|
HS Code |
176399 |
| Cas Number | 133-63-1 |
| Molecular Formula | C6H4Cl2S |
| Molecular Weight | 195.07 g/mol |
| Appearance | Light yellow to yellow solid |
| Melting Point | 49-53°C |
| Boiling Point | 252°C |
| Density | 1.44 g/cm³ |
| Refractive Index | 1.607 |
| Solubility In Water | Insoluble |
| Flash Point | 110°C |
| Smiles | Clc1ccc(S)cc1Cl |
| Synonyms | 2,5-Dichlorobenzenethiol |
| Odor | Strong, unpleasant |
| Purity | Typically ≥98% |
| Storage Conditions | Store at room temperature, tightly closed |
As an accredited 2,5-Dichlorothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,5-Dichlorothiophenol is supplied in a 25g amber glass bottle with a secure, chemical-resistant screw cap and safety labeling. |
| Shipping | 2,5-Dichlorothiophenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The packaging complies with international and local regulations for hazardous materials. The shipment is labeled with appropriate hazard warnings (toxic, corrosive), and handled by trained personnel, ensuring safety during transport and storage. |
| Storage | 2,5-Dichlorothiophenol should be stored in a cool, dry, well-ventilated area away from sunlight, moisture, and incompatible substances such as oxidizing agents and acids. Keep the container tightly closed and properly labeled. Use corrosion-resistant containers. Store in a designated chemical storage cabinet, preferably for toxic or corrosive substances, and ensure access is limited to trained personnel only. |
Competitive 2,5-Dichlorothiophenol prices that fit your budget—flexible terms and customized quotes for every order.
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2,5-Dichlorothiophenol is a fine example of modern chemical manufacturing focused on both reliability and consistent quality. In our years behind the reactors, we’ve witnessed how the unique blend of two chlorine atoms and a thiol group unlocks distinctive properties. The compound’s formula, C6H3Cl2SH, seems straightforward. Yet the subtle difference of having substitutions at the 2 and 5 positions on the benzene ring influences its reactivity and selectivity in ways that bring value to synthesis and formulations. At our plant, we produce this compound in a clear, off-white to pale yellow crystalline form, a sign that the process has gone as it should.
For customers working in research or specialized industrial applications, we focus on providing 2,5-Dichlorothiophenol that meets defined purity targets, often upwards of 98%. Our years of operating glass-lined and stainless steel reactors taught us that the purification stage matters just as much as upstream synthesis, so quality control teams test every lot for limits on water, residual solvents, and trace metals. Typical melting points land between 39-42°C, with minimal deviation, and our in-house GC-MS profiles back each batch’s identity. Packaging choice affects stability over long hauls, so we rely on chemically inert bottles that withstand accidental knocks and minimize waste from degradation or leaks.
Our team has met enough seasonal temperature swings and humidity spikes to understand how storage or handling can cause off-odors, yellowing, or even impurity spikes. Through trials, we optimized conditions not just out of theory, but out of feedback from applied labs, agrochemical developers, and custom synthesis partners. This experience guides decisions behind solvent removal, inert gas blanketing, and selection of desiccants for long-term containment. Where some products only claim purity, we track it through batch logs and customer feedback, seeing the impact in reaction yields and downstream product integrity.
Our main clients include custom synthesis houses, pharmaceutical intermediates manufacturers, and fine chemical developers. Feedback from those applying 2,5-Dichlorothiophenol in thiol-based coupling reactions and heterocyclic assembly helped shape our own process design. This compound’s strong nucleophilicity and selective reactivity with electrophilic reagents make it a popular choice in stepwise organic synthesis, especially for producing sulfur-containing aromatic intermediates. Many value its performance in creating tailor-made herbicides, dyes, and even some odorant molecules for safety industries. In R&D settings, it frequently serves as a building block during early-stage drug discovery and as an active intermediate for certain crop protection agents.
