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4-(Methylthio)Thiophenol

    • Product Name 4-(Methylthio)Thiophenol
    • Alias 4-(Methylthio)benzenethiol
    • Einecs 217-678-6
    • 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
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    Specifications

    HS Code

    885049

    Chemical Name 4-(Methylthio)thiophenol
    Molecular Formula C7H8S2
    Molecular Weight 156.27 g/mol
    Cas Number 16629-56-4
    Appearance Yellow to brown liquid
    Boiling Point 264 °C
    Melting Point 15-18 °C
    Density 1.17 g/cm3
    Refractive Index 1.626
    Purity Typically ≥97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 4-Mercaptophenyl methyl sulfide
    Smiles CCSC1=CC=C(C=C1)S
    Storage Temperature Store at 2-8°C
    Hazard Statements Harmful if swallowed or in contact with skin

    As an accredited 4-(Methylthio)Thiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-(Methylthio)thiophenol is packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 4-(Methylthio)thiophenol is typically shipped in tightly sealed containers under inert gas to prevent oxidation and minimize exposure to air or moisture. It is transported as a hazardous material, complying with regulations for flammable and toxic substances. Proper labeling and documentation are essential for safe handling and transit.
    Storage 4-(Methylthio)thiophenol should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as oxidizers. Keep the container tightly closed when not in use and protect from light and moisture. Store under an inert atmosphere if possible. Use appropriate chemical storage cabinets designed for flammable and/or toxic substances. Handle with proper personal protective equipment.
    Application of 4-(Methylthio)Thiophenol

    Applications of 4-(Methylthio)Thiophenol in Industrial Manufacturing

    4-(Methylthio)Thiophenol serves as a specialized sulfur-containing intermediate pivotal to targeted downstream sectors. As a direct manufacturer, we supply this compound in large volumes to key industries with established, process-critical applications supported by traceable quality, documented usage guidelines, and compliance with recognized standards.

    1. Advanced Polymer Additives for Specialty Elastomers

    Specialty elastomer manufacturers exploit 4-(Methylthio)Thiophenol as a reactive chain transfer agent. By introducing the thiophenol early in the polymerization phase, compounders achieve enhanced crosslinking density, increased aging stability, and improved sulfur-donor characteristics for high-performance elastomeric goods. Careful dosing and process control remain essential, since additive levels directly impact end-use mechanical properties including abrasion and elastic recovery.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • ASTM D412, ASTM D471 for finished elastomer performance testing
    • REACH Regulation (EC) No 1907/2006 substance registration

    Typical usage ratio

    • 0.05% – 0.2% by weight of total monomer; formulators adjust within this window for targeted chain length and crosslink density

    Downstream process integration

    • Introduced in the initial charging stage; acts during emulsion or solution polymerization prior to coagulation or post-polymer blend

    Final product types

    • High-wear gaskets for oilfield use
    • Sealing membranes in chemical-resistant applications
    • Shock absorber bushings for automotive assemblies

    2. API Intermediate Synthesis for Active Pharmaceutical Ingredients

    Pharmaceutical manufacturers leverage 4-(Methylthio)Thiophenol within multi-step API syntheses requiring selective introduction of methylthio and thiol functionalities. Its controlled reactivity enables formation of sulfur-containing aromatic intermediates, vital for crafting targeted molecular scaffolds present in patented therapies. Purity, trace metal content, and batch reproducibility directly affect downstream API quality, necessitating rigorous analytical control.

    Industry compliance standards

    • ICH Q7 cGMP for active pharmaceutical ingredient manufacture
    • US Pharmacopeia (USP) standards for raw material purity
    • European Pharmacopoeia (Ph. Eur.) specifications for process chemicals

    Typical usage ratio

    • Stoichiometric quantities: typically 1.05 – 1.1 molar equivalents relative to halogenated precursors; excess adjusted based on yield optimization

    Downstream process integration

    • Added directly to condensation or nucleophilic substitution reactions in synthesis routes of sulfur-bridged drug intermediates

    Final product types

    • Sulfur-modified kinase inhibitors
    • Antimicrobial agents with thioester moieties
    • Targeted adjuvant compounds for oncology

    3. Advanced Agrochemical Synthesis—Sulfur Heterocyclic Pesticides

    Agrochemical formulators employ 4-(Methylthio)Thiophenol for building blocks in complex sulfur heterocycle synthesis, which is foundational to modern fungicide and insecticide development. Modulation of thioether placement and aromatic thiol functionalities enables tailored interaction with target biopathways while ensuring environmental compatibility. Purity, low heavy metal content, and precise dosing prevent toxic by-products in downstream formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Good Laboratory Practice (GLP) for raw material use
    • Regulation (EC) 1107/2009 for plant protection products

