|
HS Code |
796095 |
| Cas Number | 637-88-7 |
| Molecular Formula | C6H6OS |
| Molecular Weight | 126.18 |
| Appearance | Yellow to brown liquid |
| Boiling Point | 259-261°C |
| Density | 1.24 g/cm3 |
| Purity | Typically ≥98% |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.617 |
| Flash Point | 177°C |
| Synonyms | 3-Mercaptophenol, m-Hydroxythiophenol |
| Smiles | C1=CC(=CC(=C1)S)O |
| Inchikey | WOOXMYMCYAIEDO-UHFFFAOYSA-N |
| Storage Temperature | Store at 2-8°C |
As an accredited 3-Hydroxy Thiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, tightly sealed with screw cap, labeled with hazard symbols and product details. Protective outer carton included. |
| Shipping | 3-Hydroxy Thiophenol is shipped in tightly sealed containers to prevent exposure to air and moisture. The chemical is packed in accordance with regulations for hazardous materials, often in amber glass bottles to protect from light. Appropriate hazard labeling and documentation are provided to ensure safe handling during transport. |
| Storage | 3-Hydroxythiophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. Protect from moisture and light. Use appropriate chemical storage cabinets, and ensure clearly labeled containers. Personal protective equipment must be worn when handling. Store according to local chemical safety regulations. |
Competitive 3-Hydroxy Thiophenol 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!
Over the years, our team has spent considerable time developing and refining 3-Hydroxy Thiophenol for reliable, practical use across demanding research and production settings. In our facility, every batch follows stringent controls to assure high purity and predictable behavior in downstream applications. The primary chemical structure, combining a thiol group and a hydroxyl group on a thiophene ring, makes this compound a versatile building block for modern synthetic chemistry. Direct experience with its handling shows a strong and distinctive odor and a sensitivity to oxidation, traits common to many thiol-bearing chemicals but managed here through careful process control and dedicated storage conditions.
In our operation, we produce 3-Hydroxy Thiophenol with HPLC purity above 98%, and water content always falls below 0.5%. This dry, off-white to pale yellow crystalline powder packs well in inert atmospheres. The melting range usually sits between 33 and 35 degrees Celsius; deviations outside of this range often indicate contamination or partial oxidation, which our QC team monitors daily. By sticking strictly to fresh, reagent-grade input materials and sterile glass-lined reactors, we avoid batch-to-batch drift and minimize trace sulfurous side-products. Analytical chemists in our lab report a reliable assay value, usually confirmed by both NMR and GC/MS, so we feel confident users won’t face performance issues hidden behind paperwork.
Handling thiol reagents calls for real attention, not just for workplace safety, but for process yields. Over time, we noticed that exposure to air or trace iron salts can quickly degrade the compound, creating colored byproducts. To avoid this, we direct operators to use sealed transfer lines and maintain a nitrogen blanket during all stages of filling, packing, and re-packing. By using solid-state containers with snap closures, even low-level humidity never reaches the drum contents, ensuring the properties remain stable up to the stated shelf life. These practical measures come from years of troubleshooting shipping losses and customer complaints from the early days, where oxygen ingress led to performance loss on arrival.
Chemically, 3-Hydroxy Thiophenol brings a blend of nucleophilicity and aromatic reactivity not present in traditional phenolic or straight-chain thiols. During pilot campaigns, customers using it as a precursor for custom thioethers and heterocyclic drugs saw higher selectivity and faster conversion at moderate temperatures, as opposed to using analogues such as 4-hydroxythiophenol or plain thiophenol. Our technical support group often discusses its role as a sulfur source in the construction of advanced materials, ranging from semiconductors to photoactive polymers, where precision placement of the thiol and hydroxy groups on the ring matters for the downstream performance.
Our regular clientele includes research groups and process engineers aiming to introduce both hydroxyl and thiol functionalities into complex molecules. In-catalyst development, the compound forms a reliable ligand under mild conditions, without needing excess activation steps. Process observation shows good compatibility in Suzuki and Buchwald-Hartwig couplings when paired with palladium complexes—a result our chemists confirmed repeatedly, especially when customers require specific regioisomer outcomes. Scale-up runs in our facility proved that 3-Hydroxy Thiophenol performs robustly at both 100-gram and 50-kilogram scales, making it suitable not only for lab research but for pilot and larger manufacturing campaigns.
Nothing sabotages a synthesis faster than degraded reagents. After learning this through hard-earned experience, we standardized all 3-Hydroxy Thiophenol packaging in vacuum-sealed, amber glass bottles for small orders, and multi-layer polyethylene-lined drums for larger consignments. Shipping under cooling conditions further preserves shelf life, and our field teams run quality spot checks on arrival. End users often ask about repacking—our stance remains strict: open only under inert conditions, and reseal immediately. On the rare occasion of visible discoloration, our technical hotline guides through re-purification or disposal to avoid downstream contamination.
Feedback from process chemists points out clear differences between 3-Hydroxy Thiophenol and its close relatives, such as 2- and 4-hydroxy thiophenols, or even unsubstituted thiophenol. Our experience confirms these opinions. In side-by-side syntheses, the 3-position hydroxy group offers unique reactivity, particularly in forming regioselective bond formations. While 2-hydroxy analogues sometimes promote self-condensation or disproportionation, our product resists those paths, minimizing process loss and impurity generation. Compared to simple phenol-thiol combinations, the fused heteroaromatic structure of 3-Hydroxy Thiophenol brings stability and solubility in mixed organic solvents, especially DMF and toluene, improving procedural flexibility in crowded syntheses.
