Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Fluorothiophenol

    • Product Name 2-Fluorothiophenol
    • Alias 2-Fluorobenzenethiol
    • Einecs 211-892-1
    • 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

    757854

    Chemical Name 2-Fluorothiophenol
    Cas Number 1973-53-5
    Molecular Formula C6H5FS
    Molecular Weight 128.17 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 179-181 °C
    Melting Point -8 °C
    Density 1.22 g/cm3
    Refractive Index 1.600
    Flash Point 70 °C
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms o-Fluorothiophenol; 2-Fluorobenzenethiol

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

    Packing & Storage
    Packing Sealed amber glass bottle with screw cap, labeled "2-Fluorothiophenol, 10 grams," featuring hazard warnings and chemical information.
    Shipping 2-Fluorothiophenol is shipped in tightly sealed, chemically resistant containers under refrigerated conditions to prevent degradation and reduce vapor emissions. It is classified as a hazardous material (flammable and toxic), requiring appropriate labeling and documentation according to international transport regulations. Handle and store away from sources of ignition and incompatible chemicals.
    Storage 2-Fluorothiophenol should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, well-ventilated area away from heat, moisture, and incompatible materials such as strong oxidizers. Store in a chemical fume hood and clearly label the container. Avoid exposure to light and sources of ignition.
    Application of 2-Fluorothiophenol

    Applications of 2-Fluorothiophenol in Industrial Manufacturing

    2-Fluorothiophenol serves as a critical intermediate in several advanced manufacturing sectors, delivering specific reactivity and molecular features necessary for high-value specialty chemical production. Below outlines key application areas based on real downstream industries, with process and compliance details guided by customer specification and regulatory requirements.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical producers use 2-fluorothiophenol as a nucleophilic building block in the synthesis of thioether- or thioester-containing active pharmaceutical ingredients (APIs). The material provides a direct route for introducing both fluorine and sulfur atoms into aromatic cores, required for bioactivity in certain antimicrobial, anti-inflammatory, and CNS-active pharmaceuticals. Manufacturers carry out thioetherification or aromatic substitution reactions under controlled atmosphere and precise stoichiometry, meeting cGMP standards for traceability and impurity control.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • FDA 21 CFR 210/211 (for API sites in the US)

    Typical usage ratio

    • 0.9–1.2 molar equivalent relative to aryl halide substrate, adjusted based on target molecule substitution pattern and impurity profile requirements.

    Downstream process integration

    • Charged during early-stage arylation, usually after solvent charging and inerting; combined with catalysts such as Pd(OAc)2 or Ni(II) complexes in multi-step batch or flow synthesis units.

    Final product types

    • API intermediates for antimicrobial drugs
    • Small molecule kinase inhibitors
    • CNS-drug precursors
    • Gram-scale reference standards

    2. Agrochemical Intermediate Production

    Leading crop protection formulators rely on 2-fluorothiophenol for manufacturing selective herbicides, fungicides, and insecticides that require a fluorothiophenyl moiety. The compound integrates into thioether or benzothiazole frameworks, enhancing rainfastness and resistance to photodegradation. Operators incorporate 2-fluorothiophenol in multi-step syntheses, coupling it with chlorinated or nitrated aromatics in controlled reactors, maintaining compliance with agrochemical regulations concerning raw material sourcing and permitted impurity levels.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC No 1907/2006) registration for chemical intermediates
    • China GB 2763 pesticide residue standard (for export-oriented agchem)

    Typical usage ratio

    • 8–15% by mass of overall synthetic input in multi-step herbicidal or fungicidal active production, adjusted to endpoint HPLC specifications

    Downstream process integration

    • Added to reactor after initial aromatic backbone is assembled; reacts in nucleophilic substitution or cyclization steps, followed by in-line filtration and purification prior to downstream formulation blending.

