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2-Hydroxythiophenol

    • Product Name 2-Hydroxythiophenol
    • Alias Thiophenol-2-ol
    • Einecs 202-933-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    810789

    Chemical Name 2-Hydroxythiophenol
    Synonyms 2-Mercaptophenol, o-Mercaptophenol, o-Hydroxythiophenol
    Molecular Formula C6H6OS
    Molecular Weight 126.18 g/mol
    Cas Number 1121-37-5
    Appearance Yellow to brown crystalline solid
    Melting Point 36-39°C
    Boiling Point 221°C
    Density 1.26 g/cm3
    Solubility In Water Slightly soluble
    Pka 7.0 (phenolic OH), 6.6 (thiol SH)
    Smiles C1=CC=C(C(=C1)O)S
    Inchi InChI=1S/C6H6OS/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

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

    Packing & Storage
    Packing 2-Hydroxythiophenol is packaged in a 100g amber glass bottle with a secure screw cap, labeled with hazard warnings and details.
    Shipping 2-Hydroxythiophenol is shipped in tightly sealed containers to prevent leakage and degradation, stored under cool, dry, and well-ventilated conditions. Packaging complies with relevant hazardous material transport regulations, as the compound may be flammable and toxic. Handle with appropriate protective equipment during transportation to ensure safety and environmental protection.
    Storage 2-Hydroxythiophenol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizing agents and acids. Keep the container tightly closed and protected from light and moisture. Use containers made of materials compatible with thiols and phenols, and always store under a fume hood or in a chemical storage cabinet designed for volatile organosulfur compounds.
    Application of 2-Hydroxythiophenol

    Applications of 2-Hydroxythiophenol in Industrial Manufacturing

    Our production-grade 2-Hydroxythiophenol supports critical transformation steps as a thiol-aromatic intermediate across selected sectors, enabling downstream partners to achieve precise molecular outcomes in advanced chemical processing chains. Presented below are principal application scenarios verified through ongoing customer usage and industry adoption, each supported with current compliance guidance, technical integration, and downstream product output details.

    1. Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers rely on 2-Hydroxythiophenol as a sulfur-containing synthon in API intermediate synthesis, including specific cephalosporin side chain expansions and thiol-aryl coupling formations. In these routes, our material enables selective introduction of thiol and phenolic moieties, enhancing substrate specificity during beta-lactam nucleus modification. QA/QC teams monitor raw material traceability and batch purity as required under medicinal supply protocols throughout process validation and scaling to commercial quantities.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • USP General Chapters (Where relevant for intermediates and reference standards)
    • EMEA Guidelines on Process Validation (EMA/CHMP)

    Typical usage ratio

    • 0.5–2.2 molar equivalents against target substrate, depending on thiol introduction step and reaction yield optimization during route scouting and scale-up; adjusted for impurity profile control

    Downstream process integration

    • Charged into nucleophilic substitution or coupling reactors after initial aromatic halogenation or sulfonation, under anhydrous conditions, typically in the early-to-mid synthesis block of multi-stage pharmaceutical manufacturing sequences

    Final product types

    • Beta-lactam antibiotic intermediates (e.g., cefadroxil, cefazolin side chains)
    • Thioether-functionalized fine chemicals
    • Sulfur-modified pharmaceutical precursors for custom synthesis houses

    2. Polymer Crosslinking Agents for Specialty Resins

    Resin blenders and polymer compounders utilize 2-Hydroxythiophenol as a functional crosslinker in certain phenolic, epoxy, and polyurethane resin systems. Its reactive ortho-hydroxyl and thiol sites permit controlled crosslink density increases, leading to enhanced adhesion, chemical resistance, and mechanical resilience in final resin matrices. R&D and production teams must document raw material intake and in-process blending data to meet performance and certification standards for engineered polymer goods.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • ISO 14001 Environmental Management (for specialty resin production)
    • ASTM D3960 (Polymer content for resins)
    • REACH Authorisation (for notification and restriction in the EU market)

    Typical usage ratio

    • 0.1–0.5 weight % in phenolic and epoxy resins, optimized via bench trials for application-specific mechanical property balance and VOC compliance

