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2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate

    • Product Name 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate
    • Alias 2-FITMPI
    • Einecs 630-611-6
    • 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

    568448

    Product Name 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate
    Cas Number 139888-86-7
    Molecular Formula C8H3F4NO
    Molecular Weight 205.11
    Appearance Colorless to pale yellow liquid
    Boiling Point 80-84°C at 20 mmHg
    Density 1.38 g/cm3
    Refractive Index n20/D 1.484
    Solubility Reacts with water
    Smiles C1=CC(=C(C=C1N=C=O)F)C(F)(F)F
    Storage Temperature 2-8°C
    Purity Typically >97%
    Synonyms 2-Fluoro-5-trifluoromethylphenyl isocyanate

    As an accredited 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, sealed with PTFE-lined cap, labeled with chemical name, hazard symbols, manufacturer, and batch number.
    Shipping 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate is shipped in tightly sealed containers, under a dry, inert atmosphere to prevent moisture exposure. It is packed in accordance with hazardous material regulations (UN 2206: Isocyanates, Toxic), and includes appropriate hazard labeling, documentation, and use of secondary containment to ensure safety during transit.
    Storage 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate should be stored in a tightly sealed container, under a dry, inert atmosphere such as nitrogen or argon. Keep it in a cool, well-ventilated area, away from moisture, heat, and incompatible substances (e.g., amines, alcohols, acids, and bases). Proper storage minimizes decomposition and prevents hazardous reactions or exposure to toxic vapors.
    Application of 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate

    Applications of 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate in Industrial Manufacturing

    2-Fluoro-5-(trifluoromethyl)phenyl isocyanate serves as a precision intermediate in multiple high-value segments of the chemical industry. As an original manufacturer, we supply this compound directly to companies engaged in crop protection, advanced material synthesis, pharmaceutical intermediates, specialty coatings, and other demanding sectors. Below, we outline several concrete downstream use cases based on real industrial practices, detailing compliance, practical use ratios, integration stages, and representative final products.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical producers utilize this isocyanate for building advanced urea, carbamate, or heterocyclic insecticides and herbicides. Its electron-withdrawing functional groups improve target molecule stability and bioactivity in crop protection agents. Production teams introduce it at the active core assembly stage, reacting it with particular amines or polyols according to target molecule specifications. Compliance regulations, toxicological thresholds, and process control remain stringent to ensure final safety and efficacy in field applications.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Quality
    • REACH Registration (EU Regulation No 1907/2006)
    • US EPA Pesticide Registration Requirements (FIFRA)
    • ISO 9001:2015 Certified Quality Systems for Fine Chemicals

    Typical usage ratio

    • 0.8–1.1 equivalents relative to amine functional groups in target molecules
    • Adjustment depends on impurity profile and batch scale; excess limited to under 10% to minimize waste

    Downstream process integration

    • Introduced in condensation or coupling steps after structural scaffold formation
    • Requires temperature control (20–40°C) and low-moisture conditions
    • Post-reaction, intermediates are immediately purified by crystallization or column chromatography
    • QC testing for residual isocyanate below 200 ppm before formulation

    Final product types

    • Selective herbicides (e.g., phenylurea derivatives)
    • Systemic insecticides
    • Novel fungicidal actives
    • Pre-mix pesticide formulations

    2. API Intermediate for Targeted Pharmaceuticals

    Key pharmaceutical manufacturers source this compound for synthesis of advanced intermediates in active pharmaceutical ingredient pipelines, particularly fluorinated aromatic urea and carbamate-based APIs. It enters the process at the intermediate stage reacting with appropriately substituted aniline or aliphatic amine derivatives. Precise stoichiometry, cGMP controls, and analytical verification ensure regulatory compliance and product quality for global markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP <823>, <795> and EP Monographs as applicable for intermediate materials
    • FDA 21 CFR Part 211 and Part 314 (US)
    • Chinese Pharmacopoeia and GB Standards for Registered Drugs

    Typical usage ratio

    • 1.00–1.05 molar equivalents relative to nucleophile
    • In multi-step APIs, excess kept below 5% to minimize side products and control batch cost

    Downstream process integration

    • Charged to reactor vessels during amide bond formation
    • Strict in-process controls on temperature (10–25°C) and reaction time
    • Immediately proceeds to hydrolysis, neutralization or extraction steps depending on API route
    • Final API purification includes HPLC and NMR confirmation of structural integrity

    Final product types

    • Fluorinated anti-inflammatory drug precursors
    • CNS-acting small molecule intermediates
    • Enzyme inhibitor scaffolds
    • Targeted kinase inhibitor routes

