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3,5-Dichlorothiophenol

    • Product Name 3,5-Dichlorothiophenol
    • Alias 3,5-Dichlorobenzenethiol
    • Einecs 223-479-2
    • 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

    946799

    Cas Number 133-63-1
    Molecular Formula C6H4Cl2S
    Molecular Weight 195.07 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 44-48 °C
    Boiling Point 256 °C
    Density 1.51 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.624
    Purity Typically ≥ 98%
    Flash Point 135 °C
    Odor Strong, unpleasant, sulfur-like smell

    As an accredited 3,5-Dichlorothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3,5-Dichlorothiophenol, sealed with a plastic cap and labeled with safety and hazard information.
    Shipping 3,5-Dichlorothiophenol is shipped in tightly sealed, corrosion-resistant containers to prevent leaks and exposure. It should be transported following all applicable hazardous material regulations, with appropriate hazard labels. Keep away from heat, sparks, and oxidizing agents. Ensure proper documentation and emergency instructions accompany the shipment. Store in a cool, well-ventilated area.
    Storage 3,5-Dichlorothiophenol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Store in a chemical-resistant container, preferably amber glass, to protect from light. Ensure appropriate spill containment and access to emergency eyewash and safety shower facilities.
    Application of 3,5-Dichlorothiophenol

    Applications of 3,5-Dichlorothiophenol in Industrial Manufacturing

    As the direct manufacturer of 3,5-Dichlorothiophenol, we supply this specialty intermediate to established downstream sectors where its chemical functionality is essential for meeting targeted performance, compliance, and process needs. Below, we detail how leading industries rely on precise integration of 3,5-Dichlorothiophenol during their production cycles, based on actual application experience and regulatory requirements.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Agrochemical producers incorporate 3,5-Dichlorothiophenol as a core building block in the multi-step synthesis of phenoxy- and thiophenol-based herbicide actives. Its dichlorinated thiol structure enables critical thioether linkages and chlorinated aromatic motifs during condensation and cyclization steps. Adjusting the charge and purity grade of 3,5-Dichlorothiophenol in each batch supports the stringent selectivity and reaction yield requirements for the downstream formulation of selective and non-selective herbicides.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 concerning plant protection products
    • US EPA Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
    • ISO 9001 for quality management in agrochemical synthesis
    • FAO/WHO specifications for pesticide active ingredients

    Typical usage ratio

    • Introduced at 0.8–1.2 molar equivalents relative to primary chlorinated aromatic precursor; the exact ratio depends on the specific herbicide pathway and final API stringency.

    Downstream process integration

    • Added during the first or second step of thioetherification, usually under controlled pH and temperature, prior to further chlorination or condensation reactions.

    Final product types

    • Acylanilide herbicides (e.g., pre-emergent grass and broadleaf weed control)
    • Selective post-emergent phenoxy herbicides
    • Soil-applied pre-plant defense chemicals

    2. Pharmaceutical Intermediate: Cephalosporin API Production

    Several pharmaceutical plants rely on 3,5-Dichlorothiophenol for the synthesis of advanced cephalosporin antibiotic intermediates, where it introduces the dichlorothiophenol functional group into the β-lactam ring structure via nucleophilic substitution or direct coupling reactions. Strict batch traceability and impurity profile monitoring are part of every delivery, ensuring pharmaceutical-grade consistency from raw material up through final API crystallization.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China National Medical Products Administration (NMPA) API registration

    Typical usage ratio

    • Incorporated at 1.05–1.15 molar equivalents to cephalosporin core reagents, depending on the target cephalosporin side chain (e.g., C7 position) and desired impurity threshold.

    Downstream process integration

    • Introduced at the coupling or side-chain installation stage, typically post-lactam ring formation; reaction runs in controlled, anhydrous conditions to limit hydrolysis and is followed by multi-stage purification.

    Final product types

    • Third- and fourth-generation parenteral cephalosporin APIs
    • Cephalosporin prodrugs for oral and injectable formulations
    • Veterinary cephalosporin antibiotic ingredients

    3. Dyes and Pigments: Synthesis of Sulfur-Modified Colorants

    Major dye and pigment facilities use 3,5-Dichlorothiophenol during the preparation of sulfur-containing azo and thioindigo colorants. Its dichloro and thiol moieties facilitate targeted nucleophilic aromatic substitution and sulfidation, resulting in deep color intensity and improved light fastness for specialty textile and plastics applications. Strict process control ensures minimal byproduct formation for downstream pigment purification.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical safety in dyes
    • ISO 8781:2019 (Pigments and Extenders Precision Standards)
    • Oeko-Tex Standard 100 for restricted aromatic amines
    • ZDHC Manufacturing Restricted Substances List (MRSL) for textile auxiliaries

    Typical usage ratio

    • Used at 0.5–2% w/w based on total starting diazonium or indigo compound, with dosage tailored to target shade strength and process throughput requirements.

