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2-Chlorothiophenol

    • Product Name 2-Chlorothiophenol
    • Alias 2-Chlorobenzenethiol
    • Einecs 212-207-9
    • 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

    362862

    Cas Number 107-59-5
    Molecular Formula C6H5ClS
    Molecular Weight 144.62
    Appearance Clear to yellowish liquid
    Boiling Point 191-193°C
    Melting Point -30°C
    Density 1.34 g/cm3
    Flash Point 75°C
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Smell Pungent, unpleasant odor
    Refractive Index 1.624 at 20°C

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

    Packing & Storage
    Packing The 2-Chlorothiophenol is packaged in a 100g amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2-Chlorothiophenol should be shipped in tightly sealed containers, away from light, heat, and incompatible materials such as oxidizers. It must be handled by trained personnel, labeled according to hazard regulations, and transported as a hazardous material, following all relevant local and international shipping, packaging, and documentation requirements.
    Storage 2-Chlorothiophenol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as oxidizing agents. Keep the container tightly closed and protected from light. Use chemical-resistant containers, ideally glass or compatible plastic. Ensure proper labeling and store away from direct sunlight, moisture, and heat to prevent degradation or hazardous reactions.
    Application of 2-Chlorothiophenol

    Applications of 2-Chlorothiophenol in Industrial Manufacturing

    2-Chlorothiophenol is a critical intermediate for synthesizing advanced agrochemicals, pharmaceuticals, dyes, and polymer additives. As an upstream manufacturer, we supply high-purity grades for targeted industrial applications requiring precise formulation and process control. Below we detail actual downstream sectors, illustrating compliance frameworks, dosing practices, and integration steps as used by leading producers.

    1. Synthesis of Agrochemical Active Ingredients

    Producers of crop protection chemicals use 2-Chlorothiophenol as a sulfur source in the synthesis of thiocarbamates and heterocyclic fungicides. Application often focuses on triazole and thiazole ring construction, where strict impurity thresholds and batch traceability are enforced. Continuous-flow or batch esterification and coupling integrate the material during key condensation or halogen exchange stages, directly prior to active molecule formation. End users adjust loading based on targeted active concentration and required byproduct specifications.

    Industry compliance standards

    • ISO 9001:2015 quality management protocols
    • REACH registration for agrochemical intermediates (EU)
    • China GB 4839 and EPA TSCA reporting (US)
    • Adherence to FAO/WHO pesticide specifications

    Typical usage ratio

    • 5–15% by mass of total intermediate batch, dependent on desired ring incorporation and byproduct limits. Higher loading required for more complex rings or when downstream yield is a concern.

    Downstream process integration

    • Thiophenol introduction at the cyclization or acylation step of fungicide or herbicide synthesis following initial halide activation
    • Temperature-controlled addition in closed reactors to minimize volatilization and off-gassing
    • Integration within multi-step syntheses with in-process HPLC monitoring for conversion
    • Final batch purification using crystallization or column techniques to control residual sulfur content

    Final product types

    • Triazole-based fungicides (e.g., propiconazole)
    • Thiocarbamate herbicide intermediates
    • Thiazole-based insecticides
    • Custom field-crop protection actives

    2. Pharmaceutical Intermediate for Antimicrobial Compounds

    Active pharmaceutical ingredient (API) manufacturers employ this thiophenolic compound in key thiol substitution and coupling steps for anti-infective and CNS-active drugs. It serves as a nucleophile for aromatic substitution reactions, facilitating synthesis of benzothiazole and other sulfur-containing drug cores. GMP protocols require precise tracking, filtration, and stripping procedures to ensure residual levels meet regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP, JP, EU Pharmacopoeia specifications for intermediates
    • FDA DMF (Drug Master File) compliance for regulated markets
    • Specific customer and market authorisation documentation (e.g., CEP in Europe)

    Typical usage ratio

    • 2–7% by mass, based on the molar equivalent needed for nucleophilic aromatic substitution. Adjusted per the complexity of the final active’s chemical structure.