Distinguishing 2,5-Dichlorothiophenol from its positional isomers and analogues helps chemists choose the right reagent for their protocol. Chemically, analogues like 2,4-dichlorothiophenol or 2,6-dichlorothiophenol show subtle but significant shifts in reactivity because chlorine substituents at different ring positions either activate or deactivate aromatic substitution and alter electron density. In practice, some users report that 2,5-dichloro isomers allow for more controlled downstream chemistry, especially where ortho or para effects matter for selectivity. Compared to mono-chlorinated thiophenol, the dichloro variant displays higher chemical stability in storage, with less tendency to oxidize or volatilize, translating to lower handling-related loss. This has been confirmed in our long-term storage studies and reported by clients running scale-up projects who noticed improved shelf-life.
Unlike generic thiophenols, the double chlorine groups impart increased electron-withdrawing character, affecting pKa and favoring processes where suppressed side reactions make or break an entire synthesis. For example, customers attempting certain nucleophilic aromatic substitutions found that the specific substitution pattern of the 2,5 variant eliminated extraneous ring activations, leading to higher-purity end products. In dye manufacturing, this difference alone can mean more vibrant final pigments and less need for downstream purification.
As a manufacturer who moves several tons per year, we learn from each client’s hurdles. Some report miscibility issues when using traditional solvents, leading us to optimize our drying and packing. The volatility of thiophenols, along with their characteristic odor, poses workplace challenges. Our facility design includes dedicated exhaust systems and scrubbers based on air flow models tested during several pilot batches. During scale-up with customers, we found that slow addition of the compound under cooled conditions controls exotherms and minimizes side product formation. These steps reflect years of troubleshooting and direct collaboration with experienced chemists on the user end.
Some feedback flagged concern about degradation products in older lots, especially under high humidity. We responded by switching to batches where residual moisture never exceeds 0.1%. Not every change was easy: transitioning to high-purity nitrogen blanketing required replacement of legacy valves and seals, and shipping protocols had to meet both local regulations and customer-specific demands. This history means that our product remains trusted even by long-term buyers who remember earlier challenges and appreciate the honest, practical approach we bring to supply and support.
Legislation for chemical handling and shipment changed considerably over the past decade, especially for compounds with strong odors or reactive groups. We navigated updates in international chemical transportation guidelines, making sure documentation and packaging stood up to regulatory audits. We check every outgoing shipment for labeling accuracy, from UN numbers to hazard pictograms, and back that information with on-request batch data. Quality assurance rests not just on routine batch testing, but awareness of customer audits and random third-party checks. Errors, even rare ones, lead to both in-house review and open reporting with affected clients. This way of working is not just good practice, it’s an expectation shaped by real-world partnerships.
Consistent feedback is that batch-to-batch consistency outpaces that of some regional competitors. Our repeat buyers—ranging from midsize labs developing patent filings to industrial scale partners—comment that the streamlining of order fulfillment and documentation adds as much value as the substance itself. It’s not enough to claim stock; actual production scheduling and real-time tracking keep shelves full when others post “out of stock” notices. Adjustments, such as shifting shift patterns to handle demand spikes at planting or patent deadlines, grew out of open communication and decades of market learning.
On rare occasions when a customer flagged a spec discrepancy, the response involved both immediate investigation and shared root-cause analysis. Product recalls, though infrequent, have always proceeded with minimum red tape. We learned that transparency upfront—sharing COA details before order confirmation, not just on delivery—builds trust and minimizes surprises. Customers using automated feed systems especially appreciate our attention to granule uniformity and batch labeling, which shrinks downtime and waste.
Many users find that reactivity with certain electrophiles can lead to unexpected byproducts unless careful control of temperature and solvent polarity is maintained. Over the years, we recorded several field reports highlighting the impact of subtle formulation tweaks. For instance, slightly drier solvent and controlled base addition can improve conversion yield by up to 5–8% for some coupling reactions, according to collaborative projects with pesticide formulators. Based on these partnerships, our technical support includes real-world tips tested at both bench and industrial scale. For particularly sensitive transformations, we provide additional batch data on minor impurities or trace metals, since past cases linked unexpected side reactions to trace contaminants below standard reporting thresholds.
