|
HS Code |
383341 |
| Cas Number | 2974-88-7 |
| Molecular Formula | C6H4Cl2S |
| Molecular Weight | 195.07 g/mol |
| Appearance | Yellow to brown crystalline solid |
| Melting Point | 39-41 °C |
| Boiling Point | 224 °C |
| Density | 1.49 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.636 |
| Flash Point | 107 °C |
| Synonyms | 2,3-Dichlorobenzenethiol |
| Smiles | C1=CC(=C(C(=C1)Cl)S)Cl |
| Pubchem Cid | 19033 |
| Ec Number | 221-017-6 |
| Odor | Pungent |
As an accredited 2,3-Dichlorothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2,3-Dichlorothiophenol, 25g," features hazard symbols, batch number, safety instructions, and tamper-evident seal. |
| Shipping | 2,3-Dichlorothiophenol is shipped in tightly sealed containers made of suitable materials, typically under inert gas to prevent oxidation. It should be packed and labeled following hazardous materials regulations, stored away from heat, sparks, and incompatible substances. Handle with appropriate personal protective equipment during transport to prevent spills or exposure. |
| Storage | 2,3-Dichlorothiophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to light, moisture, and extreme temperatures. Label the container clearly, and store it in a designated chemical storage area with secondary containment to prevent accidental release. |
Applications of 2,3-Dichlorothiophenol in Industrial Manufacturing2,3-Dichlorothiophenol serves as a critical intermediate in several specialized chemical manufacturing sectors. Our material integrates into downstream formulations where high purity, controlled reactivity, and consistent traceability are essential for large-scale production. The following scenarios outline its real-world applications in detail, including regulatory frameworks, processing flows, dosage specifics, and end-product types. 1. Agrochemical Active Ingredient SynthesisManufacturers use 2,3-Dichlorothiophenol as a key thiol building block in producing specific herbicide and fungicide actives. Its dual halogen and thiol functionalities allow selective substitution and coupling reactions during the assembly of certain triazole and chloroacetanilide-based molecules. The material directly supports stages requiring precise sulfur introduction under controlled reaction temperatures, with outcome quality dependent on raw-input trace impurities and batch consistency. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Pharmaceutical Intermediate ProductionDownstream pharmaceutical APIs that demand selective aromatic thiol functionality rely on 2,3-Dichlorothiophenol during early-stage intermediate assembly. Its controlled reactivity supports sequential halogen-substitution steps in the synthesis of molecules used in anti-infective and anti-inflammatory drugs, where purity profiles directly impact clinical reliability and regulatory approval rates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dye and Pigment Intermediate ManufacturingChemicals producers incorporate 2,3-Dichlorothiophenol in the synthesis of specialty sulfur dyes and metal-complex colorants. Its ortho-dichloro structure facilitates the creation of thiophenol-derived chromophore segments essential for color depth and stability in final pigments. Material purity and batch uniformity underpin both the intensity and fastness of finished dyes, particularly for textile and leather applications where regulatory controls on impurities and by-products are stringent. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Veterinary Active Ingredient ManufacturingChlorinated thiophenol structures form an integral part of certain veterinary API syntheses, particularly where targeted substitution reactions yield pharmaceutical agents for animal health formulations. 2,3-Dichlorothiophenol’s stable supply chain and traceable quality parameters meet the requirements of animal drug synthesis, where residual contaminant control and batch homogeneity affect eventual formulation and dosing accuracy for veterinary medicine markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Making 2,3-dichlorothiophenol starts in the same halls where we handle other demanding syntheses for the agrochemical and pharmaceutical sectors. Our batch reactors run with purpose here, and each run reflects years of fine-tuning. It’s not just a matter of mixing this or that. Care goes into the selection and pre-treatment of precursors, monitoring reaction kinetics, and capturing off-gases—details that stand between a clean batch and a problematic one. We’ve come to know every quirk in this chemistry, from the odor intensity to the risks of trace dibenzothiophene formation in certain conditions.
With 2,3-dichlorothiophenol, chlorine atoms sit on the benzene ring at positions two and three. The physical purity can make or break the outcome in downstream synthesis. Impurities like isomeric dichlorothiophenols—notoriously hard to purge—affect both the reactivity and the toxicity profile. A crowded supplier market delivers a range of variants; some are made with less control, leaving higher levels of these impurities. We use a sequence of vacuum distillation steps, sometimes two or three times per batch, until the assay consistently hits upwards of 99% by GC. Every batch matters, especially for active pharmaceutical intermediate makers, where contaminants invite compliance headaches.