    Downstream process integration

    • Direct inclusion at nucleophilic aromatic substitution steps for sulfur group introduction on benzene systems
    • Followed by base- or acid-catalyzed cyclization
    • Critical in final derivatization prior to salt-formation or crystallization of API
    • In-process quality control using LC-MS or GC for tracking residuals

    Final product types

    • Benzothiazole antimicrobials
    • Sulfur-containing anti-tuberculosis agents
    • Thioether-based CNS compounds
    • Custom API scaffolds for research and early-phase clinical supply

    3. Dye and Pigment Intermediate

    Manufacturers of sulfur-based colorants use 2-Chlorothiophenol as a functional group donor, especially in azo and heterocyclic dye synthesis. This material allows direct formation of chromophoric groups, providing color stabilization and improved fastness in synthetic textiles and plastics. The raw thiophenol enters during condensation or coupling reactions where controlled reactivity ensures final hue consistency and minimal unwanted byproducts in pigment grades.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substance levels
    • EN 71-3 (Europe) for colorant safety in toys and textiles
    • REACH Annex XVII for dye intermediates (EU)
    • Textile Eco-Cert and ZDHC MRSL guidelines

    Typical usage ratio

    • 10–30% by moles in dye coupling reactions, adjusted for chromophore intensity and shade accuracy. Lower levels for tint dyes, higher for saturated pigments.

    Downstream process integration

    • Incorporation during azo coupling or immediately after diazotization
    • Reacts in closed jacketed vessels to control exothermic profile
    • Removal of excess precursor and neutralization via liquid-liquid extraction post-reaction
    • Final filtration and drying with colorimetric QC against standard boards

    Final product types

    • Azo dyes for synthetic fibers
    • Heterocyclic sulfur pigments for plastics
    • Technical printing inks
    • Textile and leather dyes

    4. Polymer Additive Synthesis

    Producers of specialty polymer additives and stabilizers use 2-Chlorothiophenol for introducing reactive sulfur atoms into polymer chains, improving heat resistance and UV stability. The compound participates in chain transfer or crosslinking reactions. Careful dosing ensures polymer matrix integrity and end-use compliance in automotive, electrical, and packaging fields.

    Industry compliance standards

    • ISO 14001 for environmental management in manufacturing sites
    • UL 94 (Flammability of Polymeric Materials) for electrical applications
    • FDA 21 CFR 177.2600 for indirect food-contact materials (where applicable)
    • RoHS compliance for electronics and electrical sectors (EU)

    Typical usage ratio

    • 0.5–3% by total polymer mass in additive concentrates; exact ratio tailored to target crosslink density and application temperature range.

    Downstream process integration

    • Added as a functionalized building block during melt blending or solution polymerization
    • Introduction timed after initial monomer formation and before final curing or extrusion
    • Real-time process monitoring for sulfur integration using FTIR or titration
    • Masterbatch production for concentrated additive delivery

    Final product types

    • Polyolefin and styrenic stabilizers
    • Heat-resistant engineering plastics
    • UV-stabilized automotive polymers
    • Specialty elastomer protective additives
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    Certification & Compliance
    More Introduction

    2-Chlorothiophenol: A Manufacturer’s Perspective on Quality and Application

    Understanding 2-Chlorothiophenol in the Chemical Landscape

    Years of experience standing on a production floor have taught us that certain ingredients quietly define the success of entire downstream sectors. 2-Chlorothiophenol is one such chemical—a blend of reactivity and selectivity that shapes the way many chemical reactions move forward. In a world where both performance and safety dictate how manufacturers operate, this compound has found its niche. The chemical formula—C6H4ClSH—captures its essence, a chlorinated aromatic ring with a thiol functional group, co-existing in a single molecule. This unique pairing brings characteristics that other monotonic aromatics cannot deliver to synthesis outfits, especially in pharmaceuticals, agrochemicals, and dye manufacture.

