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HS Code |
509520 |
| Chemical Name | 4-Mercaptophenol |
| Cas Number | 123-39-7 |
| Molecular Formula | C6H6OS |
| Molecular Weight | 126.18 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 47-51 °C |
| Boiling Point | 174-175 °C (at 20 mmHg) |
| Solubility | Slightly soluble in water, soluble in ethanol and ether |
| Density | 1.25 g/cm³ |
| Smiles | C1=CC(=CC=C1S)O |
| Inchi | InChI=1S/C6H6OS/c7-5-1-3-6(8)4-2-5/h1-4,7-8H |
| Synonyms | p-Mercaptophenol; 4-Hydroxythiophenol |
As an accredited 4-Mercaptophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Mercaptophenol is supplied in a sealed amber glass bottle, 25 grams, with a tamper-evident cap and clear hazard labeling. |
| Shipping | 4-Mercaptophenol is shipped in tightly sealed containers to prevent contamination and minimize exposure to air and moisture. It should be packed according to international regulations for hazardous chemicals, labeled with appropriate hazard warnings, and transported under cool, dry conditions. Protective measures ensure safety during handling and transit. |
| Storage | 4-Mercaptophenol 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, well-ventilated area away from light, moisture, and incompatible substances like strong oxidizers and bases. Store at room temperature or lower, and label containers clearly to ensure safe handling and prevent contamination. |
Applications of 4-Mercaptophenol in Industrial ManufacturingAs a direct manufacturer with deep expertise in aromatic thiol chemistry, we reliably supply 4-Mercaptophenol for specialized downstream sectors. Each target industry below demonstrates where customers consistently integrate this raw material to enable specific end-product value and performance. Our application insights draw from formulation experience, compliance knowledge, and collaboration with process engineers worldwide. 1. Photopolymer Manufacturing for Photoresist FormulationsWithin the semiconductor and PCB fabrication industry, formulators use 4-Mercaptophenol as a key chain-transfer agent in photoresist systems. Its role is crucial in controlling polymer molecular weight during free radical polymerization, resulting in consistent photo-patterning precision crucial for sub-micron lithography processes. Manufacturers leverage its unique reactivity to tune profile properties, such as imaging resolution and dissolution rates, which directly influence etching performance and yield. Industry compliance standards
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2. Silver Surface Modification in Conductive InksIn printed electronics manufacturing, production engineers select 4-Mercaptophenol to form self-assembled monolayers (SAMs) on nanoparticulate silver surfaces, enhancing ink print stability and electrical performance. It functions by binding strongly to silver via thiol groups, preventing agglomeration during dispersion and sintering. This molecular interface also improves adhesion to substrates, essential for fine-line printing and device longevity in RFID, touchscreen, and sensor applications. Industry compliance standards
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3. Polymer Crosslinking Agent for Epoxy and Acrylic SystemsFormulation chemists in high-performance coatings and adhesives incorporate 4-Mercaptophenol as a functional crosslinker or co-monomer to adjust network density, cure rates, and chemical resistance in both epoxy and acrylic-based systems. The thiol enables thiol–epoxy and thiol–ene reactions under UV or heat, offering flexible ways to engineer hardness, elongation, and solvent resistance for industrial finishes exposed to demanding chemical or thermal environments. Industry compliance standards
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4. Intermediate for Active Pharmaceutical Ingredient (API) SynthesisChemical process engineers in pharmaceutical contract manufacturing organizations (CMOs) utilize 4-Mercaptophenol as a building block in multi-step API syntheses, particularly for organosulfur drugs and molecules requiring aromatic thiol intermediates. The compound offers ortho/para selectivity in nucleophilic aromatic substitution and enables late-stage thiol-functionalization under GMP manufacturing, ensuring batch traceability and impurity management for regulated markets. Industry compliance standards
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5. Corrosion Inhibitor Additive in Metalworking FluidsIndustrial fluid formulators employ 4-Mercaptophenol as a specialized corrosion inhibitor additive for water-based metalworking fluids, especially those designed for non-ferrous alloys and precious metals. The thiol group selectively adsorbs to metal surfaces, forming a passivating film that hinders oxidative degradation, pitting, or tarnishing during cutting, grinding, or lubrication, even in high-load manufacturing environments where stable and long-lasting protection is critical. Industry compliance standards
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6. Analytical Reagent for Mercury Detection AssaysProducers of environmental monitoring solutions integrate 4-Mercaptophenol as a complexing reagent in kits and laboratory diagnostics for quantitative mercury detection. The aromatic thiol forms colored or fluorescent complexes upon reaction with Hg(II) ions in sample matrices, enabling sensitive visual or spectroscopic measurement of trace environmental mercury for industrial, municipal, and water laboratory settings. Industry compliance standards
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In our labs, 4-Mercaptophenol, also recognized as para-mercaptophenol or 4-hydroxythiophenol, shows its real character through both its chemistry and the many roles it plays across industries. We've been crafting this compound for years, and with every batch, we focus on everything that matters in practical use—from its purity, odor, handling, to how it interacts with other materials in the workflow. Most of what gives this compound its reputation centers around the unique pairing of its thiol and phenol groups on the benzene ring. This difference stands out clearly once you compare it to isomers like 2-mercaptophenol or alternatives in the benzenethiol family.