2,3-dichlorothiophenol is used plenty in synthesizing crop protection agents and complex dyes. Customers working at the third and fourth stage of a synthesis count on each drum to behave identically. Subtle batch-to-batch variation unnerves them—this compound’s reactivity doesn’t forgive poorly controlled acidity or oxidizable byproducts. We've learned to collect and reprocess mother liquors rather than toss them, since they often contain recoverable product that, after scrubbing and redistillation, meets full-grade specs. Some of our oldest clients routinely ask about trace residue content—not just for technical curiosity, but because they’ve caught other vendors off guard with erratic purity profiles.
Process reliability and documentation back every shipment. We plot every assay curve and watch for the single aberrant batch. If a chromatogram flags a blip, our lab drills into it. Quality doesn't happen by accident here. Every operator gets training on solvent handling (with old-school safety drills, not just a SOP printout), since a single solvent swap mistake can drag a product out of spec and slow multi-ton campaigns by a week or more.
Some customers want this compound for sulfur-containing phenol intermediates—sometimes pharmaceuticals, sometimes agricultural actives, occasionally custom dyes. To each, the value of quality lands differently. The pharma crowd obsesses over possible trace halogenated side-products; a technical grade often will not pass muster. Agrochemical makers may tolerate more, but only up to a known threshold, since breakdown products can taint field trials or compromise shelf stability. Both prefer a supplier who backs up claims with lot-by-lot analysis rather than “standard” paperwork borrowed from a reference batch.
Tonnage buyers tend to set strict specs for melting point ranges, sulfur content, and total halide load. Not because the spec sheet says so, but because experience shows what types of trace organohalogens can end up in final actives. We learned early to tailor our reaction conditions—temperature ramps, base strength, time on stir—to pull the curve tight, rather than chase purity through late-stage fixes when problems already crept in. Improvements upstream in the process pay off downstream in less scrapped material. Some colleagues who work in pharma synthesis tell us the difference between an easy day and a headache comes down to this product’s melt point holding steady within a narrow band.
Many European and North American buyers used to accept generic imports of dichlorothiophenol, not paying close attention to where the chlorine atoms landed on the ring. That created problems in consistency and sometimes in legal compliance. The 2,3-isomer carries particular reactivity compared to its 2,4- or 2,5- cousins; the way it enters nucleophilic substitution or coupling reactions is different. The position of those chlorine atoms isn’t trivial. With 2,4-dichlorothiophenol, for example, you might see easier off-target alkylation, which rarely works for the syntheses certain plant protection agents demand.
We’ve encountered odd batches from the global market—off-odors, low melting points, even an iridescent cast from trace polychlorinated phenolic impurities. Domestic regulations started catching up once downstream users reported anomalies. Now, we support each shipment with batch-level documentation and welcome technical audits by our clients. There’s no substitution shortcut for getting the right isomer, made with controls tight enough that each lot stays in spec no matter how big the campaign gets.
Differences show up fast in end use. In our own applications lab, we measure the way our 2,3-dichlorothiophenol behaves in forming thioether linkages and compare it with the performance of 2,4- and 2,5- analogues under identical conditions. The results are never interchangeable. A sharp drop in yield with the wrong isomer, or the appearance of unexpected side products, tells us as much as a thousand words on a data sheet.
Rising calls for sustainable chemistry don’t leave compounds like 2,3-dichlorothiophenol untouched. Our customers in Europe and North America often ask for assurance that we don’t run afoul of REACH or other regional guidelines that have specific limits on polychlorinated biphenyls and dioxins. We've invested in continuous monitoring to assure negligible emissions, rerouting spent gases through multilayer scrubbing towers. Not a glamorous detail, but an important one when regulatory eyes regularly review stack emissions and wastewater logs.
Some in our industry have looked for greener pathways, like using alternative chlorination reagents or reclaiming chlorine from waste streams, but these efforts rarely bring down production costs and often introduce unpredictable byproduct patterns. A few of the “green chemistry” pilots yielded product outside of critical melting point specs—good enough for research, not for scaled industry. Based on our experience, established chlorination still rules the day for assuring quality and price-point stability.
Over the last decade, consolidation among raw material suppliers made sourcing precursors for 2,3-dichlorothiophenol more competitive. Some years, lead times double. We built up qualified supplier lists across three continents, verified for both quality and reliability. This way, production rarely lags even when regional political events or energy shifts cause price swings in benzene, sulfur, or chlorine supplies.