    A Closer Look at the Chemistry

    We prepare 2-Chlorothiophenol as a clear to pale yellow liquid, with faint but noticeable sharp notes in odor common to aromatic thiols. Our product typically runs at a purity over 99 percent by GC, with moisture content monitored at each batch stage to keep levels below 0.1 percent. This tight control does not materialize overnight; it takes fine-tuned distillation, thoughtful separation steps, and hands-on process monitoring. Many chemicals come from the same starting materials, but the tricks lie in getting the right product isolated, free from heavy-metal contamination, excess side-products, or sulfurous residues. These details turn a basic specification into a tool chemists rely on in high-stakes environments.

    Commercial value does not spring from a stockpile of specs, but from delivering consistency at scale. Purity matters in two ways: sharp batch-to-batch control keeps downstream catalysts alive and stops unwanted side reactions; low impurity footprints cut back on waste streams and environmental headaches.

    The Manufacturing Path: Balancing Scalability, Safety, and Purity

    Traditional synthesis starts with chlorination of thiophenol or thiolation of chlorobenzenes, then moves through distillation to eliminate heavy and light fractions. Our operations challenge standard routes by eliminating persistent sulfur residues in the final product. Upstream, we monitor reactor temperature gradients through automation. Downstream, we actively check for escaped hydrogen sulfide and chlorinated byproducts. Manufacturing this compound never becomes routine; new regulatory guidance (coming in from markets in the EU or North America), raw material swings, and environmental reporting requirements shape daily decisions. Waste gas capture, recycle, and destruction systems must adapt, requiring frequent upgrades and operator training. These layers are not simply regulatory hoops—they make the compound safe to use and handle, both in our shop and in customers’ reactors.

    Applications: What Makes 2-Chlorothiophenol Stand Out

    Within pharmaceuticals, 2-Chlorothiophenol often features as a sulfur donor in the construction of biologically active thioether and thiazole motifs. Many blockbuster medicines—antimicrobials, anti-inflammatories, CNS agents—trace their molecular backbone to a properly functionalized aromatic thiol. Our customers in the pharmaceutical sector appreciate the batch documentation and trace impurity control because process yields, impurity flags, and ultimate regulatory submissions tie directly back to raw ingredient integrity.

    Agrochemical companies draw on the same unique chemical reactivity, but look for robust, cost-effective supply chains and the ability to scale up pilot runs to multi-ton lots. They convert 2-Chlorothiophenol to intermediates that go on to become improved herbicides, fungicides, and crop-protectant agents. The molecule’s distinctive reactivity profile allows for selective functionalization—a chlorine atom ortho to the thiol provides access to specific sulfide linkages and coupling reactions, promoting efficiency where other thiols might falter or waste raw material through overreaction.

    Dye and pigment manufacturers use 2-Chlorothiophenol for advanced chromophores and specialty colorants. Its precise introduction into conjugated ring systems allows finely tuned hue adjustments and lightfastness in specialty inks and textiles. Not every thiol or aromatic halide performs this reliably in acidic or basic dye baths; the combination of chlorine and sulfur in this skeleton provides robust color properties, especially in demanding applications like automotive coatings and digital printing.

    Differences Compared to Related Chemicals

    In a world full of choices—chlorobenzenes, thiophenol, and other halogenated or sulfhydryl-substituted benzenes—small changes make major differences downstream. Thiophenol, missing the chlorine, reacts more aggressively, often forming unwanted dimers or cross-linked byproducts under strong conditions. This can tack on extra workup steps for the customer and increase solvent requirements, trashing the process economics. Simple chlorobenzenes require multi-stage functionalization to deliver the desired end-use sulfur chemistry, generally using harsher reagents and conditions with lower selectivity and greater environmental impact.

    In comparison, 2-Chlorothiophenol’s dual substituents offer a unique blend. The sulfur group gives nucleophilicity and chelation, while the chlorine atom moderates activity, supports directed ortho-metallation, and opens the door for tailored substitution patterns. In heterocycle synthesis, such as making benzothiazoles, this means fewer cleaning and purifying steps, less waste, and higher throughput. In years past, synthetic chemists juggled trial-and-error with less selective reagents. The rise in availability of this specific compound shortened process development cycles and cut out much chemical ‘deadwood.’ This benefit shows clearly on the shop floor: smaller solvent inventory, faster batch turnaround times, and minimized hazardous waste treatment bills for our clients.