Quality 4-Mercaptophenol leaves our reactors as a solid crystalline substance, usually off-white to pale yellow—occasionally more yellow if stored long or exposed to moisture. The faint, yet lingering, sulfur odor is often a reminder to those who work closely that this is a thiol through and through. Our product typically lands at purity above 99%, since lower grades usually trigger issues both in lab work and manufacturing lines. Even around minor impurities, the reactivity profile shifts, and applications like sensitive surface modifications or organic syntheses see the effects right away.
We see the highest volumes of this compound moving out for use in surface science, especially for self-assembled monolayers on gold substrates. The thiol group binds strongly with gold, making this compound favored in biosensor construction, certain medical devices, and research setups investigating surface chemistry. Years ago, we worked closely with teams fabricating test sensors—not only did they need reliable batch-to-batch consistency, but even minor variations in crystallinity affected the time it took to anchor molecules on a gold slide. From our position, that told us to invest in not just quality control, but also process modifications to minimize subtle batch differences.
Outside of surface applications, 4-Mercaptophenol serves as an intermediate in organic syntheses, dye manufacturing, and in polymer research. Its dual functional groups open wide possibilities for downstream reactions. Researchers utilize the hydroxyl group for further derivatization, while the mercapto (thiol) group often targets conjugation or coupling with metals and other organics. Some pharmaceutical projects turn to this molecule as a launching pad for crafting custom ligands or fine-tuning biological probes.
Our clients rarely settle for just knowing the CAS number or chemical formula. Real daily work relies on knowing the typical form, handling requirements, and the details that influence performance. We produce 4-Mercaptophenol in several particle size ranges, mainly tailored for those needing fine powders for rapid dissolution or larger crystals for easier filtration in synthesis. Packaging matters too—smaller lots packed in amber glass prevent light exposure and minimize oxidation, which can alter reactivity fast.
Consistency is the anchor. Our refining steps knock down unwanted sulfur-containing byproducts, and extensive drying cycles lower water content. More than once, we’ve had conversations with partners who ran into unexplained interference peaks during spectroscopic analysis, only to trace the issue back to trace oxidized thiols or phenolic byproducts in lower-cost material from other sources. Tighter control at our end created fewer downstream headaches on theirs.
We stay close to industry norms in terms of assay (purity), melting point, and heavy metal thresholds. Typical melting point for our high-grade product sits firmly between 86-88°C. Moisture content hovers below 0.1%—the sweet spot for minimizing clumping and errant side reactions in sealed environments. Sulfur and metal impurity levels routinely test well below the detection limits required in analytical or pharmaceutical work. Chromatographic purity checks, not just titration or color tests, show the minor impurities that influence tough applications.
Chemistry offers a few ways to get similar functional effects, sometimes by using isomeric alternatives or other aromatic thiols. Over years of direct dialogue with chemists, we’ve seen the differences play out in multiple applications. The main distinction comes down to where both the hydroxyl and thiol groups sit on the ring. With 4-Mercaptophenol, both functional sites are in para positions, reducing internal steric hindrance and providing distinct reactivity compared to ortho- or meta-isomers like 2-mercaptophenol. This spatial arrangement gives better access when using the molecule as a linker or building block. In surface science, for example, the para position boosts signal clarity in many detection schemes, particularly in surface plasmon resonance experiments.
Using a different aromatic thiol, such as thiophenol, strips away the hydroxyl group and limits options for further functionalization. Chemists in polymer research and dye synthesis often need both reactive handles; taking one away usually forces them into workaround syntheses, introducing more steps, reagents, or purification headaches. Other competitors—such as para-aminothiophenol—swap the hydroxy for amino, creating a new set of reactivity and safety concerns. In some synthetic schemes, this swap increases toxicity risks, narrows the set of compatible reaction partners, or triggers instability under the desired conditions.
We’ve noticed that in biological surface modification, researchers often face non-specific binding or reduced selectivity when switching to analogues. The dual functionality of 4-Mercaptophenol sets a balanced stage for crafting surfaces with precise molecular recognition features. Those met with throughput bottlenecks or inconsistent bioactivity usually trace it back to substitutions or inferior para-mercaptophenol quality.
We keep handling straightforward but strict. Unopened product stays in cool, dry spaces, sealed tightly and away from reactive agents like strong oxidizers or bases. Many labs notice the thumbprint smell—sulfur—but know it never lingers beyond a quick cleanup. Dust control, good ventilation, and use of gloves prevent most unwanted exposure. In our facility, even with experienced staff and good safety routines, we see that working with open containers for long periods can intensify air concentration, so we recommend short handling periods or use of fume hoods.
From raw material through final product, we track every container with a batch and lot number, detailed production record, and shelf-life check. Freshly prepared batches look and behave consistently. If a bottle spends months on a shelf in a humid room, it doesn’t take long for clumping or color shift to crop up. Stable containers make downstream work easier for our customers; those who keep stocks tightly sealed and consider regular inventory turnover rarely confront surprises.
