Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3,4-Dimethoxythiophenol

    • Product Name 3,4-Dimethoxythiophenol
    • Alias 3,4-Dimethoxybenzenethiol
    • Einecs 251-849-6
    • 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
    VTB
    Specifications

    HS Code

    516531

    Chemical Name 3,4-Dimethoxythiophenol
    Molecular Formula C8H10O2S
    Molecular Weight 170.23 g/mol
    Cas Number 7154-77-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 143-144 °C at 15 mmHg
    Density 1.16 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >= 98%
    Flash Point 155 °C
    Storage Conditions Store at 2-8 °C, tightly closed, away from light
    Refractive Index 1.589 (lit.)

    As an accredited 3,4-Dimethoxythiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,4-Dimethoxythiophenol is supplied in a 25g amber glass bottle with a secure screw cap and chemical hazard labeling.
    Shipping 3,4-Dimethoxythiophenol is shipped in tightly sealed containers made of compatible materials to prevent leakage and exposure. It should be stored and transported at room temperature, away from heat, ignition sources, and incompatible substances. All packages are clearly labeled and compliant with relevant chemical transport regulations to ensure safety during shipment.
    Storage 3,4-Dimethoxythiophenol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong oxidizing agents, and incompatible materials. Properly label containers and store them in a dedicated chemical storage cabinet, preferably for flammable or reactive substances, and ensure compliance with all safety regulations.
    Application of 3,4-Dimethoxythiophenol

    Applications of 3,4-Dimethoxythiophenol in Industrial Manufacturing

    As a specialized chemical raw material supplier with direct production capability, we provide 3,4-Dimethoxythiophenol to customers operating precision processes in pharmaceuticals, agricultural chemicals, advanced electronic materials, high-performance polymers, photoinitiators, and fine chemical synthesis. Below are its established application areas, with details on regulatory compliance, practiced formulation usage, process integration, and downstream product categories.

    1. Pharmaceutical Intermediate Synthesis

    3,4-Dimethoxythiophenol functions as a key intermediate in the manufacture of advanced pharmaceutical molecules, especially for API (Active Pharmaceutical Ingredient) building blocks where sulfur substituents improve pharmacokinetic properties or serve as reactive handles for further derivatization. Medicinal chemistry protocols typically use this compound for thioetherification, sulfur bridge formation, and as a nucleophile in heterocycle construction. Pilot runs and multi-ton GMP batches require precise inventory traceability and conformance to regulatory test methods for residual solvents and elemental impurities.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <826>: Residual Solvents Testing
    • EU GMP, Part II
    • Specific customer pharmacopoeia monographs dependent on API

    Typical usage ratio

    • 0.2% – 4% molar equivalent relative to total substrate, with exact ratio determined by step dosage in synthetic scheme and process yield targets

    Downstream process integration

    • Batch addition at the nucleophilic aromatic substitution or S-arylation step
    • Post-reaction purification by solvent extraction and crystallization
    • Complete material reconciliation within GMP batch record

    Final product types

    • Target APIs for cardiovascular, oncology, and neuroactive therapeutics
    • Advance intermediates for contract development and manufacturing organizations (CDMOs) producing specialty sulfur-containing molecules
    • Custom reference standards and impurity markers

    2. Crop Protection Active Ingredient Manufacturing

    The compound is incorporated into synthesis flows for specific thiophenol-based fungicides and herbicides, giving high selectivity profiles for modern agrochemical formulations. Agrochemical groups use it to introduce sulfur functionality, enabling novel structure-activity relationships and photo-stable pesticide molecules. Raw material shipments must comply with regional environmental and worker safety legislation, in addition to documented safety data for process operators.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (Europe)
    • US EPA 40 CFR Part 158 (Pesticide data requirements)
    • China GB/T 1604-2014: General Rules for Pesticide Production
    • ISO 9001:2015 for manufacturing traceability

    Typical usage ratio

    • 0.5% – 3% by weight relative to reaction mass, modulated following development trials for desired product purity

    Downstream process integration

    • Integrated in multi-step syntheses for specific active compounds
    • Introduced during sulfenylation or cross-coupling with halogenated intermediates
    • Followed by in-line quality checks for unreacted starting material

    Final product types

    • Systemic fungicides for cereals and fruits
    • Herbicidal actives with improved degradation profiles
    • Formulation intermediates for emulsion concentrates and suspension concentrates

    3. High-Performance Polymer Synthesis

    3,4-Dimethoxythiophenol is utilized as a chain terminator, chemical modifier, or functional monomer in the manufacture of sulfur-containing engineering plastics, such as polythioethers and aromatic polyethers. Plastic formulators require tailored addition of such modifiers to engineer properties like flame retardancy, chemical resistance, and dielectric strength, especially for cables, electronic encapsulants, and specialty films. Batches must pass environmental and materials compliance assessments, including restricted substances and leachables.

