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2-Chloro-6-Fluorobenzylthiol

    • Product Name 2-Chloro-6-Fluorobenzylthiol
    • Alias 2-Chloro-6-fluorobenzenemethanethiol
    • Einecs 'EINECS 401-040-7'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    826160

    Productname 2-Chloro-6-Fluorobenzylthiol
    Casnumber 936940-31-5
    Molecularformula C7H6ClFS
    Molecularweight 176.64
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥97%
    Density Approximately 1.33 g/cm³ at 25°C
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 2-Chloro-6-fluorobenzyl mercaptan
    Smiles Clc1cccc(F)c1CSH
    Inchi InChI=1S/C7H6ClFS/c8-6-3-1-2-5(9)7(6)4-10/h1-3,10H,4H2
    Storagetemperature Store at 2-8°C

    As an accredited 2-Chloro-6-Fluorobenzylthiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, sealed with a screw cap, labeled with hazard warnings, chemical name, CAS number, and supplier details.
    Shipping 2-Chloro-6-Fluorobenzylthiol is shipped in tightly sealed containers to prevent leaks and exposure. It should be packaged according to regulations for hazardous materials, protected from moisture, heat, and incompatible substances. Shipping must comply with international and local chemical transport guidelines, ensuring clear labeling and appropriate documentation for safe handling and delivery.
    Storage 2-Chloro-6-Fluorobenzylthiol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from heat sources, acids, strong oxidizing agents, and incompatible substances. Store under inert gas (such as nitrogen) if possible, and ensure the storage area is equipped with appropriate spill control and ventilation.
    Application of 2-Chloro-6-Fluorobenzylthiol

    Applications of 2-Chloro-6-Fluorobenzylthiol in Industrial Manufacturing

    As a primary manufacturer of 2-Chloro-6-Fluorobenzylthiol, we deliver this specialty intermediate to key downstream producers. Our clients apply this material in advanced chemical synthesis across several specialized industries. We ensure precise compositions and compliance throughout the integration into established processes.

    1. Pharmaceutical Active Ingredient Synthesis

    Many pharmaceutical companies use this compound as a building block for synthesizing small molecular APIs, including targeted cancer therapies and rare disease treatments. It acts as a functionalized thiol for introducing thioether or sulfide moieties during advanced stage organofluorine molecule construction. The compound’s fluoro-chloro substitution supports pharmacokinetic tuning and metabolic stability in final actives.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for API Manufacturing
    • EU EudraLex Volume 4 GMP, Part II
    • US FDA 21 CFR Part 211
    • Chinese Pharmacopoeia monograph cross-reference (for intermediates)

    Typical usage ratio

    • Applied at 1.2–1.5 molar equivalents for substitution steps, depending on substrate reactivity and desired conversion
    • Final ratio adjusted according to reaction monitoring data and impurity profiles

    Downstream process integration

    • Input in late-stage condensation and nucleophilic aromatic substitution on activated heterocycles
    • Usually charged to reactor after solvent volume control and temperature ramping
    • Integrated with real-time in-process analytical methods (HPLC, MS) to minimize side-products

    Final product types

    • Tyrosine kinase inhibitors (custom pharmaceuticals)
    • Active metabolite analogs for rare disease study
    • Control substances for regulated research

    2. Crop Protection Intermediate Manufacturing

    Large agrochemical processing companies use this raw material for synthesizing sulfur-containing fluorinated intermediates in commercial herbicide and pesticide production. The unique benzylthiol motif enhances binding properties and improves environmental degradation profiles. This positions the material as a critical input during batch production of next-generation crop protection agents for regulated markets.

    Industry compliance standards

    • ISO 9001 Quality Management in Agrochemical Production
    • FAO/WHO specifications for technical active ingredients
    • REACH Annex VII–X (EU registration, where applicable)
    • China ICAMA pesticide intermediate registration rules

    Typical usage ratio

    • Utilized at 0.9–1.3 parts by weight relative to core aromatic halide reagents
    • Ratio adjusted based on target pesticide synthesis route and environment safety study feedback

    Downstream process integration

    • Feeds the sulfur introduction step before final oxidation or ring closure
    • Pre-mixed with base or reducing agent to control side-reactions
    • Material charged by closed-feed system under nitrogen atmosphere for operator safety

    Final product types

    • Selective herbicides for resistant weeds
    • Next-generation fungicides with improved environmental profiles
    • Pre-cursor materials for registered pesticide actives

    3. Advanced Electronic Material Precursor

    Specialty chemical manufacturers serving the electronics sector incorporate this compound for tailor-made fluorinated benzylthio derivatives. These downstream chemicals play crucial roles in the development of photolithographic photoresists, OLED intermediates, and certain specialty coatings for semiconductors. The robust aromatic sulfide linkage contributes to chemical resistance and electronic properties tuning.

