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2-Phenylthiophene

    • Product Name 2-Phenylthiophene
    • Alias 2-Phenylthienyl
    • Einecs 212-846-4
    • 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

    103282

    Chemical Name 2-Phenylthiophene
    Cas Number 2614-17-5
    Molecular Formula C10H8S
    Molecular Weight 160.24 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 270-272 °C
    Density 1.118 g/cm³ at 25 °C
    Refractive Index 1.630
    Solubility In Water Insoluble
    Flash Point 110 °C
    Smiles c1ccc(cc1)c2cccs2

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

    Packing & Storage
    Packing Amber glass bottle labeled "2-Phenylthiophene, 25g." Features hazard warnings, CAS number, batch number, and supplier logo for identification.
    Shipping 2-Phenylthiophene is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be stored and transported in a cool, dry, well-ventilated area, away from incompatible substances. Proper labeling and documentation are required, and handling must comply with all relevant safety and regulatory guidelines for hazardous chemicals.
    Storage 2-Phenylthiophene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep it separate from strong oxidizers and acids. Proper chemical labeling is essential. Handle in accordance with standard laboratory safety procedures and ensure access to safety equipment such as eyewash stations and fire extinguishers.
    Application of 2-Phenylthiophene

    Applications of 2-Phenylthiophene in Industrial Manufacturing

    As a direct manufacturer of 2-Phenylthiophene, we deliver this intermediate to leading chemical sectors with rigorous technical guidance and tailored specifications. Here, we outline verified downstream application scenarios where our material integrates with industrial processes, fulfilling precise compliance, formula, and product development needs.

    1. Pharmaceutical Intermediates: API Synthesis

    2-Phenylthiophene serves as a specialized building block for heterocyclic core structures in the synthesis of various pharmaceutical active ingredients, notably anti-inflammatory and central nervous system agents. Our production meets the strict impurity profiles demanded for regulated API routes, supporting scale-up from pilot to full GMP batch campaigns.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EMA guideline on the chemistry of APIs (EMA/CHMP/QWP/130310/2012 Rev 1)
    • USP <467> Residual Solvents
    • European Pharmacopoeia monographs (when used in reference to intermediates)

    Typical usage ratio

    • Forms 10–25% of the molecular input during fragment coupling steps; exact percentage varies by drug candidate and reaction conditions.

    Downstream process integration

    • Directly involved in Suzuki, Heck, or Stille cross-coupling reactions at stage two or three of API route development.
    • Introduced following initial halogenation or lithiation steps to produce target pharmaceutical scaffolds.

    Final product types

    • Small molecule drug substances targeting pain, inflammation, or neurological conditions
    • Advanced pharmaceutical intermediates (APIs-in-progress)
    • Research compounds for clinical candidate optimization
    • Custom reference standards for pharmaceutical QC

    2. Electronic Materials: Organic Semiconductor Precursors

    The aromatic and sulfur-containing structure of 2-Phenylthiophene makes it suitable as a regulated precursor for advanced organic semiconductors, including thiophene oligomers and polymers for application in OLED displays and organic field-effect transistors (OFETs). This feedstock enters high-purity routes where electronic grade purity and batch consistency are mandatory.

    Industry compliance standards

    • JEITA ET-7304 (Japan Electronics and Information Technology Industries Association, organic semiconductor quality guidelines)
    • IEC 62899 (Printed Electronics)
    • RoHS (Restriction of Hazardous Substances Directive, for end applications)
    • In-house proprietary material purity specifications (≥99.9%) for electronic downstream partners

    Typical usage ratio

    • Composes up to 30% of starting monomer batches, adjusted between 10%–35% depending on target polymer properties and film application.

    Downstream process integration

    • Fed into chemical vapor deposition or solution polymerization processes to create functionalized thiophene-based monomers and polymers.
    • Used in pre-polymerization functional group modification steps for device-specific tuning.

    Final product types

    • OLED active materials for display and lighting
    • Organic photodetector substrates
    • Semiconducting polymers for printed electronics
    • OFET devices for flexible sensors and circuits

    3. Agrochemical Synthesis: Fungicide and Herbicide Precursors

    Chemical manufacturers leverage the unique heterocycle of 2-Phenylthiophene during multi-step agrochemical synthesis. It acts as a bridging unit or aromatic modifier in the creation of fungicidal and herbicidal actives, offering targeted spectrum and metabolic stability. Compliance focuses on trace impurity control and environmental safety within the crop protection sector.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH Regulation (EC) No 1907/2006, for precursor registration and tracing
    • ISO 9001:2015 Quality Management Systems (applicable to batch consistency and traceability)
    • OECD guidelines for chemical testing (pertinent to downstream R&D toxicity evaluations)

    Typical usage ratio

    • Acts as a scaffold or functional substituent at rates of 5–15% relative to starting reagents per batch, modified as per product potency and synthetic yield targets.

