|
HS Code |
668162 |
| Iupac Name | 4-[(4-hydroxyphenyl)disulfanyl]phenol |
| Common Name | 3,3'-Disulfanediyldiphenol |
| Molecular Formula | C12H10O2S2 |
| Molecular Weight | 250.34 g/mol |
| Cas Number | 2668-19-7 |
| Appearance | Off-white to light yellow powder |
| Melting Point | 170-174 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.38 g/cm³ |
| Smiles | C1=CC(=CC=C1O)SSC2=CC=C(C=C2)O |
| Inchi | InChI=1S/C12H10O2S2/c13-9-1-5-11(6-2-9)15-16-12-7-3-10(14)4-8-12/h1-8,13-14H |
As an accredited 3,3'-Disulfanediyldiphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3,3'-Disulfanediyldiphenol is packaged in a sealed, amber glass bottle with a screw cap, labeled with safety information. |
| Shipping | 3,3'-Disulfanediyldiphenol should be shipped in tightly sealed containers, protected from moisture, heat, and incompatible substances. Handle with appropriate chemical precautions. Ship according to applicable local, national, and international regulations, including hazard labeling. Use secondary containment to prevent leaks during transit and ensure proper documentation accompanies the shipment. |
| Storage | 3,3'-Disulfanediyldiphenol should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture, heat, and direct sunlight. Use appropriate chemical storage cabinets if available, and ensure containers are properly labeled. Always follow relevant safety and local regulatory guidelines for chemical storage. |
Competitive 3,3'-Disulfanediyldiphenol prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing chemicals like 3,3'-Disulfanediyldiphenol involves more than just keeping to a recipe. Experience with phenolic compounds, especially those containing sulfur bridges, gives a window into both the challenges and the payoffs of investing in specialized intermediates. We have seen customers across polymer, coating, electronics, and specialty additive fields come in looking for alternatives to standard bisphenols, driven primarily by demands for higher heat resistance, stronger adhesion, or enhanced oxidative stability. Over the years, we made it a priority to produce 3,3'-Disulfanediyldiphenol with a sharp eye on purity, reproducibility, and scale, all while responding to these highly specific needs.
Let’s start with some structure. 3,3'-Disulfanediyldiphenol, known by its CAS number 2668-19-1, connects two phenol rings with a disulfide bridge. Compared to simple bisphenols, this molecular tweak does a lot of heavy lifting. The sulfur-sulfur bond sits between the aromatic rings, creating a backbone with a distinct set of physical and chemical properties. Customers often ask how this compares to standard bisphenol A or its chlorinated cousins. One of the main things that sets this compound apart is how the disulfide linkage changes both flexibility and redox behavior, opening up possibilities that aren’t available with other common bisphenols.
Producing 3,3'-Disulfanediyldiphenol starts with careful raw material control, particularly with the sulfur reagents. Purity matters, because small traces of unreacted thiol or oxidized byproducts propagate downstream in resin production, affecting both shelf life and performance. Before scaling up, we spent months refining our crystallization protocol to ensure that the product consistently reaches assay requirements above 99 percent, with residual sulfur impurities well below 50 ppm. Water content can sneak in during final processing, but we use vacuum drying and a controlled environment to keep this below the detection threshold. Every batch gets run through HPLC and elemental analysis, because we’ve learned over the years that customers rarely have time to troubleshoot a bad intermediate.
Some of the polymer people we work with have shifted away from conventional dithiol-based hardeners for epoxy resins, choosing 3,3'-Disulfanediyldiphenol as a chain extender or modifier. The disulfide bridge gives cured resins better flexibility than their conventional competitors while still offering resistance to thermal degradation. We often hear from customers struggling with embrittlement in their composites, and the added toughness that comes from disulfide linkages gives their products a longer lifespan and better resistance to repeated stress. Formulators in electronics and copper-clad laminate factories have validated the compound for its thermal and oxidative stability. Featuring this material in solder mask and high-performance PCB substrates lets device manufacturers push operating temperatures higher, keeping failures low even under tough cycling.
In adhesives, we have seen 3,3'-Disulfanediyldiphenol enable higher wet adhesion, especially on metal and oxide-rich surfaces. The sulfur bridge imparts a natural affinity for transition metals, and its reactivity makes it a good candidate for vulcanization catalysts and adhesion promoters. Customers who came in using standard bisphenols for their adhesives often discovered that their products peeled or let go when exposed to moisture or mild acids. Once they switched to a disulfide-bridged variant, complaint rates dropped.
We’ve walked production lines and pilot plants alongside the technical teams of our customers, studying where the difference really shows up. For example, in the world of photoresists and photopolymers, many suppliers look for crosslinkers that handle both electron beam and thermal curing. The redox properties of the disulfide bond in our product make it uniquely suited to act as a co-initiator in certain UV-cured systems. Handled properly, 3,3'-Disulfanediyldiphenol participates in radical-induced crosslinking without causing premature dark curing, solving a problem that cost our clients real money in lost batches. Resin manufacturers using our product report improved shelf stability and fewer issues with premature hardening under storage.
Thermoplastics manufacturers setting up continuous lines want materials that run at higher temperatures and withstand mechanical loads over months or even years. The oxidative stability and resilience to chain scission that comes with the disulfide bond have impressed technical directors looking for alternatives to better-known bisphenols. Sometimes the conversations go beyond classical comparisons. For instance, as fire safety standards evolved, the halogen content in several common additives came under scrutiny. 3,3'-Disulfanediyldiphenol offered a non-halogenated route to comparable or higher flame retardance, giving customers peace of mind about reaching new benchmarks for RoHS or REACH compliance.