    Industry compliance standards

    • IPC-4101C (Printed Circuit Board Base Materials)
    • RoHS Directive 2011/65/EU (Heavy metal and organohalogen control)
    • REACH SVHC List (Substance notification)
    • UL 94 flame rating compatibility for final polymers

    Typical usage ratio

    • Reacted at 0.6–1.0 parts per 100 parts base monomer, as determined by desired resin load
    • Adjusted following pilot-scale electrical property and stability testing outcomes

    Downstream process integration

    • Added post-polycondensation or grafting onto polymer backbones for resist materials
    • Integrated via automated metering unit with in-line viscosity control for coatings
    • Requires careful solvent selection to maintain purity during high-value synthesis

    Final product types

    • Photoresist precursor solutions for semiconductor processing
    • OLED material intermediates
    • Antistatic and dielectric specialty coatings

    4. Specialty Fine Chemical Synthesis

    Producers of high-value specialty chemicals utilize this material to introduce both halogen and thiol groups in complex, multi-stage syntheses. Such compounds find further use in custom ligand development, probe molecule design, and advanced laboratory reagents, primarily for organizations operating under ISO-accredited laboratory frameworks.

    Industry compliance standards

    • ISO 17025 Laboratory Quality Systems
    • Sigma-Aldrich Laboratory Reagent Specifications (reference for specialty grades)
    • GHS/CLP hazard labeling for chemical supply
    • JIS K 0050 (Japanese chemical reagent testing methods)

    Typical usage ratio

    • Included at 1.0–2.5 equivalents, highly dependent on target substitution degree and multi-step conversion yields
    • Ratio set by NMR or chromatography-based monitoring of real-time reaction progress

    Downstream process integration

    • Acts as key intermediate for nucleophilic substitution and cyclization reactions
    • Usually introduced after intermediate purification to avoid mixed-sulfur byproducts
    • Controlled addition via syringe pumps in small and pilot-batch runs

    Final product types

    • Specialty laboratory reagents for analytical chemistry
    • Custom ligands for metal ion chelation research
    • Probe molecules and standards for mass spectrometry applications
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Chloro-6-Fluorobenzylthiol: A Closer Look From the Manufacturer’s Side

    Everyday in specialty chemical manufacturing brings a new challenge, and 2-Chloro-6-Fluorobenzylthiol stands out as one of those molecules that keeps our team engaged and focused. Speaking as the people who spend our days in the plant and our nights reviewing process data, this compound isn’t just another line on a product list. Its utility and the craftsmanship involved in making it meet high standards set it apart from many others in our catalog.

    What Distinguishes This Compound From the Rest?

    2-Chloro-6-Fluorobenzylthiol falls into the category of halogenated aromatic thiols, and it occupies a unique space in the world of chemical synthesis. Many of our customers approach us looking for building blocks for their active pharmaceutical ingredients or advanced agrochemical intermediates. They ask for selectivity, purity, and a process that can be trusted batch after batch. We know that in this field, details matter. The presence of both chlorine and fluorine substituents on the aromatic ring allows for altered reactivity, leading to reaction profiles that aren’t possible with simpler benzylthiols or single-substituted derivatives.

    We see requests for 2-Chloro-6-Fluorobenzylthiol rising every season, and most inquiries come from teams developing new molecular scaffolds. That makes sense—adding chlorine and fluorine onto a benzylthiol framework delivers a specific balance of electronic effects. In pharmaceutical R&D or advanced polymers, tiny shifts in electron density often decide if a reaction shines or fizzles out. Many clients mention how this compound provides a distinct edge over unsubstituted benzylthiol or mono-halogenated versions because of its dual halogen pattern.

    Production Insights: How We Approach Manufacturing

    Manufacturing 2-Chloro-6-Fluorobenzylthiol is more demanding than many people realize. Our process begins long before the first drums are filled. Every step must control for by-products and impurities, especially given the reactivity of halogenated aromatic systems. We’ve learned to pay attention to raw material sourcing. Not all chlorinated or fluorinated benzaldehydes perform the same during synthesis, so vetting suppliers is a mandatory step.