    3. High-Performance Polyurethane Material Synthesis

    Advanced materials manufacturers employ this isocyanate for specialty polyurethane synthesis, imparting chemical resistance, hydrophobicity, and stable dielectric properties. This compound is dosed in prepolymer or polymer formation steps, typically reacting with selected diols or polyols. Quality assurance protocols focus on batch homogeneity, free monomer content, and polymer chain structure to satisfy demanding electrical, automotive, and fluid-handling applications.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty materials
    • ASTM D257 for electrical insulation materials
    • RoHS 2011/65/EU for restricted substances in material components
    • REACH Annex XVII for aromatic isocyanates

    Typical usage ratio

    • 0.9–1.2 NCO/OH ratio as calculated by titration, adjusted for polyol equivalent weight and targeted crosslink density
    • Correction during pilot to ensure physical property targets (tensile, elongation, glass transition temperature)

    Downstream process integration

    • Dosed to reactor with diol/polyol under inert atmosphere
    • Simultaneous or sequential addition based on mixing performance
    • Post-reaction degassing, followed by casting, extrusion, or foaming operations
    • End-use QC includes hardness, electrical, and chemical stability testing

    Final product types

    • Polyurethane prepolymers for electronics encapsulation
    • Chemical-resistant coatings and linings
    • High-purity elastomer components
    • Coating dispersions for automotive underbody applications

    4. Specialty Reactive Dyes and Colorants Manufacturing

    The compound acts as a coupling isocyanate in advanced aromatic dye synthesis, creating chromophores with enhanced colorfastness and solvent resistance. Dye manufacturers prepare intermediates using diazotization or amidation pathways, with this isocyanate tailored for high-yield reactions. Final dye batches undergo strict color strength, purity, and residue checks for export to textile and polymer coloration markets.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substances in textiles
    • ZDHC MRSL for dye manufacturing inputs
    • REACH Substance Restriction for azo and isocyanate-based dyes
    • ISO 787/1 for general methods of testing pigments and extenders

    Typical usage ratio

    • 0.95–1.05 equivalents to main dye-forming amine or hydroxyl groups
    • Very tight ratio control (within 3%) to maximize color development and minimize hydrolysis byproducts

    Downstream process integration

    • Charged after completion of diazo coupling or amine protection; typically under chilled conditions (5–15°C)
    • Colorant intermediates isolated via filtration and solvent swap prior to final dye coupling
    • Batch isocyanate monitoring ensures below 100 ppm unreacted for product safety
    • Final QC protocols include lightfastness and pH stability checks

    Final product types

    • Aromatic reactive dyes for cotton and nylon finishing
    • Solvent-based colorants for plastics
    • Disperse dyes for polyester fiber
    • Specialty pigment intermediates for inks and coatings

    5. Performance Additives in Fluoropolymer Modifier Production

    Manufacturers in the high-performance plastics sector adopt this isocyanate for the synthesis of tailored fluorinated modifiers and crosslinkers. It anchors reactive functional groups onto perfluorinated or partially fluorinated backbones, enhancing compatibility with host polymers. Integration usually occurs in functionalization or terminal modification steps, with special attention to solvent selection and temperature management to preserve fluorine content.

    Industry compliance standards

    • ASTM D543 for chemical resistance of plastics
    • UL 94 flammability tests (as applicable for downstream articles)
    • ISO 14001 for environmental management in production
    • REACH SVHC screening for persistent organic content

    Typical usage ratio

    • 0.7–1.3 equivalents relative to fluoropolymer chain ends, based on targeted end-group density
    • Adjusted according to viscosity and reactivity of host polymer system

    Downstream process integration

    • Reactive dosing in melt-kneading or solution-blending stage
    • When used as chain extender, pre-mixed with other reactive additives under dry N2
    • Intermediate purification by solvent extraction or membrane filtration to remove side products
    • Comprehensive FTIR and elemental analysis before pelletization or film casting

    Final product types

    • Fluorinated additive masterbatches
    • Performance modifiers for PVDF or PTFE blends
    • Chemical-resistant membranes
    • Fluoropolymer-based sealants
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    Certification & Compliance
    More Introduction

    Introducing 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate: A Direct Perspective from the Manufacturer

    Purposeful Innovation in Aromatic Isocyanates

    As a chemical manufacturer with direct experience in developing and scaling aromatic isocyanates, our team knows every batch’s importance—chemical consistency translates directly to outcomes in downstream applications like pharmaceutical development and advanced material engineering. Among dozens of isocyanates that we manufacture, 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate stands out in both structure and practical results. This compound—often referred to in-house by our synthesis team as a “workhorse isocyanate” for functionalization—serves a niche of researchers and specialty developers seeking improved reactivity and unique substitution patterns.