    Downstream process integration

    • Inserted into intermediate coupling steps after halogen or nitro group installation, leading to final formation of sulfur-aryl actives.
    • Undergoes further chlorination or methylation for tailored field efficacy profiles.

    Final product types

    • Systemic and contact fungicides for cereal and vegetable crops
    • Pre- and post-emergence herbicides
    • Sulfur-heterocycle based plant protection agents
    • Experimental agrochemicals for field trials

    4. Specialty Dyes & Pigments: High-Performance Colorants

    In the specialty dye industry, formulators select 2-Phenylthiophene as a segment for synthesizing thiophene-azo and sulfur-containing chromophores. These high-value colorants demonstrate excellent thermal and photochemical stability for use in industrial coatings, inks, and fibers requiring European and North American toxicological compliance.

    Industry compliance standards

    • EN 71-3:2019 (Migration of certain elements for coatings, toys and textiles)
    • Oeko-Tex Standard 100 (for dyes on textiles and garments)
    • REACH Annex XVII and SVHC regulations for pigment ingredients
    • ISO 9001 quality control for batch color reproducibility

    Typical usage ratio

    • Utilized at 3–8% of theoretical yield during coupling with diazonium or activated aromatic compounds, depending on shade intensity and processing method.

    Downstream process integration

    • Engaged in sulfonation or nitrosation reactions to build photo-stable colorant molecules
    • Applied before final purification, milling, and dispersion steps in dye manufacturing

    Final product types

    • High-temperature stable textile dyes
    • Solvent-dispersible colorants for inks and coatings
    • Specialty pigments for plastics and synthetic fibers
    • Photostable colorant intermediates

    5. Fine Chemicals: Research and Analytical Standards

    Academic and commercial laboratories utilize our high-purity 2-Phenylthiophene as a reference standard or synthetic intermediate for custom molecule development, NMR calibration, and chemical library synthesis. Material handling focuses on exact composition and lot traceability to meet global analytical methodologies and laboratory audit requirements.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for the competence of reference material producers)
    • GLP (Good Laboratory Practice) OECD Principles
    • ACS Reagent Chemical Purity Criteria
    • Internal SOPs for analytical sample chain of custody

    Typical usage ratio

    • Weighed at 0.1–2.0% (w/w) in multi-compound NMR or GC-MS calibration mixes, or as needed for targeted organic synthesis projects.

    Downstream process integration

    • Added directly to organic reaction vessels for molecule assembly
    • Used in analytical lab sample standardizations

    Final product types

    • Chemical reference standards for method validation
    • Specialty fine chemicals for research
    • Diagnostic and forensic test kits
    • Custom analytical reagents
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    Certification & Compliance
    More Introduction

    Introducing 2-Phenylthiophene: Chemistry in Action

    Why 2-Phenylthiophene Earns Respect in Modern Chemistry

    Few aromatic compounds offer versatility and performance like 2-Phenylthiophene. At our chemical plant, generations of process engineers have watched demand for specialty thiophenes rise steadily, and 2-Phenylthiophene stands out each time. Its chemical backbone—a fusion of a phenyl group to the second position of a thiophene ring—gives it unique electronic characteristics compared with untouched thiophene or conventional biphenyl structures. That simple adjustment triggers big differences downstream, both in how it behaves in a reaction and how its derivatives function in final applications.

    On the manufacturing floor, we always look at how an aromatic compound sits not only in a textbook, but in the reactor, in the distillation columns, and at the lab bench where chemists trial sample lots. Over years of batch and continuous syntheses, 2-Phenylthiophene keeps proving itself reliable to purify and consistent in physical form. Reasonable melting and boiling points coupled with good stability let us standardize isolation and packing procedures. Consistency at scale means our partners use each drum knowing what they’re getting.

    Behind these properties sits a clear chemical structure you can rely on. 2-Phenylthiophene’s configuration—not a random mixture, not an isomeric tangle—avoids the headaches some other sulfur heterocycles bring. We prepare it by coupling appropriately substituted thiophenes, then refining through robust crystallization and distillation pathways developed by our process chemists. Since we run dedicated thiophene lines, we’ve ironed out the typical hurdles: sulfur contamination, aromatic substitution side-routes, and the need for precise temperature management throughout production. The result: as close to unimpeachable purity as laboratory analytics allow. Our routine lot testing by NMR, GC-MS, and HPLC ensures you’ll find clear signals rather than mysterious peaks.

