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2-(4-Methoxyphenyl)Thiophene

    • Product Name 2-(4-Methoxyphenyl)Thiophene
    • Alias 4'-Methoxy-2-thienylbenzene
    • Einecs 642-183-5
    • 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

    789590

    Chemical Name 2-(4-Methoxyphenyl)thiophene
    Molecular Formula C11H10OS
    Molecular Weight 190.26 g/mol
    Appearance Solid, often white to light tan
    Melting Point 54-56 °C
    Boiling Point 324-326 °C
    Cas Number 10586-30-4
    Smiles COC1=CC=C(C=C1)C2=CC=CS2
    Density 1.17 g/cm³ (estimated)
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Refractive Index 1.622 (estimated)
    Pubchem Cid 3131570

    As an accredited 2-(4-Methoxyphenyl)Thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25g of 2-(4-Methoxyphenyl)Thiophene, labeled with chemical details, hazard symbols, and handling instructions.
    Shipping 2-(4-Methoxyphenyl)thiophene is typically shipped in sealed containers under inert atmosphere to prevent contamination and degradation. The packaging complies with chemical safety regulations, labeled with hazard information. It should be transported at ambient temperature unless otherwise specified, and handled by authorized personnel following appropriate safety guidelines for organic chemicals.
    Storage 2-(4-Methoxyphenyl)thiophene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from strong oxidizing agents and moisture. Proper chemical storage standards should be followed, and access should be limited to trained personnel. Ensure the storage area is equipped with appropriate spill containment measures.
    Application of 2-(4-Methoxyphenyl)Thiophene

    Applications of 2-(4-Methoxyphenyl)Thiophene in Industrial Manufacturing

    As a specialist manufacturer of 2-(4-Methoxyphenyl)Thiophene, we supply this advanced intermediate to several high-value industrial sectors. Our clients utilize this material strictly in sectors with established, regulated pathways, focusing on speciality chemical synthesis rather than broad commodity processing. The sections below illustrate real production environments where downstream manufacturers rely on our product for its specific structural reactivity, impurity profile, and integration into demanding process flows.

    1. Pharmaceutical Intermediate Synthesis for Thienopyridine Antiplatelet Agents

    Pharmaceutical manufacturers utilize 2-(4-Methoxyphenyl)Thiophene as a key building block in complex, multi-step syntheses of thienopyridine core structures, including intermediates targeted at antiplatelet drugs like ticlopidine analogues. The methoxy- and thiophene-substituted motif facilitates targeted substitutions and regioselective functionalization in the heterocyclic assembly, influencing yield and impurity control for GMP compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. guidelines for pharmaceutical intermediates (as per ICH Q11 and local MAH requirements)
    • 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals (United States)
    • EU EudraLex Volume 4 – GMP (Europe)

    Typical usage ratio

    • 10%–18% of total batch input as a core intermediate by weight, adjusted for target molecule and downstream yield, based on stoichiometry in stepwise synthesis pathways.

    Downstream process integration

    • Added in Step 2 or 3 of multi-stage organic synthesis, following halogenation or Suzuki–Miyaura coupling.
    • Integrated after in situ generation of boronic acid or Grignard intermediates (depending on final active substance target).
    • Requires controlled nitrogen or inert gas environment for process consistency and impurity minimization.
    • Undergoes transformation via coupling and cyclization in the assembly of biologically active heterocycles.

    Final product types

    • Thienopyridine analogues (e.g., advanced intermediates for ticlopidine, clopidogrel derivatives)
    • API pre-intermediates supplied to downstream conversion houses
    • Pharmaceutical reference compounds for QC/analytical use
    • Documentation-grade intermediates for use in DMF submissions

    2. Advanced Materials: OLED and Organic Semiconductor Synthesis

    Producers of specialty optoelectronic materials integrate 2-(4-Methoxyphenyl)Thiophene into conjugated oligomer and polymer structures for high-performance organic electronics. Its electron-rich thiophene ring, modified with the 4-methoxyphenyl substituent, enables fine-tuning of charge-transport and photophysical properties in semiconducting layers, essential for OLED displays and photovoltaic modules.