    Model and Specifications—The Details Matter

    Our 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate leaves the reactors under the identifier CAS 76338-11-3. What sets its model apart isn’t the paperwork but the effort spent refining the process to yield a clear, pale liquid with predictable purity margins. Customers typically see colorless to light yellow appearance—often determined by storage and aging, never by incomplete reactions. Purity checks usually surpass 98% by GC; trace impurities—chloride, acid residues, phenolic byproducts—are minimized because side reactions in isocyanate chemistry compound rapidly. Every kilogram reflects not just overhead work but targeted improvements, like running extra drying and fractional distillation steps when a downstream client develops a new catalyst system sensitive to even minor contaminants.

    The boiling point edges just under 120°C at reduced pressure, and our engineers confirm that consistent handling protocols are critical—not just for product integrity, but to avoid hazards sometimes overlooked by less-experienced handlers. Typical packing uses amber glass or specialty HDPE with inert gas purging because isocyanates tend to form insoluble ureas with tiny moisture traces. Uncontrolled humidity leads to loss of product and, worse, inconsistent downstream performance. That’s why efforts from synthesis to packing revolve around real-world laboratory challenges.

    Why Choose This Structure? Substitution Patterns and Outcomes

    The decision to introduce both a fluorine atom at the ortho position and a trifluoromethyl group at the para offers clear advantages in reactivity and selectivity. Many users of aromatic isocyanates know the frustration of side reactions swelling as simple phenyl isocyanates interact with nucleophiles. This compound, built on our custom fluorination and Friedel-Crafts methodology, resists over-reactivity while maintaining a strong electron-withdrawing footprint. The result—regioselective transformation rates tend to stay high with nucleophilic aromatic substitution partners, especially in pharmaceutical intermediate steps.

    Comparing to classic phenyl isocyanate, or even less-substituted fluoro derivatives, the double force of fluorination and trifluoromethylation impacts both electron density and steric outcome. Our technical staff have seen these effects firsthand in pilot-stage cross-coupling reactions, yielding products with higher chemical yields, less tar, and lower demands for post-workup purification. For those working in medicinal chemistry or agrochemicals, these characteristics reduce bottlenecks in early-phase compound screening because the isocyanate group integrates reliably and without trace instability.

    Real-World Usage Cases and Insights from Our Clients

    Over decades of manufacturing experience, we build close connections with chemists—from major multinational R&D labs to smaller specialty outfits. Many share feedback on how and why they’ve leaned into this specific isocyanate. Typical applications fall into two broad areas: synthesis of urea and carbamate derivatives intended for biological testing, and as a building block in high-performance polymer development. The reactivity balance—boosted by the electron-poor aromatic ring and stabilized by our purity standards—often makes the difference in difficult transformations.

    In medicinal chemistry, small-molecule drug candidates using the 2-fluoro-5-(trifluoromethyl)phenyl motif show desirable metabolic stability and reduced liability from enzymatic oxidation, compared to rings lacking fluorination. This is not a theoretical benefit—it’s a tangible result seen in late-stage screening, as reported by client development teams. Isocyanate-based transformations with this compound allow fast access to structurally novel ureas, a key pharmacophore in kinase and protease inhibitors.

    From a polymer standpoint, the isocyanate moiety offers selective reaction with diamine and diol partners, yielding resins with precise control over cross-linking density and thermal properties. Customers developing specialty coatings take advantage of the unique ring structure, finding that the dual electron-withdrawing groups increase thermal resistance and chemical inertness in the final cured formulation. Our manufacturing notes log multiple cases where drop-in replacement of this isocyanate against standard phenyl-based variants raised glass transition temperatures and extended resistance to hydrolysis—truly valuable for demanding end-uses, such as electronics encapsulants or medical device coatings.

    Meeting and Overcoming Challenges—A Manufacturer’s Perspective

    The chemistry behind isocyanate manufacture remains unforgiving. Trace moisture during production or storage ruins whole reactor batches, and minor variations in feedstock quality show up months later as downstream complaint tickets. We’ve addressed these issues by pushing for process route innovation—switching to direct fluorination at tightly controlled temperatures, refining trace acid removal, and adopting continuous-flow setups for critical reaction steps. Our staff tracks each improvement not just in terms of yield or purity, but by how much earlier customers can use the delivered product without extra preparation.

    Safety requirements shape our production floor, as isocyanates pose serious respiratory sensitization risks. Automated now replaces manual transfer wherever possible, less from regulatory pressure and more for our own peace of mind. Encapsulation, regular gas monitoring, and multi-stage scrubbing help keep production steady and our team healthy. Every kilogram of 2-fluoro-5-(trifluoromethyl)phenyl isocyanate reflects not just chemistry but deliberate, people-centered refinement based on what we’ve learned the hard way.

