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2-Fluorophenyl Isothiocyanate

    • Product Name 2-Fluorophenyl Isothiocyanate
    • Alias 2-FITC
    • Einecs 228-961-7
    • 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

    112441

    Chemicalname 2-Fluorophenyl Isothiocyanate
    Casnumber 61272-77-3
    Molecularformula C7H4FNS
    Molecularweight 153.18
    Appearance Colorless to pale yellow liquid
    Boilingpoint 77-80°C at 2 mmHg
    Density 1.22 g/cm³
    Flashpoint 87°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., chloroform, ethanol)
    Synonyms 1-Isothiocyanato-2-fluorobenzene
    Refractiveindex 1.608-1.610

    As an accredited 2-Fluorophenyl Isothiocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams, sealed cap, labeled with chemical name, formula, CAS number, hazard symbols, and safety information.
    Shipping 2-Fluorophenyl Isothiocyanate is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a hazardous chemical and must comply with local and international transport regulations. Appropriate labeling, documentation, and handling precautions ensure safe transit and delivery to laboratories or industrial facilities.
    Storage 2-Fluorophenyl Isothiocyanate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store under inert atmosphere if possible to prevent decomposition. Label the container clearly and handle with appropriate personal protective equipment.
    Application of 2-Fluorophenyl Isothiocyanate

    Applications of 2-Fluorophenyl Isothiocyanate in Industrial Manufacturing

    2-Fluorophenyl isothiocyanate serves as a specialized intermediate in multiple sectors. Our direct manufacturing processes ensure consistent quality and reliable supply for downstream producers in regulated fields. Below, we detail specific application areas, integration into industrial workflows, and associated compliance standards.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Integrators in pharmaceutical manufacturing use 2-fluorophenyl isothiocyanate as a building block in certain non-biological APIs, especially in heterocyclic and urea-derivative drugs. It enters nucleophilic substitution and cyclization reactions, providing functionalization crucial for pharmacologically active molecules. Its reactivity supports the preparation of kinase inhibitors, antineoplastic agents, and anti-inflammatory compounds. Manufacturing quality, traceability, and impurity controls strictly follow pharmaceutical guidelines from sourcing through final purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) standards for intermediates (where applicable)
    • European Medicines Agency (EMA) API registration requirements
    • Current Good Manufacturing Practice (cGMP) Part 211

    Typical usage ratio

    • Added at 0.8–1.6 molar equivalents relative to the amine nucleophile, depending on downstream synthesis stoichiometry
    • Adjusted based on expected conversion and impurity profile in multi-step synthesis

    Downstream process integration

    • Introduced during nucleophilic aromatic substitution or urea formation steps
    • Utilized in closed reactors under inert atmosphere with inline monitoring
    • Direct feeding into batch or continuous reactors for process scale-up

    Final product types

    • Intermediate compounds for kinase inhibitors
    • Urea-linked anticancer drug intermediates
    • Sulfonamide-based anti-inflammatory agents
    • Custom heterocyclic small molecules

    2. Agrochemical Synthesis for Custom Pesticides and Herbicides

    Agrochemical manufacturers employ 2-fluorophenyl isothiocyanate for custom synthesis of selective herbicide intermediates and crop protection actives. The compound acts as a coupling reagent or thiourea precursor, functionalizing aromatic rings that impart specificity and environmental persistence. Processing typically requires high-shear mixing and gradual addition to minimize heat evolution and promote high-purity yields. All operations comply with international chemical safety and agricultural substance controls.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 certified manufacturing
    • Regulation (EC) No 1107/2009 (EU plant protection products)

    Typical usage ratio

    • Dosage of 1.2–1.3 molar equivalents per acylation substrate in herbicide intermediate formation
    • Ratio determined by desired product selectivity and purification scheme

    Downstream process integration

    • Added to reaction mass during initial condensation stage
    • Employed under controlled pH and temperature to enhance coupling efficiency
    • Post-reaction workup includes solid-liquid extraction and phase separation

    Final product types

    • Pre-emergence herbicide intermediates
    • Custom thiourea-based pesticide scaffolds
    • Aromatic sulfonylurea herbicide pre-products
    • Specialty crop protection compound bases

    3. Polyurethane and Polymer Additive Production

    Producers of specialty polyurethane elastomers and engineering plastics use 2-fluorophenyl isothiocyanate as a synthesizer for isothiocyanate-terminated additives. These additives enhance polymer chain reactivity or impart low-flammability characteristics. The chemical may enter pre-polymerization stages, typically reacting with polyols or chain extenders to tailor molecular weight and branching. Strict controls prevent residual isothiocyanate content in final products, aligning with technical and regulatory standards for industrial plastics.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) Regulation (EC) No 1907/2006
    • ISO 9001 Quality Management for polymer manufacturing
    • RoHS Directive (Restriction of Hazardous Substances) for electronics polymers
    • ASTM D3574 (polyurethane foam test methods)