    Industry compliance standards

    • IEC 62899-202 – Printed electronics technical requirements (OLED applications)
    • ISO 9001:2015 – Quality Management for specialty chemical batch traceability
    • RoHS 2011/65/EU compliant raw material sourcing
    • TÜV SÜD/UL-recognized process safety for electronic component manufacturing

    Typical usage ratio

    • 1–6 mol% in total monomer feedstock during copolymerization or oligomer assembly, adjusted by targeted electronic bandgap and final device requirements.

    Downstream process integration

    • Direct polymerization using Suzuki or Stille coupling to yield electron donor-acceptor conjugated systems.
    • Introduction into pre-formed oligomer frameworks via stepwise cross-coupling and subsequent film deposition.
    • Purification through sequential column chromatography and recrystallization to eliminate trace metals.
    • Final material applied as active layer in spin-coating, vapor deposition, or inkjet formulations.

    Final product types

    • Organic light-emitting diode (OLED) active materials
    • Organic field-effect transistor (OFET) channel layers
    • OPV (organic photovoltaic) donor-acceptor blends
    • Custom functional materials for flexible display panels

    3. Agrochemical Intermediate for Heterocyclic Herbicide Synthesis

    Agrochemical formulators employ 2-(4-Methoxyphenyl)Thiophene as a protected heteroaromatic synthon in the synthesis of selective post-emergence herbicides. This compound's specific substitution pattern increases precursor reactivity, allowing for controlled functional group insertion and precise downstream oxidation or sulfonation steps for desirable environmental fate and herbicidal activity profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO 2022 revision)
    • ISO 9001:2015 – Batch quality and traceability
    • REACH Regulation (EC) No 1907/2006 for new agrochemical intermediates
    • GLP (Good Laboratory Practice) where required for study submissions (OECD Principles)

    Typical usage ratio

    • 7–15% by weight in multi-step synthesis, determined by stoichiometric balance and conversion yield of target active ingredient.

    Downstream process integration

    • Used upstream in the aromatic acylation step to generate protected thiophene intermediates.
    • Further processed via in situ sulfonation or oxidative cyclization to build active herbicidal motifs.
    • QC analytical controls at each coupling/functionalization stage to monitor isomeric purity.
    • Transferred directly to subsequent formulation labs post-intermediate isolation.

    Final product types

    • Thienyl-based post-emergence herbicide actives
    • Intermediates for selective grass or broadleaf weed control agents
    • Custom crop-specific herbicide molecules under development
    • Reference standards for environmental fate research

    4. Dye and Pigment Intermediate for High-Fastness Colorants

    Specialty dye and pigment manufacturers incorporate 2-(4-Methoxyphenyl)Thiophene into chromophore precursors to achieve improved lightfastness and thermal stability in premium colorants. The integration of this moiety into extended aromatic cores modulates π–electron distribution, directly affecting tint strength and stability for use in technical textiles, inks, and automotive coatings.

    Industry compliance standards

    • OEKO-TEX Standard 100 (applicable to textile dye raw material purity)
    • ISO 9001:2015 for specialty pigment traceability
    • EN 71-3 (Safety of toys – migration of certain elements) for pigment applications in children’s products
    • REACH Substances of Very High Concern (SVHC) registration/exclusion

    Typical usage ratio

    • 0.5–3% by weight in dye or pigment synthesis, tuned for color depth, shade, and target substrate compatibility. Higher ratios applied for deep black or high-intensity shades.

    Downstream process integration

    • Enters at the initial condensation stage to form core chromophoric structures.
    • Subjected to further derivatization (sulfonation, diazotization, or coupling) to craft color-conditioning side groups.
    • Purification by filtration and vacuum drying post-coupling for downstream blending.
    • Final blending with dispersants and stabilizers for compatibility in waterborne or solvent-based systems.

    Final product types

    • Technical textile colorants (for sportswear, uniforms, protective fabrics)
    • High-fastness automotive and industrial coatings
    • Premium inkjet and laser printing dyes
    • Customized pigment preparations for specialty plastics and composites
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    Certification & Compliance
    More Introduction

    2-(4-Methoxyphenyl)Thiophene: One Manufacturer’s View

    Understanding the Compound

    Every batch of 2-(4-Methoxyphenyl)thiophene we produce reflects years of attention to detail and a drive to support users in diverse applications, from development of advanced organic electronics to pharmaceutical intermediaries. Our process starts with clear intent: deliver material that chemists and engineers can trust, because direct feedback from downstream applications keeps us sharp. The backbone of this compound—a thiophene ring bearing a para-methoxyphenyl substituent—finds value wherever conjugated systems or aromatic substitutions prove necessary for molecular engineering or bioactivity optimization.