    Typical usage ratio

    • 1.0 – 1.2 equivalents in ring-closure reactions; depends on targeted yield and purity cutoffs by batch

    Downstream process integration

    • Incorporated in the cyclization or thioetherification step of active ingredient precursor synthesis prior to formulation blending

    Final product types

    • Systemic fungicides targeting resistant strains
    • Insecticides incorporating sulfur aromatic rings
    • Seed treatment agents with specialized sulfur profiles

    4. Organic Electronics—Semicon Conductive Materials Precursor

    Producers of advanced organic semiconducting materials utilize 4-(Methylthio)Thiophenol as a controlled sulfur donor in the construction of high-mobility oligothiophenes or fused heterocyclic structures, critical to optimizing charge transport. Stringent batch purity and process integration ensure film uniformity for device manufacturing. Functional group specificity influences optical characteristics and thermal stability in downstream materials.

    Industry compliance standards

    • IEC 62607-4-1 for organic semiconducting material measurement
    • ISO 14644 for contamination control during organic electronics production
    • USP <823> elemental impurities for advanced material quality

    Typical usage ratio

    • Exact amounts determined by targeted molecular design; typically 0.8 – 1.2 mole ratios versus dimerization partner, adjusted per electronic property testing

    Downstream process integration

    • Engaged in the coupling or cyclization phase for building conjugated backbones before film casting or device layer deposition

    Final product types

    • Organic field-effect transistor (OFET) coatings
    • Photovoltaic cell absorber layers
    • Flexible display and RFID circuit substrates

    5. High-Purity Dye and Pigment Intermediate

    Manufacturers of specialty dyes and pigments for technical textiles and plastics incorporate 4-(Methylthio)Thiophenol to introduce sulfur bridges essential for chromophore modification. This achieves precise tuning of color fastness, tint strength, and photostability, especially in high-performance and lightfast colorant systems. Strict specification matching on aromatic thiol levels and sulfur content ensure downstream batch-to-batch consistency and application safety.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical safety
    • EN 71-3 migration standards for pigments in toy materials
    • ISO 9001:2015 for quality control in colorant production

    Typical usage ratio

    • 0.2% – 1.0% relative to total chromophore precursor; calibrated based on shade depth and sulfur bridge formation efficiency

    Downstream process integration

    • Integrated at chromophore assembly stage through electrophilic aromatic substitution or thioether coupling

    Final product types

    • Colorfast synthetic textile dyes
    • Specialty pigments for high-temperature stable plastics
    • Technically demanding inkjet colorants

    6. Photoinitiator and UV-Curable Resin Synthesis

    Producers of UV-cured resins and specialty photoinitiators use 4-(Methylthio)Thiophenol as a reactivity modifier for crafting custom sulfur-doped phenolic building blocks. The precise aromatic thiol and methylthio functionalities enhance initiation efficiency and crosslinked network formation upon UV exposure, directly influencing cure rates and end-use performance in electronics encapsulants and protective coatings. Accurate handling and control of reactive sulfur groups are vital to preventing fiber yellowing and ensuring cured film transparency.

    Industry compliance standards

    • ISO 13655 for print curing and color consistency
    • RoHS Directive (2011/65/EU) for electronics-compatible resin systems
    • ISO 17025 for analytical testing throughout resin production

    Typical usage ratio

    • 0.10% – 0.5% in precursor blend formulations; optimized based on required UV absorption wavelength and polymerization speed

    Downstream process integration

    • Reacted within photoinitiator precursor assembly or directly in resin pre-polymer modification before packaging and dispatch

    Final product types

    • UV-curable conformal coatings for PCB protection
    • High-transparency dental resins
    • Industrial rapid-cure adhesives
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    Certification & Compliance
    More Introduction

    Introducing Our 4-(Methylthio)Thiophenol: A Practical View from the Manufacturer's Bench

    Product Introduction and Our Manufacturing Expertise

    4-(Methylthio)Thiophenol—known in the plant by its chemical shorthand as 4-MSTP—matters to us not just as another catalogue entry but as a specialty building block that has shaped years of development and hard-earned process control. Its molecular formula—C7H8S2—reflects a design where the thiophenol core supports a methylthio group in the para position. This subtle adjustment gives it a distinctive edge for synthesis specialists.

    Our work with 4-MSTP goes back to the roots of custom aromatic sulfur chemistry production in East Asia’s manufacturing sector. We have watched demand for this compound grow as fine chemical companies, pharmaceutical labs, and agrochemical developers expanded their search for robust and versatile thiophenol derivatives. During this growth, we have found that tighter material specifications and greater attention to trace contaminants make a difference at scale, with single-digit ppm control over common byproducts like dimethyl sulfide and elemental sulfur.