    Specifications Matter on the Production Floor

    We produce batches in a range of custom and standard purities. Most fine chemicals users work with reagent-grade 2-Phenylthiophene, where purity sits at 98.5% or higher by GC. Trace sulfur byproducts—of critical interest in electronics and pharmaceuticals—remain tightly controlled, thanks to our multi-stage distillation. Each batch undergoes loss-on-drying and residual solvent testing to confirm low thresholds, so the material does its job without adding headaches for formulators. Color, clarity, melting range—all match international expectations and help customers scale quickly with minimal requalification. Each container’s lot integrity and traceability give regulatory teams peace of mind.

    Because we handle large and small volumes, our team adjusts handling and packing to user demands. For laboratory synthesis, small ampoules or bottles give researchers quick and clean access; for intermediate or industrial use, stainless drums and composite containers keep the chemistry safe and line-ready. And unlike some substituted thiophenes—which attract attention for instability or strong odors—2-Phenylthiophene arrives in a stable, low-odor solid or liquid state (depending on temperature and batch size), easing handling and storage across applications. Chemists reach for this compound when they need confidence in their reaction sequences, not mystery in the drum.

    Applications Rooted in Real-World Needs

    On the user end, applications for 2-Phenylthiophene keep multiplying. In the years since we adopted it as a routine product, we’ve seen sharp growth in demand from OLED and organic semiconductor manufacturers. The reason lies in the molecule’s aromatic structure and sulfur content. When researchers build conjugated polymers—those backbone structures that carry electrical charge or emit light efficiently—the phenyl attachment on the thiophene modifies the electronic landscape, enhancing charge mobility, shifting absorption and emission spectra, and improving film-forming properties. That subtle electronic effect offers a direct benefit that unmodified thiophene or simple biphenyl can’t deliver.

    We get a steady stream of requests from R&D teams in specialty pigment and dye houses, too. The balance of aromaticity and sulfur leads to unique colorfastness and photostability. In dye synthesis, that sulfur atom twists the chromophores, letting artists and technicians achieve color shades that last longer under stress. Drug development also leans on 2-Phenylthiophene. The compound’s scaffold forms the basis for designing bioactive molecules targeting inflammation, cancer, and infection. Unlike more exotic heterocycles—often fussy or hazardous—our 2-Phenylthiophene supports green chemistry goals by coming cleanly from manageable feedstocks, and it integrates easily into robust medicinal synthetic routes.

    Teams working on advanced lubricants and additives benefit from the compound’s stable yet reactive profile. Unlike plain thiophene, which might oxidize unpredictably, the phenyl substitution buffers against degradation, granting longer shelf-life and more predictable performance in boundary lubrication environments. We continue to monitor the market and partner with R&D teams, always trading real data and experiences, not corporate speculation.

    Practical Differences from Standard Thiophenes and Analogues

    Some customers ask why they can’t just use simple thiophene or other aryl-substituted heterocycles in these applications. From years of working with these molecules—not spreadsheets or catalogs, but real reactors and product runs—we see clear differences that go beyond lab curiosity. Thiophene itself tends toward volatility; its boiling point is much lower and it often brings more aggressive odor. That complicates handling in larger-scale or open-vessel applications. And its electron-rich nature means it can be oxidized or substituted in ways that turn up side-reactions and process waste.

    Add a phenyl group at the 2-position, and things change. You get a slight boost in molecular weight and boiling point, and a fundamental shift in resonance distribution through the ring system. For synthetic chemists, that means new reactivity, better control in cross-coupling or electrophilic substitution, and a pathway toward functionalized products that stick to their design specs. Compared to 3-Phenylthiophene, which turns up in the literature but rarely in manufacturing plants, the 2-substituted version shows better scalability and more straightforward purification. Fewer unfamiliar byproducts appear at workup—something our quality team tracks batch by batch.

    We have also fielded cross-comparisons with biphenyl and phenyl-substituted furans. Biphenyl builds polymers and advanced materials, but lacks the tunable sulfur chemistry key to some optoelectronic properties. Phenyl-furan analogues offer partial overlap in application space, though most break down or polymerize faster, and can’t handle the same thermal or oxidative load in high-temperature processing. Our technical sales and support chemists work hand-in-hand with clients, not just to fill orders but to solve synthesis or process problems using these physical and chemical insights. We don’t ship abstract “solutions”—we rely on what performance feedback and testing results tell us.

    Process Control, Analytical Diligence, and Continuous Improvement

    Rolling out a specialty chemical like 2-Phenylthiophene challenges every part of a chemical plant, from sourcing high-quality starting materials to minimizing emissions. Our plant uses continuous monitoring and strict purification steps to keep contaminants out of your end products. Retaining a lean, refined process helps us drive down cost, match purity targets, and produce as greenly as we can. Each run gets three points of analytical verification—at raw material intake, post-reaction intermediate, and finished product. Our QC lab brings decades of hands-on analytical skill, not just fancy instrumentation: each batch gets a human in the loop, reviewing spectroscopic, chromatographic, and physical data against both internal and international criteria.

