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2-Fluorothioanisole

    • Product Name 2-Fluorothioanisole
    • Alias 2-Fluorophenyl methyl sulfide
    • Einecs 214-042-1
    • 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

    151273

    Cas Number 456-55-3
    Molecular Formula C7H7FS
    Molecular Weight 142.19
    Iupac Name 1-fluoro-2-(methylsulfanyl)benzene
    Appearance Colorless to pale yellow liquid
    Boiling Point 75-77°C at 15 mmHg
    Density 1.18 g/cm3 at 25°C
    Melting Point -38°C
    Smiles CSC1=CC=CC=C1F
    Refractive Index 1.556
    Solubility Insoluble in water, soluble in organic solvents
    Synonyms o-Fluorothioanisole

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

    Packing & Storage
    Packing 2-Fluorothioanisole, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling.
    Shipping 2-Fluorothioanisole is shipped in tightly sealed containers, protected from light and moisture. It must be handled in accordance with relevant regulations for hazardous chemicals, including appropriate labeling and documentation. Transport may require secondary containment and temperature control, with the package clearly indicating flammability and toxicity hazards to ensure safe delivery.
    Storage 2-Fluorothioanisole should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area, separate from incompatible materials such as strong oxidizers. Proper chemical labeling and secondary containment are recommended to prevent spills. Limit access to trained personnel and ensure appropriate safety measures are in place.
    Application of 2-Fluorothioanisole

    Applications of 2-Fluorothioanisole in Industrial Manufacturing

    As a direct manufacturer of 2-Fluorothioanisole, we serve strictly defined industrial sectors where this intermediate delivers unique value in downstream synthesis and specialty chemical processing. Below, we outline verified commercial application scenarios, detailing regulatory compliance, specific formulation inputs, integration steps, and the types of finished goods produced by our customers.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Major pharmaceutical companies utilize 2-Fluorothioanisole as a key building block in the preparation of various thioether- and fluorinated-containing drug molecules, especially for targeted synthesis of heterocyclic APIs. It supports fluorination patterns critical in next-generation small molecule therapeutics and is added early in multi-step synthetic protocols leading to compounds for oncology, CNS, and anti-infective therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP regulations for finished pharmaceuticals)
    • EU Guidelines for GMP for Medicinal Products (EudraLex Volume 4)
    • Relevant local Pharmacopoeias (USP, EP, JP) for process intermediates

    Typical usage ratio

    • 0.5% to 3% of total batch input, calibrated according to the required yield of thioether-substituted intermediates; adjusted based on scale-up validation and impurity control constraints.

    Downstream process integration

    • Introduced in the early or mid-point of chemical synthesis, typically during nucleophilic aromatic substitution, Grignard-type coupling, or as a precursor for sulfoxide or sulfone conversion under controlled oxidation conditions.

    Final product types

    • Active pharmaceutical ingredients (APIs) for anti-cancer therapies (e.g., small molecule kinase inhibitors)
    • Precursor for CNS and anti-infective agent synthesis
    • Intermediates for fluorinated heterocyclic compounds
    • Custom reference standards for pharmaceutical R&D

    2. Agrochemical Synthesis: Herbicide and Fungicide Production

    Leading crop protection companies select this thioanisole derivative as a functionalized intermediate for the synthesis of advanced phenoxy- and thioether-based herbicides, as well as certain systemic fungicides. Its use allows precise placement of fluorine atoms, which enhances environmental stability and bioactivity in final formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO Code of Conduct)
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for chemical manufacturing quality management
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, EU)

    Typical usage ratio

    • 1% to 5% of reaction batch input, with exact proportion depending on required fluorine incorporation for target compound; adjusted in structure–activity optimization during pilot and commercial scale-up.

    Downstream process integration

    • Typically added at the functionalization stage, entering Mannich, Suzuki, or selective oxidation reactions leading to the active ingredient core structure; may be subjected to subsequent chlorination or methylation steps post coupling.

    Final product types

    • Broad-spectrum phenoxy herbicides
    • Systemic fungicides for cereals and vegetables
    • Pesticidal intermediates with fluorinated or thioether components
    • Pre-formulated actives for agrochemical toll manufacturing

    3. Fine Chemical Building Block for Electronic Materials

    Producers of high-performance electronic chemicals introduce this compound as a strategic aryl-thioether precursor during synthesis of specialty monomers and advanced functionalized polymers. Integration of the fluorinated aryl moiety confers enhanced dielectric properties and thermal stability, supporting microelectronic and display technology material requirements.