    As a producer, purity isn’t a number we check off, but something we enforce at every stage. With our model number MPT-204, we routinely track purity above 98%. This isn’t window dressing for a catalog. In laboratories chasing optoelectronic breakthroughs, even small traces of unrelated aromatics or oxidized sulfur will affect performance. The routine feedback we get from researchers tells us that downstream processing or additional recrystallization wastes both time and material, so we take extra care during column purification and monitor every output via NMR and MS. Each lot matches spectra for identity; each test run verifies melting point consistency. Our standard appearance is an off-white crystalline solid, stable when protected from light and air, free from the tars or off-odors that mark a rushed synthesis.

    Application Insights from the Manufacturing Floor

    Colleagues in academia and industry route their orders to us for a couple of main reasons. For those working in organic semiconductors, especially in research areas exploring polymers and small molecules for OFET or OLED manufacturing, the electron-rich backbone and substituted ring give this molecule more than just another “input” role. Its structure lets users tweak electronic properties, with the methoxy group pushing electron density and modifying stacking in thin films. Several teams pushing for sharp absorption edges or fine-tuned emission spectra came to us after trouble with inconsistent material performance from less direct-sourced suppliers. Careful attention to purity pays off during vapor deposition, spin-coating, or polymerization, where stray metal or non-paraffinic residues can spoil device performance.

    Another set of projects comes from those working in medicinal chemistry. 2-(4-Methoxyphenyl)thiophene can act as a building block for heterocyclic compounds under active study in the search for anti-inflammatory and anticancer molecules. The para-methoxyphenyl group offers a key spot for late-stage functionalization, and sulfur heterocycles stay in demand as core fragments in patented leads. We keep a dialogue with customers so that, should an order request above the laboratory scale come in, we have their process knowledge on hand and can adjust batch size, storage, and shipment accordingly. Working at scale, our focus shifts to safeguarding batch homogeneity: chemists investing months on target molecules or analog screens do not want to troubleshoot starting material at the pilot plant.

    What Sets Our Process Apart

    Over the years, we learned that not all 2-(4-Methoxyphenyl)thiophene offers the same value in practice. Running side-by-side comparative analyses, we observed that materials coming through bulk trading chains often contain minor isomeric impurities—sometimes from cross-coupling side paths, sometimes as a result of incomplete protection or workup. Those stray substances won’t show glaring problems under a TLC lamp, but they crop up during scale-up or instrument calibration, sometimes giving headaches when customers can't explain baseline drifts or odd byproducts. Our reactors run under atmospheres that eliminate moisture and air exposure; we automate temperature ramping and phase monitoring to block formation of byproducts. Our purification steps resist “shortcuts” that could bump throughput but risk introducing cross-contamination. Every release batch faces full spectroscopic profiling: the forty minutes spent now saves days of troubleshooting for customers later.

    Talking about differences isn’t just about process flowcharts. For a chemist in a resource-stretched lab, our product means fewer blank runs and more reproducibility. Any new derivative project—especially those testing bioactivity or charge carrier mobility—relies on uniform starting compounds. We partially attribute the higher reproducibility in device testing and in combinatorial reactions to the absence of ortho-methoxy isomers and oxidized tars in our final material. Chemists who depend on subtle structure-activity correlations—those hunting for new non-planar aromatics, for example—report sharper SAR trends with our thiophene compared to “off-the-shelf” options. The same feedback resurfaces among customers making cross-coupling libraries, where spurious starting impurities create splitting in NMR or ghost peaks in LC/MS chromatograms.

    Meeting Specific User Needs

    We frequently talk with synthetic chemists about what matters most at the bench level. Many get their hands dirty with transition metal catalysis, photochemistry, and late-stage coupling. For those aiming to expand the substrate scope in C–H activation or Suzuki coupling, starting material integrity proves critical. The sharp melting point of our product—typically matching published values for high-purity samples—gives chemists faster verification that the right structure came off the column. Users shifting to continuous flow or microreactor synthesis praise the low batch-to-batch variation in our thiophene. Their equipment needs standardized inputs due to short residence times. We keep our internal documentation on specification lots open for partner review, so anyone scaling work up or differentially quantifying trace palladium or other metals can check our figures directly. For scale-ups headed to pilot, we rerun elemental analysis and impurity profiling, not relying on a months-old certificate.