    Industry compliance standards

    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • RoHS Directive 2011/65/EU (European electronics)
    • ISO 14001:2015 for Environmental Management
    • EN 60216: Electrical Insulating Materials—Thermal Endurance

    Typical usage ratio

    • 0.1% – 1.2% by weight based on polymer formulation, precisely controlled according to target mechanical and functional requirements

    Downstream process integration

    • Monomer feed dosing during melt polycondensation or solution polymerization
    • Catalyst-assisted copolymerization step
    • Post-reaction stabilization prior to pelletizing or extrusion

    Final product types

    • High temperature-resistant wires and cable insulation
    • High-performance films for electronics and automotive environment
    • Specialty membranes and coatings for filtration and corrosive media

    4. Photoinitiator and UV-Curable Resin Component Manufacturing

    This chemical is used as a precursor and intermediate in synthesizing novel photoinitiators and UV-crosslinkable additives. Its electron-rich thiophenol group provides reactivity for developing tailored UV absorbers and radical-generating structures required in high-speed printing inks, photoresists, and 3D printing resins. Photochemical process workflows require exact dosing and careful removal of byproducts, adhering to stringent purity benchmarks specific to electronics, printed circuit boards, and digital image applications.

    Industry compliance standards

    • EN ISO 4892-2: Plastics—Methods of Exposure to Laboratory Light Sources
    • China GB/T 26398: Photoinitiator Compounds for UV-Curable Materials
    • REACH SVHC compliance for photoinitiator raw materials
    • ASTM D7767: UV Cure Analysis in Coatings and Resins

    Typical usage ratio

    • 0.3% – 2.5% by weight in the initial building block synthesis, adjusted based on desired UV absorption range and curing response

    Downstream process integration

    • Key starting material for constructing thioether-linked photoinitiator scaffolds
    • Added to condensation or coupling step in photoinitiator intermediate synthesis
    • Subsequent formulation and QC analysis for photoinitiator product lots

    Final product types

    • UV-curable coating additives
    • Photoresist compounds for semiconductor lithography
    • High-efficiency free radical photoinitiators for inkjet and PCB industries

    5. Fine Chemical and Specialty Intermediate Production

    Specialty fine chemical manufacturers employ 3,4-Dimethoxythiophenol as a customizable building block for a range of aromatic sulfur compounds. It serves as a reagent in the assembly of bespoke molecules for fragrance modifiers, dye intermediates, and custom reagents in organic synthesis. Customers require lot-specific documentation on analytically verified purity and batch homogeneity, as well as regulatory support for downstream analytical compliance certificates.

    Industry compliance standards

    • ISO 9001:2015 Certification for Fine Chemical Synthesis
    • Certificate of Analysis (COA) requirements—IR, NMR, and GC-MS characterization
    • Compliance with applicable TSCA (US) or REACH registration for specialty chemicals
    • Control over aryl thiol residuals per distribution agreement

    Typical usage ratio

    • 0.2% – 2.5% by weight in targeted syntheses based on molecule complexity and function of sulfur aromatic group in end-use

    Downstream process integration

    • Functionalization step in dye or aroma intermediate manufacture
    • Used as a key starting block in sulfenylation or demethylation protocols
    • Profiling via HPLC or LC-MS to ensure absence of unknown impurities

    Final product types

    • Colorant intermediates for textiles and paper
    • Fine aroma chemicals for downstream blending
    • Analytical reagents for QA/QC laboratories
    Free Quote

    Competitive 3,4-Dimethoxythiophenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3,4-Dimethoxythiophenol: Product Insight from the Manufacturer’s Perspective

    Real-World Knowledge Behind 3,4-Dimethoxythiophenol

    Our facility has spent years developing and refining 3,4-Dimethoxythiophenol, a compound that, while not as famous as some other aromatic thiols, has gained a practical reputation among chemists and engineers for its distinct combination of sulfur functionality and dual methoxy groups on a phenol backbone. The product comes out of the reactor as a pale yellow to light brown liquid with a characteristic sulfurous aroma often noticed by anyone who has ever handled phenol derivatives. If you work with organosulfur compounds, you appreciate how the precise nature of substitution patterns influences both reactivity and isolating the material. The 3,4-dimethoxy substitution has a habit of imparting a degree of electron density to the ring, which can have subtle effects in both synthesis and downstream application.

