Anhui Liwei Chemical Co., Limited
Products

2-Hydroxythiophenol, (2-Mercaptophenol)


    • Product Name 2-Hydroxythiophenol, (2-Mercaptophenol)
    • Alias 2-Mercapto-1-hydroxybenzene
    • Einecs 200-695-1
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    878256

    Name 2-Hydroxythiophenol
    Alternative Name 2-Mercaptophenol
    Molecular Formula C6H6OS
    Molar Mass 126.18 g/mol
    Cas Number 1121-31-9
    Appearance Yellow to brown solid or liquid
    Boiling Point 264 °C
    Melting Point 36-39 °C
    Density 1.26 g/cm³
    Solubility In Water Slightly soluble
    Pka 8.95 (phenolic OH)
    Smiles C1=CC=C(C(=C1)S)O
    Inchi InChI=1S/C6H6OS/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

    As an accredited 2-Hydroxythiophenol, (2-Mercaptophenol) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Hydroxythiophenol (2-Mercaptophenol) is supplied in a 25g amber glass bottle with secure, chemical-resistant screw cap labeling.
    Shipping 2-Hydroxythiophenol (2-Mercaptophenol) should be shipped in tightly sealed containers, protected from light and moisture. It must be packed in accordance with local, national, and international regulations for hazardous chemicals, as it may be classified as a flammable and toxic substance. Appropriate hazard labeling and documentation are required during transit.
    Storage 2-Hydroxythiophenol (2-Mercaptophenol) should be stored in a tightly closed container under an inert atmosphere, such as nitrogen, in a cool, dry, and well-ventilated area away from light and sources of ignition. It should be kept away from oxidizing agents and acids. Refrigeration (2–8°C) may be beneficial to prolong shelf life and minimize decomposition. Handle with appropriate personal protective equipment.
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    Certification & Compliance
    More Introduction

    2-Hydroxythiophenol (2-Mercaptophenol): Experience in Manufacturing and Its Role in Modern Synthesis

    Introduction to 2-Hydroxythiophenol: Direct from the Manufacturing Floor

    Working in chemical synthesis over the years, certain molecules stand out for their reliability and versatility. 2-Hydroxythiophenol, also identified as 2-Mercaptophenol, always holds a place in my own production lists because of its unique combination of a thiol and a phenolic group on a benzene ring. Manufactured in our plant under strictly controlled conditions, this compound arrives as a pale yellow to slightly brown crystalline solid, carrying a distinct but manageable odor characteristic of thiols. Our experience confirms that by sticking to a hands-on, carefully monitored process from raw input selection through to final packaging, we deliver a product that researchers and manufacturers can put to work right away—without hesitation over purity or consistency.

    Specifications and Quality: Lessons Learned from Practice

    In the manufacturing shop, cutting corners on quality never pays. We routinely achieve purity levels above 99%, based on HPLC and GC testing, because even a fractional impurity in 2-Hydroxythiophenol can disrupt sensitive reactions. This is a compound that tolerates no sloppiness—whether you're scaling up an organic synthesis, developing pharmaceuticals, or producing specialty polymers. Attention spans during crystallization and filtration cannot slip; air exclusion during synthesis is a must, since both phenolic and thiol groups may oxidize if left unprotected.

    We store and pack 2-Hydroxythiophenol using air-tight, inert containers, usually amber glass or HDPE bottles. In my experience, even mild exposure to air or light will deepen the product color and can raise peroxide levels—markers of instability. Consistent monitoring in-house remains non-negotiable before anything leaves the warehouse.

    Applications: Why 2-Hydroxythiophenol Remains a Workhorse

    On the application side, I have watched customers use 2-Hydroxythiophenol in a remarkable breadth of settings. The combination of a reactive phenol and a thiol on the same benzene ring does not appear often, and this molecular layout leads to strong demand in downstream organic synthesis. Nucleophilic addition and substitution processes go smoothly thanks to the electron-rich thiol at the ortho position, enabling routes to heterocycles or coupler intermediates, often in a single step.

    We regularly supply this compound for building sulfur-containing pharmaceuticals and agrochemicals. The thiol group often acts as a key handle for tethering target molecules or introducing further functional groups, one step at a time. In the dye and pigmentation space, 2-Hydroxythiophenol can behave as a chelating agent, making it valuable for applications requiring precise coloration or metal ion control.