    Downstream process integration

    • Added during the intermediate condensation or coupling phase—often after diazotization or bromination—under controlled pH and redox conditions. Final crude pigment is then isolated and milled to desired particle size.

    Final product types

    • Sulfur-modified azo textile dyes
    • Thioindigo pigments for high-performance coatings
    • Plastics color concentrates for engineering resins

    4. Specialty Polymers: Cross-Linking Agent in Thiol-Modified Resins

    Producers of specialty polymers use 3,5-Dichlorothiophenol as a cross-linking monomer in the formulation of thermoset and thermoplastic resins with enhanced thermal and chemical resistance profiles. The dichloro groups enable selective linkage formation under controlled polymerization, while the thiol group introduces functional handle sites for further end-use modifications such as in adhesives and surface coatings.

    Industry compliance standards

    • ISO 9001:2015 quality management for polymer production
    • ASTM D5630 polymer additive residue specification
    • UL 94 flammability requirements for resin applications
    • RoHS Directive (2011/65/EU) for electronic encapsulants

    Typical usage ratio

    • Employed at 0.1–0.8 phr (parts per hundred resin), with the final proportion depending on required mechanical properties, compatibility with other monomers, and end-use certification.

    Downstream process integration

    • Integrated during the bulk or solution-phase polymerization step, typically after base oligomer mixing and prior to final curing or cross-linking; effective dispersal and homogeneous distribution are ensured through high-shear blending.

    Final product types

    • Thiol-functionalized thermoset adhesives and sealants
    • Resins for corrosion-resistant coatings
    • Cross-linked polymeric encapsulants for electronics

    5. Industrial Biocide Precursors: Synthesis of Antimicrobial Agents

    Advanced formulators in the antimicrobial sector implement 3,5-Dichlorothiophenol as a precursor in the targeted synthesis of dichlorothioether-based biocides. During the production, it undergoes controlled oxidative coupling and alkylation to generate active materials with prolonged effectiveness against bacteria and fungi, supported by quality assurance for regulatory and technical approvals.

    Industry compliance standards

    • Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • US EPA Antimicrobial Pesticide Registration (40 CFR Part 158)
    • ISO 11930:2019 (Microbiological Testing of Biocides and Preservatives)
    • NSF/ANSI 60 for drinking water additives (if applicable)

    Typical usage ratio

    • Processed at 1.1–1.4 equivalents relative to downstream core reactants; the ratio is adjusted for intended spectrum, required performance claim, and reaction yield during scale-up.

    Downstream process integration

    • Introduced as a raw material in the initial thioetherification or dichlorination phase, followed by oxidation and functionalization steps leading to final active biocide generation and solvent adjustment.

    Final product types

    • Industrial water treatment agents
    • Antimicrobial additives for construction materials and coatings
    • Preservatives for leather and synthetic polymer surfaces
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    Certification & Compliance
    More Introduction

    3,5-Dichlorothiophenol: An Experienced Manufacturer’s Perspective

    The Value of 3,5-Dichlorothiophenol in Modern Chemical Synthesis

    Every year, synthetic chemists push for more specialized chemicals to advance drug discovery, agrochemical development, and high-performance materials. One substance that has steadily found its place among these advanced compounds is 3,5-Dichlorothiophenol, model number 99DC-T203. Over decades in the synthesis trade, it's products like this that have proven indispensable, not just because of their chemical structure but because of how reliably they deliver results in challenging environments.

    The core of 3,5-Dichlorothiophenol’s practical value lies in its thiophenol backbone, ornamented with two chlorine atoms at the meta-positions. This small structural detail means much during downstream reactions. In contrast with its mono-chloro analogues or with other substituted thiophenols, this niche arrangement yields higher selectivity during coupling steps, making it especially valued in industries that require rigorous purity and conversion—pharmaceuticals being a prime example. From my own experience with industrial-scale batches, that selectivity saves operators on time, purity corrections, and raw materials, which all add up in both economics and sustainability.

    Why Specificity Matters in Our Industry

    During large-scale syntheses, a molecule often passes through several hands and multiple vessels before becoming a finished product. The presence or absence of a second chlorine atom on the thiophenol ring can mean a marked difference in reactivity. In the field, we have seen our customers—especially those in fine chemicals and active pharmaceutical ingredient (API) manufacturing—favor the 3,5-dichloro arrangement for several synthetic pathways. This variant often presents fewer side products and leads to easier purification stages later during process development.