    Typical usage ratio

    • Incorporated at 1–2% by weight into pre-polymer mix depending on targeted modification
    • Adjusted for molecular weight of base polymer and reactivity profile

    Downstream process integration

    • Reacted with primary alcohol or amine groups during pre-polymer preparation
    • Inline metering and gradual addition to reactor for uniform dispersion
    • Monitored using FTIR and viscosity profiling before final polymerization

    Final product types

    • Flame-retardant polyurethane foams for transportation or insulation
    • Isothiocyanate-functionalized engineering plastics
    • Solid elastomers for industrial rollers and pads
    • Reactive polymer cross-linkers

    4. Specialty Dye and Pigment Manufacturing

    Colorant and dye manufacturers utilize 2-fluorophenyl isothiocyanate as an amine derivatization agent during synthesis of custom azo and sulfur dyes. The compound introduces fluorinated phenyl groups to enhance colorfastness and solvent resistance. Processing requires accurate temperature control and reaction time optimization to avoid over-derivatization or side-product formation. Strict compliance with industrial dye standards facilitates downstream use in textiles, coatings, and high-performance inks.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile chemical safety
    • EN 71-3 (Safety of toys – migration of certain elements) for pigments
    • REACH Annex XVII restrictions on aromatic amines
    • ISO 787/1 (General methods of test for pigments and extenders)

    Typical usage ratio

    • Used at 0.9–1.2 molar equivalents per amine group in dye coupling reactions
    • Adjusted for desired chromophore intensity and application medium compatibility

    Downstream process integration

    • Charged to synthesis vessel post-diazotization
    • Blended under controlled agitation with chromogenic base
    • Purification by crystallization or chromatographic separation

    Final product types

    • Light-stable azo dyes for synthetic fibers
    • Fluorinated pigment dispersions for high-end coatings
    • Sulfur dyes for technical textiles
    • Solvent-resistant ink components
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    Certification & Compliance
    More Introduction

    2-Fluorophenyl Isothiocyanate: Insights from Direct Production Experience

    Understanding the Value of 2-Fluorophenyl Isothiocyanate

    Producing 2-Fluorophenyl Isothiocyanate every day, we see firsthand how this compound supports researchers and downstream manufacturers in the pharmaceutical and agricultural sectors. With the steady demand for isothiocyanate derivatives, this fine chemical offers a unique position due to its precise reactivity and versatility in synthesis. Our facilities work directly from raw fluorinated benzene sources, keeping full oversight on purity and controlling byproducts in a way that helps downstream results stay predictable and consistent.

    The molecular structure of 2-Fluorophenyl Isothiocyanate features a fluorine substitution at the ortho position on the phenyl ring, giving a specific combination of electron-withdrawing properties along with an active isothiocyanate function. Researchers appreciate this balance, as it impacts reactivity differently compared to unsubstituted phenyl isothiocyanate or other ring-substituted versions. From our testing and feedback from advanced synthesis labs, this profile makes the compound a solid building block for manufacturing pharmaceuticals, agrochemicals, and specialty intermediates—particularly in cases where selectivity and regio-specific transformations define project success.

    Traditionally, isothiocyanates like the parent phenyl variant serve as cornerstones in urea and carbamate synthesis. Introducing a fluorine atom at the two-position shifts the electron density of the ring in a distinct way; this plays out in the selectivity during nucleophilic addition reactions. In hands-on terms, clients often point out improved control in bioconjugation experiments and peptide functionalization when using 2-Fluorophenyl Isothiocyanate compared to mono- or para-fluoro variants. This difference doesn’t just come from the structure on paper—it translates to cleaner conversions and higher yield, both in multikilo batch processes and specialized lab runs.

    Specifications Guided by End-Use Feedback

    Every lot that leaves our site undergoes chromatography profiling, moisture quantification, and residual solvent assessments, using techniques we have honed over years of production. Final purity routinely measures above 98%, confirmed by HPLC and NMR analyses. The most frequent specification requests involve control over trace halogenated impurities and residual solvents. We specifically monitor and keep limits on residual dichloromethane and toluene, since their presence can counteract sensitive catalytic steps in further manufacturing. From what chemists report, having confidence in this level of purity allows for more streamlined process validation and fewer troubleshooting cycles during scale-up.

    Physical characteristics like melting range and appearance rarely surprise us; the compound typically appears as a pale yellow oily liquid at room temperature. It stays stable under cool, dry storage, but shows sensitivity to moisture and light with extended exposure. Packaging reflects this: we rely on amber glass containers, sparged with nitrogen, for every shipment above 500 grams, based on oxidation episodes observed in earlier years. Rapid turnovers and lean inventory mean our material spends minimal time in warehouse transit, which helps maintain stability until it reaches its destination. By processing customer returns and shelf samples ourselves, we track how handling and packaging tweaks pay off in actual shelf life and usability.