    Industry compliance standards

    • IEC 61249-2-21 for electronic base materials
    • RoHS Directive (2011/65/EU) for hazardous substance control
    • ISO 14001:2015 for environmental management in electronics manufacturing
    • REACH (EC No 1907/2006) for fine chemical precursors

    Typical usage ratio

    • 0.8% to 2% based on the monomerization feedstock mass, tailored for targeted functional group density within the polymer backbone.

    Downstream process integration

    • Fed into specialty monomer synthesis through selective C–S or C–F bond formation, followed by polymerization or co-polymerization, sometimes via sulfoxide crosslinking or further organofluorine modifications depending on required polymer functionality.

    Final product types

    • Dielectric polyarylene-based films for semiconductor packaging
    • Photoresist materials for integrated circuit fabrication
    • Functionalized aromatic polymers used in flexible displays and OLED devices
    • Specialty monomers for niche electronic applications

    4. Advanced Scent Compound Synthesis in Fragrance Industry

    Several leading aroma chemical producers employ the thioanisole derivative as a niche precursor during the synthesis of sulfur- and fluorine-enriched odorant molecules, aiming to create highly stable, high-impact note components for fine and luxury perfumery. The unique electronic profile imparts distinctive top and middle note enhancements for specialty fragrance formulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Code of Practice
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • ISO 9001:2015 for fragrance chemical manufacturing
    • REACH registration for aromatic chemical components

    Typical usage ratio

    • 0.2% to 1% as a specialty intermediate, with tuning based on intended olfactory intensity and performance of the finished compound within the fragrance blend.

    Downstream process integration

    • Integrated into sulfur-containing odorant synthesis pathways, typically via etherification or oxidation followed by advanced esterification or aldehyde functionalization, finalized via purification for trace impurity removal before fragrance compounding.

    Final product types

    • Concentrated aroma chemicals for fine fragrance creation
    • Signature scent bases for premium personal care products
    • Odorant intermediates for household and fabric care fragrance systems
    • Trace components in niche, custom-designed fragrances
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    Certification & Compliance
    More Introduction

    2-Fluorothioanisole: Experience from the Plant Floor

    Introduction to a Trusted Product

    Work in the chemical manufacturing business teaches the difference between hype and results. 2-Fluorothioanisole (also known as 1-fluoro-2-methylthio-benzene, CAS 456-47-3) never attracted front-page headlines, but its reliability speaks for itself through years of production runs and bulk customer feedback.

    Every batch starts with benzene ring chemistry. Over the years, the formula has stayed the same: a single fluorine atom at the ortho position, a methylthio group at the para. This sounds simple on paper, but purity and integrity tell the real story. Through direct synthesis and in-house distillation, we keep unwanted byproducts from sticking around, sharpening selectivity and improving yield. Laboratory work can make a flask of clean product; plant work makes thousands of kilograms with identical specs, time after time. This is the difference end users notice.

    For those who handle daily inventory, the product’s faint aromatic odor and oily clarity are subtle but unmistakable. Storage can create headaches with some organosulfur chemicals, but 2-fluorothioanisole’s shelf stability shows its value. Drum after drum, month in and month out, it keeps color and composition without surprise oxidations or polymerizations. In our own yards, drums that have sat for more than a year still meet original analysis.

    Why 2-Fluorothioanisole Matters in Industry

    For practitioners, this chemical most often serves a specific industrial purpose: it’s a building block for pharmaceutical intermediates, custom syntheses, and high-performance agricultural chemicals. Synthetic chemists prefer 2-fluorothioanisole where other anisoles stumble. The electron-withdrawing fluorine fine-tunes the aromatic ring’s reactivity, shifting nucleophilic substitution and increasing compatibility with specialty catalysts. Processes that use this molecule tend to feature in patent-protected routes, where every molecular tweak pays dividends.