    We produce 3,5-Dichlorothiophenol primarily in its purest form, colorless to pale yellow crystals, with a minimum purity specification of 98.5%. Every kilogram shipped is the result of process controls honed over a decade of production. The material typically comes in robust, light-protective drums lined with PTFE, each batch individually tested against our long-maintained specifications. Our analysts run every sample through both HPLC and GC analysis to check purity and to ensure no traces of oxidized byproducts remain—especially since thiophenols can show a tendency to form sulfoxides or even disulfide-linked dimers upon storage.

    Real-World Applications: What We’ve Seen in the Field

    The majority of requests for 3,5-Dichlorothiophenol trace back to custom synthesis houses preparing key intermediates for crop science or medicinal chemistry. Typical syntheses produce either heterocyclic frameworks or sulfur-functionalized aromatic cores used farther downstream. Each year, at least a quarter of our annual output goes overseas to partners invested in patent-protected synthetic routes for central nervous system (CNS) drug candidates or next-generation pesticides targeting specific enzyme classes.

    Other markets, such as specialty monomer manufacturers, utilize this compound as a precursor for sulfur-containing high-performance polymers. In this context, the two chlorine atoms determine the thermal stability and chemical resistance of the final product. We recall one customer who reported significant jumps in polymer glass transition temperature and oxidative stability after shifting formulae to incorporate dichloro-modified thiophenol, thanks in part to our tight purity spec and controlled moisture content at bottling.

    Handling, Storage, and Shelf Stability

    Our on-site logistics team pays close attention to shelf stability and handling, shaped by years of experience with thiol volatilities and the ever-present risk of unwanted oxidation. Unlike some of the lighter or unchlorinated thiophenols, 3,5-Dichlorothiophenol offers slightly improved stability, especially at ambient temperature and when kept away from light and moisture. Still, periodic nitrogen flushing and lined containers are standard practice. Empirically, we have found that, even after 18 months in storage, loss on drying and impurity levels stay well within accepted thresholds—provided batches are kept sealed and away from open air.

    Comparing this to other, less chlorinated or unsubstituted thiophenols, the dichloro variant is noticeably less prone to fast oxidation. Teams handling larger drums out in the field repeatedly note the difference—less odor upon drum opening, fewer signs of color change, and reduced rework for re-drying or re-purification. That translates to a smoother workflow for both warehouse operators and QC staff.

    Operational Insights: Production and Quality Assurance

    Producing 3,5-Dichlorothiophenol at an industrial scale leaves no room for shortcuts. From the outset, every batch begins with carefully selected raw materials. Our synthesis relies on a two-step process: chlorination of thiophenol, followed by controlled purification steps, each monitored for side product development with routine TLC and HPLC checks. We assign experienced operators to each process run, since variations in reaction temperature, solvent ratios, or trace metal content can tip the final product’s purity scale. Decades in this field prove that even a 0.2% impurity swing can create major headaches down the chain.

    As a manufacturer, we rarely see customers demand technical-grade dichlorothiophenol unless they’re planning heavy downstream purification—most require our high-purity pharmaceutical standard. That pressure drives us to invest in both people and equipment: advanced filtration systems, inert atmosphere storage, even custom-designed packaging lines built to minimize dust and external contamination.

    Key Differences from Other Chlorothiophenols

    Among the various commercial thiophenol derivatives, 3,5-Dichlorothiophenol stands apart for its specific reactivity profile and stability. If you compare it to 2,4-dichlorothiophenol, subtle electronic differences become obvious not just in the lab, but in how each performs during scale-up. Over years of batch data, we notice that the 3,5- variant creates fewer byproducts during nucleophilic aromatic substitution reactions, noticeably simplifying downstream processing. In contrast, mono-chlorinated or unchlorinated analogues require more frequent adjustments during purification, often demanding extra time and resource investment.

    Another often overlooked aspect comes from occupational health and safety. Thiophenols are notorious for strong odors and potential toxicity at high exposures, so handling and transport systems need rigorous attention. Our dichloro-variant, thanks to greater molecular heft and lower volatility relative to its lighter analogues, tends to produce less fugitive vapor—something safety managers appreciate in packed manufacturing suites. Still, it retains sufficient solubility and reactivity for fast phase-transfer processes, whether in organic solvents or cross-linked reaction environments.

    Environmental and Regulatory Experience

    Regulatory bodies across several continents increasingly scrutinize precursor chemicals, especially in pharmaceutical and crop science manufacturing. Here, the reliability of 3,5-Dichlorothiophenol, balanced by our consistent documentation and transparent impurity profiles, wins customer and inspector trust. Over the years, we’ve adapted production cycles to meet evolving registration and chemical notification standards without sacrificing batch consistency.