    Final product types

    • Precursor to benzothiazole-based pesticides
    • Intermediates for sulfur-containing herbicides
    • Building blocks for systemic fungicides
    • Sulfur-fluorine hybrid insecticidal actives

    3. Advanced Dye & Pigment Synthesis

    Manufacturers in the specialty dye sector use 2-fluorothiophenol to impart unique photophysical properties and chemical resistance to colorants applied in plastics, fibers, and high-performance coatings. The aromatic thiol reacts with diazo or electrophilic partners to form sulfur-bridged dye structures, leading to improved fastness and resistance to oxidative degradation. The compound supports high-purity pigment manufacture under close quality system control, limited by standards for residual organosulfur.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice
    • DIN EN 71-3: Toy safety—migration of certain elements (for pigment use in toys)
    • ISO 9001 for pigment and dye batch traceability
    • Oeko-Tex® Standard 100 (for synthetic textile dyes)

    Typical usage ratio

    • 2–7 mol% relative to base pigment aromatic ring, tailored by ultraviolet absorbance and shade requirements after small-scale pilot batches

    Downstream process integration

    • Fed directly into dye coupling reactors; undergoes sulfidation or bridge-forming reactions, followed by precipitation and pigment finishing.

    Final product types

    • Light-resistant textile dyes
    • Plastic mass-pigmentation agents
    • Performance automotive coatings pigments
    • High-durability printing inks

    4. Specialty Polymer Modification

    Producers of engineered polymers apply 2-fluorothiophenol as a functional chain transfer agent in the synthesis of sulfur- and fluorine-containing polymers, or as a reactive end-capper for custom polyarylenes. Incorporation improves polymer dielectric properties and enhances chemical resistance for application in electronics and membrane technologies. Material addition must meet polymer-grade purity benchmarks and follow quality protocols to prevent cross-contamination during extrusion or solution polymerization.

    Industry compliance standards

    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • ISO 14001 Environmental Management for chemical processing
    • ISO 10993-5 Biocompatibility (for medical-grade polymers)
    • RoHS Directive (2011/65/EU) for electronics polymers

    Typical usage ratio

    • 0.05–1 wt% relative to monomer feed for chain transfer modification, adjusted in pilot based on target polymer molecular weight and end-group analysis

    Downstream process integration

    • Charged after initial monomer solvation, reacting during the exothermic polymerization phase; unreacted thiol removed with vacuum stripping prior to extrusion or pelletization.

    Final product types

    • Fluorinated engineering plastics
    • Conductive polymer compounds
    • Specialty polymer membranes
    • Polyarylene-based dielectric films

    5. Custom Organic Electronics Materials

    Organics-based electronics firms source 2-fluorothiophenol to synthesize thioether-bridged molecular semiconductors and organic light-emitting diode (OLED) precursors. The compound introduces both sulfur and fluorine into π-conjugated systems, allowing for precise tuning of charge mobility and thermal properties. Purity control and process documentation align with tight electronic material QC benchmarks, supporting scalable synthesis for device manufacturing.

    Industry compliance standards

    • IEC 61249-2-21: Halogen-free electronic materials
    • JEDEC JESD22-A108 (Temperature, Moisture, and Bias Life Test for semiconductors)
    • ISO 14644 for cleanroom synthesis of organic microelectronic materials
    • REACH (EC) 1907/2006 registration for high purity intermediates

    Typical usage ratio

    • 1–5 mol% versus base polycyclic substrate, frequently adjusted per photophysical property measurements during scale-up optimization

    Downstream process integration

    • Added after precursor oligomer formation in coupling steps; purification through chromatography and crystallization before device fabrication.

    Final product types

    • OLED emitter precursors
    • Molecular semiconductors
    • Organic field-effect transistor (OFET) materials
    • Light-harvesting dye-sensitizer intermediates
    Free Quote

    Competitive 2-Fluorothiophenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Fluorothiophenol: Performance and Practical Use in the Chemical Industry

    Direct Manufacturing Experience with 2-Fluorothiophenol

    Over the past decade, shifts in specialty chemicals have kept our factory on its toes, but few compounds have earned as much attention from our researchers and production engineers as 2-Fluorothiophenol. Chemists out in the lab value its straightforward reactive profile, and the plant team respects the compound’s manageable handling requirements. This aromatic thiol, distinguished by a fluorine atom bonded to the number two position on the ring, continues to carve out a practical place in modern synthesis. As direct manufacturers, we have studied its quirks, learned from customer feedback, and found its real strengths in a range of demanding applications.