    As a manufacturer, we have learned to respect the handling of thiol intermediates. Their odor is pronounced, and leaks in the plant never go unnoticed. Over the years, we’ve adopted closed systems and improved ventilation to protect both workers and the environment. That’s not just compliance—it makes daily operations safer and avoids production delays. Downstream, we track trace impurities more carefully than with most other bench compounds. Our quality control team uses HPLC, NMR, and GC-MS to pick up even the faintest signals of unwanted by-products. Clients trust our certificate of analysis because every line reflects real effort on the shop floor.

    Purity, Consistency, and Customer Needs

    Standard purity levels for 2-Chloro-6-Fluorobenzylthiol are usually around 97%. In practice, many of our customers request higher purity: 98% or even 99%. We see why. Medicinal chemists and material scientists both push for that extra margin because downstream applications call for certainty—not guesswork. In our plant, we adjust distillation or crystallization steps to boost purity when needed. Each batch starts with a clear production plan, and our technicians tweak conditions on the fly if any step veers off course. That’s the flexibility people don’t often see behind chemical manufacturing; the reality is that no two product runs are completely identical, so people matter as much as machines.

    Consistency is just as critical as purity. Our clients come back to us because each batch of 2-Chloro-6-Fluorobenzylthiol behaves the same way in their hands. Many new customers have tried generic material from traders and found that the first pilot run misbehaved—yield dropped, side reactions increased, or the recovery became unpredictable. Word-of-mouth tells us that robust process control and on-site analytical capabilities give us a leg up in this market. We trace every batch from raw input to finished bottles. If a client comes back with feedback or an unexpected problem, we can walk back through the data step by step.

    Where Do Customers Use This Compound?

    Most of the 2-Chloro-6-Fluorobenzylthiol we send out lands in the hands of researchers. Some work in pharmaceutical discovery, targeting halogenated benzylthiol motifs in new drug candidates. The balance of electron-donating and withdrawing effects created by chlorine and fluorine substitutions influences biological activity—sometimes boosting metabolic stability, sometimes shifting the selectivity of receptor binding. We’ve heard from academic groups and startup biotechs that our material helped them get past a tricky synthetic bottleneck or improved the overall yield of their key intermediates.

    Another growing area of use lies in materials science, especially for the synthesis of tailor-made polymers and resins or for surface modification applications. The benzylthiol moiety presents a versatile handle for attaching the aromatic ring to various surfaces. Industries seek out this particular substitution pattern because it tunes hydrophobicity or polarity in ways that single-halogen compounds don’t achieve. Some customers report improved chemical resistance or altered refractive indices for specialty films and coatings. Agrochemical researchers also incorporate halogenated thiols into advanced formulations where they notice a marked difference in performance; for example, the tailored release of sulfur compounds enables more effective formulations in some crop-protection products.

    What Sets 2-Chloro-6-Fluorobenzylthiol Apart From Its Relatives?

    Looking at the broader class of aromatic benzylthiols, each substitution brings its own set of benefits and problems. Unsubstituted benzylthiols offer broad utility but rarely deliver the targeted effects needed for today’s advanced syntheses. Mono-halogenated derivatives like 2-chlorobenzylthiol or 6-fluorobenzylthiol can perform well in some reactions, yet clients looking for fine-tuned reactivity or specific solubility characteristics often find their limits quickly.

    Adding both chlorine and fluorine atoms onto the ring, in the positions seen in this molecule, shifts reactivity and physical properties in ways that enable unique downstream chemistry. Our customers sometimes describe reduced side-product formation or improved isolation of subsequent intermediates. In polymer or surface applications, this pattern modifies adhesion and resistance to solvents or UV breakdown. Compared to other halogenated benzylthiols, this molecule’s dual-substituted nature can reduce volatility, sharpen melting ranges, or enhance solubility in certain mixed solvents. That opens up process flexibility for both small-batch work and larger scale-up. We receive regular feedback about how these small details make a big difference as projects move from benchtop to kilo-lab and pilot-plant.

    Handling and Stewardship: Lessons Learned Over Years of Manufacturing

    Through years of production, we have developed a deep appreciation of the challenges surrounding aromatic thiols. Anyone familiar with thiol chemistry knows well the notorious odor and the potential for workplace complaints or environmental concerns. Our team invested early in active ventilation, vapor containment, and smart packaging strategies to prevent leaks and cross-contamination during shipping. We designed our shop layouts to minimize handling steps, running tight batch controls that keep everything on a schedule and avoid unnecessary storage time.

    Waste minimization makes a clear difference daily. We actively separate and recycle as much solvent as possible, which reduces both environmental burden and raw material costs over time. Hydrogen sulfide and other sulfur by-products call for reliable scrubbing systems, and we routinely update our hardware to keep workplace air, and community surroundings, at the highest safety and cleanliness levels. Teams across our facility run regular containment drills to reinforce best practices and ensure everyone understands the procedures without gaps.