    What Sets 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate Apart from Related Products?

    Over our years supplying to developers and academic partners, clear preferences emerge for certain isocyanate substitutions. The same trifluoromethyl and fluoro group combination found in this compound simply isn’t available in other commercial isocyanates. For chemists pursuing SAR studies or structure-activity optimizations, this specific pattern cannot be swapped for a para-only variant or a non-substituted ring without losing both electronic and steric advantages.

    Other isocyanates we manufacture—for instance, 4-fluorophenyl or 3-trifluoromethylphenyl isocyanate—find use where different reactivity or physical performance characteristics drive development. The ortho-fluoro, para-trifluoromethyl arrangement delivers a sharper drop in aromatic ring electron density and steers nucleophilic addition far more predictably. Our clients regularly report lower byproduct formation and a greater likelihood of successful late-stage derivatization, especially in challenging target molecules.

    We also notice differences in safety and storage. Some isocyanates polymerize or decompose under typical storage, but the molecular structure of this one provides enhanced resistance to unplanned reactions. It’s common for our larger customers to stockpile a few months’ supply with no measurable change in GC assay, provided they meet our storage recommendations. This stability pays dividends during scale-up and reduces headaches for buyers in remote locations with long shipping lead times.

    Manufacturing Stories—What Experience Has Taught Our Team

    Scaling up to multi-kilogram runs of such a specialized isocyanate means learning by sometimes hard experience. Over tightening one reactor seal, underestimating the effect of a trace catalyst impurity, or missing a subtle shift in distillation head temperature would each cost us a day’s cycle time—not to mention raw materials. Through repeated runs and direct conversations with some of the world’s closest-watchdog end users, we grew to anticipate problems before they reached the drum or bottle. Unexpected color changes or inconsistent NMR readings almost always tie back to a controllable detail at our end, and we invest in both staff education and laboratory capacity to head off avoidable errors.

    This industry doesn’t reward shortcuts. By handling these complications in-house—instead of offloading reprocessing to contract operators or simply repacking poor yields—we build a reputation on reliability. The sales team may talk about customer partnership, but in reality, the manufacturing floor hears about product fit and downstream performance issues before anyone else. This feedback closes the loop and lets us continuously improve both process and product week by week, without waiting years for process audits or regulatory cycles.

    Why We Think Our Approach Matters to Chemists

    As a direct manufacturer, we’ve come to understand that what matters most isn’t just the chemical sold, but the problem it reliably solves. Clients doing method development or considering a switch from competitor products count on our stated purity and actual reactivity to hold up under pressure. When a major client’s medicinal chemistry group moved from standard phenyl isocyanate to our fluorinated product, they cited not only higher assay confirmation but smoother reactions and a drop in troubleshooting calls. Consistency and honest quality control make these outcomes repeatable.

    We also see meaningful results in process-driven industries. Resin manufacturers on tight deadlines often run full production cycles on incoming drums after a quick check for residual moisture—they don’t have the time or resources to second-guess supplier claims. Our repeat shipments to these customers deliver both reliability and the specific technical profile that only this isocyanate provides. This practical benefit—the ability to trust product from a known source—remains the single greatest success marker for our team.

    Path Forward: Addressing Future Challenges

    Global chemical regulations keep shifting and supply chains grow more complex. Synthesizing and distributing high-spec specialty isocyanates ask us to stay nimble, anticipate supply disruptions, and preemptively invest in both raw material backstops and process improvements. Rising demand from Asia, North America, and the EU tests logistics and long-standing supplier relationships. We stay focused on core principles—documented traceability for every batch, layered safety investments for our own team, and responsiveness to unexpected changes in precursor or reagent markets.

    Continuous R&D efforts, spurred in part by challenging customer requests, lead to constant tweaks at the bench and in production. Pursuing lower-waste process technologies—like in-line drying or microreactor routes for hazardous threading steps—offers both environmental and economic payoff. The benefit radiates out to our users, as more robust manufacturing leads to tighter specifications and fewer batch-to-batch surprises.

    Progress Drives Results—Direct from Our Shop Floor

    The global market doesn’t wait, and neither do our end users. By putting direct knowledge, iterative process improvement, and consistent manufacturing execution into every batch of 2-Fluoro-5-(Trifluoromethyl)Phenyl Isocyanate, we deliver more than just a chemical. We share the value of experience that solves problems, speeds innovation, and supports the breakthroughs that keep our industry moving forward.

    From idea to pilot scale, from process troubleshooting to robust, scalable deliveries, this product owes its repeat success to the thousands of hours spent on granular details. If your next project needs the unique structural advantages and proven reliability of this molecule, you can count on a manufacturer that measures success—one batch, one customer report, one new solution at a time.