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HS Code |
674620 |
| Chemical Name | 4-(1,3-Dithiolan-2-Yl)Phenol |
| Molecular Formula | C9H10OS2 |
| Molecular Weight | 198.30 g/mol |
| Cas Number | 263177-30-4 |
| Appearance | White to off-white solid |
| Melting Point | Approx. 93-97°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1CSC(S1)C2=CC=C(C=C2)O |
| Inchi Key | OKUGFJCAENBJDE-UHFFFAOYSA-N |
As an accredited 4-(1,3-Dithiolan-2-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, secure screw cap, chemical label displaying “4-(1,3-Dithiolan-2-Yl)Phenol,” 25g net weight, hazard warnings, and handling instructions. |
| Shipping | 4-(1,3-Dithiolan-2-yl)phenol is shipped in sealed, chemical-resistant containers to prevent moisture and air exposure. Packaging complies with regulations for hazardous materials. Transportation is arranged via ground or air, labeled appropriately for chemical safety, with safety data sheets included. Handle with care, avoiding extreme temperatures and direct sunlight during transit. |
| Storage | Store **4-(1,3-Dithiolan-2-yl)phenol** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and moisture. Keep away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and physical damage. Label the storage area clearly, and ensure appropriate spill containment materials are available nearby. Use only with proper personal protective equipment. |
Applications of 4-(1,3-Dithiolan-2-Yl)Phenol in Industrial Manufacturing4-(1,3-Dithiolan-2-Yl)Phenol supports advanced chemical synthesis and specialty material manufacturing across several tightly-defined industrial sectors. As a direct manufacturer, we supply this intermediate to customers requiring consistent quality, traceable origin, and strict technical documentation. 1. Antioxidant Additive for Lubricant FormulationIndustrial lubricant producers add 4-(1,3-Dithiolan-2-Yl)Phenol as a phenolic antioxidant to synthetic and mineral oil lubricating blends. This compound stabilizes base stocks against thermal degradation and oxidative stress in high-temperature environments such as automotive engines, gearboxes, and heavy machinery. Formulators select this additive during the compounding stage, assessing precise dosage by end-use performance targets and OEM qualification tests. Advanced process control and continuous blending support reproducibility, while ongoing quality control ensures low batch variation and consistent additive performance. Industry compliance standards
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2. Polymer Stabilizer for Engineering ThermoplasticsIn plastics and polymer compounding, 4-(1,3-Dithiolan-2-Yl)Phenol functions as a high-performance stabilizer to protect against heat- and light-induced degradation. Formulators employ this additive in polyolefins, polycarbonates, and engineering resins to extend service life, preserve mechanical strength, and enhance color retention. Precise dosing takes place in extrusion or compounding lines using gravimetric feeders, and compatibility checks ensure no migration or phase separation in complex blends. Processors maintain compliant records and batch traceability for regulated applications such as automotive or electrical parts. Industry compliance standards
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3. Intermediate for Specialty Agrochemical SynthesisMajor agrochemical manufacturers use 4-(1,3-Dithiolan-2-Yl)Phenol as a core intermediate during the synthesis of select fungicidal and insecticidal actives. Integrated into multi-step batch and flow chemistry lines, the compound undergoes controlled transformations such as halogenation, alkylation, and coupling reactions. Every reaction step requires in-process verification and mass balance monitoring to meet regulatory and purity thresholds. Technical documentation and sample retention support audit readiness and registration in global crop protection markets. Industry compliance standards
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4. Precursor for Electronic Chemicals in Photoresist ProductionSemiconductor and printed circuit fabrication utilize derivatives of 4-(1,3-Dithiolan-2-Yl)Phenol as crucial intermediates for photoactive compounds in positive and negative photoresists. These application-specific materials demand ultra-high purity with tight controls on trace metals and organic impurities. Integration involves closed-system transfer, filtration, and microreactor steps, verified by in-house QC using ICP-MS and HPLC. Batch records, validation documents, and change control submissions support regulatory and customer audits within the electronics supply chain. Industry compliance standards
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5. Modifier in Epoxy Resin Hardener SystemsProducers of high-performance epoxy systems incorporate 4-(1,3-Dithiolan-2-Yl)Phenol as a reactive diluent or hardener modifier to tune curing kinetics and improve chemical resistance. This chemical enables formulators to adjust open time, modulus, and heat distortion temperature in formulated epoxies used for industrial coatings, adhesives, and composites. In-plant quality control confirms solid content and epoxy equivalent weight to ensure downstream performance for aerospace, marine, and construction sectors. Industry compliance standards
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Producing 4-(1,3-Dithiolan-2-Yl)Phenol takes more than following a formula—it demands hands-on understanding at every step. The molecule, with CAS number 65661-36-7, draws a lot of interest from professionals in specialty chemicals, pharmaceutical intermediates, and materials science for its unique combination of functional groups. Over years of refining both process and quality control, our facility has learned the nuances of this compound. Each batch reflects this attention to detail, not only in its purity but also in its consistency and suitability for demanding syntheses.