    Application in Laboratory and Industrial Processes

    Most purchases of 2-Fluorophenyl Isothiocyanate pass through to medicinal chemistry offices and pilot-scale manufacturers chasing new molecule scaffolds. In combinatorial chemistry, it acts as a reliable electrophilic partner, especially for amine and thiol functionalizations. Newer kinase inhibitor leads and certain pesticides trace their origins to these coupling steps. The introduction of a fluorine atom at ortho-position makes a consistent difference in the pharmacokinetic profiles of candidate molecules; medicinal chemists tell us about downstream boosts in bioavailability and metabolic resilience, which tie directly to this substitution pattern.

    In peptide synthesis, this compound helps in isothiocyanate-amine coupling, forming thiourea bridges used in probe labeling or as enzyme inhibitors. The ortho-fluorine gives a slight twist in the coupling kinetics and the steric outline, which can reduce off-target side reactions in labeled proteins. Unlike plain phenyl isothiocyanate, which sometimes yields broader product distributions, this fluorinated derivative supports higher selectivity, aligning with detailed analytical feedback from users. Projects in chemical biology, where the fine details of reactivity matter most, have contributed to evolving our internal handling protocols—avoiding metal contamination, minimizing hydrolysis, and ensuring rapid transfer from storage to use.

    On the agrochemical side, companies leverage this material for synthesizing fungicide and insecticide candidates that demand robust aromatic stability. The fluorine’s role in lowering metabolic breakdown rates in field conditions adds value during product development. Economies of scale matter less here, compared to the reliability of obtaining reproducible yields during pilot production. We’ve had direct conversations with R&D teams who track small differences in impurity profiles, underscoring the importance of traceability right back to our initial batch logs.

    Operational Experience: Lessons Learned in Synthesis and Quality

    Running the actual chemical reaction to make 2-Fluorophenyl Isothiocyanate draws on phosgenation chemistry as a critical step. Every shift in raw material quality—minor solvent impurities, small shifts in acid chloride content—makes itself known in isothiocyanate output. Our plant crews monitor color and IR signatures during workup, not just waiting for final analytical numbers. Most byproduct formation, particularly urea derivatives and phenylthiocarbamates, stems from wet feedlines or fluctuating pH during quench operations. Our shift leads tune metering pumps and gas feed rates to keep the reaction tight, using our own process data—not academic literature—to set real operating limits.

    Disposal and handling of spent gas streams create practical challenges; we invested early in abatement systems before regulations forced our hand, due to firsthand knowledge of the risks from airborne isothiocyanate exposures. Workers directly handling this product understand the need for sealed lines and monitored venting, based on lessons learned from smaller leaks and minor occupational exposures in years past. This hands-on vigilance ensures we meet environmental targets and, most importantly, keep our team safe.

    Controlling reaction temperature shapes overall yield and impurity load. Over the years, we’ve experimented with both batch and continuous protocols; feedback from our quality team shows tighter distributions and less side-product formation using pulse-fed reactors. Process analytical technology, including online FTIR monitoring, gives us early warnings for out-of-spec runs. By acting on these signals right away, not waiting for standard lab confirmation, we avoid sending questionable material into downstream processing. The result shows up in consistently passing audit samples drawn at random—meaning fewer headaches for technical managers, both at our end and in customer plants.

    Comparing 2-Fluorophenyl Isothiocyanate with Other Isothiocyanates

    Chemically, not all isothiocyanates behave alike. Our own production slate includes unsubstituted phenyl, para-fluoro, and various alkyl-substituted types. 2-Fluorophenyl Isothiocyanate sits in a middle ground: more reactive than most para-substituted variants, less volatile than many aliphatic alternatives. In direct testing with nucleophiles—amines, alcohols, or thiols—we chart reaction rates and isolate product yields, stacking up the ortho-fluoro compound against others. The consistent finding: the ortho-substitution provides a helpful compromise between speed and selectivity. This pattern holds true whether you’re measuring chromatographic retention or clean conversion of target functionalities in larger synthesis campaigns.

    Purely physical differences—such as melting or boiling point—rarely drive end-user preferences, but volatility and stability under ambient air make storage and handling workflows smoother. In our practice, the ortho-fluoro derivative resists hydrolysis and oxidation as long as the user follows typical precautions. Its handling profile closely matches the plain phenyl type, but it brings a noticeably different reactivity fingerprint that users can leverage in exploratory chemistry or patent-sensitive projects. Anyone who’s tried to swap in a more basic isothiocyanate mid-project—hoping to skirt limits on precursor supply—knows this isn’t a plug-and-play chemistry; those subtle shifts in electron withdrawal and steric bulk carry through to your product profile.