    Downstream process integration

    • Pre-dispersion into base resin monomer melts; fed during resin pre-polymerization or post-blend stages, followed by thermal or catalytic curing in batch reactors or continuous lines

    Final product types

    • Adhesive resins for electronics
    • High-durability coatings for industrial surfaces
    • Composite matrix binders for automotive and aerospace parts

    3. Corrosion Inhibitor Formulations for Metal Processing

    2-Hydroxythiophenol features as an active component in custom corrosion inhibitors for ferrous and nonferrous metal treatment plants. Its dual functional groups form stable chelate layers on metal surfaces during acid cleaning, pickling, or cooling system operation, resulting in reduced oxidation and improved surface retention for treated components. Product stewardship and environmental teams monitor dosing and discharge under industry regulation to prevent ecological contamination.

    Industry compliance standards

    • ASTM G31 (Laboratory Immersion Corrosion Testing of Metals)
    • ISO 8044 (Corrosion of Metals and Alloys - Basic Terms)
    • RoHS 2011/65/EU (restriction of hazardous substances in industrial maintenance chemicals)
    • REACH (for registration in corrosion inhibitor blends in the EU)

    Typical usage ratio

    • 25–400 ppm in water treatment solutions, adjusted based on metal type, system pH, and operational exposure cycles as determined via field pilot studies and coupon testing

    Downstream process integration

    • Dosed into acid wash baths or recirculated coolant lines after primary filtration and pH adjustment steps; included post-cleaning or between successive fabrication processes for component preservation

    Final product types

    • Pickling inhibitors for refinery and pipeline steel
    • Chemical cleaning agents for heat exchangers
    • Circuit board surface protectants for electronics

    4. Dye and Pigment Intermediate Manufacturing

    Synthetic dye and pigment producers use 2-Hydroxythiophenol as a crucial bridging intermediate in azo and sulfur dye production, where it enables heterocyclic ring closure and targeted thiol group insertion. Colorant manufacturers document trace thiol conversion and product color fastness according to end-user textile or plastics application needs, incorporating quality assurance checkpoints throughout batch processing.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes
    • EN 71-3 (Toy Safety - Migration of certain elements) for pigment safety
    • ISO 105-A02 (Textiles – Tests for color fastness)
    • REACH registration for pigment intermediates in the EU

    Typical usage ratio

    • 0.1–1.0 molar equivalent per dye intermediate, adjusted for color strength and purity indexing during development and scale-up

    Downstream process integration

    • Added during nucleophilic aromatic substitution or cyclization steps after the main aromatic amination or halogenation reactions, preceding final coupling or metallization

    Final product types

    • Sulfur dyes for textile fibers
    • Azo dye intermediates for polyester or nylon substrates
    • Specialty pigments for plastics and coatings

    5. Agrochemical Synthesis: Fungicide Intermediate

    Leading agrochemical formulators integrate 2-Hydroxythiophenol for targeted construction of thioether and substituted aromatic backbones essential in modern fungicide APIs. It enables high-purity molecular frameworks that deliver consistent field performance against fungal pathogens. Process engineers monitor material identity and batch filtration to minimize contamination during raw pesticide ingredient manufacture.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • ISO 9001 process controls for crop protection chemicals
    • EPA FIFRA regulations (U.S. Environmental Protection Agency - Federal Insecticide, Fungicide, and Rodenticide Act)
    • REACH Annex II for substance evaluation in agricultural products for the EU market

    Typical usage ratio

    • 0.8–2.5 molar equivalents per reaction, set per individual synthetic pathway to boost conversion and meet fungicidal purity targets set during regulatory submission trials

    Downstream process integration

    • Fed as a reaction intermediate or functional substituent after key aromatic halogenation steps; integrated prior to final oxidation or coupling in continuous and batch synthesis lines

    Final product types

    • Systemic fungicide actives (e.g., thioether-substituted benzene derivatives)
    • Broad-spectrum crop protection ingredient intermediates
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    Certification & Compliance
    More Introduction

    Introducing 2-Hydroxythiophenol: Product Insights from the Manufacturer’s Perspective

    Understanding 2-Hydroxythiophenol in Everyday Work

    Anyone in specialty chemicals soon realizes that certain compounds find their way into targeted research and production processes. 2-Hydroxythiophenol, also known in labs as o-Mercaptophenol, isn’t just another fine chemical—it comes from decades of problem-solving, feedback from process chemists, and lab-scale optimization. We produce it right here at our site with a careful hand on every batch, and that experience shapes how we approach both purity and packaging.

