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HS Code |
913509 |
| Name | 1,3-Benzenedithiol |
| Cas Number | 108-98-5 |
| Molecular Formula | C6H6S2 |
| Molecular Weight | 142.25 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 261 °C |
| Melting Point | −13 °C |
| Density | 1.228 g/cm³ |
| Solubility In Water | Insoluble |
| Odor | Unpleasant, thiol-like |
| Refractive Index | 1.632 |
| Flash Point | 126 °C |
| Ec Number | 203-630-6 |
As an accredited 1,3-Benzenedithiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Benzenedithiol is packaged in a 25g amber glass bottle, securely sealed, labeled with hazard symbols and chemical details. |
| Shipping | 1,3-Benzenedithiol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. The shipment must comply with regulations for hazardous chemicals, using appropriate labeling and documentation. Transport should be by ground or air with certified carriers, ensuring spill containment measures and emergency procedures are in place during transit. |
| Storage | 1,3-Benzenedithiol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as oxidizing agents and strong bases. Protect it from light and moisture. Use secondary containment to prevent leaks, and clearly label the storage area as containing hazardous chemicals. Store under an inert atmosphere if sensitive to air. |
Applications of 1,3-Benzenedithiol in Industrial Manufacturing1,3-Benzenedithiol serves as a specialty intermediate in advanced industrial synthesis, supporting targeted molecular design in downstream manufacturing. As a direct producer, we ensure quality and traceability from origin to application, empowering key industries to integrate this compound for precise functionalization, performance improvements, and regulatory compliance. 1. Pharmaceutical API Synthesis: Sulfur-Containing MoleculesFunctionalization with thiol groups is critical for thiolated APIs, especially in the synthesis of biologically active compounds where aromatic dithiol moieties improve pharmacokinetics or serve as reactive handles in molecular scaffolds. Our material supports scalable operations where strict traceability and consistent purity have direct implications on batch outcomes and subsequent downstream validation. Industry compliance standards
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2. Corrosion Inhibitor Additive Formulation in Lubricant and Fuel BlendsCorrosion inhibition demands precise control of additive interaction with metal surfaces and fuel matrix compositions. Our benzene-based dithiol supports the design of high-affinity, sulfur-rich inhibitors for protecting pipelines, storage tanks, refineries, and offshore drilling equipment from degrading effects of moisture and electrochemical reactions by forming persistent molecular films. Industry compliance standards
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3. Polymer Crosslinking Agent for High-Performance ResinsAromatic dithiols act as functional crosslinkers, building higher network density and chemical resistance in specialty polymers or high-performance thermoset resins. This enables targeted tuning of mechanical and barrier properties in downstream plastics and composite products, particularly where sulfur bridging links or heat/solvent stability is essential for end-use reliability. Industry compliance standards
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4. Metal Surface Functionalization in Electronics ManufacturingThe dithiol compound provides dual-thiol surface ligands for forming self-assembled monolayers (SAMs) on gold or noble metal substrates, supporting advanced microfabrication and sensor device assembly. This process improves adhesion, electrical interface stability, and enables subsequent functional group attachments for nanoelectronic devices and biosensor chips. Industry compliance standards
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Every day on the production floor, the familiar scent of thiol signals that a new batch of 1,3-Benzenedithiol has just completed its intricate synthesis. This compound, recognizable by its molecular formula C6H4(SH)2 and CAS Number 108-98-5, stands out from other aromatic dithiols not just in structure, but also in how it behaves in demanding applications. Our crew takes pride in routinely shaping this molecule into the clean, high-purity product industries count on for reliability and repeatable performance. Consistency flows from strict process controls—without them, you don’t get the tight melting point, the nearly colorless to pale-yellow appearance, or the stable storage behavior that top researchers and engineers need.
Here, we manufacture 1,3-Benzenedithiol under carefully controlled, documented conditions. The key lies in our close management of each distillation and purification step. That results in a product characterized by a purity specification exceeding 99% as measured by gas chromatography. From packing to shipment, every lot passes rigorous quality checks for content, melting range, and absence of trace metal contaminants. No batch leaves our plant until it tests free of excessive oxygen-sensitive byproducts, which can interfere with applications. Many competitors offer similar grades, but we invest in removing odor-forming residues and trace water that can hinder downstream use. After years on the line, we know how even minor impurities can disrupt multi-step syntheses or compromise sensitive catalyst work.
