Anhui Liwei Chemical Co., Limited
Products

2,5-Dihydroxy Thiophenol


    • Product Name 2,5-Dihydroxy Thiophenol
    • Alias 2,5-Dimercaptophenol
    • Einecs 224-582-8
    • 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

    716788

    Product Name 2,5-Dihydroxy Thiophenol
    Chemical Formula C6H6O2S
    Molecular Weight 142.18 g/mol
    Cas Number 1005-61-0
    Appearance White to light yellow crystalline solid
    Melting Point 125-130°C
    Boiling Point Decomposes before boiling
    Solubility In Water Slightly soluble
    Density 1.45 g/cm3 (approximate)
    Purity Typically >98%
    Odor Characteristic, unpleasant odor
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 2,5-Dihydroxybenzenethiol
    Stability Stable under recommended conditions

    As an accredited 2,5-Dihydroxy Thiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,5-Dihydroxy Thiophenol is supplied in a 25g amber glass bottle with a secure screw-cap, labeled with hazard and handling information.
    Shipping **2,5-Dihydroxy Thiophenol** is shipped in tightly sealed containers, protected from moisture and light. It should be packaged according to standard chemical regulations, labeled as a corrosive and hazardous material. Appropriate hazard handling and documentation are required during transit to prevent leaks, exposure, and ensure compliance with shipping safety guidelines.
    Storage 2,5-Dihydroxy Thiophenol should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry, and well-ventilated area away from light, moisture, and incompatible substances like oxidizing agents and acids. Store at recommended temperatures, typically in a refrigerator or a temperature-controlled chemical storage cabinet.
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    Competitive 2,5-Dihydroxy 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.

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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    2,5-Dihydroxy Thiophenol: Insights from the Manufacturer’s Bench

    Understanding the Backbone of Chemical Precision

    2,5-Dihydroxy Thiophenol stands out as a specialty intermediate for those looking to push the boundaries in fine chemical development. In our plant, the process starts long before it sees application—each batch reflects years of technical tweaking and strict process control. Among the thiophenols, this molecule’s twin hydroxy groups, at the 2 and 5 positions, open up selectivity and reactivity other analogues just can’t match. The underlying chemistry offers two accessible positions for functionalization, making it a key choice for chemists who need both reactivity and predictability without sacrificing workup downstream.

    Production Insights: What Sets Our 2,5-Dihydroxy Thiophenol Apart

    Large-scale production isn’t just about growing volume—it’s about consistent structure and purity. Our synthesis routes have gone through a dozen rounds of optimization to prevent over-sulfonation, ring degradation, or buildup of sulfur-based side-products. High-purity 2,5-Dihydroxy Thiophenol means fewer surprises in later reactions, something our long-term clients count on batch after batch. Careful control at each step, from raw material selection through post-reactor purification, means less waste and higher yields for formulators relying on downstream conversions.

    On the technical bench, this compound lands as a pale yellow crystalline solid. Moisture and light sensitivity are well-known quirks, so we designed storage and handling to keep oxidative darkening and decomposition in check. Several modifications to our dryers and packing lines have cut down on trace contaminant pickup—a recurring issue we saw years ago when ramping up capacity. Chemists see those results translated into traceable improvements in their process controls, often with tighter analytical profiles than off-the-shelf alternatives.

    Key Physicochemical Characteristics in Context

    For those familiar with thiophenols, handling volatile organosulfur compounds is never just a matter of plugging numbers into a specification sheet. Odor management, volatility at ambient temperatures, and the challenge of preventing hydrolysis all factor into our day-to-day routines. 2,5-Dihydroxy Thiophenol’s structure shifts the balance, with its added hydroxy groups dampening vapor pressure and easing some of the strong smell commonly tied to simpler thiophenols. Our experience shows that a well-dried solid, sealed against moisture ingress, avoids the development of off-odors and preserves reactivity. That translates directly into fewer handling headaches for research and production teams alike.

