain passes through multiple hands. Tight chain-of-custody monitoring directly in our facility lowers that exposure. Having our own QA team in charge from raw input to drum-filling allows early detection and correction of any deviation from target product characteristics.
We also incorporate regular stability testing, sampling materials placed under simulated shipping and customer storage. After several years of these runs, our internal data guide continuous improvements. One early summer, a temperature spike during transit identified a sterilizable flaw in our packaging sealant. That direct experience led to a packaging update, helping preserve product integrity across a wider climatic range. Third-party shippers, unfamiliar with fine isocyanate nuances, sometimes fail to flag or address these “minor” mismatches—yet users at the end of the chain bear the cost in material waste or failed synthesis runs.
Since our teams handle the entire lifecycle of 3-(Ethoxycarbonyl)Phenyl Isocyanate, we spot and address the small challenges that rarely make it to general product overviews. Hydrolysis stands out: we minimized moisture contamination by reengineering our filling lines and instituting batch-wise humidity monitoring as a standard protocol, not just a periodic compliance check.
Crystallization control caused interruptions until process optimization balanced cooling rates and agitation patterns. Slightly slowing the post-reaction temperature ramp—based on dozens of iterative test runs—resulted in more uniform crystal size, thicker filtration cake, and improved product isolation. We share these process notes with our regular customers, not because we want to boast, but because smoother downstream work helps everyone.
Disposal can perplex even experienced shops, especially those scaling up. We offer return-and-treat options for customers who don’t have in-house waste neutralization, closing the loop to reduce regulatory or workplace risks. Each year, a handful of buyers take advantage of this service, almost always after encountering stricter local waste rules—a reality we planned for in advance based on our own production audits.
The growth in fine-tuned drug discovery has pushed our 3-(Ethoxycarbonyl)Phenyl Isocyanate into new synthetic targets and biological screening libraries. Innovative startups request shorter lead times and even higher purity grades. A decade ago, this would have felt like overkill. Now, as high-throughput screening demands more predictable chemistry, our QC routines reflect that need, ramping up precision in every purification and documentation step. Having all these tools under one roof ensures rapid adaptation, unlike resellers bound to unpredictable third-party sources.
We see increased requests from green chemistry-driven projects. Work flows easier when the starting isocyanate reacts cleanly under milder conditions. The ethoxycarbonyl group allows for more controlled chemistry at room temperature or in less hazardous solvents, cutting down on energy needs and improving laboratory air quality over several thousand runs.
Years in the fine chemicals trade have shown that customers expect more than a one-off batch meeting a published spec. Repeat buyers value predictability, transparency, and the depth of experience of those doing the actual synthesis, not just logistics. We invest in regular team training, equipment updates, and frequent feedback loops with our clients—practices born out of constantly learning from the outcomes, both good and bad, as our experience grows.
If supply disruptions arise—tank cleaning, regulatory delays, or logistical hiccups—direct communication from our facility keeps users informed. We don’t outsource the hard conversations, and we keep extra inventory of critical precursors on-site. Some competitors, operating at arm’s length from production, can’t adjust as quickly or guarantee continuity for recurring orders.
Products like 3-(Ethoxycarbonyl)Phenyl Isocyanate generate valuable feedback that shapes our operation. Synthetic chemists raise application-driven clarifications. Production workers suggest equipment tweaks or packaging mods. These are logged, implemented, and measured for actual benefit. A dropped drum or a leak in a transfer line turns into a new SOP or an equipment upgrade—each improvement acts as one more confidence point for the next batch.
Routine audits of process safety and quality ensure no gap slips through unchecked. Each year, we pull random samples from storage and re-test for potency, moisture, and possible degradation. This practice, established after an internal recall many years ago, now anchors trust for repeat customers who bet their downstream results on our vigilance.
We keep a close eye on regulatory shifts and evolving market requirements. Increasingly, buyers expect digital access to real-time QC and COA data. Each batch now leaves with a traceable digital fingerprint, not just a paper certificate. Researchers pushing the limits of medicinal chemistry, materials science, or agricultural innovation don’t settle for average—they push us to refine process parameters, update documentation, and upgrade packaging.
Looking forward, we see 3-(Ethoxycarbonyl)Phenyl Isocyanate as a model case study: a specialty compound benefiting from the manufacturer’s hands-on responsibility and continuous improvement mindset. Real-world practice trumps theoretical compliance, every time, and decades of plant-floor lessons carry more weight to demanding chemists than glossy product brochures or generic datasheets.
Each bottle and drum of 3-(Ethoxycarbonyl)Phenyl Isocyanate ships out as the product of quiet but intensive work: not just chemical synthesis, but hands-on monitoring, process tweaking, user feedback, and a dedication to both safety and scientific progress. By not outsourcing or fragmenting our supply, we control for consistency, reliability, and practical responsiveness. The next time a process falters or a screen runs unexpectedly clean, experience traced back to the manufacturer’s bench will likely be the deciding factor.