1,3-Benzenedithiol, which some call meta-benzenedithiol or m-Benzenedithiol, plays several roles, but thiol-protected gold nanoparticle synthesis forms the core of its demand. In our experience, universities and electronics developers favor the meta-isomer for its ability to generate monolayers with a uniform packing density. Chain length and the positions of the thiol groups really make a difference—the meta isomer brings a unique reactivity profile when forming self-assembled monolayers (SAMs) on gold and silver substrates, compared to ortho or para isomers. Researchers working in surface chemistry have verified that meta connection sites moderate the spacing of the sulfur atoms, affecting both conductivity and binding efficiency. We receive positive feedback from teams fabricating molecular wires, sensors, and other advanced devices relying on this uniform coverage.
We’ve noticed that in copper corrosion inhibitors, meta-benzenedithiol holds a reputation for robust performance in aggressive environments. It adheres efficiently to metal surfaces, forming protective layers that limit oxidation even under harsh cycling. Our customers involved in oil and gas, as well as precision electronics, routinely request lot-by-lot certification of sulfur content and purity for such demands, underlining the necessity of tight process control on our end.
Anyone in our industry knows that dithiol chemistry comes with special challenges. Handling thiols safely and effectively, especially volatile, high-purity samples, takes experience. We’ve refined our techniques to minimize exposure to air and moisture, lowering byproduct formation and odor. The layout of our sealed reactors, transfer lines, and cold-storage rooms grew out of years refining the process. Each shift, our operators monitor pressure and temperature variations not just by equipment readings, but by the subtle changes that only hands-on workers recognize from years of experience. These behind-the-scenes details show up in downstream reliability. Customers working with competing samples often mention issues like unusually fast degradation, phase separation in organic solvents, or loss of surface reactivity—problems that trace back to lapses in purity or handling.
Where some facilities send out brownish or off-tone product, ours displays the near-white crystalline or needle-like structure researchers expect. Analytical labs often point out that our m-benzenedithiol stores with less discoloration — an indicator of lower residual acid and fewer catalyst remnants lurking in the material. This may seem minor, but with some three-component couplings common in organic synthesis, even ppm-level side products will foul yields and increase purification burdens. We’ve built our reputation by delivering well-behaved product, batch after batch.
Growing demand from advanced electronics, specialty polymers, and nano-materials manufacturers keeps us on our toes. Technological innovation in these fields has forced us to rethink everything from solvent selection to crystallization temperatures. For example, photonics researchers sometimes ask us to tailor physical characteristics, such as particle size, to facilitate dispersion in custom resins. We’ve responded by tweaking crystallization rates, mechanical sieving, and solvent exchange protocols. The feedback loop with laboratories and process engineers helps refine each production campaign, offering continuous improvement. Even the smallest step—say, a slight tweak in vacuum distillation—shows up as a boost in performance for users expecting world-class monolayer formation or chemical selectivity.
Drug discovery teams, though fewer in number, also approach us for meta-benzenedithiol as a building block for heterocyclic rings and custom ligands. In our process, we routinely screen for specific contaminants that might interfere with sensitive pharmaceutical synthesis, earning trust from these groups who’ve experienced problems with batch variability from less-focused suppliers.
After personally spending many years decanting and bottling finished product, our advice always rings practical. Store 1,3-Benzenedithiol in tight, light-resistant containers, under inert gas if possible. We use amber glass for shipping, and recommend immediate transfer under argon to minimize moisture uptake. Even small leaks compromise purity before the sample ever hits the lab bench. We recommend cold storage, ideally 2–8°C, which helps extend shelf life out beyond 12 months—our stability testing shows marked improvements over room-temperature storage in open air. If your process involves heating, ensure good ventilation and trap airborne residues to keep worker exposure in check. Spills clean up easily with adsorbent, but thorough decontamination matters, as sulfur-containing residues can persist on surfaces. Our own warehouse materials, from shelving to sealing compounds, have adapted over the years to handle the persistent thiol smell—a nuisance we now rarely encounter after refining our protocols.
Synthesizing 1,3-Benzenedithiol on scale demands both careful precursor selection and strict control of extraction and isolation steps. Early on, we adopted improved reduction methods that cut byproduct load from traditional sulfonation/reduction schemes. Today, selective catalytic hydrogenation and high-purity work-up solvents help us minimize sulfonic acid and disulfide byproducts—both culprits behind poor results in downstream applications. Our process was developed to mitigate odor emissions, reduce waste, and reuse solvents to limit our environmental impact. Over the years, we learned that not all sources of benzene sulfonic acids behave the same; trace heavy metals or halides in the starting material quickly foul the end product. Years of hands-on experience let us anticipate and catch these alterations long before they can sneak into our shipments.