    The Challenge of Odor and Handling

    Experience in the plant reveals a side to 2-Chlorothiophenol that shows up nowhere in catalog tables: the characteristic thiol odor, sharp and persistent, follows even slight leaks or minor spills. Traditional packaging and quick-turn loads expose workers and adjacent product lines if ventilation and containment systems are not kept in peak condition. Odor masks the compound’s true hazard profile; its actual toxicity rests well below many common organosulfur chemicals, but persistent exposure or careless transfer can desensitize even seasoned staff. Repeated inhalation produces discomfort and workplace complaints, so the best results come from closed loading systems, local exhaust ventilation, and personal protective gear upgrades. Each plant run brings new lessons about line integrity and drumming protocols, and periodic equipment upgrades form a regular part of our operating budget. Our in-house odor abatement techniques cut release levels to a fraction of government standards, keeping peace with neighbors, too.

    Packaging and Storage Realities

    We draw on steel drums and high-density polyethylene containers, tested over time for chemical compatibility and resistance to both corrosion and permeation. Temperature swings impact physical handling; 2-Chlorothiophenol tends to increase in vapor pressure as ambient shop temperatures ramp up, so storage inside ventilated, cool enclosures blocks pressure buildup in container heads. Package integrity is never a cost-saving shortcut—with the characteristic odor, even a pinhole or thin seam escapes detection for only a short time. We train handling crews on detection and quick-response, using gas meters and physical inspection, alongside standard PPE. No substitute exists for boots-on-the-ground awareness, especially during transfer operations.

    Compliance, Safety, and Site Integrity

    Long-term manufacturing experience highlights the constant presence of evolving regulations. 2-Chlorothiophenol occupies a space in global regulatory frameworks not as a consumer-facing risk, but as a critical intermediate subject to tracking, reporting, and secure transport rules. Our in-house compliance officers review everything from inventory controls to hazardous waste manifests. Audits from international certifiers force us to maintain documentation that synchronizes with every batch we produce. This work—meticulous and sometimes tedious—creates a solid paper trail, which both shields us from legal exposure and builds trust with customers who must validate their own supply chains.

    Our plant workers face the true risks of the job, not in theoretical hazard scores, but in routine tasks—line changes, filter maintenance, and emergency response to a minor vessel leak or process upset. Training programs for these practical scenarios must go deeper than textbook minimums. We structure our ongoing education around simulated spill response, proper PPE donning, and updated MSDS interpretation. These lived experiences show how theory and practice sometimes clash, and investing in people’s safety brings returns both measurable—fewer accidents, lower insurance premiums—and intangible, preserving morale and team cohesion.

    Sustainability and Environmental Impact

    Turning raw materials into this compound, it becomes clear how even modest improvements in yield or byproduct capture pay out across entire operating years. Many upstream chemical routes use chlorinating agents and sulfur sources that generate side streams of non-condensible gases and halogenated waste. We have re-engineered portions of the process to cut fugitive losses, reclaim solvent fractions, and recycle certain byproduct streams back as feedstock where feasible. In cases where outside disposal is unavoidable, we partner with third-party waste processors certified to handle this specific class of sulfur-chlorine organic. Our plant metrics include not just product throughput, but air emissions, water use, and offsite waste volume. Each year brings new stretch targets for efficiency and environmental stewardship, enforced as much by a sense of community responsibility as by government inspectors.

    On the demand side, interest in green chemistry and lower-impact alternatives pushes our internal development team to trial new processes—working on catalytic alternatives, continuous processing, and transition-metal-catalyzed approaches that promise fewer waste streams and greater atom economy. Upgrades are gradual, but even minor steps (improved filters, enhanced batch monitoring, automated sampling) tighten control and lessen residual impact. Customers ask about these steps because their own supply chains face similar pressure to disclose environmental credentials. Years ago, few buyers cared for life-cycle analysis; now, it’s a point of competitive distinction.