    Colleagues in material science value our product as a monomer or cross-linker during polymerization. The ortho orientation of the hydroxy and thiol sites opens up distinct reaction paths. Specialty resins and adhesives can be engineered for added strength or specific chemical resistance, taking advantage of both nucleophilic centers. Over the years, customers have shared feedback regarding improved yields and reproducibility in these kinds of advanced materials and coatings when they work with consistently manufactured 2-Hydroxythiophenol.

    Comparing 2-Hydroxythiophenol with Related Chemicals

    Working in manufacturing, close attention to the differences between positional isomers and functional group analogues is part of daily life. Many clients ask how 2-Hydroxythiophenol stacks up against alternatives such as 4-hydroxythiophenol (para isomer) or simple thiophenol.

    2-Hydroxythiophenol (ortho isomer) pairs its hydroxy and thiol groups right next to each other, a structural twist that shifts its reactivity. For example, this ortho layout enables hydrogen bonding intramolecularly, which changes solubility and melting behavior versus para analogues. Pure thiophenol, with only the -SH group and no -OH, loses much of the fine-tuned selectivity that comes from the interplay of both groups on the same ring.

    From a manufacturing standpoint, ortho-substituted compounds demand greater vigilance, as their proximity can drive side reactions during synthesis if temperature and pH controls drift. Through repeated campaigns, our crew has learned that purified ortho isomers tend to command higher trust in fine chemical fields, where downstream applications rest on predictable selectivity or reactivity. Where 2-Hydroxythiophenol provides a distinct advantage comes with reactions needing a cooperative effect between functional groups—a feature para and meta isomers often cannot match.

    Sourcing alternatives like 4-hydroxythiophenol sometimes makes sense if only one site must react. For coupled, multi-step processes and certain catalyzed polymerizations, the ortho configuration pays dividends and remains the gold standard. Our production teams have invested in process refinements over the years to guarantee that substitution patterns are controlled, avoiding contaminants like monochlorinated or disubstituted side products.

    Process Integrity: Observations on Handling, Storage, and Safety

    A lesson picked up quickly on the line is the stubborn sensitivity of 2-Hydroxythiophenol to oxygen and light. Incoming shipments of raw precursors arrive checked for water content and peroxides; even small deviations during reaction setup can spoil a batch. Quality control relies on real people with a knack for catching subtle color shifts and testing headspace for sulfurous odors.

    We built protocols around minimizing worker exposure to fumes, since the thiol group’s aroma clings even after thorough ventilation. Splash protection and gloves—nitrile, not latex—remain standard issue. Many junior operators learn this lesson on day one, as skin contact not only smells but can cause irritation.

    In storage, containment is everything. Our finished product vault uses low-humidity air and amber glass as a baseline. On several occasions, we have traced rejected lots back to failures in container integrity. Routine checks bring problems to light before customers experience any drop in performance.

    Regulatory and Environmental Considerations: Our Firsthand Approach

    Handling an organosulfur compound like 2-Hydroxythiophenol brings a specific regulatory footprint. Regional authorities call for reporting of thiol emissions and track wastewater discharge. Our compliance systems, shaped by years of audits, focus on scrubber maintenance and precise effluent monitoring. In several cases, we scaled up pilot batches just for the purpose of confirming compliance standards under real-world operating conditions before full-scale runs.

    Our plant captures off-gases using activated carbon beds, refreshing them per schedule to keep sulfur levels below thresholds. We designed containment for spills based on personal experience with the compound’s odor and staining tendencies; fast cleanup and disposal prevent lingering exposure. Our protocols keep us out of trouble—government inspectors have learned we expect them on site any day, rather than treating compliance as a once-a-year box-ticking ritual.

    Consistent Quality: How Experience Informs Every Batch

    Over the course of dozens of production cycles, patterns emerge. Slight fluctuations in starting material color or storage temperature can show up days later in the final assay as a small loss in purity. We keep logs of every batch—what worked, what failed, what we tweaked for a better outcome. Within our walls, pride comes from zero rejects after quality control review, not just the volume shipped.