The safety data looks clinical on paper, but our plant protocols evolved out of necessity rather than just regulation. The strong odor and skin sensitization potential make fully enclosed systems a must. We installed high-throughput fume scrubbing systems, and all workers in our thiophenol area wear dual-layer gloves and full-face respirators. At waste handling, oxidizing agents convert free thiol residues into less volatile sulfonic acids before sewer disposal, shrinking odor footprints and managing regulatory risks. Our internal accident logs show that while strict handling prevents major issues, even minor spills without prompt cleanup can lead to lingering odors and, in rare cases, minor allergic reactions. Sustained staff training, strict supervision, and clean workspace structures proved to be the only effective answers.
We don’t just label a drum and ship it—every batch arrives in our quality control center before leaving. Qualified staff run duplicate checks for purity, residual solvent level, heavy metals, and, where needed, chiral purity and isomer ratio. In cases where chromatographic separation highlights minor side peaks, our protocol requires full batch rejection or a tailored re-crystallization cycle. Years ago, this slowed delivery timelines, but today’s continuous-flow purification setups push throughput higher without sacrificing output standards. Several clients from the electronics sector rely on this rigorous eye; even parts-per-million sulfur variants can trigger conductivity changes in sensitive film applications, so precision is not negotiable.
Our history making 3-Hydroxy Thiophenol runs parallel to industry changes in specialty chemicals. Twenty years ago, the product mostly went to small research labs. Today, increased focus on sustainable agriculture and microelectronics expanded requests several times over. Crop science teams use the thiophenol structure as a template for targeted agrochemical synthesis, where the arrangement of reactive groups guides design. In semiconductor modification, polymer teams build on the unique reactivity at both the sulfur and oxygen sites to tune dielectric properties or create new surface treatments. Conversations with formulators and scientists influence how we approach scale-up and adapt batch sizes, meaning our plant flexes output as customers push new boundaries in their markets.
We welcome technical requests and feedback, not only as a business necessity but because open dialogue often uncovers small improvements we can implement rapidly. Over the years, this led us to introduce just-in-time production schedules, allowing fresher batches on delivery and reducing time-in-transit degradation. Regular technical round-tables with user groups push us to review and adjust additive lists, test alternative packaging, and update process documentation. This interactive approach puts practical knowledge in the hands of end-users and provides a channel for industry-wide best practice sharing.
Direct feedback often flags recurring problems like moisture-induced clumping, subtle discoloration, and possible performance dips in complex syntheses. In each case, we implement actionable improvements. Using bulk desiccant liners and minimizing headspace air in shipping containers dramatically improves shelf stability and minimizes moisture hit. Regular site visits to customer plants reveal user-side issues—such as prolonged exposure during manual dosing—which we address through training seminars and on-site demonstrations of best-in-class transfer methods. If oxidation occurs, we support purification through straightforward methods like column chromatography or short-path distillation, guiding users without exposing them to unnecessary processing hazards.
Our 3-Hydroxy Thiophenol complies with REACH pre-registration rules, and we keep safety documents aligned with global standards, including GHS labelling and transport hazard codes. Regular audits and third-party testing ensure no drift from compliance status. Large-scale users in the EU and North America appreciate this transparency and often specify our documentation for regulatory filings. In new product applications—such as advanced battery electrolyte manufacturing—our regulatory affairs team works closely with partners to furnish everything from impurity profiles to disposal advice, reducing project delays and clearing path for innovation.
Feedback does not stop once product leaves our docks. Regular contact with application chemists, plant engineers, and laboratory scientists keeps us tuned in to shifting needs. Sometimes a nuance in solvent compatibility changes the preferred solvent system. Other times, reduced particle size or alternative delivery format enables better integration with robotic dosing units. One cycle reinforced that even minor changes in temperature or storage atmospheric composition can alter how 3-Hydroxy Thiophenol performs in real-world situations. We take such findings seriously and update internal protocols quickly.
Drawing on decades of in-house synthesis experience, we invested heavily in real-time monitoring and process automation to avoid product drift and subpar performance. This isn’t just a marketing story—it reflects hundreds of adjustments led by our frontline staff and ongoing learning from the field. Each drum contains a product traceable down to the shift that synthesized it, allowing full accountability and swift root cause analysis for any user concern. Practical application support stems from hands-on knowledge, not just theoretical expertise. Real use-cases from specialty synthesis validate what structured testing often cannot capture.
Delivering a product that fits not only the spec sheet but the real-world bench or reactor is our constant aim. 3-Hydroxy Thiophenol, as it emerges from our reactors, benefits from a chain of improvements, each forged by practical necessity and direct customer input. While market forces and applications shift, attention to detail at every stage ensures that the chemical arriving at a researcher’s work station is robust, predictable, and safe to deploy. We remain committed to refining manufacturing, quality systems, and technical support as end-user needs grow and evolve. Our journey with 3-Hydroxy Thiophenol reflects the broader pattern in chemical manufacturing: innovation built on transparency, practical learning, and open exchange with those who use our products to make the next leap forward.