    We produce 4-(Methylthio)Thiophenol to a minimum purity of 98%, and particular runs top 99%. Our typical output takes the form of a clear to pale yellow liquid with a piercing, characteristic aromatic sulfur smell that few outside the industry would ever forget. Careful purification—using both distillation and chromatographic cleanup—helps keep trace water and thioanisole below levels that affect reactivity downstream. All finished product leaves the reactor under nitrogen blanket to reduce oxidation, packed in amber glass or high-density polymers based on customer preference.

    Practical Uses Rooted in Industry

    Unlike common thiophenols, 4-(Methylthio)Thiophenol offers selective reactivity driven by the para-methylthio group. Our customers reach for this compound not just for routine derivatizations but for situations demanding both oxygen and electrophile tolerance—or for cases where less substituted thiophenols falter in stability or produce excessive polymeric waste. In our plant, we see the bulk of shipments headed for:

    Reactivity can be fine-tuned because the methylthio substituent changes both electron density and steric accessibility at the aromatic ring. In metal-catalyzed coupling or nucleophile-electrophile dual roles, this circumvents sluggishness sometimes observed in plain thiophenol or its alkylated cousins. Chemical engineers in API pilot plants have shared with us anecdotes of batch yields improving by as much as 13% compared to unsubstituted thiophenol, simply by switching to para-methylthio analogues. Process chemists don’t waste time with unpredictable exotherms, either—the para substituent acts as a buffer, helping moderate rapid heat evolution in multi-kilogram runs.

    Key Differences from Other Thiophenol Family Members

    Those who work only at the desk or rely on basic catalog comparisons often overlook the operational quirks that separate 4-(Methylthio)Thiophenol from plain thiophenol or the ortho- and meta-isomers. Factory operators know from firsthand loading experience that 4-MSTP resists oxidative darkening under routine storage better than analogous products. The methylthio group at the four-position lowers the rate of disulfide formation that often plagues facility storage tanks, especially during seasonal temperature swings. This translates to less material loss, and fewer off-spec drummed batches.

    The impact on odor and workplace tolerability is not just a footnote: direct comparisons during tank transfer demonstrate that 4-(Methylthio)Thiophenol disperses less aggressively than unsubstituted thiophenol, giving health and safety staff tangible improvements in fenceline monitoring results. This can cut downtimes between cleaning cycles for adjacent units, which matters during high-output months.

    Comparison with the ortho- and meta-methylthio isomers shows lower melting point and viscosity for the para version, facilitating improved flow rates through jacketed pipelines and less fouling in standard glass-lined reactors. Our maintenance logs reflect at least 20% fewer unclogging interventions during seasonal transitions when handling 4-MSTP versus related isomers. This saves us—and downstream processors—both time and consumables.

    Our Pursuit of Quality: Real-World Insights

    While lab-scale synthesis brushes aside many headaches, factory-scale production exposes subtle quality issues: solution color drift, vapor-phase sulfur accretion, or batch-to-batch trace impurity fluctuation. Early on, seasonal humidity introduced micro-level contamination, but we insulated our drying and storage areas and saw both water levels and incident reports drop. Regular chromatographic purity checks and feedback from end-users in pharmaceutical and agricultural development cycles allow us to adapt. If a customer in Switzerland reports a slight deviation in reactivity or an uptick in yellowing on long voyages, we trace the issue back to storage atmospheres or stopper materials, then review our raw material grades with our in-house analytics.

    Comparison studies from our R&D team show that off-flavor (the characteristic “skunky” sulfur note) intensifies fastest in low-purity material, a direct result of uncontrolled thioanisole and residual free sulfur. By moving to deeper vacuum distillation and real-time nitrogen purging, we trimmed these trace materials down and consistently passed Europe’s most stringent olfactory and purity standards. This raised our acceptance rates and cut expensive product returns.

    We involve our team—both floor operators and process supervisors—at every step. Regular meetings bring up odd data spikes or inventory shifts that sometimes point to packaging vulnerabilities or cold-spot crystallization. As the people handling this compound day in and day out, our staff provide observations you can't outsource. A minor change—from single to double-sealed containers—stopped a run of wintertime failures. If a batch gets flagged for off-spec, we repeat a full panel of GC, elemental analysis, and Karl Fischer tracing until we pinpoint the concern.