    Supporting Research and Scale-Up

    Collaboration with clients does not stop at the warehouse door. Large pharma and specialty chemical innovators increasingly demand more than a product certificate—they want insight into batch reproducibility, trace impurity profiles, and scale-up support. Our technical team maintains open lines with project scientists, sharing analytical data and collaborating on troubleshooting. One key lesson: the fine details in starting material quality can spell success or setback in late-stage scale-up. That’s why we operate surplus pilot reactors so we can run custom syntheses on short notice, adjusting key parameters to support client process development work.

    Technical data transfer is another area where we set our practices apart. As new clients arrive, we log every production run, analytical trace, and shipment history. These archives come in handy for troubleshooting, regulatory submissions, or patent filings. When a customer needs a special grade—lower metal contamination, tighter sulfur content, or distinct particle size—we can often draw directly from our production records to design the next run, skipping guesswork and shortening lead times. This degree of technical continuity stands out less in routine purchasing discussions but pays off when research timelines tighten and flexibility makes the difference between missing or making a market window.

    What Challenges Remain?

    Producing halogenated aromatics like this compound always brings regulatory and environmental watchfulness. Disposal of process waste containing both halogens and sulfur ranks among the most closely monitored steps in modern chemical manufacturing. Our plant invests heavily in effluent treatment and abatement technologies because short cuts can backfire quickly—whether through regulatory penalties or community complaints. Reliable production means thinking beyond a single order to the long-term relationship with local authorities and neighbors.

    Another persistent challenge comes from the market side. Prices on some pharmaceutical and agrochemical raw materials move more in response to regulations, logistics, and geo-politics than to manufacturing cost alone. The same can be said about rare halogenated feedstocks. We hedge by locking in agreements with trusted suppliers and maintaining backup sources, but unexpected delays or raw material swings can disrupt even the best-managed schedules. Regular conversations with purchasing and supply-chain teams across our organization help us see risk building early and take preventive steps that keep customers’ projects on track.

    On a practical level, we find education about safe handling and use always needs reinforcement, especially as our material reaches new markets. Not everyone is familiar with the safe storage and usage of aromatic thiols. We invest time writing clear handling guides, running webinars, and sending out reminders about PPE and ventilation best practices. Sometimes clients reach out after a first batch arrives with questions about solvent compatibility or downstream mixing. Our technical support team stands ready to answer as part of our commitment to seeing projects through safely—not just making a sale and moving on.

    Continuous Improvement and Customer Feedback

    Manufacturing doesn’t stand still. Our process teams regularly debrief after production runs to capture what went well and where things can improve. We try new purification strategies, experiment with feedstock alternatives, and adjust process steps to shave off unnecessary delays. Many improvements come directly from customer input. For example, tweaks to particle sizing or dryness specifications usually originate from application-specific demands—a polymer scientist needing a perfectly uniform batch, or a pharmaceutical team worried about residual moisture in a key intermediate. Those feedback loops shape our operating procedures and our priorities for capital investments across the plant.

    We take pride in troubleshooting. When customers encounter an unexpected by-product or a reaction that stalls out, they often share experimental details with us, and our process chemists run parallel tests or simulations. A batch that looked perfect in characterization but threw off a trace contaminant on use can cause days of investigation. We track those cases obsessively until a solution emerges, and those lessons feed back into both plant training and future product runs. The net effect is a steadily improving cycle of process optimization that serves all our customers, not just the ones who first flagged an issue.

    Looking Ahead: The Future of Halogenated Benzylthiol Chemistry

    Demand for high-purity, reliable aromatic thiols with advanced substitution patterns shows no sign of slowing down. As pharmaceutical and materials sciences push into ever-more specialized territory, molecules like 2-Chloro-6-Fluorobenzylthiol take on enhanced importance. Our experience tells us that success depends as much on technical rigor as it does on communication and flexibility—qualities that rarely make it into a data sheet but matter at every stage from lab bench to commercial production.

    We continue investing in analytical tools, process automation, and operator training to keep quality levels at the top of the industry. Partnerships with customers, supplier relationships across continents, and continual operations review create a resilient foundation for whatever the next market trend may be. We remain committed to delivering a material that researchers and product developers can stake their reputation—and future breakthroughs—on. For us in manufacturing, that’s not just a goal; it’s a source of pride earned daily in the plant and in every successful project that moves forward because the chemistry works right from the start.