    Feedback tells us that customers value the security of source control. As a chemical manufacturer, there’s no warehouse juggling of drums bought from various importers. Every lot arises from a known batch, made in facilities overseen by our core team. We hold data files and analytical results on-hand, not offloaded onto logistics middlemen who can’t answer technical questions. This direct model brings accountability. If a problem arises during application, a chemist reaches someone who runs the equipment, not a sales desk. We feel this approach pays off: publications coming from users of our thiophene often cite cleaner analytical spectra and fewer side products in coupling reactions or aromatic substitutions.

    Key Differences from Other Manufacturers’ Material

    Discussions with contract labs and research facilities tell us many sources of 2-(4-Methoxyphenyl)thiophene resemble one another on basic descriptors, but diverge when put to the test. For starters, not all manufacturers maintain in-house purification capacity at scale. Some rely on outsourced distillation or non-dedicated multi-use columns. We invested in reactor lines and filtration designed exclusively for sulfur- and methoxy-functionalized aromatic systems. This allows us to minimize cross-contamination, a common issue in plants producing both halogenated and methoxy-function compounds in the same vessels.

    Our speed in delivery often comes from skipping reinspection, not from cutting synthetic steps. We stand by direct quality control done on-site, monitoring each phase from initial chlorination or bromination of the thiophene through to the Ullmann coupling, workup, and crystallization. Internal records show that each time we encountered unexpected polymerization or trace phenol contaminants, it dated back to a material-handling slip; none of our best lots came from efforts to rush or short-circuit purification. Every crystallizer, every flask, and each nitrogen line are logged for maintenance. Coordinating with customers who run scale-dependent projects—especially in electronics—means we store safety margins of inventory after each batch, sealed and monitored for changes in moisture content or color as an early warning of degradation.

    Feedback loops matter. Users alert us when trace byproducts or changes in solubility appear. If a lab in Switzerland or Japan identified an infrequent impurity in their reaction outputs, we dig through process logs and, if needed, tweak reaction times, solvent systems, or column loading. This keeps rare problems from becoming the norm. Crafting product stories behind each analysis, our chemists anticipate downstream needs like flame ionization detection, microelemental analysis, or vapor phase transfer without waiting for the purchaser to discover a problem days after material intake.

    Chemical Identity and Handling in Practice

    2-(4-Methoxyphenyl)thiophene stands out among its analogs. The para-methoxy group on the phenyl ring changes both electronic and solubility properties versus non-substituted phenylthiophenes. Our product dissolves easily in acetonitrile, dichloromethane, and most aromatic solvents. We’ve tracked user experiences during solution-phase polymerizations: ease of dissolution at standard concentrations translates to consistent results in spin coating and layer deposition. The melt and crystallization points of our material track closely with published analyses, avoiding surprises in thermal cycling applications.

    In both small-molecule and polymer chemistries, subtle differences in the starting material matter greatly for properties like charge mobility, absorption onset, and film homogeneity. Technicians in OLED fabrication report that cleaner material yields less device failure and higher uniformity under photoluminescence mapping, correlating directly with reduced baseline drift during operation. Pharmaceutical partners synthesizing trial candidates choose our 2-(4-Methoxyphenyl)thiophene because chromatographic profiles match those needed for regulatory documentation and repeat analysis.

    For reference, pure 2-(4-Methoxyphenyl)thiophene comes as a crystalline or powdery solid. It must be kept away from light and strongly oxidizing environments; we package it in tightly sealed bags within amber containers, providing an oxygen barrier. Our attention to fine particulate and dust management comes from past incidents where a small spill or powder spread compromised the integrity of neighboring batches. We recommend handling only in gloveboxes or well-shielded fume hoods for applications involving sensitive polymerizations or organometallic reactions. Customers doing trial runs for combustion or thermal decomposition studies appreciate access to micro-sublimation or further purification on request; this supports results for grant and publication submission.