Waste management from thiophenol residues—a common headache—also prompted us to connect clients with disposal specialists versed in sulfur chemistries. Our plant has piloted byproduct recovery schemes based on these conversations, funneling certain streams towards internal recycling or safer oxidation before neutralization. Many customers, especially those under stricter environmental scrutiny, look for suppliers who demonstrate not just product stewardship, but improvements in process waste handling rooted in lived experience and plant investment.
Our technical support builds directly from what we learn in our own operations and from customers who bring back process feedback. It’s become routine for our chemists to troubleshoot synthetic bottlenecks or suggest tweaks for cleaner reaction profiles. The on-site team fields questions ranging from apparatus fouling to solvent compatibility. We learned long ago that direct phone calls solve more problems than endless looped email chains or digital ticketing. Application-specific advice—whether advice on reactor charging protocols, solvent swaps, or quenching procedures—grows out of cumulative handling and observation, not merely theoretical best practices.
We’ve helped multiple clients develop tailored extraction methods for isolating product from tough matrices, often sharing insights from our lab scale optimization runs. When clients report back successful tweaks or faster workup methods, we often build those into our in-house documentation. This information ends up guiding not just new buyers, but existing partners who take on new projects with daunting targets.
Advances in agrochemical and pharmaceutical development added new demands for purity and documentation. In the past five years, researchers synthesized increasingly complex molecules, with heightened need for ultra-pure building blocks. We address this trend by continuously updating our analytical programs, broadening NMR, LC-MS, and non-routine impurity testing. Open communication with formulators lets us anticipate new analytical requests or delivered forms (such as pre-dissolved concentrates or custom blends).
Sustainability pressure affects suppliers throughout the chain. We took action on greener process alternatives: reviewing routes starting from less hazardous chlorinating agents, recycling spent solvents with modern distillation skids, and leveraging catalysis for improved yields. While many suppliers talk about green chemistry, adopting changes requires risk-taking and full buy-in from plant staff. Over several pilot campaigns, we transitioned to cleaner fuels for boiler units and paired these with remote emissions monitoring. These steps cost time and capital but, as feedback from both customers and on-site personnel suggests, result in safer, more responsible supply.
Over the years, buyers expressed surprise at the performance boost of using carefully controlled batches for reactions where run-of-the-mill substitutes didn’t perform as needed. We see this most clearly in projects where selectivity, low impurities, or minimal off-odors directly affect final product quality. Those working on exploratory chemistry or niche formulations especially benefit from working closely with a source manufacturer willing to respond directly to technical and logistical challenges.
Trust in a supply partner, especially for high-impact intermediates like 2,5-Dichlorothiophenol, is built not only through reliability, but also through continuous knowledge sharing and transparent incident response. Across thousands of kilos and countless transactions, our team works to capture problems, collect user insights, and circle this hard-won information back into product improvements. As chemistry and regulation evolve, so do the expectations for clarity and partnership from those who run the reactors and fill the drums.
Our engagement with clients extends into joint development of new derivatives and custom blends. Increasingly, those in fine chemical and pharmaceutical development seek not just standard off-the-shelf products, but modular building blocks for fast-changing project needs. The in-house R&D group, staffed by chemists with both plant and lab backgrounds, coordinates these projects not by copy-pasting existing processes, but by tailoring solutions informed by what worked (or didn’t) for similar targets in the past. No process is static, just as market needs keep shifting.
Moving forward, industry trends point to growing demand for detailed documentation, cleaner production routes, and support packages based on end-use risk and regulatory complexity. Building new capacity for 2,5-Dichlorothiophenol remains a continual process, guided by direct buyer input and firsthand lessons learned on plant floors. As expectations move higher, we adapt, learning from both the tough days and the successes shared by everyone handling this complex molecule from start to finish.