    Model and Specifications Driven by Consistency

    Our main offering comes as 2-Fluorothiophenol with a purity exceeding 98%. This purity matters most for clients using it in fine chemical intermediates or pharmaceutical research, where trace impurities can disrupt multi-step syntheses. Experienced chemists often remark on the compound’s clean spectral footprint and dependable reactivity profile, especially when compared with isomeric or unsubstituted thiophenols. The physical form stays consistent batch after batch: a clear, colorless to pale yellow liquid, with a distinct, recognizable thiol odor.

    From synthesis all the way to dedicated storage, each kilogram is stabilized and sealed to minimize oxidation and contamination. Analytical records—NMR, GC, HPLC—stand behind every lot. We have worked side-by-side with end-user teams to verify that process equipment does not impart additional byproducts or degrade the thiol group, since reliability in purity remains non-negotiable for downstream applications.

    Understanding the Structure and Its Impact on Reactivity

    The unique signature of 2-Fluorothiophenol comes from the fluorine’s influence on the benzene ring and the thiol group’s high nucleophilicity. The ortho-fluorine intensifies electron withdrawal compared to unsubstituted thiophenol. Synthetic chemists familiar with electrophilic aromatic substitution point out that this impacts both the acidity and the reactivity of the thiol moiety. In our day-to-day runs, we measure this effect during alkylation and coupling reactions, especially when building custom intermediates for clients in pharmaceuticals and agrochemicals.

    If a customer has relied on 4-fluorothiophenol or standard thiophenol, transitioning to the ortho-substituted molecule can bring sharper reactivity or increased selectivity, but not without careful adjustment to protocols. We see this most often in conversations with researchers scaling up pilot batches for bioactive compound synthesis, where yield improvements finely hinge on subtle changes in the electron environment around the aromatic core.

    Reliable Usage Across Key Industries

    End-users in pharmaceuticals, crop protection, and dye manufacturing tap into 2-fluorothiophenol’s utility as a building block for more elaborate aromatic compounds. For fine chemical producers, it offers a faster route to sulfonamide and thioether derivatives. Our product tends to go into multi-step syntheses, often finding its final home as a protected sulfur handle or as part of fluorinated scaffolds with bioactive properties.

    Clients frequently approach us with projects focused on fluorinated benzothiazole formation, artificial sweetener development, or kinase inhibitor research. In these settings, the ortho-fluorine proves its worth by reducing byproduct formation or simplifying downstream purification. Many report that coupling and thiol-ene reactions proceed under milder conditions, saving both time and solvent costs.

    Quality Control and Batch Consistency

    Factory staff monitor every kilo throughout the entire production process, with tracking down to raw material source, temperature controls in key reactor stages, and closed-system transfers to shield the compound from oxidative air. Incoming feedback from advanced research teams often comes long after our sample batches have shipped. They confirm that having a trustworthy chain of custody and consistent assay results elevates the value of each drum.

    Occasionally, laboratories challenge us by needing smaller test lots or custom purity ranges. With full command over synthesis and bottling, we can adjust specifications without risking loss of product fidelity. The familiarity we have built with the compound’s volatility and sensitivity keeps our operations lean, reduces waste, and addresses unexpected demands in real time. This responsiveness stands as one of the hallmarks of true direct manufacturing, one that resellers cannot match.

    Difference from Unsubstituted and Other Fluorothiophenols

    Many chemists turn to simple thiophenol due to its cost efficiency and readily available supply. In cases where less selectivity suffices, plain thiophenol often maintains its dominance. Yet, the ortho-fluorine in 2-fluorothiophenol introduces a set of chemical behaviors unmatched by its para-substituted or non-fluorinated peers. Specifically, it tunes the chemical environment to offer advantages in regioselectivity and product yield during oxidative disulfide formation or coupling steps.