    Supporting the Chemical Community: From Bench to Bulk

    As manufacturers, we often speak with chemists who want to push 2-Chlorothiophenol performance even further—tighter impurity controls, custom formulations, new packaging sizes, or regulatory document supplementation. Each request becomes a project: adapting batch protocols, training QC teams to new signal thresholds, or investing in custom filling lines for specialty customers. Sometimes, process bottlenecks or unexpected impurity profiles challenge the whole line, sending both plant managers and researchers back to the drawing board. We invite those challenges as the best lessons come from close collaboration between operations and R&D crews.

    External partnerships shape the landscape even more. We keep open lines of communication with customers trialing new reactions, with academic partners designing new routes, and with technical consultants adapting our product to pilot plants. These relationships shape what we prioritize in process improvements—whether a pharmaceutical client needs tighter trace analysis, or an agrochemical producer demands extra capacity during growing season. Direct feedback from downstream users informs where to dial in purity or optimize cost efficiency. This ongoing dialog is not just about business—it’s the foundation of long-term trust that sustains both our plant and the industries we serve.

    Pushing Technical Boundaries with a Continuous Improvement Mindset

    The chemical sector has always understood the value of precision and adaptability. 2-Chlorothiophenol brings together both. By focusing on feedstock quality, careful process design, and real-world feedback, we continue to refine the product. Technological investments—real-time gas analytics, microprocessor-controlled reactors, and in-house spectroscopy—have reduced off-spec batch rates and shortened production cycle times. Every plant run helps us learn more about the molecule, and every shipment deepens our experience as true makers, not mere handlers or brokers.

    Our workforce reflects these values. Operators move from line worker to team lead with a detailed understanding of both chemical principles and practical plant dynamics. Their input identifies shortcuts, potential risks, or hidden inefficiencies that would otherwise go unreported. Engaged workers help prevent accidents before they start. Company-wide focus on continuous improvement means integrating small upgrades—automatic drum handlers, improved thermal monitors, umbrella gas sensors—into day-to-day routine. Chemical manufacturing demands this attitude because raw materials do not always behave as theory predicts, and contingency planning for process upsets is simply part of the engineering toolkit.

    Looking Forward: Market Dynamics and the Future of 2-Chlorothiophenol

    The chemical world never stands still. Changing pharmaceutical pipelines spark new interest in building-block chemicals with better ecological profiles and tighter performance windows. We track those shifts, watching how regulatory environments change use patterns for chlorine- and sulfur-containing compounds. Demand for 2-Chlorothiophenol rides on trends in active ingredient launches, expansion cycles in dye manufacturing, and short-term swings in agricultural policy and climate. As a manufacturer, keeping ahead means retaining flexibility, both in plant scheduling and inventory management, repeatedly reviewing supply contracts and sourcing backups for critical feedstock.

    Shifts to greener, more sustainable chemistry routes will continue to test legacy manufacturing processes. Our approach relies on transparency with customers, readiness to invest in plant upgrades, and a mindset prepared for the unexpected. No two plant runs look precisely alike, but each builds toward the higher standards the industry—and downstream sectors—expect. Each shipment arrives not as a faceless commodity, but as the product of cumulative experience, hands-on stewardship, and careful balancing between safety, regulatory expectation, and technical potential.

    Final Thoughts on Making a Difference in Specialty Chemicals

    The journey of 2-Chlorothiophenol from plant to bench has shaped both our technical expertise and business philosophy. Consistency, safety, and speed are not abstract slogans—they are the backbone of sustainable production. Differences from generic aromatics or less specialized thiols lie not only in molecule design, but in the careful methods of manufacture, handling, and ongoing product refinement. Daily effort from production chemists, QC teams, engineers, and operators knit together each batch, with decisions informed by experience, real-world feedback, and technical curiosity.

    We view every kilogram that leaves our site as a promise delivered to those down the line—synthesizers in pharma, innovation teams in dyes, and chemists fine-tuning crop-protection agents. Fewer process surprises, tighter impurity controls, and greater user confidence come from a manufacturing mindset built on learning and plain hard work. The chemical may be small in scale compared to bulk commodities, but the standards it sets and the solutions it enables ripple far and wide. This is why, without fanfare or shortcuts, we continue refining the way 2-Chlorothiophenol is made, understanding its application, and supporting the innovators who rely on it.