    Experience-Driven Improvements and Solutions

    Manufacturing has a way of exposing weak points; we treat every complaint or nonconformity as a real opportunity to improve. A few years ago, a batch developed an unexpected coloration after long-distance shipping in hot weather. Examination traced the issue back to packaging insulation, not to the synthesis itself. Following this, we overhauled our logistics and began automated temperature monitoring during transport. Consistently, newer batches arrived pristine, with zero recorded discoloration or loss. Tracking shipments through data loggers gave us an edge: any sign of temperature spike or pressure loss leads to immediate review of transport protocols and can trigger a preventive recall of marginal containers.

    Not all improvements focus on disaster prevention. Repeated requests for gram-scale packaging led us to set up smaller-scale, automated weighing and pouching units. Researchers avoiding excessive handling or wishing to minimize bench contamination can opt for pre-weighed portions, sealed inertly. Some research groups campaign for even tighter trace metal specifications; in response, we started batch-specific palladium and copper quantification, making those figures directly available for purchasers working in metal-catalyzed synthesis. Feedback helped us realize that some users in microelectronics or pharmaceutical screening prefer certificates showing every residual byproduct above 10 ppm, even if current regulations only ask for 100 ppm. Our documentation now tracks to a finer standard, matching needs dictated by next-generation R&D.

    Direct connections between manufacturer and end user make a difference. When a team encountered a downstream cyclization failure using imported material, our consult with their lead chemist uncovered an interference from a minor, ring-opened contaminant. By comparing MS and NMR, we tied the impurity directly to a different vendor’s synthesis route. Ironically, the issue became a case study in the value of single-source accountability, strengthening our internal batch controls and extending the philosophy to other thiophene analogs.

    Supporting Future Directions

    We see users exploring 2-(4-Methoxyphenyl)thiophene in solar energy capture, organic light-emitting diodes, sensors, and as a core fragment in new drug synthesis. Each new territory stresses the need for reliable, reproducible input. Our process adapts over time: we’ve invested in new filtration media, solvent recycling, and crystallization technologies. Pilot projects sometimes push for custom analogs; our experience with 2-(4-Methoxyphenyl)thiophene often smooths the path, letting us troubleshoot derivatization steps or offer up alternative protecting group strategies based on real-world experience. By having crystal structure, impurity map, and reactivity notes on hand, we help partners avoid months of trial and error.

    Increasingly, we supply material for multi-kilogram projects, not just research scale. As a manufacturer who tracks every kilogram’s origin, handling, and analytic result, we have built trust that’s not easy to replicate. Batch-to-batch continuity comes straight from our process data. Institutional users who write methods or standard operating procedures for broader rollouts rely on this continuity. No blind repacking or trans-shipping enters our system; we see every order as a direct line to the next innovation or regulatory filing.

    The Practical Impact of Direct Manufacturing Experience

    For us, the value of 2-(4-Methoxyphenyl)thiophene starts with hands-on mastery of the compound, not just paperwork. We’ve been present for bench-scale runs where early solvent choices affected product color and purity. We adjusted columns midway through scale-up after hearing feedback from users working in high-sensitivity environments. We learned how to read the subtle signs of a healthy batch: hue, grain size, flow, and even the way it settles in a weighing vial. Our staff gets trained not just in process operation, but in recognizing variant signatures in melting or spectral reading, because one person’s hunch sometimes stops a bad outcome from creeping further downstream.

    Our story with 2-(4-Methoxyphenyl)thiophene is ongoing, shaped by daily feedback and a culture of fix-it-first. Providing this compound means more than filling a barrel—it means knowing what’s inside, knowing what matters to people using it, and always keeping process improvement in sharp focus. Whether it’s a single gram for academic study or a drum for a pilot run, our dedication to quality and support rests on direct experience, not glossy catalogs or third-party reassurances.

    Real-world chemistry rarely rewards shortcuts. Most labs don’t have time to re-purify, and nobody wants to lose valuable signal in the final application because a starting material carried in a contaminant from an unknown batch. We continue to take the time needed to analyze, monitor, and package each lot with care. As new uses for 2-(4-Methoxyphenyl)thiophene unfold, we stay close to the action so users receive a compound that reflects practical, ongoing mastery as much as technical sheets and spectra.