    During synthesis, we dial in melting point and color as leading indicators of impurity levels. Any shift hints at ring-substituted byproducts or polymerization side-reactions. Our technicians run thin-layer chromatography and HPLC on each lot—not because of regulations, but because years in the trenches have shown that tighter process control prevents a cascade of problem-solving later. The result: a product with a reproducible baseline, ready for application in advanced chemical transformations.

    Why Formulators and Researchers Choose This Molecule

    Our conversations with customer labs often highlight the gap between bench chemistry and reliable scale-up. 2,5-Dihydroxy Thiophenol bridges that divide. Its chemical stability during stepwise synthesis—even in the presence of strong base or acid—means fewer protection and deprotection cycles in organic synthesis. In real-world terms, that’s less time spent tweaking processes and more time advancing new molecules, whether in electronic materials, active pharmaceutical ingredient (API) intermediates, or custom catalysts.

    In the dye and pigment sectors, 2,5-Dihydroxy Thiophenol’s pattern of substitution gives predictable coupling in azo and quinoid pathways. Skilled formulators leverage the ortho- and para-positioned hydroxy groups for symmetry in polymer backbones or signal transducers in sensor applications. We’ve seen direct feedback from coatings manufacturers using this compound to build more resilient sulfur bridges within polymer chains, improving both colorfastness and mechanical strength.

    Comparison with Other Thiophenols: Performance on the Line

    Out in the compounding and R&D labs, many have tried to substitute simpler thiophenols or their mono-hydroxy cousins. These alternatives show limitations quickly. Mono-hydroxy structures lack the same balance of reactivity and steric accessibility; processes relying on substitution at both ortho and para positions run into yield bottlenecks and side-product issues. We’ve fielded plenty of support requests from teams who tried to retrofit their process with 4-hydroxy-thiophenol or unsubstituted thiophenol, only to find color stability, odor release, or conversion efficiency compromised.

    Compared to dihydroxy benzene derivatives lacking the thiol group, 2,5-Dihydroxy Thiophenol opens a new branch of sulfur-based crosslinking. The sulfur moiety alters nucleophilicity and redox behavior, bringing complexation and chelation potential to applications in metal recovery, catalysis, and specialty resins. Based on direct scale-up trials in our own development lab, the unique positioning of the thiol and hydroxy groups supports smoother downstream transformations in multi-step syntheses.

    How Applications Drive Production Choices

    Production never happens in a vacuum. Early demand centered on niche catalyst development in process chemistry, but over the last decade, applications have expanded. Today, requests come from teams scaling up advanced ligands for sensors, researchers working on anti-oxidant additives in specialty coatings, and polymer engineers seeking to bridge aromatic systems with controlled sulfur content. Each market shift triggers a conversation with our process engineers: What tolerances really matter? Should we tighten residual metal content or focus on specific chromophore purity?

    Smaller pilot lots sometimes call for deliberately controlled impurity profiles, enabling mechanistic studies or new downstream modifications. In electronic materials, for instance, customers often request characterization data beyond standard specs—trace metals, moisture content, or even crystallography details—because such parameters predict how the product performs in deposition or crosslinking steps. Our team has learned to work directly with clients during development, sharing investigator-level findings as part of the product release. This transparent collaboration keeps improvements grounded in real-world outcomes, not just QC paperwork.

    Environmental, Health, and Safety—Strategies Beyond Compliance

    On the production floor, responsible stewardship of 2,5-Dihydroxy Thiophenol starts long before packaging. We’ve worked through the challenge of controlling organosulfur emissions at every stage, building in closed reactor systems, scrubbing technology, and careful solvent recovery. Worker exposure—a factor many overlook—dropped significantly once we shifted from manual transfer to automated charging systems. The smell of volatile thiols might have once meant complaints around the facility, but ongoing engineering controls and proactive housekeeping helped minimize nuisance and risk.