Most requests for this product focus on high-purity, low-moisture solid forms, as purity over 98% remains the expectation for research and development as well as manufacturing needs. Consistency in melting point, solubility, and physical appearance directly impacts downstream applications, especially where trace contaminants can derail sensitive reactions. Our investments in batch analytics, spectral confirmation, and critical drying steps pay off in minimized lot-to-lot variability. In the lab, we've seen how even subtle differences influence yield and reproducibility—it's why each batch comes with detailed analytic records, not just standard certificates.
In practice, 4-(1,3-Dithiolan-2-Yl)Phenol often serves as a key intermediate, particularly where sulfur-containing frameworks are important for biological or advanced material properties. The compound’s structure—blending a phenolic ring with a dithiolan group—brings challenges and strengths. The phenolic hydroxyl remains reactive under a range of conditions, while the dithiolan ring provides distinctive chemical reactivity that’s not easily replicated with more common thiol compounds. Our production line applies dedicated glass-lined reactors to minimize contact with metals, since traces of iron or copper from stainless steel can trigger unexpected side reactions or color changes in the finished product. These operational choices come from daily lessons on the plant floor, not by-the-book promises.
Light, temperature, and oxygen management makes a difference, too. The compound reacts to prolonged exposure to ambient air or heat, with gradual color changes signaling shifts in purity. We store the finished product under nitrogen and cool conditions to preserve its pale beige crystalline form, because experience shows that even overnight mishandling leads to quality dips that show up in end-use applications like pharmaceutical synthesis or polymer modification.
End-users approach this building block from many technical angles. In pharmaceuticals, medicinal chemists value the ability to introduce a robust and versatile dithiolane unit into lead compounds. This structure acts as a metabolic shield or reaction handle for further transformations. In our discussions with development teams, we’ve seen 4-(1,3-Dithiolan-2-Yl)Phenol pushed through multi-step synthesis—as a precursor to heterocyclic scaffolds and sulfur-rich fragments that conventional chemistry struggles to access in high yield.
Material science applications demand the same reliability. Research into sulfur-based polymer additives and functionalized advanced coatings leverages the compound for both its reactive phenol moiety and the dual thioether bridge offered by the dithiolan group. These features allow tailoring of polymer backbone features, electrical conductivity, or specific binding characteristics. Direct feedback from collaborating R&D labs taught us that certain reaction pathways only proceed reliably with a product free from oxidized impurities and stabilized against trace acids or bases. Each request for application support reinforces how crucial strict quality standards are—not in theory, but on the bench.
Plenty of phenol derivatives fill the market, but few tote the sulfur content and structural complexity of 4-(1,3-Dithiolan-2-Yl)Phenol. Compared to simple thiophenols, this compound integrates both aromatic hydroxyl and a five-membered dithiolane ring. In synthesis, this brings extra selectivity and new reaction channels, letting researchers or manufacturing chemists access frameworks not easily reached with regular phenolic compounds.