    Compared to other thiophenols, our 3,4-Dimethoxythiophenol gets its edge in particular niche roles. You won’t find this molecule on every shelf, but researchers and technical experts in pharmaceuticals, agrochemicals, and material science come to us specifically for the way our process delivers high chemical purity and minimal residual sulfur contaminants. Our technicians run GC and NMR on each lot, minimizing thiol oxidation by keeping batch turnover tight and storage under nitrogen. In this chemical segment, it is easy to underestimate the impact of trace oxygen and moisture on shelf life and utility; we have learned the hard way how even small changes in storage conditions can degrade the product or lead to batch rejection.

    Meeting Industry Expectations and Real Application Challenges

    3,4-Dimethoxythiophenol plays a unique part in modern synthetic chemistry. Organic synthesis labs working on new drug scaffolds, for example, sometimes need thiolated aromatic compounds with selective electron-donating substituents. The two methoxy groups on the aromatic ring change the electronic landscape, giving chemists leverage in forming C–S bonds or in modulating reactivity in multi-step syntheses. Often, our clients are racing against the clock with competitive projects. Having reliable, well-characterized product in stock beats hunting through import logs and customs paperwork for something shipped from another continent.

    Some of our long-term partners use 3,4-Dimethoxythiophenol as an intermediate. In custom synthesis, the options for substitution are nearly endless, but the 3,4-dimethoxy configuration confers useful selectivity not easily achieved with more generic thiophenol variants. We supply to R&D departments in both established pharmaceutical companies and emerging biotech firms. Several have spoken to us about an improvement in yield and reduction in byproducts when using our material compared to batches from casual traders or brokers. Even our own QC team can tell the difference under the hood: sharper melting point profiles, cleaner end-stage HPLC signals, and less “unknown” content in their own pilot runs.

    In agricultural research, 3,4-Dimethoxythiophenol sometimes finds its way into projects on sulfur-containing crop protectants and experimental herbicides. It is not one of the most commonly talked-about building blocks in this field, but where selectivity or site-specific metabolism is needed, the methoxy pattern again brings value. We have consulted on cases where swapping to our product allowed a formulation team to eliminate undesirable residues, improving not only efficacy but environmental safety and process reproducibility—two topics always flagged in regulatory audits.

    Manufacturing Realities: From Raw Materials to Finished Compound

    Producing 3,4-Dimethoxythiophenol at scale challenges both the technical team and the operations crew. The building blocks required, usually substituted anisoles or phenols, demand careful sourcing to avoid isomeric impurities. Every time we refine our distillation or extraction steps, we shave weeks off downstream purification and minimize waste load. For those who have never set foot in a mid-scale chemical plant, the difference between a batch processed in open vessels and one done under inert – with water scavenging and constant monitoring – is more than laboratory trivia; it impacts whole months of inventory schedules and customer confidence.

    Working hands-on with this material, it is clear that slight deviations in temperature, pH, or even mixing speed during the key thiolation step can alter the product spectrum. We train our operators to pick up on aroma changes and color shifts, which often tell the story long before lab analytics send back the formal numbers. Sulfur chemistry, despite decades of tradition, responds strongly to the human factor. In our operation, even the drum labels reflect which technician oversaw each batch—a mark of accountability that helps when tracking down root-cause issues.

    Comparing with Other Substituted Thiophenols

    The market presents several choices for aryl thiols. 4-Methoxythiophenol, 2,5-dimethoxythiophenol, even unsubstituted thiophenol all have roles, but the difference often lies more in customer experience than it does on paper. Some of the most noticeable disparities come in reactivity: with two methoxy groups at the 3 and 4 positions, the electronic effects become more pronounced than in monomethoxy variants or plain thiophenol. This can influence coupling yields, selectivity, and, crucially, the odor profile that so often plagues operators and maintenance crews. Our quality tracking shows that downstream purification often runs more smoothly with our 3,4-dimethoxy product compared to the more oxygen-sensitive 2,5-isomer.

    Customers who switch to our product after using third-party or distributor-sourced material often report smoother processing — less tar, lower rates of thiol oxidation, and, when running reactions on the bench, faster “clean-up” times. In real industrial settings, time saved during filtration, resin work-up, or even simple bottle handling translates to lower labor costs and fewer replacement parts in the handling systems. We see this most prominently in pilot-scale or contract manufacturing runs where timelines are tight and every kilogram matters.

    Customer Experience: Consistency, Traceability, and Trust

    As direct manufacturers, we pay attention to details that sometimes get lost in distributor networks: the origin of raw materials, the age of each batch, the storage environment, the calibration of the GC-FID equipment. More than once, our process engineers have addressed a customer’s complaint about “strange results” by tracing back an anomaly to a supplier’s contaminated drum or incorrect labeling. Transparency is embedded into our batch records, and every customer can trace the material from the very first synthesis step through to the shrink-wrapped container on their loading dock.