    In the field, 2-Hydroxythiophenol (C6H5SH with a hydroxy group at the ortho position) stands apart from its isomers and related thiols. Chemists rely on its particular reactivity: both the phenolic OH and the thiol SH can enter into selective transformations, which means this molecule steps into roles that no simple phenol or monothiol matches. We’ve listened to researchers at pilot plants and academic labs telling us that no substitute gives the same results in certain cross-coupling, ligand design, or surface modification work.

    Production Reality: Batch, Purity, and Hands-On Control

    From manufacturing, control of 2-Hydroxythiophenol requires more than off-the-shelf operation. Each batch starts from high-grade starting materials, and we dedicate reactors that never see cross-contamination from unrelated products. Controlled atmospheres are critical—both to limit oxidation of the thiol function and to prevent off-odors from spreading outside the plant. Our staff monitor every intermediate, not just the finished product, since instability or side-product carryover build up fast in the aromatic thiol business.

    We guarantee purity at levels targeted by modern synthetic chemists, usually exceeding 98% by HPLC. That just covers the main compound—color, trace sulfur byproducts, and volatile impurities all get checked in parallel. Years ago, clients regularly had to post-purify commercial batches they bought from trading houses. Challenging application development projects—like defensible trace analysis, anchored ligands for catalysts, or specialty polymers—quickly taught us the dollars lost from batches that barely scrape past minimum requirements.

    Conversations with End-Users: Where 2-Hydroxythiophenol Makes a Difference

    We’ve made hundreds of shipments of 2-Hydroxythiophenol to both companies and universities; it’s the ground-level conversations with formulators and research staff that shape our view. Synthetic chemists tell us our material offers consistency in nucleophilic aromatic substitution. That’s not just a talking point—the ortho arrangement leads to distinct selectivity, which others have confirmed in practice.

    On the surface chemistry side, researchers use 2-Hydroxythiophenol to create SAMs (self-assembled monolayers) on gold and other metals. Here, trace contaminants or slight oxidation lower yields or add inconsistency to the surface attachment process. Purity means better reproducibility: fewer failed runs. We've had clients come to us after piercing odors or yellow-brown discoloration plagued them in trials with less rigorously controlled material.

    Beyond pure R&D, companies working on anti-corrosion treatments or specialized sensors use our batches as feedstock for more elaborate syntheses. Our role often extends to providing technical support, especially for scale-up, since 2-Hydroxythiophenol degrades or darkens unless handled cooled and shielded from oxygen. Years of operational tweaks have taught us where bottlenecks lie: everything from transportation planning to the right inert packaging feature in our own drums or ampules.

    What Sets 2-Hydroxythiophenol Apart from Alternatives

    Chemists may ask, “Why not use simple thiophenol, or para-hydroxythiophenol, or a dihydroxybenzene thiol?” It always comes down to what’s needed in the synthesis or application. The ortho arrangement sets up unique hydrogen bonding opportunities, and its electron distribution differs from para isomers. In semiconductor cleaning, a slight shift in reactivity alters residue left on a wafer. In asymmetric catalysis, only this molecule fits the coordination environment some ligands demand.

    Thiophenol offers strong nucleophilicity, but its uses are limited in more specialized transformations since it lacks the additional coordinating group. Even where para- or meta- isomers exist, their steric profiles and chemical selectivity change downstream results. Over time, our team has run controlled side-by-side tests. We’ve confirmed that substituting other phenolic thiols—even at high purity—reduces regioselectivity or slows reaction rates in some target applications. Measuring this in-house gives our customers clear data, separating guesswork from evidence.

    On another front, customers sometimes look for cost savings in multi-purpose phenolic or thiol blends. The reality often stings: loss of performance in fine electronics, bioconjugation, or surface treatments costs more than a direct material swap saves. Repeat requests for traceability and supply chain transparency come from those who already got burned by lesser material. Being the manufacturer, we know exactly where every batch comes from, what modifications apply, and what testing regime each customer faces.