    From an economic standpoint, the synthesis route for 2-Fluorophenyl Isothiocyanate runs longer and draws on higher-cost fluorinated starting materials, which affect both price and batch sizing. We have learned how to stretch yields during workup, recovering solvents and reducing byproducts, but producing at scale always means balancing cost per kilo against purity and delivery lead time. Global events—shifts in fluorinated benzene pricing or regulatory updates—feed directly into our production planning and inventory strategy, based on weekly operational reviews. This kind of coordination only becomes possible because we oversee our own lines and keep the entire value chain from raw material intake to final shipment under one roof.

    End-User Support Informed by Real-World Use

    Beyond the numbers, we engage directly with application chemists and operational buyers, troubleshooting project hiccups and sharing data from our own in-plant testing. Our technical support team includes operators with years of experience, not just sales reps or call center staff. When a client runs into unexpected chromophore peaks during QC or sees unusual tint in a large batch, our process chemists review the actual campaign records and sample history instead of relying on generic guidance.

    Patterns in customer issues teach us where process controls tighten up final outcomes. If a repeat buyer flags deviations in appearance or minor IR shifts, we compare campaign logs and run investigation batches to verify root causes. Some of our process improvements have come straight from conversations with academic collaborators or scale-up partners who run longer validation runs and manage more real-world process variability than a simple trial batch can show. In these partnerships, information flows in both directions: we implement upstream changes to filter particle fines or reduce headspace gas, and in turn, clients see easier downstream purifications or increased reproducibility.

    Contributing to Safer and More Predictable Chemistry

    Producing isothiocyanates at industrial scale brings a set of responsibilities that go well beyond shipping barrels. In thicker detail, 2-Fluorophenyl Isothiocyanate’s value comes from what it makes possible in the hands of scientists and manufacturers—faster lead optimization in drug discovery, tighter control in bioconjugation, longer shelf stability in specialty intermediates. Users rely on traceability back to each batch record, and our own operators rely on hard-won knowledge in handling, abatement, and process troubleshooting.

    We have watched the regulatory and technical standards around isothiocyanates sharpen year by year. Technical managers look for predictable documentation—COAs that map to real, observable data points—but also for evidence of learning and improvement over repeated campaigns. Our role includes compiling customer feedback cycles, integrating real incident data, and supporting rapid investigation or batch pulls if required. Customers report fewer surprises when details like impurity carryover, hydrolysis sensitivity, or packaging shifts surface quickly and are acted upon with transparency. Keeping a tight loop between plant floor, QC lab, and client site cuts down on costly delays or rework further down the line.

    Challenges and Our Solutions on the Shop Floor

    Solvent management forms a practical challenge in the synthesis flow. Over time, collecting and recycling solvent fractions not only improves environmental compliance, but saves cost per batch. Small investments in distillation column maintenance pay off through increased recovery rates and tighter solvent purity ranges, which directly benefit product quality. Waste stream tracking and onsite abatement—filtration, carbon scrubbing, and careful pH neutralization—stem from firsthand experience with the nuisance and risk that uncontrolled emissions can produce. By using data collected from years of changeover and maintenance cycles, we have developed a rhythm of preventive checks that keeps our emission levels well below both local and international guidelines.

    Process safety stays high on our priority list. Exposing staff to isothiocyanate vapors or accidental splashes carries known risks. Training programs, built on reports from previous incidents, shape plant protocols—not just paperwork for auditors, but live drills and routine PPE checks. As requirements evolve, we adapt our procedures faster than formal regulation demands, out of respect for the chemical and for our teams who handle it. This commitment shows up in turnover data and in operator conversations: a plant run by seasoned staff brings fewer unplanned shutdowns and a better product experience for everyone down the supply chain.

    Moving Forward: Supporting Next-Generation Synthesis

    Reflecting on our ongoing work with 2-Fluorophenyl Isothiocyanate, our perspective has shifted from simply making and shipping a molecule, toward being stewards of technical and operational progress in specialty chemistry. We see our compound in flow chemistry platforms, late-stage functionalization campaigns, and novel biological labeling strategies. Each cycle of feedback shapes how we invest in analytical upgrades, process tweaks, and collaborative development.

    As market requirements evolve and new end-uses surface, customers expect us to lead with technical transparency and reliability. We consider reliability more than a tagline—a concrete outcome of real experience, detailed log keeping, and problem-solving on the floor. With every kilogram produced, tracked, and shipped, we reinforce our commitment to the chemists, scientists, and process engineers who convert this stand-alone intermediate into the next wave of applied chemicals and healthcare solutions.