    Even within our own facility, the expectation for repeat performance drives us to tweak reaction conditions, fine-tune purification, and adjust post-synthesis handling based on each year’s experience. Repeat customers keep us honest; they are quick to notice if a product behaves differently in a formulation or causes an unexplained drop in yield. This feedback loop sharpens our internal standards and leads to incremental changes year after year, such as changing solvent grades, improving nitrogen purity, or switching to glass-lined reactors in certain parts of our process.

    Market Context and Evolving Demand

    Unlike commodity chemicals, where every batch looks and feels the same across vendors, specialty aromatic thiols like 3,4-Dimethoxythiophenol sit in a different class. Each ton produced reflects past lessons—process bottlenecks identified, failed syntheses that never left the lab, and collective experience from hundreds of bench and plant chemists. It also reflects our reading of market signals: inquiries from formulation chemists, research proposals that call for functionalized aromatic thiols, and regulatory changes requiring tighter impurity profiles.

    Recently, a shift toward greener solvents and process intensification has impacted how we look at batch optimization. Some of our customers have begun seeking higher-concentration formulations, seeking to lower shipping weights and improve process chemistry yields. In response, our team has explored in-line extraction, recycling of process solvents, and alternative waste treatment—all strategies aimed at keeping our product in step with customer demands and sustainability standards. It is a constant balancing act, as one process change can improve cost but risk decreasing purity or shelf life if not implemented carefully.

    Regulatory and Environmental Considerations

    Handling and producing aromatic thiols, including 3,4-Dimethoxythiophenol, brings its own health and safety priorities. Our plant teams work within strict guidelines to monitor air quality, mitigate accidental releases, and train operators on safe handling. It isn’t just about ticking boxes; minor releases of sulfur-containing vapors can bring both odor complaints and scrutiny from local agencies. Our system of carbon scrubbing and negative pressure workspaces aims to capture any fugitive emissions. For those people accustomed to working with these compounds, even tiny improvements in odor control make the daily environment much more manageable—and keep relations with our community positive.

    Raw material traceability combines with a focus on reducing hazardous waste at every step. In recent years, new European and North American regulations have led us to retool certain process steps—not for simple compliance, but because the new approaches often help us improve on cost, reproducibility, and batch-to-batch security. Sometimes these changes mean working more closely with local authorities, sharing operating data, or inviting auditors inside to observe practices firsthand. These are not hurdles; they become everyday parts of running a plant with an eye toward longevity and responsibility.

    Building on Experience: What Sets a Manufacturer Apart

    What never changes is the value that comes from cumulative experience. Every challenge from a customer—about a sticky product, a shipment delay, a failed batch run—drives us to look again at how we synthesize, package, and support 3,4-Dimethoxythiophenol. We maintain an archive of process data not because of outside certification requirements but because time and again, a trend in reactivity, unexpected impurity spikes, or slight changes in physical character can be spotted years after the fact by comparing notes and chromatograms across multiple campaigns.

    Direct communication helps us solve problems more quickly for users in the field. If a client’s new process leads to increased volatility, or they find an unknown side product forming in large-scale trials, our technical experts step in—not with pre-written answers, but informed by what our operators and chemists have faced firsthand. The laboratory may be where certification happens, but the manufacturing floor is where insight takes shape. Adjustments made after real feedback—such as holding times, tank coatings, or small additions of stabilizer—often wind up generating benefits across the production stream, not just for the “problem case” that starts the investigation.

    Looking Toward the Future with 3,4-Dimethoxythiophenol

    What comes next will hinge on changes in demand, shifts in regulation, and advancements in synthetic methodology. We have ongoing projects aimed at improving selective functionalization of the aromatic core, and many of our partners are already investigating pathways that use 3,4-Dimethoxythiophenol as a stepping stone to more complex sulfur-containing ring systems. As flow chemistry and automated synthesis step further into the mainstream, our focus stays on providing a clean, reliable starting material—something that enables discoveries without introducing unknown risk at the start.

    Those involved day-to-day with these materials know that small advances at the supplier level can make all the difference in both research and manufacturing. Despite global disruptions, from raw materials to transportation, we maintain direct engagement with our customers, reviewing their process changes and listening to what works. Sometimes, progress means integrating AI-driven analytics in process monitoring; at other times, it means swapping a clutch on a forty-year-old pump to keep the line running. Our credibility comes from the trust established over repeated projects, not from claims made on a specification sheet.

    The world of specialty chemicals is built on details: knowing the precise impact of a methoxy group, understanding the volatility and reactivity implications of a sulfur atom placed just so, and delivering a product that matches not only the certificate but also the unwritten expectations of people actually running the chemistry. In this ongoing journey, 3,4-Dimethoxythiophenol serves as a testament to what careful manufacturing, honest communication, and steady adaptation deliver to users worldwide.