Some customers consider 1,3-dithiolan-substituted products as interchangeable, but experience tells us otherwise. Every adjustment—whether swapping in a methyl group or changing the ring orientation—alters solubility, reactivity, and downstream performance. For example, the unique ring and phenol combination resists certain oxidations, allowing it to survive harsher conditions than thiol-phenol systems. We've tracked cases in our QC labs where small shifts in structure led to significant changes in melting point and UV response, both critical for pharma and specialty materials.
There's also an availability gap in the market. Large catalogs may list dozens of phenolic or thioether products, but the practical challenge revolves around supply reliability and analytical traceability. As a manufacturer, controlling the process from incoming raw materials to finished product ensures trace-level impurities are identified, and customers aren’t left searching for explanations when a reaction fails. Our teams troubleshoot problems directly, based on field data and real instruments, not just literature values.
Routine analysis in our lab includes HPLC, NMR, IR, and, whenever required, mass spectrometry for deeper impurity profiling. These aren't simply quality boxes to check. Over years, we’ve found that periodic issues—like low-level thioether oxidation or phenolic discoloration—never show up in basic assays but emerge in field reports of inhibited downstream reactions. We invest in advanced analytics for each batch and respond to trends in the data, not just regulatory minima. This approach came out of working hand-in-hand with development chemists, who want more than a certificate—they want actionable details on side-products and data consistency.
On the production side, stepwise refining and purification always return bigger dividends than a post-synthesis polish. Our operators know where process drift introduces impurities, from minor variations in kettle temperature or stir speeds to the timing of work-up steps. Small changes in filtration, crystal growth, or drying reveal themselves only with practical experience, not from procedural guides alone. Sticking to tight temperature bands and precise solvent ratios proves especially important because crystal habit and size affect not just appearance but processability, blending, and reactivity.
Few users realize how much packaging design can improve actual working performance. Years of shipping to varied climates taught us that the standard powder bottle or simple drum just doesn’t cut it for this compound. We pair moisture-proof, oxygen-limiting containers with minimal headspace, since ambient humidity triggers clumping and starts subtle decomposition. Even in well-run labs, a poorly sealed jar can compromise days of work. Because of that, we select specific packaging types and secondary enclosures based on finished product stability testing. If users report clumping or off-odors, we backtrace packaging batches to identify and solve the packaging problem rather than blaming user handling.
Transport logistics bring their own challenges. In our shipments, delays at border or customs stations sometimes stall the reagent under varying temperature regimes. To counter that, we recommend and provide cold-chain solutions for key customers, especially for larger-scale synthesis or international shipments. Warehousing protocols on our site involve 24/7 environmental monitoring and regular audits, since even a few hours of warehouse downtime—say, from a power outage—has led to real, measurable product degradation.
Bench-scale purity and performance don’t always predict scale-up success. We’ve partnered with clients moving from grams to multi-kilogram and even ton-scale batches. At these scales, the sensitivity of 4-(1,3-Dithiolan-2-Yl)Phenol to minute process variables becomes obvious. Reaction kinetics shift, solvent exchanges become harder to manage, and equipment residue can change every lot’s profile. We run pilot batches to capture these variations, offering tailored technical advice for users scaling beyond the lab, because a single out-of-specification delivery carries real costs—not only for our customers, but for us and our reputation.
Sending bulk material globally also brings regulatory and documentation hurdles. We maintain documentation that exceeds customary compliance, allowing seamless import clearance for most jurisdictions. In the field, we’ve helped customers by providing supplemental analytics or stability data on request, especially when seeking approval for regulated manufacturing environments.
Multiple chemists in our own technical team have handled this compound in varying settings, learning what works and where hazards hide. With a phenolic group and two thioether links, certain standard phenol-handling habits don’t apply. Staff follow enhanced personal protective routines—not because labels say so, but because early exposure symptoms and dermal reactivity can be tricky. Training new personnel ends up relying as much on worked examples as on documentation. Our EHS audits emphasize hands-on practice, since no written checklist replaces the careful habits earned through real handling.
