|
HS Code |
717184 |
| Iupac Name | 4,4'-(1,1-Dioxido-3H-2,1-benzoxathiole-3,3-diyl)bis(2-chlorophenol) |
| Molecular Formula | C18H10Cl2O4S |
| Molecular Weight | 409.24 g/mol |
| Cas Number | 3346-97-0 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 215-218°C |
| Solubility In Water | Insoluble |
| Boiling Point | Decomposes before boiling |
| Density | 1.55 g/cm³ (approximate) |
| Synonyms | Dichlorfenil, 2,2'-Dichloro-4,4'-sulfonylbisphenol |
| Pubchem Id | 2898 |
| Flash Point | >250°C |
| Logp | 5.78 |
| Smiles | C1=CC(=C(C=C1Cl)O)C2=C(C3=CC(=C(C=C3S(=O)(=O)O2))Cl)O |
As an accredited 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25-gram amber glass bottle, sealed with a screw cap, and labeled for chemical laboratory use. |
| Shipping | The chemical 4,4'-(1,1-Dioxido-3H-2,1-benzoxathiole-3,3-diyl)bis(2-chlorophenol) is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous material, requiring compliance with local, national, and international transport regulations. Appropriate labeling and documentation accompany each shipment to ensure safety and regulatory compliance. |
| Storage | Store 4,4'-(1,1-Dioxido-3H-2,1-benzoxathiole-3,3-diyl)bis(2-chlorophenol) in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Clearly label the container and ensure access is restricted to trained personnel. Follow standard laboratory chemical storage protocols. |
Competitive 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Our team has been manufacturing 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) for several decades at our dedicated facility. Those familiar with specialty chemicals know how challenging it can be to obtain high-purity benzoxathiole structures, especially where functional groups like 2-chlorophenol are positioned with precision. Our technicians work with carefully sourced feedstocks, and we monitor each stage—starting from raw material verification, through stepwise oxidation, cyclization, and ending with high-vacuum purification.
What separates this compound in practical use comes down to stability, solubility, and functional application. We pride ourselves on delivering material that consistently displays bright off-white granules, low impurity profiles, and reliable batch homogeneity. Analytical reports show a typical purity of 99% and a moisture content controlled under 0.2%. Consistency doesn’t just come from routine; it grows from an understanding of how even a small deviation introduces headaches downstream. We have witnessed firsthand what trace contaminants do to process yields during scale-up.
Manufacturing this benzoxathiole derivative presents less leeway for error than many aryl-substituted phenols. We work with melting points consistently within a 3°C spread, checked by automated DSC analysis. Bulk density and particle size distribution make a real difference for customers measuring in grams or tons. Several users in advanced polymer systems prefer a tighter sieve cut, so we calibrate milling equipment to pass through a 100-mesh screen. Clumping must be avoided since bridging during automated dispensing disrupts the entire batch schedule. We ship in both fiber drums and multi-layer antistatic liners.
Solubility in organic solvents such as dichloromethane and DMF enables compatibility with a wide range of formulating processes, which matters more than most realize before upscaling. We periodically test for trace organic byproducts using two-dimensional GC-MS and confirm structure integrity by NMR, since even minor byproduct uptake tends to compromise the targeted performance in end-use applications.
Our experience with 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) began in resin modification, but end-users have taken it much further. The unique bis(2-chlorophenol) configuration activates sites on the polymer backbone that aren’t achievable with simpler chlorinated phenols or even other sulfone-bridged analogues. The result is greater thermal resilience and chemical compatibility. Finished resins show tighter crosslinking, improved flame retardancy, and higher resistance to UV degradation. This direct feedback loop with formulators has been invaluable, as we’ve adapted our process in response to bottlenecks shared by technical teams.
For the engineered plastics segment, real success comes from replacing legacy stabilizers and phenolic antioxidants with this compound. In-house testing—benchmarked against conventional bisphenol and non-halogenated options—shows an uptick in high-temperature creep resistance, particularly important for aerospace-grade polyimide and PEEK blends. Some teams report increased transparency in finished films, which has encouraged demand within specialty optoelectronic substrates.
Chlorinated diphenol-based additives such as this aren’t limited to polymers. Our partners in industrial coatings find that this molecule delivers outstanding barrier properties, especially when curing at elevated temperatures. Precisely matched melting and softening points allow for easy blend-in during compounding.
The pharmaceutical and agrochemical sector, always searching for novel building blocks, has found the reliability of our product’s purity profile enables straightforward derivatization. Lower impurity loads reduce post-synthetic purification, saving hundreds of hours of labor in pilot and kilo-lab facilities yearly.