    For some, the default shift is toward 4-fluorothiophenol, believing positional substitution has little impact. In actual industrial syntheses, our feedback contradicts this. We see measurable differences in reactivity and byproduct profiles. The ortho variant reduces over-reduction in ring systems and increases the stability of intermediates bearing electron-deficient substituents. Plant managers working in colorant development have also shared that the ortho-fluorine keeps product color more stable, reducing the risk of discoloration after prolonged storage.

    We avoid overstating subtle improvements. Not every process benefits equally, and the switch from one positional isomer to another merits careful process review. Our long-term clients in pharmaceutical discovery, for example, only commit to using ortho-fluorine substitution when the synthetic challenges justify the extra cost and supply chain controls.

    Handling and Practical Safety Considerations

    Direct production brings hands-on experience with the material’s handling quirks. 2-Fluorothiophenol emits a strong, often unpleasant aroma in open air, so our transfer lines and storage tanks use inert gas blankets. This keeps both product quality and plant air safe. Even though the compound avoids some of the volatility pitfalls seen with smaller thiols, operators still prioritize full PPE and ventilated enclosures for filling and sampling operations.

    Unlike some reactive fluorinated aromatic compounds, 2-fluorothiophenol remains fairly predictable at room temperature. Its controlled oxidation profile lets us manage storage without relying on exotic cooling or specialty drums, but we recommend turning stock regularly and avoiding extended sunlight exposure.

    Waste minimization matters. Our process engineers designed in-line recovery and neutralization steps to handle wash fluids and off-spec product. This benefits both the environment and the economics of large campaigns. Our QC team logs every production run, ensuring traceability and rapid recall capabilities if contamination or out-of-tolerance impurities are ever spotted, supporting both our own standards and the end-user’s audit demands.

    Application Development: Real-World Examples

    One of the fastest growing uses for 2-fluorothiophenol involves the synthesis of fluorinated benzenesulfonamides. Several medicinal chemistry groups rely on our batches for clean conversion to sulfinate esters, where even trace-aged thiophenol can sabotage pharmaceutical safety profiles. Their feedback revealed that ortho-fluorination lets them push conversions to higher yield without needing drastic pH or radical initiator adjustments.

    Another strong application shows up in custom dye synthesis, especially for specialty textiles and fluorescent labels. Here, the ortho-fluorine helps achieve consistent hue and intensity under a range of temperatures. Our process engineers cycle samples through accelerated aging conditions before bulk shipping, making sure dye-makers don’t see pigment degradation on the customer’s end.

    For advanced materials start-ups developing new electron-transporting polymers, 2-fluorothiophenol lets them tailor building blocks for greater efficiency. Its solubility profile, unique versus other isomers, means fewer troublesome purification steps, particularly in solvent mixes used for OLED and organic photovoltaic development.

    Pain Points in Supply and Solutions That Work

    Historically, interruptions in the global supply chain for intermediates like 2-fluorothiophenol have threatened project timelines, especially for groups working on fast-turn drug discovery or pilot-scale specialty materials. Several years back, a key feedstock shortage forced us to engineer a more reliable sourcing agreement with local suppliers. Contingency contracts, buffer inventories, and on-site quality testing keep our customers insulated from most commodity price swings and delivery snags.

    There remains concern among buyers about the risk of adulteration or mislabeling, especially as downstream regulatory audits tighten. By managing synthesis and bottling directly, we step past one of the most common points of failure found with third-party resellers who split batches across different suppliers.

    Customers raise purity concerns, particularly as they move from gram-scale investigations to multi-kilogram campaigns. We’ve responded by offering comprehensive batch documentation, including impurity profiles and storage history, not just a COA. This transparency forms the backbone of trust for collaborative development and repeat purchasing decisions.

    Feedback Loops with End-Users: A Manufacturer’s Perspective

    Direct engagement with clients keeps our process improvement cycle running. Over the years, we have received insight from process chemists ramping up to pilot scale, as well as from academic groups and start-ups experimenting at the analytical scale. They share data on reaction efficiency, report where bottlenecks form, and describe what makes our version of 2-fluorothiophenol function well—or where hurdles remain.

    We turn these lessons into real actions: filter redesigns to cut post-filtration residue, customized drum linings to dodge unwanted catalytic activity, and live shipment tracking to prevent site-to-site blend-ups. The point is not perfection, but constant improvement rooted in day-to-day experience, never theory alone.