It’s not lost on us that a quality failure in such a highly reactive compound can cause far-reaching headaches. We still get requests from users burned by off-spec arrivals: resinous mass in the drum, failure to dissolve, or, worst of all, new impurity peaks in their downstream API projects. Years ago, we partnered directly with customers’ R&D teams, drilling into how our product behaves in their syntheses. Open data-sharing—HPLC traces, impurity maps—proved more convincing than a certificate-of-analysis with vague numbers. This back-and-forth helped us improve base washing and vacuum cycling, leading to better and more consistent output.
We shy away from fancy packaging choices. Instead, our focus is on containment and transit predictability. Sealed fluorinated drums keep ambient air and moisture out, since hydrolysis—even slightly—risks corrosive byproducts. Tanks shipped by sea stand up to weeks in changing climates; we track in-transit temperatures and humidity because the first sign of swelling or yellowing tells us something slipped at the packaging stage.
It took trial, error, and tough reviews from more demanding clients to get this part right. Lessons came from minor incidents, not big disasters: a single misfit drum cap, a tag unreadable after customs inspections, a lading slip with the wrong UN code. We now log and double-verify each shipment, because a lost or mislabeled drum causes regulatory paperwork that burns days and angers downstream users who can’t afford a stoppage.
Not all chemical manufacturers are the same. We bring years of specialization, with batch-to-batch tracking built into every aspect of our process. Routine pre-sale and after-sale support lets technical teams reach the right chemist, not a salesperson. Our clients often call with synthesis questions about reactivity with their chosen halogenated or nitrated partners; our applications support team gives real-world troubleshooting, not copy-paste advice from a spec sheet.
Documented process transparency anchors both trust and regulatory comfort. Customers in Germany care deeply about REACH registrations, and those in the US need assurance on EPA limits. Our internal compliance team keeps tabs on the changing global regulatory landscape, and we don’t wait for customer complaints before responding to shifting standards. This approach protects long-term relationships and stability in supply, even when the market shifts or governments recalibrate compliance criteria.
Raw material volatility sits at the top of challenges for most chemical manufacturers. Rather than hedge futures, we diversified suppliers and invested in expanded on-site storage. These steps cushion us from sudden outages in the benzene or sulfur market. We also constantly monitor in-plant yields for signals that a precursor’s spec has drifted—small differences in supplier purity levels affect final assay values. By building traceability into every tank and drum, we reduce the risk of a small error scaling up into a major product recall.
Handling chlorinated sulfur compounds carries clear risks: exposure, spills, and the odd exothermic runaway. We run regular training on live scenarios for our operators—responding to venting, swapped supply lines, or a missed phase cut in a batch sequence. Roots of process safety lie in muscle memory, not just checklists.
Waste treatment needs real consideration. Spent reaction mixtures too rich in organochlorines go through both neutralization and multi-stage stripping before release. The cost is not trivial, but there’s no shortcut that doesn’t lead to compliance failures.
Customer problems don’t always come tied to a specification. We’ve responded to concerns in the field, such as off-smells during product use, minor phase separation in older product, and the unwanted presence of a trace impurity after months in storage. Open conversations—with sample batches supplied for joint troubleshooting—helped us isolate causes, update internal specs, and improve protocols for packaging and shipment. This back and forth with end users gives us ground-level insight that guides our continuous improvement.
Supplying 2,3-dichlorothiophenol is about more than just controlling process parameters or delivering a chemical in a steel drum. We supply clients who use this compound in the synthesis of key intermediates, pest control agents, and dye manufacturers. Each group brings a different set of problems, asks distinct questions about impurity carryover, and presses their own priorities about shelf life and compliance.
We’ve learned that durability in this business depends on listening. End users in agriculture repeatedly ask for detailed impurity maps; pharma buyers check for residual halogenated aromatics at sub-ppm levels. Rather than send out a generic certificate, we tailor analytical results to their own needs, sometimes running custom analyses or reference syntheses to assure the 2,3-dichlorothiophenol performs flawlessly in their real-world processes.
Long-term, our role as a manufacturer links both trusted chemistry output and a willingness to take feedback on product performance. We hold ourselves to a simple standard: every kilo of 2,3-dichlorothiophenol shipped matches the expectations of experienced customers—on assay, on processability, on safe handling, and on regulatory risk. Our own experience makes clear that shortcuts in this area always show up downstream, and so we invest in getting the first steps right.
Experience drives improvement. As the field continues to evolve, new purity demands appear, in line with stricter standards imposed by both the pharma and agrochemical worlds. Our work isn’t finished. We actively invest in process developments, more precise analytic methods, and tighter controls at every stage of synthesis and shipment. Expertise is never static; lessons from the drum floor and the application lab shape every step forward in 2,3-dichlorothiophenol production.