The main differences relative to more common bisphenol or simple phenol compounds can be traced to the sulfone group at the core and the dual 2-chlorophenol arms. We’ve confirmed, in our own thermal analysis, a marked increase in decomposition temperatures compared to bisphenol A, making this material a more robust choice for formulations exposed to harsh environments. While Bisphenol F exhibits decent thermal stability, the added electron-withdrawing sulfone and ortho-chlorine groups in our compound extend performance windows and help suppress undesirable free-radical generation.
Within the sulfonated aromatic family, alternatives often bring non-uniform color, larger particle sizes, or higher residual solvent content. Consistency takes a back seat when supply chains shift. We’ve had to step in as a direct source for end-users who switched from bulk resellers and noticed new problems: lumpy dispersions, unpredictable haze in films, or a yellow tint in high-purity polymers. Our direct control over quality and traceability accounts for reduced troubleshooting cycles.
Some resin manufacturers opt for less chlorinated options to address regulatory and downstream biodegradability, yet performance losses become obvious under even moderate stress. This compound, on the other hand, achieves a balance between regulatory requirements and end-use reliability when appropriately applied in non-food, industrial uses. We review regulatory updates proactively and maintain transparent reporting, so partners make informed decisions on formulation strategies.
From a manufacturing standpoint, producing 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) calls for rigorous equipment maintenance and staff training. Every production batch represents years of accumulated knowledge—from glass-lining kettle internals to avoid contamination, to real-time HPLC monitoring during sulfonation steps. We have seen how overlooked minor process variables—like local humidity, feedstock color, or agitation speed—can spiral and affect purity, flow properties, and shelf-life. Batches flagged for deviation are never released.
Learning from a decade of customer feedback, we instituted fully segregated production lines for different chlorine loadings. Maintaining sharp separation between product families helps prevent cross-contamination, the source of much frustration among compounders. Each drum is accompanied by a certification of analysis listing batch, analytical technique, and chromatograms.
Since the structure incorporates both sulfone and chloro-aromatic functionalities, waste streams carry extra compliance obligations. Our plant manages these effluents through closed-loop solvent recovery and on-site neutralization. We view environmental compliance as an extension of product integrity: trace residuals are tracked until verified neutralized.
Those who specify this product often arrive after a bad experience with cheaper substitutes. Value comes from lower troubleshooting overhead and higher yields over multiple production cycles. Fast, reliable deliveries matter more to our partners than marketing brochures ever could. We maintain forward inventory in several regional warehouses, reducing supply volatility and improving planning. While chemists care about structure and purity, plant managers insist on steady drum availability, calibrated to seasonal demand swings.
We have built long-term partnerships not by just shipping product, but by listening to reports from the field—whether it’s a line shutting down due to dust contamination, or a color drift in the masterbatch output. These insights cycle back into our process development. It isn’t glamorous, but this is where quality originates. The most expensive mishaps happen in implementation, not in the spec sheet.
Materials science progresses by iterating on technique and chemistry. Trends in the advanced materials world demand finer particle sizes or lower halogen content. In our shop, lean process initiatives and new filtration technologies help us meet these evolving needs. We see increasing requests for compliance documentation, such as full origin tracing and impurity mapping, especially from multinational customers in electronics and aerospace.
We take part in technical consortia examining both new applications for benzoxathiole chemistry and emerging environmental requirements. Several customers are running trials substituting polybrominated additives with our sulfone-bridged product. Their results reinforce what we see in our own QA data—this compound offers a route to both fire retardancy and lower toxicity hazards.
Manufacturing new compounds is always a process of refinement. Our chemists are already piloting derivatives with alternate halogen distributions and new blocking groups, steering the chemistry toward higher performance and lower environmental impact. Customer requests often set our R&D schedules. When someone asks, “Can this be made with a narrower melting range?”—we don’t see it as a niche request, but as part of our roadmap for the next generation.
The work involved in making, packaging, and delivering 4,4'-(1,1-Dioxido-3H-2,1-Benzoxathiole-3,3-Diyl)Bis(2-Chlorophenol) creates value far beyond the drum. Each shipment draws on years of experience, lessons learned from both success and failure, and direct dialogue with users who push the boundaries of polymer, electronic, and industrial chemistry. The product’s technical profile stands out, but it is the everyday vigilance—batch by batch, drum by drum—that matters most to our reputation.
We welcome ongoing conversations, audits, and feedback, not just as compliance, but as part of a culture built around continuous improvement. We keep learning, troubleshooting, and improving, so partners and customers can count on consistency, reliability, and fresh solutions for new ideas in high-performance materials.