    Specifications: Beyond Paper to Practical Application

    Spec sheets only show half the story. We supply 2-Hydroxythiophenol as fine crystalline solid, pale to light yellow, with careful control over water and air access from the minute it leaves the reactor. Glass ampules or lined drums with tight seals prevent premature darkening and avoid off-odors that signal stray oxidation. We listen when clients report preferences between bulk versus small packs; reactivity and shelf life matter more than ease of handling for most projects at gram-to-multikilogram scales.

    Stability is always a concern. Even trace metal ions or excess air can catalyze unwanted side reactions. Over the years, we’ve improved packaging—from pre-cleaned anti-static bottles to vacuum-sealed options—so the product our customers receive performs without a hitch. For large-volume clients, lab trials expand into pilot quantities and custom bulk packaging—with sampling at every interval. Our technical manager tracks each lot through outgoing QA and field feedback.

    Transportation for this chemical stays closely monitored. 2-Hydroxythiophenol carries pungent odors typical for aromatic thiols. Storage recommendations at customer sites call for sealed containers, cool environments, and gloves to avoid extended contact. We don’t just pass on rules; we send end-users guidance born from field-tested experience—minimizing spillage risks, exposure to oxygen, and batch-to-batch contamination.

    From Lab-Scale Roots to Global Distribution

    Our manufacturing story began with modest batches supporting academic routes to new ligands and intermediates. Now, we ship to companies developing biosensors, high-cost coatings, and even utilities exploring corrosion abatement. The feedback loop matters: chemists return with results, both good and bad, and we adjust how we control process variables—temperature, atmospheric control, recrystallization solvents.

    Building scale in production of 2-Hydroxythiophenol meant working through staff training, quality programs, and constant review of environmental controls. Aromatic thiols demand skilled technicians—missteps can mean lost raw materials or safety incidents. Our team runs through regular audits, not just for compliance but for continuous improvement. It means less downtime, steadier production, and more consistent outcomes for those downstream.

    Regional regulations matter more now than they did a decade ago. It’s easier said than done to adapt, but customers working under REACH or strict US frameworks need documentation and batch-level traceability that we provide automatically. Regulatory support—meeting every environmental and workplace standard—comes from process knowledge, not just legal compliance. Whenever we see new rules hit, we review long before deadlines force hasty changes.

    Facing Challenges: Oxidation, Handling, and Logistics

    In practical terms, aromatic thiols like 2-Hydroxythiophenol challenge both manufacturing and user operations. Left exposed for too long, the compound darkens or acquires odors signaling unstable byproducts. Our facility leverages nitrogen purges at purification and packing, and fills each container with low headspace to limit exposure. Shipping partners stay briefed on temperature and hazardous goods demands. These measures didn’t come from manuals—they evolved from real losses and rejected shipments early on.

    Clients sometimes overlook on-site protocols after delivery. Overheating, leaving containers open on the bench, or using inadequate gloves let odors and instability become problems. We communicate often with end-users and purchasing agents, sharing field learnings and troubleshooting steps. Some problems reach us in the form of failed syntheses or surface modification results—our experience helps close gaps, whether it's a contamination issue, improper storage, or questions about downstream application.

    We invested in quality improvements based on actual disruptions—not theoretical risk. Air monitors and rapid containment mean nearly zero atmospheric release outside our plant. For customers, these lessons translate to safe storage, better waste handling, and less troubleshooting. Our team has seen all the mistakes. As a result, guidance supporting safe and effective use of 2-Hydroxythiophenol is more than boilerplate; it comes from long-term observation and detailed incident tracking.

    Continuous Improvement Motivated by Real-World Use

    Client engagement drives much of our work. Any new process or bulk order typically follows a period of pilot shipments and detailed feedback. Our plant integrates feedback to resolve not just major, but the small yet nagging, process issues: annoying crystallization in valves or caking during transfer, discoloration after long storage, or batch-to-batch odor variation. The team addresses each with a mix of better raw materials, fine-tuned purification, revised packing, or staff retraining.