    In our plants, production and QC teams hear from customers who work under regulatory and production pressure. With tighter EPA and REACH constraints, the margin for error tightens. A consistent product lets them keep their own process streamlined. We’ve watched R&D groups move from regular thioanisole derivatives to the fluorinated version, driven by a need for specific polarity, metabolic resistance, or improved downstream stability. Unlike generic methylthioanisole, the fluorinated derivative resists aerobic degradation and shows cleaner performance in catalyst-driven carbon-fluorine coupling steps, which can make all the difference at scale.

    Technical Characteristics That Stand Out

    Throughout hundreds of runs, several technical traits come up in internal meetings:

    Reliability Across the Supply Chain

    Sourcing specialty chemicals comes with risk. Delays in shipment, quality fluctuations, or shipment in suspect containers can ruin a production schedule. Our team was asked during a recent audit how we address these points. Every drum leaving the factory gets tested individually for basic specs: GC purity exceeds 99.0%, water well below 0.2%, low non-volatile residue, capped with tamper-evident seals and full tracking back to the original batch.

    Once shipped, we track complaint rates and return records. Over the past three years, deliveries of 2-fluorothioanisole ran at a return rate below 0.4% across all global shipments—a figure that speaks to plant-level diligence. Most rejections—rare as they are—resulted from transit damage, not product itself.

    Users in the pharmaceutical and agrochemical sectors know the cost of off-spec batches. For customers operating multi-step syntheses, even minor impurities set off chain reactions with major financial consequences. That’s why trust builds not through big claims but through steady, long-term performance: every drum full, every analysis matched, no substitution, no dilution, no last-minute “adjustments.”

    Practical Safety Lessons from Years of Experience

    Safety doesn’t sell like a product feature, but it matters most in daily work. Early in my career, I saw the aftermath of poor handling practices—even with “routine” chemicals. Sulfur-containing aromatics require tight controls. Though 2-fluorothioanisole’s volatility remains moderate compared to lighter benzenes, inhalation and skin contact protection never become optional. Local exhaust and personal protective equipment are routine, not special measures. On one occasion, a leaking drum in the truck dock reminded the entire crew to double-check seals and lift handling. That episode led to our policy of always double-validating shipment closures and instructing third-party logistics providers face to face, not just through emails.

    Waste disposal, too, takes planning. Chlorinated solvents and mineral acids handle most process residues, but neutralization and careful segregation keep our waste streams manageable. Local regulations now require batch-specific tracking for organosulfur waste; our system now prints barcoded waste manifests long before drums leave the yard. Such logistics issues don’t show up on sales brochures, but long-term operators know their significance.

    Comparison with Other Aromatic Thioanisole Derivatives

    Customers often ask about the true difference between 2-fluorothioanisole and thioanisole or other mono-substituted aromatic thioethers. The answer depends on your route and reactivity targets.

    Fluorination, especially at the ortho position, introduces a subtle change in electron distribution within the ring. In palladium-catalyzed cross-couplings, this allows the molecule to resist overactivation and improves selectivity in carbon-heteroatom bond formation. Thioanisole alone works for general methylthio functionalization; but for late-stage pharmaceutical intermediates, extra stability against oxidation and a tailored ring activation profile give the fluorinated version an edge. This means less tarring, crisper GC traces, and smaller rejection lots—not theory, but the outcome of years of lab and plant data review.

    Physical handling between the two is comparable; both have manageable vapor pressures, pour easily from steel drums, and show little reactivity towards common rubbers and valve seals. But the difference starts to show at the reaction kettle. Yield improvements and lower byproduct rates lead to savings over several campaign runs—a fact not always visible during initial cost comparison. We share these observations with users running 10,000-liter syntheses, not just folks at the gram scale.

    Compared to the para-fluorinated or meta-fluorinated variants, the ortho isomer hits a distinctive note. Our team often reviews literature and customer UPLC data showing that para and meta substitutions do not block electrophilic attack at the same sites, leaving potential for unwanted side products. Ortho-fluorination makes a difference in regioselective outcomes. Batch data from pilots in North America and Asia show improved conversion efficiency when 2-fluorothioanisole substitutes its isomeric relatives.

    Usage Stories from the Field

    Hearing from users in the field offers perspective unavailable from spec sheets. Pharmaceutical groups in Europe send regular feedback after receiving drums for their development projects. In one case, a research division saw a boost in final step yields by switching from para- to ortho-fluorinated thioanisole. Fewer isomeric byproducts emerged during purification, shaving days from downstream processing.