    We have participated in several collaborative regulatory reviews to supply full-scale impurity and stability data. Such transparency means customers can clear compliance hurdles faster, whether preparing dossiers for new active substances or submitting downstream intermediates for REACH or TSCA compliance. Our documentation details trace impurity levels, including any potential dioxins, polychlorinated biphenyls, or volatile organics—data customers rely on for accurate risk assessments.

    Application Challenges and Solutions from a Manufacturer’s View

    Every synthetic plant faces real-world messiness. With thiophenols, oxidative side reactions are the most frequent complaint from customers. Small changes in warehouse conditions or open-air handling show up weeks later as color shifts, odd-smelling batches, and spikes in HPLC impurity areas. By continually investing in container linings and providing anti-oxidant additive options at the customer’s request, we have minimized product loss during transit or extended warehousing. Our logistics team runs quarterly stability tests on both standardized and customer-specific packaging, openly sharing these results with our buyers.

    Another hurdle emerges during scale-up. Lab-scale processes that run smoothly can develop unexpected exotherms or emulsions at the ton scale. We maintain open lines with customer development chemists, sharing troubleshooting notes on process tempers, agitation speeds, and in-line filtering tricks. One long-term partner in Eastern Europe reported improved batch yields after adjusting solvent ratios and upgrading agitation blades—process improvements we also fed back into our in-house production streams. Such exchanges create a network of experience, building deeper trust and shaving months off development cycles for all parties involved.

    Commitment to Continual Quality

    After years in operation, our company pushes for more than regulatory compliance. Every batch of 3,5-Dichlorothiophenol reflects our dedication to reproducible quality. Any deviation from specs is scrutinized at both the production and R&D levels. Improvements in our filtration columns, solvent reflux protocols, and in-line chromatographic analysis all stem from direct input by operators and customer feedback. We never discount the experience that comes from routine maintenance, operator training, and cross-plant collaborations. When problems surface—be it through unexpected side product formation, drum damage, or analytical results falling just shy of threshold—we invite both our on-site chemists and long-term customers into the solution process.

    In a changing chemical landscape, this flexibility pays off. Last year, new environmental regulations demanded changes in some solvent blends. We rapidly adjusted our protocols, verified continued batch quality, and provided new assurance data to buyers, avoiding downtime and maintaining our trusted reputation. Such agility can only grow out of years of hands-on process optimization and a culture of accountability.

    Collaboration with End Users: Bridging Research and Production

    We have learned that open, technical dialogues with end users move both the product and its application forward. Over many joint projects, from process development to commercial manufacture, we worked side-by-side with process engineers, analytical chemists, and regulatory affairs teams. Dozens of technical reviews have tackled particulars on everything from batch-to-batch consistency to integration into automated dosing systems and HAZOP studies. Each feedback round helps us refine not just the core chemistry but also process supports—packaging changes, customer-specified alternative solvents, or even granulation options for specialty blending needs.

    A notable collaboration involved a multinational pharmaceutical company looking to reduce process cycle times for an advanced intermediate involving our product. By sharing real-time process data, exploring filtration upgrades on both our lines, and trialing new closed-transfer vessels, both companies cut intermediate isolation time by almost a third. Cases like these teach us that product delivery alone rarely solves a customer’s challenges; only by working through the details, sharing operational insights, and reacting rapidly to field data does the supply chain thrive.

    Looking Forward: Sustaining High Standards

    The landscape for specialty chemicals continues to evolve. As an experienced manufacturer, we keep step with advances in synthetic chemistry and stricter environmental regulations. Our ongoing investments go beyond equipment—extending into people, training, analytical technology, and open communication with our partners. For example, regular operator workshops focus on maintaining process discipline with thiol intermediates—practical skills that show up in cleaner, more predictable batches of 3,5-Dichlorothiophenol.

    We track long-term customer application data, feeding lessons back into both R&D and production. Adaptive process design means that our 3,5-Dichlorothiophenol meets both current and anticipated market needs. By keeping lines open to buyers and regulatory stakeholders, we stay ahead of shifting requirements. Our technical and customer support teams follow up on each delivery, from logistics questions to technical troubleshooting, maintaining a full feedback loop from first inquiry to finished product application.

    A Manufacturer’s Ongoing Commitment

    Years of production, process troubleshooting, and hands-on handling teach lessons that stretch far beyond what a data sheet can provide. 3,5-Dichlorothiophenol, as it leaves our site, represents more than a batch number—it embodies the work of analysts, plant operators, logistics teams, and the chemists who answered hard questions to keep quality consistent. In the high-stakes world of advanced chemistry, that unity of expertise remains the best safeguard for both product performance and the reputation of those who rely on it. As demand for precision and reliability grows, our approach stays grounded in transparency, collaboration, and steady innovation.