    Design input loops have also taught us to offer batch reservations for high-frequency research organizations, smoothing the transition from early R&D to multi-site manufacture. We catalog technical bulletins describing subtle differences seen across applications, but we place the greatest trust in what our routine production and QC logs show us each month.

    Environmental Responsibility: Putting Practice into Action

    Our stewardship goes beyond compliance papers or simple disposal permits. Directly producing 2-fluorothiophenol, we have adopted closed reactors, solvent recycling loops, and multi-stage air scrubbing. The odors intrinsic to thiol chemistry can provoke local concern, so we designed plant upgrades to keep emissions firmly below regulatory limits.

    Disposal guidelines for spent or off-spec 2-fluorothiophenol batches match real-world needs. Sulfurous by-product streams filtered out for controlled incineration, and spent process water receives oxidation to neutralize thiol traces before site release. These methods stem directly from lessons learned during pilot-plant commissioning and later scale-up, where the cost of accidental releases taught valuable lessons no textbook could replace.

    This commitment forms a large part of the reassurance we offer to buyers with strict product stewardship goals, particularly in regulated industries like pharmaceuticals or agrochemicals. Much of our improvement comes from formally logging environmental deviations and acting on findings, not letting them slip through the cracks.

    Addressing Challenges in Production and Shipping

    2-Fluorothiophenol does not tolerate long journeys without controlled conditions. From years of export, we know that extended transit during hot months raises risks for both stability and safety. We prioritize temperature-monitored storage and use tight-sealed, inert-lined containers. Each batch receives run-specific labeling, reducing the potential for mismatched goods and ensuring traceability for every shipment.

    Working with logistics partners who understand flexibility and proper documentation pays dividends. Flat-footed shippers and third-party warehouses outside the industry often mishandle specialty chemical goods. Every container travels with detailed shipping instructions, and we require real-time shipment status from partners on export routes. Importers have told us that having a truly transparent document trail—backed by in-house certificates and shipment tracking—cuts their inland customs headaches in half.

    For local buyers, we can arrange split shipments or custom-repackaging services. In these cases, drums ship out directly from production warehouses, never exposed to unnecessary handling stages.

    Supporting Research Teams with Technical Guidance

    Our technical staff takes pride in supporting researchers at all levels—from early exploratory work up to late-stage scale-up. Guidance focuses on practical advice for making 2-fluorothiophenol fit into existing reaction steps with minimal surprises. Whether a group tackles nucleophilic aromatic substitution or explores late-stage functionalizations for small-molecule drugs, we offer firsthand knowledge on which bases, solvents, or working temperatures prove most compatible.

    Research groups repeatedly mention the benefit of being able to consult directly with our synthesis and QC experts, instead of navigating a faceless distributor. This guidance saves both money and weeks of troubleshooting. Many discover subtle tips, such as how to store open containers for short periods or stabilize reaction mixtures during scale-up, often making the difference between a successful pilot and a stalled project.

    We archive technical suggestions and feedback so they inform improvements for future users. This loop keeps packaging and handling protocols real-world ready and aligns our operation not with abstract service models, but tangible experience in the laboratory and production hall alike.

    Conclusion: Manufacturer Commitment to Quality and Partnership

    Operating as the direct manufacturer of 2-fluorothiophenol, we focus on experience, not just the molecular formula or a purity number on a label. Every decision, from sourcing to shipping, flows from an understanding rooted in hands-on work and open dialogue with customers. Success comes down to reliable delivery, quick responses to unique project needs, strict attention to safety and the environment, and the readiness to solve challenges as they emerge—not in theory, but in daily practice.

    This substance has evolved into a trusted material for hundreds of research and industrial users not because of a brand or a bullet list of features, but from a foundation of consistent quality, real technical support, and proactive troubleshooting. We hold ourselves accountable for every lot, not just what leaves the gate, but in how it works in the customer’s hands a continent away. That’s how commitment earns its meaning and why 2-fluorothiophenol remains a mainstay product among contemporary aromatic thiols.