    We have learned the importance of tweakable process windows. Running at the edge of parameter drift—temperature, pressure, catalyst rate—lets an operator see potential process upsets before they affect a full batch. We chart every process variable, storing data for future troubleshooting or documentation. If even a trace of off-spec material shows up, isolation and corrective action routines kick in automatically, flipping lots to quarantine and avoiding cross-contamination downstream. Feedback from customer labs also loops directly back into our QA improvements, not just into yearly audits.

    Customers in electronics, pharmaceuticals, and research rely on us not just for a drum of chemical, but for a partnership. We publish key analytical spectra for transparency, answer technical questions with real experience, and back up claims with facts anyone can verify. Supplying a high-stakes industry means we stay responsive, continuing to refine synthesis and shipping procedures as industry standards shift and application landscapes widen.

    Supporting Downstream Innovation from the Source

    A specialty molecule’s true test comes once it reaches the hands of creative chemists, formulators, and engineers designing the next generation of materials or drugs. 2-Phenylthiophene, with its balanced reactivity and reliable performance, continues to open doors for innovation. The feedback loop between our production team and our most demanding customers gives us both the real-world performance stories and the granular analytical data needed to keep improving.

    Research teams in photovoltaic materials report the impact on device efficiency and stability when using this critical building block. Pharmaceutical researchers cite robust coupling yields and fewer purification headaches, getting new leads from bench to animal studies with minimal surprises. Those on the fabrication line for displays or sensors mention improved throughput, fewer failed batches, and a better-controlled safety profile compared with less predictable analogues. Academic articles and patent filings following the material’s integration into new architectures often cite synthesis and application details that align directly with the reality of our process findings.

    Our role as a manufacturer keeps us grounded in what matters: high-purity, consistent 2-Phenylthiophene, delivered safely, with technical clarity and process traceability end to end. We track feedback, listen to real user needs, and incorporate relevant regulatory, sustainability, and design elements as they evolve. Regular dialogue with downstream users keeps us honest, adjusting specs and batch sizes where science, safety, or practicality demand changes.

    Addressing the Challenges: Availability, Regulatory, and Environmental Demands

    The shift toward stricter regulation, higher purity expectations, and sustainability means we can’t stand still. We face constant pressure on solvent handling, waste stream minimization, and long-distance logistics. Our technical group works side by side with environmental teams to tighten solvent recycling, reduce water usage, and turn spent material into usable feedstock for adjacent syntheses. Over time, more of our runs use green chemistry approaches, phasing out older reagents or practices that don’t meet new emissions or waste targets. That means partners can incorporate 2-Phenylthiophene into their own green portfolios or low-impact product lines without worry.

    Meeting compliance in all shipping and labeling keeps the supply reliable as cross-border controls update. Our regulatory group tracks both export documentation and regional chemical registry needs. Ongoing dialogue with authorities and customers means delays get caught early—batches don’t sit in customs limbo or get flagged for incomplete paperwork. Our approach: solve paperwork, compliance, and handling concerns before they make it to the customer’s loading dock or bench.

    A material is only as useful as its consistent delivery—and the ability to meet sudden spikes in demand. Our manufacturing planners continuously monitor inventory, capacity, and market signals, keeping production nimble and responsive. Careful raw material qualification and long-term supplier partnerships take the sting out of market volatility; we don’t run on speculative sourcing and avoid supply slack that might endanger your program. And because we stay focused on core products like 2-Phenylthiophene, expertise compounds across every production run. We learn, adapt, and keep getting better, batch after batch.

    A Commitment to Chemistry that Works

    Manufacturing and supplying 2-Phenylthiophene means much more than filling an order. We consider ourselves a part of the entire journey from raw material to invention. Each improvement in process, each new use case, and each technical inquiry makes its way back to our factory floor. For us, it’s about blending modern technology with chemical craft, learning from what works, and being realistic about challenges. If you build materials, design drugs, or push electronics innovation, you know the value of solid, reliable feedstock. That’s what we aim to provide—day in and day out, with hands-on experience, accountable manufacturing, and an earned reputation for getting it right.

    Let us know where your own work takes 2-Phenylthiophene next. Our teams are always ready to share results, answer hard questions, and work through the gritty details that separate a catalog product from a chemistry breakthrough. That’s not rhetoric—it’s the outcome of years doing the work, side by side with the real innovators who rely on our chemistry.