    Waste streams containing thiol-bearing residues require special treatment; oxidation protocols and dedicated handling systems split these from broader plant effluents. Some of these solutions grew out of hands-on problem-solving by our shift leaders, who saw bottlenecks in filter press cleaning or spent solvent handling. Now, those lessons fuel both productivity and community safety. Although regulations guide our minimum standards, many of our operational controls began as grassroots initiatives, founded by feedback from the people who blend, filter, and package the product daily.

    Partnering with the Next Generation of Innovators

    Customer feedback never trickles in on a schedule. A university researcher calls at midnight with a question about unforeseen reactivity; a coatings manufacturer flags an irregular color shift during scale-up. These real-world touchpoints drive our focus—troubleshooting root causes and sharing decades of insight rather than just reference values on paper. Sometimes that means adapting analytical protocols, such as introducing rapid IR screening for batch-to-batch verification or conducting joint trials in a customer’s processing line.

    We bridge the knowledge gap by leveraging internal expertise, many of whom came up themselves as bench chemists or plant techs before leading development projects. This experience base pays dividends: practical guidance on solvent choice, work-up, and even how to stage temperature ramps for optimal conversion. One pharma client, facing repeat fouling during alkylation, reached out for advice and ended up collaborating with our team to revamp their entire reaction sequence. The result: fewer purification headaches, a safer work environment, and improved throughput.

    Tracing Reliability from Raw Material to Application

    Each batch of 2,5-Dihydroxy Thiophenol starts with feedstocks selected by both analytical result and supplier transparency. Down the chain, years of supplier relationships and materials audit keep quality stable. Even so, occasional hiccups—like a shipment showing slight sulfur spec deviation—prompt rapid sheltering and trace-back, not blanket rejection. Keeping the dialogue open with suppliers means we catch and correct issues before they ever impact production.

    Once in-reactor, attention shifts to kinetic control: catalyst loading, pH police, and the elimination of side reactions through real-time monitoring at key points. Experience showed that minor deviations during sulfonation or hydroxy protection cascaded into larger downstream purification challenges. Tweaks to our quench protocols improved throughput and, in turn, allowed us to offer tighter lead times for pilot and production orders.

    Many of the quality systems we maintain grew from mistakes we learned from, not just outside auditing. Early on, a too-rapid filtration step led to incomplete solvent removal and instability in warehouse storage. Repeating that process in slower stages, coupled with in-process NMR and mass spec confirmation, eliminated the issue for good. These real-time course corrections build supply reliability for the end user, whether they’re a Fortune 100 formulator or a bespoke research group.

    Customization, Innovation, and the Value of Manufacturer Know-How

    Research never stops. As a manufacturer, we receive requests for tailored variants: alternate salt forms, pre-blended reagent kits, or purified product for analytical standards. For those working in pharmaceutical or electronic domains, the conversation often includes documentation at the level of detailed trace impurity profiles or custom solvent packaging. Our plant team thrives on these challenges, adopting modular production lines able to switch between different downstream processing demands.

    Regular investment goes into lab-scale piloting and side-by-side application tests with partner sites. Sometimes an adjustment in crystallization discipline or a fresh approach to drying saves thousands in end-user process costs. We’ve learned the value of speed and responsiveness over bare-bones spec compliance; quick adaptation lets us keep pace with both regulation and technological innovation.

    Continuing the Tradition of Hands-On Chemical Manufacturing

    On the manufacturer’s floor, chemistry never stays static. Every new batch of 2,5-Dihydroxy Thiophenol carries the weight of accumulated experience—years of process development, customer troubleshooting, and partnership-driven improvement. For those working at the cutting edge of chemical synthesis, from pharmaceuticals to pigments to sensors, this compound provides a flexible, robust building block. No one molecule solves every challenge, but produced with care and insight, 2,5-Dihydroxy Thiophenol opens up opportunities that extend far beyond the specification sheet.

    Our commitment remains rooted in practical benefits—cleaner reactions, reliable downstream performance, open-door expert support. As applications keep changing, insight from the plant floor and project bench will shape new approaches to both product and process. In the end, reliable chemical manufacturing is built person-to-person, batch-by-batch, with adaptability and know-how guiding every drum out the door.