    On the agrochemical side, a Brazilian customer reported that the stability profile of 2-fluorothioanisole allowed cleaner formulation blending, which proved critical during summer storage in humid conditions. Their technical team highlighted that other methylthio derivatives grew off-colors in a matter of weeks, affecting spray solution clarity and market acceptance. Consistency in appearance and odor won them over.

    We often draw insights from domestic pilot plants that run continuous flow setups rather than batch reactors. In a recent flow synthesis installation, the low viscosity and predictable thermal behavior of 2-fluorothioanisole simplified pumping regimes and reduced downtime. These details rarely get reported beyond the plant floor, but they shape purchasing and operational decisions more than most realize.

    Regulatory Considerations

    Chemical compliance now ranks alongside quality and cost in importance. REACH, TSCA, and other regional chemical inventories put pressure on supply chains. All our batches, whether shipped to the EU, US, or domestic markets, follow a single set of internal documentation. Our compliance officers reference updated registration dossiers and quarterly audits to catch changes in export or storage restrictions.

    Routine analysis of residual solvents and heavy metals ensures conformance, even as regulations move the goalposts. We keep a record of customer audits showing our plant’s track record: zero serious nonconformance findings over six consecutive years of EU and North American customer audits. It’s also the reason we train every new production chemist in legal and documentary procedures, not just reaction execution.

    Applications in Next-Generation Synthesis

    In mainstream organic synthesis, 2-fluorothioanisole builds value as either a starting material or protected intermediate for routes leading into fluorinated benzene derivatives. Recent advances in C-F bond-forming reactions and organosulfur cross-couplings have moved this molecule up the priority list for both academic and industrial routes. Several innovator and generic pharma customers confirm that it integrates smoothly in Suzuki and Buchwald-type couplings with rare catalyst fouling events.

    Specialty polymer developers find a fit for the unique balance of nucleophilicity and oxidative patience. In one reported case, a R&D group developing electronics-grade conjugated polymers leveraged 2-fluorothioanisole’s specific substitution pattern to control bandgap width and improve temperature stability—a reminder that aromatic chemistry still surprises even after decades at the bench.

    Challenges That Come With Growth

    No chemical surpasses its market’s needs without obstacles. As emerging regions ramp up synthesis of advanced intermediates, supply chain capacity and regional logistics become sticking points. A surge of interest in 2-fluorothioanisole over the past two years brought growing pains: increased raw material volatility, competition in shipping lanes, and new compliance documentation requirements. Solutions developed out of necessity included diversifying logistics partners, investing in new corrosion-resistant drum hardware, and installing a secondary purification column to maintain continuity even with upstream hiccups.

    Energy prices also feed into cost structure. Our site’s management made the decision last year to retrofit distillation columns for higher energy recovery, limiting overhead without affecting purity. The results improved both carbon footprint and bottom line—a measure that gained approval in ESG audits and customer environmental reviews.

    Looking Ahead: What Improved Production Means for You

    Demands for cleaner, more specialized ingredients get louder with every year. Our journey with 2-fluorothioanisole shows that success comes from improvement, not just keeping up. Incremental gains in purity, safer handling methods, and better documentation transform the daily experience for users all the way through to final product packaging.

    We listen closely to feedback from formulators, QC labs, and process engineers on what works—and what doesn’t. A decade of experience confirms that direct relationships between producer and customer, without middlemen diluting the conversation, lead to faster troubleshooting and innovation. We continue to adapt our production lines, sample policies, and data sharing practices based on what end users actually face in their process rooms.

    Conclusion: Confidence Born from Practice

    2-Fluorothioanisole doesn’t succeed because of hype, but because it delivers on what matters: reliable specs, proven stability, practical suitability for advanced chemical syntheses, and steady support along the way. No single batch defines a manufacturer’s reputation; it’s the sum of all the work behind each drum, the day-in and day-out attention, and the open conversations with users who depend on product integrity to build their own results. For those looking to partner in long-term aromatic chemistry, our experience with 2-fluorothioanisole offers a foundation built on lived reality, careful improvement, and honest delivery.