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3-(Ethoxycarbonyl)Phenyl Isocyanate

    • Product Name 3-(Ethoxycarbonyl)Phenyl Isocyanate
    • Alias Ethanol 3-isocyanatobenzoate
    • Einecs 403-150-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 3-(Ethoxycarbonyl)Phenyl Isocyanate

    Applications of 3-(Ethoxycarbonyl)Phenyl Isocyanate in Industrial Manufacturing

    As 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 Production

    Leading 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

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC 1907/2006)
    • TSCA Inventory (for US market supply)
    • RoHS Directive 2011/65/EU (for applications in restricted electronics elastomers)

    Typical usage ratio

    • Ranges from 5% to 20% by weight in prepolymer formulation, adjusted for target hardness, elongation, and processing flow; exact proportion depends on desired Shore A/D rating and end-use flexibility parameters.

    Downstream process integration

    • Charged during isocyanate prepolymer synthesis, following polyol dewatering and before exothermic chain extension; batch, semi-continuous, or continuous blending lines implement metered dosing for reaction control.

    Final product types

    • Industrial scraper blades
    • High-abrasion conveyor rollers
    • Custom-molded vibration dampers
    • Wear-resistant sheets for mining or heavy equipment

    2. Synthesis of Polyurethane Coatings for Electronics Encapsulation

    This 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

    • UL 94 Flammability (V-0/V-1 for electronics)
    • IPC-CC-830 (Coating Qualification and Performance Specification for Printed Circuit Board Assemblies)
    • IEC 60695-11-10 (Fire hazard testing in electronics)
    • RoHS 3 (EU 2015/863)

    Typical usage ratio

    • In formulated encapsulation systems, typically 8% to 15% by weight relative to polyol content, with the precise figure modulated to achieve dielectric strength and thermal cycling tolerance as specified by OEM qualification protocols.

    Downstream process integration

    • Mixed immediately prior to casting during two-component potting operations; reaction with polyols initiates polymer network formation under degassed, low-moisture conditions to prevent bubble defects on encapsulation lines.

    Final product types

    • Printed circuit board (PCB) conformal coatings
    • Sensor encapsulation gels for automotive and medical electronics
    • LED driver encapsulation materials
    • Micro-controller module pottings

    3. Synthesis of Aromatic Polyurethane Adhesives for High-Performance Laminates

    Adhesive 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

    • EN 204/D4 (European standard for water resistance in wood adhesives)
    • ISO 4587 (Adhesive joint shear strength)
    • GMP EC 2023/2006 (for food-packaging adhesives where required)
    • ASTM D1002 (Lap shear testing for metal assemblies)

    Typical usage ratio

    • Formulators incorporate 3% to 12% by weight, according to substrate compatibility and required open time; the lower end applies to rigid laminates, while flexible packaging adhesives require tighter molecular control at higher ratios.

    Downstream process integration

    • Added in the isocyanate curing stage, after base polyol and plasticizer blending; introduced in solvent-based or 100% solids systems, typically with controlled mixing to regulate exotherm and maintain uniform molecular crosslinking.

    Final product types

    • Aerospace interior structural adhesives
    • Automotive lightweight composite panel bonding
    • Flexible multilayer film adhesives for food and medical pouches
    • Hardwood and engineered wood bonding systems

    4. Intermediate for Agrochemical Active Ingredient Synthesis

    Major 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

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 17025:2017 (Lab testing in intermediate and actives QC)
    • Good Manufacturing Practice (GMP) for Active Substances used as Starting Materials (EC No 1252/2014, EudraLex Volume 4)
    • US EPA Pesticide Registration Requirements

    Typical usage ratio

    • Generally applied at stoichiometric equivalents (1:1 molar ratio) in targeted urea/carbamate coupling reactions; actual charge may be varied ±5% depending on downstream yield and workup losses in continuous or batch operation.

    Downstream process integration

    • Introduced during the late-stage intermediate coupling step, typically following alkylation or halogenation; addition is closely monitored under inert atmosphere to control side-product formation during high-temperature, solution-phase synthesis.

    Final product types

    • Aromatic urea-based herbicides
    • Phenylcarbamate insecticides
    • Selective pre-emergence weed control actives
    • Intermediate compounds for further heterocycle synthesis in crop protection lines

    5. Building Block for Custom Polyurethane Optical Materials

    Producers 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

    • ISO 13485:2016 (Medical device optical components, for relevant lens applications)
    • ASTM D1003 (Haze and Light Transmission of Transparent Plastics)
    • REACH (regulatory compliance for supply into the EU optical market)
    • RoHS (Restriction of Hazardous Substances, for optical electronics applications)

    Typical usage ratio

    • Custom optical polymer formulations employ 6% to 14% by weight isocyanate charge, precisely titrated to achieve target refractive index and transmission clarity per customer application, with fine adjustments made during pilot line trials.

    Downstream process integration

    • Added as a primary isocyanate component post-filtration of base diol mixture; reacted in anhydrous, filtered glassware or cleanroom batch reactors, under color-controlled conditions to comply with optical industry consistency criteria.

    Final product types

    • Polyurethane films for imaging sensor windows
    • Light-guiding optical sheets
    • Laser-protective viewing panels
    • Custom-molded optical lenses for analytical instrumentation
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    Certification & Compliance
    More Introduction

    Introducing 3-(Ethoxycarbonyl)Phenyl Isocyanate: From Synthesis to Real-World Applications

    Direct from the Source: Our Expertise in Fine Chemical Manufacturing

    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.

    What Sets 3-(Ethoxycarbonyl)Phenyl Isocyanate Apart?

    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.

    Model and Specifications: Standards Shaped by Real-World Use

    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.

    Practical Applications: Experience in the Field

    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.

    From Bench to Bulk: Manufacturing Know-How

    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.

    Quality Built on Feedback

    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.

    Comparative Advantages over Other Phenyl Isocyanates

    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.

    Beyond the SDS: Real Handling Experience

    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.

    Solutions to Common Issues: Practical Strategies Unlocked by Experience

    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.

    Emerging Trends and Demands

    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.

    Long-Term Reliability in Partnership

    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.

    Continuous Improvement: Listening to Chemists and Operators Alike

    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.

    What the Next Generation Demands

    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.

    Conclusion: Rooted in Experience, Ready for Innovation

    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.