    Sustainability pressures keep rising. While 2-Hydroxythiophenol isn’t produced in bulk like other aromatics, each kilo impacts local and broader environments. Internal waste streams get managed by capture and reprocessing rather than venting or dumping. Our chemists design routes to maximize yield, avoid batch failures, and reduce energy costs—all proven by tracking each lot through cradle and delivery. End users trust that our documentation matches reality.

    Occasionally, we get requests to modify composition or purification routes for ultra-specialized needs, such as high sensitivity analytical work or semiconductor projects. Our technical staff partner closely, building out small custom campaigns. These projects often teach lessons we then apply to the regular production flow. Small changes in raw material source or process temperature have outsized effects on stability, purity, and ease of use.

    Feedback Loop: Users, Researchers, and the Manufacturing Team

    We learn the most from the chemists—synthetic, analytical, and process teams—who report problems months or years after a sale. Failures in a catalyst run, discoloration of a gold-coated substrate, or an off-note in a batch of polymer additives spark detailed conversations. Our technical support takes these calls seriously because they drive the next improvement cycle. Over time, tweaks in manufacturing and logistics lead to better yields, cleaner reactions, and less troubleshooting for everyone.

    Publishing test data means showing real-world variability, not just glossy best-case numbers. We report anonymized batch data trends—on purity, byproducts, and stability—to our largest customers so they see the same reliability we live with. Trust builds on openness, and we don’t filter out anomalies when reviewing process changes. The mistakes become case studies for future hires and partners.

    By staying rooted in actual experience, our team builds both product and community. Long-term customers rely on our institutional memory about what does and doesn’t work. Some have built whole synthetic routes around the attributes peculiar to our 2-Hydroxythiophenol.

    A Compound That Brings Value Beyond the Beaker

    Why does 2-Hydroxythiophenol remain necessary in many fields? The answer grows clearer after years of production, technical calls, and solved customer challenges. Its unique molecular structure offers a combination of phenolic and thiol reactivity in one scaffold. Chemists need it for distinct substitutions that neither analogs nor easier-to-make alternatives supply. The ortho position influences coordination behavior in ligand design, which impacts final catalyst performance in the factory and the paper.

    Our process puts control into every stage—raw materials, careful atmosphere management, stepwise purification, and tailored packing—because correct handling at each point ensures clients waste no time purifying, cleaning, or repeating entire trials. These touches may sound simple but arise from decades of cumulative process knowledge.

    Cutting corners isn’t just cost dangerous. You see it in extra purification steps slotted into lab schedules, the need to dispose of off-color or strongly odorous samples, and the project delays caused by inconsistent results. We’ve built our model to instead supply reliably clean, correctly labeled 2-Hydroxythiophenol every time it leaves the door.

    Supply chain confidence grows out of traceability, not marketing. From our reactors to customer loading bays, we track every container. Batches carry quality certifications—supported by both in-process and outgoing testing—that stand up to regulatory inspection, research scrutiny, or process-scale validation. This supply integrity matters in every field, whether a graduate student carries out a single flask-scale modification or a company runs through drums per month.

    Looking Ahead: Ongoing Learning and Innovation

    Chemical manufacturing never stands still. Our team reviews new literature and market developments, watching for opportunities to improve process performance, reduce waste, and support innovative end-use directions. Customers suggest, challenge, and inspire change: New applications in electronics, advanced polymer building blocks, or next-generation surface coatings prompt tweaks in synthesis or logistics. Sometimes, simple process improvements make the biggest difference for everyone involved.

    2-Hydroxythiophenol has never been a mass-market product, but its role in research, specialty manufacturing, and advanced applications keeps evolving. As regulatory expectations around the globe intensify, we meet those demands in real-time, keeping communication open and documenting every improvement. Our commitment is to deliver reliable, high-purity product, informed by experience, and supported by technical conversations grounded in actual use—not sales promises.

    We welcome researchers, production experts, and technical managers who need more than a simple listing or a batch spec. Our feedback-driven, open approach to manufacturing ensures each lot delivers what’s expected—because that’s what years of lessons, challenges, and partnerships have taught us works best.