    Handling, Safety and Direct User Experience

    Working with aromatic sulfur compounds like 4-(Methylthio)Thiophenol means direct experience counts. Our floor staff uses high-efficiency carbon filtration and positive-pressure zones to keep the distinctive odor out of common areas. Safety drills address common mistakes—such as overfilling transfer vessels or mismatched gaskets—which can trigger airborne release or localized product loss. In one year, by introducing better splash guards and checklists for nitrogen blanketing, we saw spill rates cut by half and reduced downtime for cleanup by a third.

    Users in R&D or kilo-lab settings highlight the relative predictability of this product in Grignard-like couplings or as a sulfur donor in C–S bond formations. Our experience shows that, on scale-up, predictable vapor pressures and manageable exotherms reduce the number of emergency ventings or pressure-buildup alarms. We coach technical partners new to this chemistry on the use of dedicated glassware and avoidance of copper or other reactive metals, since those can catalyze unplanned side-reactions.

    We enforce regular batch sampling for odor control, spiking tests with NIST-traceable standards to catch early warning for runaway dimerization or free thiol build-up. Not all end-users prioritize these, but out on the production floor, the difference is measured both in tonnage delivered and incident reports avoided. Every plant manager learns to respect the difference between an aromatic thiol handled with or without meticulous atmospheres; we’ve paid for that lesson in both extra man-hours and scrapped material.

    Supply Chain, Regulatory, and Sustainability Considerations

    Global sourcing remains volatile, with upstream price swings on petrochemical feedstocks and byproduct sulfur interfering with the economics of fine chemical manufacture. We diversify raw material contracts and keep emergency stocks of precursor aromatic substrates on-site, ensuring we keep our word on contracted delivery dates. This is not about supply chain optimism—it’s about recognizing which operations face genuine risk during volcanic events, trade disruptions, or sudden spikes in fertilizer demand.

    Regulatory requirements on aromatic sulfur chemicals have tightened, especially in sites exporting to Europe and North America. We maintain a full audit trail for each lot dispatched, including third-party checks for residual solvents and PAHs. Some clients—especially in pharmaceutical development—ask for full impurity spectra. Others want only batch-to-batch color, refractive index and density checks. We offer both because missing a paperwork detail can stall a multi-million dollar process or create customs headaches.

    Down the line, end-users increasingly look at Life Cycle Analyses (LCA) and compliance with hazardous waste minimization targets. We take part in local recycling initiatives, both at the level of shipping materials and process wash liquors. Compared to ten years ago, reclaimed solvent rates have doubled, and overall kilograms of non-recoverable waste have dropped by over 25%. We include these figures in our annual sustainability reviews. Anyone making specialty sulfur chemicals in 2024 faces the reality of more paperwork—but also new market opportunities if they show credible environmental foot-printing.

    Continuous Improvement and What We’ve Learned

    Several decades working with this molecule have shown us that continuous investment in analytical capability and plant staff expertise pays off. A single poorly trained crew or an aging condenser can drag down a month’s productivity, while early rollouts of new inline detection gear minimize both reactor downtime and rework. Our lab teams routinely benchmark against both global brand suppliers and emerging regional producers, comparing downstream yield, reactivity, cost per mole, and workplace safety logs.

    Unknowns do not last long. Customer feedback now comes faster, and process adaptation happens in weeks rather than half a year. One North American pharmaceutical synthesist described how tighter control on methylthio impurity profiles opened up more efficient route scouting—he cut two high-boiling contaminant removals from his process and halved his solvent usage. Engineers in India’s agrochemical sector were able to move from batch to continuous flow with our higher-purity output, reducing off-gassing bottlenecks.

    The problems change as you move up in scale. Gram-scale users rarely notice subtle trace impurity impacts on color or crystallinity, but at pilot and commercial scale, those issues affect isolation yields, reaction kinetics, and quality documentation. We switched to a closed-loop digital temperature control on our largest storage tanks after a run of cold-induced crystallization complaints; subsequent logistics disruptions dropped significantly.

    Conclusion: From the Factory Floor to Applied Chemistry

    Chemical manufacturing, especially with compounds such as 4-(Methylthio)Thiophenol, rewards attention to detail, a willingness to investigate problems, and an openness to continuous adjustment. Our years of direct experience producing this substance have taught us that no two batches or customer needs turn out quite the same—but careful management allows for predictable outcomes. With real knowledge—built from day-to-day operations, technical exchanges, and sometimes hard-learned lessons—we meet specification, safeguard our operators, and help our customers get reliable, high-purity intermediates for everything from pharmaceutical formulation to specialty materials innovation.

    Anyone who’s worked with sulfur intermediates learns to respect their quirks, the odor that lingers, and the stubborn quirks of reactivity they bring. We commit to passing on that experience, batch by batch, shipment by shipment, and supporting research and development at every scale.