    Our process puts emphasis on skilled operators. The machinery exists to automate steps, but human expertise remains at the core of our operation for a reason. Colleagues learn to pick up deviations on sight or smell, reporting upstream to halt problems before they grow expensive. For 2-Hydroxythiophenol, this approach prevents the downstream headaches that come from a faulty lot in someone else’s lab.

    Customer Feedback and Real-World Partnerships

    Years working with clients in pharmaceuticals, polymers, and specialty chemicals has built a feedback loop. Those working on novel drug candidates share which impurity profiles might block regulatory acceptance. Coatings customers bring data on which batch runs give haze-free dispersion. We pass along blends and variations, always tracking how small tweaks in process impact the final feel or reactivity of the compound in the field.

    This ongoing dialogue improves our process with every order. Beyond simply meeting specifications, real-world user experience becomes our baseline for where improvements must happen. On many occasions, modifications suggested by a trusted research client find their way back into our batch record templates, forming the next round of process upgrades.

    Practical Differences from Other Thiols and Phenols

    Being on the manufacturing side, I can say that 2-Hydroxythiophenol cannot be swapped for basic thiophenol or hydroquinone when the chemistry gets sensitive. Substituting even a seemingly close isomer often changes reaction mechanism or leaves products with poorer yields.

    Compared to plain phenol or simple alkyl thiols, our product brings reactivity not only at the sulfur but at the oxygen position. Chemists running aromatic substitutions, Michael additions, or oxidative couplings get to choose directionality. Our application results prove that, for some key reactions, this flexibility means higher selectivity and shorter synthesis cycles.

    Alternative thiols rarely bring similar nucleophilicity when placed at other positions. A phenol with the hydroxy at the para position, for example, forfeits the subtle hydrogen bonding behavior and the ease of directed ortho metalation. It also lacks the same chelating ability for certain metal ions—a difference that comes into play in pigment and electronics applications.

    Process Transparency: Sharing What Really Happens

    Clients often say they appreciate knowing what takes place between order and shipment. Instead of hiding shortcomings, our team chooses to surface challenges as part of our narrative. If a batch falls outside specs, nobody waits for an investigation—production pauses, root causes are found, and lessons are relayed to R&D and customer service.

    Our commitment is to keep the process chain open. We keep communication flowing, not just on product grades and lot traceability, but about shelf-life, best storage advice, and the minor flags we pick up long before outsiders see a trend. Relationships thrive on trust; from our side, that grows out of process visibility and a willingness to explain the story behind every bottle of 2-Hydroxythiophenol delivered.

    Future Directions: Investment in Reliability

    From our perspective, the role of 2-Hydroxythiophenol will continue to grow as downstream industries explore more sulfur and oxygen functional group chemistry. In battery materials and advanced electronics, the right molecule brings a measurable boost in performance—battery cycling, charge transport, or film stability in coatings, for instance.

    To keep pace with evolving demands, we invest back into the plant floor—automation where it adds speed without removing skilled oversight; regular updates to QC instrumentation; training that turns every team member into a process owner, not just a machine minder. These choices pay off through fewer recalls, less downtime, and a reputation our customers trust.

    Why Sourcing Direct from the Manufacturer Matters

    Our experience proves that direct relationships between manufacturer and user set the stage for better outcomes. By maintaining control from start to finish—raw material vetting, production, packaging, and shipment—we guarantee attributes like purity, particle size, and shelf stability. Feedback loops run tighter, miscommunications drop, and customers access not only a product, but our collective expertise in putting it to use.

    Other suppliers, including distributors and middlemen, simply cannot pass along the same depth of technical judgment or willingness to interface during troubleshooting. Innovation and reliability in 2-Hydroxythiophenol production rest on knowing the customer’s frustrations as well as our own. Over decades, this approach shows up in lower rates of return, shorter time to market for new formulations, and collaborative advances that benefit both sides.

    Conclusion

    Making 2-Hydroxythiophenol isn’t just a matter of following set recipes. It grows from uncounted rounds of practice, from technician know-how, from the willingness to tweak and learn through feedback, and from disciplined attention at each step. Listening to chemists and engineers who rely on this molecule, and then shaping our process to their real requirements, gives us an advantage. Quality, reliability, and deep chemical understanding cannot be substituted or simulated—they must be built, day by day, on the manufacturing floor.