We face special challenges scaling up, as increased vessel size brings new mass transfer and heating dynamics. Our engineers use sophisticated agitation and stepwise reagent addition—skills honed over dozens of campaigns—to guarantee every lot satisfies the target purity. At every checkpoint, we confirm structural identity not only by standard IR and NMR, but also by testing reactivity in model monolayer assembly or cross-coupling reactions. Many customers have switched to our product after finding other sources inconsistent batch-to-batch—a concern that traces back to variable small-scale laboratory practices unsuited to production scale.
Our support team stays in direct contact with researchers and manufacturers using 1,3-Benzenedithiol worldwide. We solicit feedback and routinely receive notes about higher efficiency in gold nanoparticle assembly, more predictable corrosion inhibition, and easier purification steps, compared to less-refined competitors. When incidents do occur, such as detection of low-level contaminants that slip through, our investigation traces root causes and leads to process upgrades. One example involved detection of trace iodide in a medical device customer’s downstream synthesis; pinpointing the issue to an upstream reagent shift helped us institute new supplier audits and analytical screens. This iterative approach strengthens both our product and the wider scientific community relying on it.
Several long-term partners use our product in organic electronics research, reporting higher charge mobility and device uniformity due to the predictable assembly behavior imparted by the clean meta-dithiol structure. Their published papers cite low background current and increased shelf-life for stored materials. We actively track literature, cross-examining public findings with our analysis to foresee evolving requirements. This cycle—engaging with researchers while constantly reviewing in-house data—sets our product lines apart and keeps them ready for future technical challenges.
Some believe all dithiols are interchangeable, but our years on the ground show otherwise. Differences between meta-, para-, and ortho-benzenedithiol go far beyond structural formulas. Positions of the thiol groups dictate the orientation and density of self-assembled monolayers, which in turn control electrical properties and chemical reactivity. Our analytical staff detect slight shifts in melting point and solubility in CH2Cl2, hexane, or THF, depending on batch purity and isomeric constitution. Those details decide whether a new organic device works, or an industrial corrosion inhibitor passes field tests.
We invest in differential scanning calorimetry and high-resolution mass spectrometry to verify every variable. Years of conversations with laboratory process engineers proved that even subtle off-target isomeric contamination can wreck a carefully designed experiment or slow down a pilot production run. Our obsessive attention to inventory storage and changed shipment methods over time to prevent cross-contamination, and proprietary barcoding allows for full traceability on every container. Production logs—painstakingly handwritten in the early days, now digitized—have become vital in debugging issues as they arise. This backstory, and continued reinvestment in process control, separates us from third-party resellers and bulk chemical traders who typically lack such a deep stake in their product’s outcome.
Our commitment to sustainability plays out in more than marketing slogans. Production of 1,3-Benzenedithiol generates specialized sulfurous waste streams; we recover and reprocess sulfur-containing solvents and minimize vented emissions through closed-loop systems. We run analytical screens on our effluents before discharge, as environmental compliance demands vigilance. Beyond compliance, we see waste reduction as an engine for cost savings and better workplace safety. Partnering with local recyclers and solvent manufacturers, we set up return cycles that lower our raw material footprint. Customers increasingly request full traceability, so we document every inbound shipment of reagents and every quality-control data point through our integrated management platform—a practice that helps clarify any questions raised years after delivery.
Looking ahead, we see the application scope for 1,3-Benzenedithiol expanding further into high-performance sectors. Biomedical device surfaces, new classes of conductive polymers, and next-generation photovoltaics all require a stable, pure, and predictable dithiol source. We stay in close contact with researchers scaling up from benchtop to pilot scale, offering technical support based on our direct factory experience. As specifications grow stricter and regulatory bodies demand more detail, we continue building on our legacy of hands-on, detailed chemical manufacturing. Our alignment with evolving research practices and feedback-driven process improvement keeps our product trusted among those who understand why purity, reliability, and deep manufacturing experience matter.
Crafting 1,3-Benzenedithiol is both a science and a craft. Our plant has grown with the world’s demand, adapting not just to the needs of specialty chemistry, but also to the lessons written in every well-documented batch record and every call from a chemist who counts on us for that one crucial detail. Those stories, told from our side of the manufacturing line, explain best why and how 1,3-Benzenedithiol stands apart from the crowd.