We track incoming safety reports, supplier analytics, and new toxicological findings. If an update affects exposure or transport advice, we revise our material guides and communicate these changes promptly to end users who need actionable, workaday information, not regulatory jargon. Over the years, customers and partners exchanging incident reports with us have prevented more than one close call on the bench or in shipping.
Our position as a manufacturer isn’t only about output. Chemists and formulators often approach us for troubleshooting tricky reactions, optimizing yield, or qualifying a new application. With direct access to batch records, hands-on process specialists, and the ability to tweak production conditions at short notice, we bring a practical, solution-focused perspective. In several case studies, switching grade or refining handling protocol helped unlock new routes for difficult syntheses. Raw data and bench experience matter more than theory when a synthetic pathway falters, and we commit resources to give application support when the literature alone falls short.
Recently, a customer in the biomaterials sector reached out after observing unexpected discoloration in a functionalized polymer batch. Drawing on our compound-specific experience, we identified the likely cause not as a process impurity but as a result of micro-level contamination from their in-plant glassware. Detailed discussion, shared analytical spectra, and phone consultations rapidly solved the matter—protecting both their timeline and our shared reputation for reliability. It’s this willingness to go beyond the warehouse that brings development and progress to new products leveraging 4-(1,3-Dithiolan-2-Yl)Phenol.
R&D never stands still. Teams in our plant conduct ongoing stress-testing—exposing sample batches to temperature cycling, accelerated oxidation, and prolonged light exposure to pinpoint shelf-life limits and detect weak spots before they translate into field complaints. We invest in scaling greener process options, exploring how to cut down on solvent waste without sacrificing product consistency. Each improvement comes backed by a bevy of comparative data, not just lab bench theory. Subtle tweaks in crystallization or filtration methods have cut energy costs and residual waste, lessons earned through sustained trial and error.
We also watch for emerging substitution trends. Compound classes shift in and out of favor in pharmaceutical and material innovation. Direct dialogue with both suppliers and customers often uncovers promising derivatives or application pivots that demand a nimble manufacturing response. Instead of defending the compound against every new market challenge, we look for niche solutions—such as customizing particle size for certain automotive coatings or supplying a stabilized grade for bioactive conjugates. The flexibility stems from close familiarity with both core process and downstream needs, sustained by daily engagement with users whose trust we value.
Handling feedback isn’t only a customer service formality; it drives internal change. A few years ago, persistent feedback about occasional clumping forced a full process review. It turned out that minor humidity fluctuations in the final drying room, not visible in general conditions monitoring, produced the issue. We retrofitted environmental controls and switched to a more robust sealed container for shipments. Transparent incident notation and follow-up form a loop from production to application and back. Users return because they find their concerns translated into real improvements, not just apologies or technical bulletins.
We champion fact-based dialogue because speculation in specialty chemicals quickly leads teams astray. Customers have requested ad hoc analytical runs when suspecting cross-contamination from other raw materials. Rather than brushing off concerns, we set up specific tests, report the actual findings, and recommend handling countermeasures to prevent recurrence. This approach distills years of day-to-day problem solving into shared gains, helping everyone produce better, safer, and more valuable outcomes with 4-(1,3-Dithiolan-2-Yl)Phenol.
Producing and supplying 4-(1,3-Dithiolan-2-Yl)Phenol involves more than churning out a line item for a catalog. Attention to process, honest feedback loops, and willingness to learn from mistakes keep our standards high and our customers’ trust intact. Technical facts guide improvements while shared field experiences steer advisory support in directions that matter. Batch after batch, the goal remains steady: deliver material that meets real needs, not just theoretical ones.
Day in, day out, this approach means end-users receive a compound defined not only by structure and purity, but by reliability, pragmatic support, and continued responsiveness—qualities shaped by manufacturing on the ground, rather than armchair theory or remote documentation. The strength of 4-(1,3-Dithiolan-2-Yl)Phenol in the laboratory or plant lies as much in the underlying manufacturing story as in the sum of its atoms, a reality that shapes both our outlook and our daily work.