Some customers initially underestimate the oxidative sensitivity of the thiol group. We’ve fielded plenty of troubleshooting calls over unexplained side reactions. Extra oxygen in the headspace or exposure to UV ends up oxidizing the thiol, shifting mass balance in analytical methods or blocking intended surface reactions. We spent years developing packaging that reduces the risk while keeping everything manageable for both research and large-scale operations.
Efficient synthesis generates byproducts, some with environmental considerations—a fact easy to overlook for those not on the manufacturing side. Waste trace thiols and phenolic substances require careful treatment before disposal. We route all liquid and solid waste streams to controlled neutralization and scrubbing steps. Years ago, we expanded our treatment plant to handle peaks in production, making sure nothing inconsistent ends up in outgoing effluent. Most low-volume producers skip or minimize these steps, but cutting corners increases long-term risk.
We routinely monitor our wastewater streams for oxidized sulfur species and phenol derivatives. Partnering with third-party labs helped us uncover trace contaminants and opens up exchange of best practices. We’re not content with just meeting minimum regulatory standards. The investments show up in fewer regulatory complications and smoother, more predictable production runs. Customers that need to manage downstream waste streams appreciate our transparency—and it shapes the way they plan for their own compliance needs.
Solvent recovery and recycling also drives our process. Most of the solvent used for crystallization and purification gets cycled through closed loops, cutting down on both environmental impact and operating costs. By focusing early on efficient process design, we maintain both high product output and responsible waste management.
Raw material costs shift due to global sulfur price swings and changes in phenol derivative demand. Over the past few years, supply disruptions and shipping constraints impacted lead times, especially for unusual particle sizes or packaging volumes. We keep safety stock on hand to manage abrupt shifts, but sometimes even that gets stretched if demand spikes across multiple industries at once.
Our approach to pricing stays tied closely to batch quality. High-purity, low-impurity material doesn’t just cost more to make—it saves downstream issues, reduces product rejects, and simplifies compliance for our customers. In tough market cycles, competitors undercutting with lower-priced, higher-impurity material might attract short-term buyers. Over the long haul, repeat customers return after running into reliability issues in their own lines. Several clients tried alternates, experienced surface fouling or product discoloration, and came back once they added up time spent troubleshooting versus slightly higher up-front price.
Market pressures force constant process review. We avoid shortcuts for faster output when it could risk batch quality. Honest, clear communication matters far more than one-off sales—many of our key customer relationships start with technical conversations, repeat shipments, and troubleshooting help, then expand naturally into bigger partnerships.
From our post, we see common issues: delayed shipments, unpredictable performance from off-spec or old material, interaction challenges with sensitive metals or polymers, and occasional regulatory hurdles. Each has pushed us to refine both process and communication.
Shipping delicate thiols cross-border requires paperwork and attention to shelf life. We maintain close relationships with couriers and run regular logistics reviews. Our approach—test shipping stability, use double-sealed containers, and label for temperature and light sensitivity—lets most shipments arrive with material in prime condition. Delays occasionally happen; keeping spares in customer hands avoids production stops on their end.
Performance unpredictability can usually be traced back to either formulation drift over time or minor contamination. We run side-by-side quality tests with customer-archived samples, helping labs isolate process changes or equipment issues. Detailed COA reports, updated with every order, provide confidence that specification changes are intentional, not accidental.
Speaking frankly to peer manufacturers, regulatory demands for phenolic compounds and sulfur-containing chemicals keep tightening. Our early adoption of extra vapor and liquid containment, regular environmental audits, and transparent reporting has kept us ahead of changing rules. Using best practices for our size helps reassure both inspectors and client compliance teams.
We’re watching demand for 4-Mercaptophenol grow as newer biosensing platforms, nanotechnology, and drug development strategies mature. Researchers want cleaner surfaces, tighter functionalization, and documented provenance for every molecule. Requests for isotope-labeled or special-purity batches come more often now. We respond by keeping our process design flexible—smaller reactor runs, more targeted quality checks, and close attention to lot-traceability.
Application development shapes production choices. For surface science labs, we focus on keeping the thiol group free from oxidation; for synthetic organic chemists, we offer custom batch sizes and added drying steps. For those building larger devices or scaling up, we look for ways to shave time without sacrificing our quality guarantees.
Closing feedback loops between field users and our reactors helps us spot subtle new requirements. Our technical team keeps open lines with both research and production, catching practical feedback—like the need for anti-static packaging in especially dry climates, or tighter crystal size control for automated synthesis machines.
Our experience with 4-Mercaptophenol roots itself in routine, careful control—detailed tracking, real human troubleshooting, and investment in waste management and process flexibility. As the role of this molecule continues expanding in both fundamental research and practical applications, the value of consistency, clear communication, and honest reporting only grows. By staying grounded in the needs of those actually using the product, and owning every step from raw material to finished batch, we continue tightening the bond between manufacturing reliability and real-world scientific progress.