The pharmaceutical industry—always cautious about new intermediates—has tested our compound as a building block for sulfur-rich active pharmaceutical ingredients. In this field, the reproducibility of every batch stands paramount. We maintain batch records, analytical data, and full lot traceability for any pharmaceutical customer interested in validation, because in our experience, a claim of purity is only as valuable as the data behind it.
Production rarely stands still. Over the years, customers have brought us requests for custom particle sizes, improved filterability, or tighter color indices. Turbidity, residual iron contamination, and even bulk flow have turned into battlegrounds for downstream processability in specialty uses. After seeing the pain downstream, we invested in in-situ controls, applying real-time monitoring of pH and redox conditions to prevent color drift and metal contamination. Each customer batch report includes a breakdown on heavy metals and volatiles, not as a marketing gimmick, but because these numbers tell us—and our customer’s production chiefs—what to expect sharply and simply.
Stringent global regulations demand evidence and assurance. Major customers have asked if our 3,3'-Disulfanediyldiphenol meets limits on residual organic solvents and banned byproducts. We developed a solvent-recovery process that not only keeps emissions low but delivers a cleaner compound at the end. Independent audits have forced us to prove our product meets or beats current environmental and worker safety standards. Internal teams check final products for BTEX, PAHs, and any residues mandated by regional regulations. This isn’t an afterthought; regulatory noncompliance has real costs, and our investment in green chemistry practices has paid back through customer loyalty and smoother approvals.
Traceability remains a constant theme in specialty chemicals. We upgraded our documentation systems with batch-specific certificates of analysis, supported by independently validated labs. International customers, especially those supplying electronic, food-packaging, or medical sectors, require a level of transparency that off-the-shelf documentation can’t reach. Our own plant has responded by opening up on-demand batch records, so partners have direct evidence of compliance every time they order.
From sheet molding to top-tier high-frequency electronics, customers rarely stick to a single “ideal” grade. Granule size, melting point consistency, and dust suppression factor into every line restart and scale-up. We’ve adapted our production runs to offer a small, but meaningful, range of size cuts. Large-volume partners have required tailored drying and packaging, as some process lines suffered clogging with fines or bridging in standard drums and sacks. We field these requests with tweaks to drying cycles, optional anti-cake additives, and upgrades to liner systems. The effort pays off when clients report reduced downtime and cleaner plant audits.
Some of the largest demands land on logistics and shelf life. Specialty phenolics have a reputation for oxidation and color shift during storage. Years back we switched from open bins to sealed packaging flushed with inert gas, which stopped yellowing and surface crusting on products sitting for six months or more. Time and again, customers have expressed relief at pulling open a barrel of our product and finding it matches last month’s sample in both appearance and performance.
Discussions around “why use this compound” nearly always come back to the difference in the disulfide bridge. Compared to bisphenol A and bisphenol S, customers notice clear variations in both performance and handling. The disulfide linkage holds a delicate balance—too much reactivity, and storage stability becomes an issue; not enough, and downstream reactivity doesn’t deliver. Over years of refinement, we’ve tuned our process to keep oxidants and stabilizers at the necessary levels. This approach controls the redox profile of the product batch after batch.
In high-performance polymer applications, our customers have watched their resins maintain flexibility without sacrificing structural performance. In electronics, the added sulfur brings better bonding to metal substrates and improved resistance to thermal cycling. Adhesive producers report unmatched wet strength on stainless steel and aluminum surfaces, a point that most commercial bisphenols struggle with. Environmental compliance officers reading our data sheets find a lower halogen content, helping clients move into new markets where regulatory pressure keeps tightening.
While it’s tempting to just look at lab data, practical day-to-day use shapes these conclusions. Plant users handling thousands of kilos every week come back, not for theoretical advantages, but for the real operational benefits—less dust, more consistent flow, and fewer clogs. The biggest win comes from stable, high-purity lots, which allow process parameters to stay tight without frequent re-tuning. In very few cases do we see other phenolic monomers that offer the durability, flexibility, and safety profile of high-purity 3,3'-Disulfanediyldiphenol.
Long-term customers challenge us to improve continuously, not only in product but also in support. We keep close tabs on shifts in global regulations, customer preferences, and end-use requirements. As additive restrictions and performance standards evolve, so does our synthesis. Much of our innovation comes out of feedback—requests for lower extractables, faster dissolution in specific solvents, tighter color and clarity all drive our process tweaks.
We don't claim every customer will need 3,3'-Disulfanediyldiphenol, but those that do often find us after testing what other products cannot deliver. Customers who face high heat, repeated flex cycles, and need for metal compatibility in their products tend to discover the compound’s strengths right away. Some arrive after facing warranty claims due to inferior resin flexibility; others want to avoid halogenated alternatives.
It’s not enough to make a product and ship it. Each step, from raw material qualification to packaging and logistics, makes a difference downstream. We partner with our clients on new application trials, engage with R&D as they design next-generation products, and trace every lot from reactor to delivery. A point of pride stems from seeing a customer’s process line running better because of our upstream investments. This is where the expertise of a true chemical manufacturer shines—not simply in the ability to duplicate a molecule, but in ensuring that every gram stands up to the test of the real world.
Years of working with phenolic and sulfur chemistry have taught us that technical mastery and responsive manufacturing make the difference. 3,3'-Disulfanediyldiphenol stands as a testament to this approach, offering a platform for higher-value, safer, and more resilient products across industries. Each batch leaving our plant is backed by knowledge, real-world feedback, continuous improvement, and a commitment to customer partnership.
We welcome inquiries from partners looking to improve the performance, safety, or value of their products. Our experience shows that innovation starts with understanding—and we bring both the technical skill and hands-on manufacturing experience needed to deliver.