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3-Thiophen-2-Yl-Benzaldehyde

    • Product Name 3-Thiophen-2-Yl-Benzaldehyde
    • Alias 3-(2-Thienyl)benzaldehyde
    • Einecs 629-725-1
    • 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

    810356

    Chemicalname 3-Thiophen-2-Yl-Benzaldehyde
    Molecularformula C11H8OS
    Molecularweight 188.25 g/mol
    Casnumber 67439-80-7
    Appearance Yellow to orange solid
    Meltingpoint 52-56°C
    Purity Typically >97%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC=C(C=C1)C=O.C2=CSC=C2
    Inchi InChI=1S/C11H8OS/c12-8-9-3-1-2-4-10(9)11-5-6-13-7-11/h1-8H
    Storagetemperature Store at 2-8°C

    As an accredited 3-Thiophen-2-Yl-Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, labeled "3-Thiophen-2-Yl-Benzaldehyde", includes hazard symbols, batch number, and expiry date.
    Shipping 3-Thiophen-2-Yl-Benzaldehyde is shipped in sealed, chemical-resistant containers to prevent contamination and degradation. It should be transported under ambient temperature with appropriate labeling, according to local and international regulations for hazardous chemicals. Ensure packaging prevents leaks, complies with UN packaging standards, and includes a safety data sheet (SDS) for recipient reference.
    Storage 3-Thiophen-2-Yl-Benzaldehyde should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, ideally in a designated chemical storage cabinet. Always follow safety guidelines, avoid moisture exposure, and ensure appropriate labeling to prevent accidental misuse or contamination. Store separately from incompatible substances.
    Application of 3-Thiophen-2-Yl-Benzaldehyde

    Applications of 3-Thiophen-2-Yl-Benzaldehyde in Industrial Manufacturing

    3-Thiophen-2-Yl-Benzaldehyde serves as a critical intermediate in several specialty chemical value chains. By leveraging its functionalized aromatic structure, downstream industries incorporate this raw material at precisely defined stages to synthesize advanced molecules that meet rigorous product quality and regulatory demands. Below, we detail recognized industrial applications of this compound based on verified market adoption and sector-specific compliance requirements.

    1. Organic Electronic Materials: OLED Intermediate Synthesis

    Advanced display and lighting manufacturers rely on this benzaldehyde derivative to construct thiophene-containing functional materials, forming part of emissive layers in OLED devices. Formulators appreciate its ability to introduce extended conjugation and modulate charge-transport properties. The compound integrates within multi-step syntheses to yield high-purity small-molecule organic semiconductors, subject to strict electronic material purity controls to prevent performance-inhibiting defects in finished displays or lighting components.

    Industry compliance standards

    • IEC 62341 (OLED panel evaluation and reliability standards)
    • JEITA ED-1538 (Evaluation method for organic electronic materials)
    • ISO 14001 (Environmental management in electronics manufacturing)
    • RoHS Directive for restricted substances

    Typical usage ratio

    • 0.1–1.5 molar equivalents relative to the targeted di- or triarylamine or hole-transport moiety, with adjustments based on target layer thickness and optical density

    Downstream process integration

    • Introduced during Suzuki, Stille, or Knoevenagel cross-coupling steps
    • Purification via column chromatography or preparative HPLC before functional coating formulation
    • Final solution blending with host materials prior to evaporation or inkjet printing

    Final product types

    • Active OLED display panels (smartphones, TVs)
    • OLED lighting modules
    • Wearable flexible electronic components
    • Organic photodetectors

    2. Pharmaceutical Active Intermediate for Thienyl-Containing APIs

    Leading pharmaceutical manufacturers incorporate this building block during synthesis of active pharmaceutical ingredients containing thiophene or benzaldehyde scaffolds. The compound sees frequent use in processes requiring Scifinder-listed thienyl-based pharmacophores, particularly in anti-inflammatory, central nervous system, and oncology research programs. Chemists control input levels to adjust for downstream reaction quenching, aiming to meet international pharmacopoeia standards for residual content and compound integrity.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient production
    • USP, EP monographs on final drug substance purity
    • 21 CFR Part 210/211 (US FDA cGMP guidelines)
    • EDQM CEP submission requirements

    Typical usage ratio

    • 1.0 mole per thienyl- or benzaldehyde-derivative formation, with downstream ratio tailored to batch scale-up and impurity profiling parameter outcomes

    Downstream process integration

    • Added during Grignard condensation, Friedel–Crafts alkylation, or reductive amination stages
    • Stringent in-process controls for unreacted intermediate and potential impurities
    • Exhaustive QC by HPLC and NMR prior to isolation or API downstream reactions

    Final product types

    • Thienyl-containing small molecule drugs (e.g., CNS therapies, antitumor candidates, anti-inflammatory agents)
    • Regulated pharmaceutical intermediates
    • Reference standard materials for preclinical screening
    • API process validation lots

    3. Specialty Agrochemical Synthesis

    Several multinational agrochemical processors employ the compound as a core intermediate for thienyl-benzyl based actives with applications in crop protection. Typically integrated into synthetic routes for fungicides or herbicides, the material’s addition aligns with manufacturing guidelines that limit elemental impurities, guaranteeing acceptable downstream product registration for agricultural use. The input ratio and process steps undergo adjustment dependent on bioefficacy data and resistance management protocols for target geographies.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • OECD Guidelines for the Testing of Chemicals—Agricultural chemicals section
    • ISO 9001 for chemical batch process management
    • Globally Harmonized System (GHS) for chemical labeling

    Typical usage ratio

    • Ranges from 3–15% by mass in the core reaction step, variably set according to active content targets and downstream mixture stability studies

    Downstream process integration

    • Initial condensation or nucleophilic addition with thienyl or aryl nucleophiles
    • Purification by distillation or crystallization prior to formulation blending
    • Quality assessment for residual solvents and byproduct profiles before registration sample dispatch

    Final product types

    • Agrochemical technical concentrates (fungicide, herbicide, or seed treatment intermediates)
    • Bulk actives shipped for post-formulation abroad
    • Pre-formulated crop protection solutions for regulated markets

    4. Functional Dye and Pigment Development for Advanced Materials

    Manufacturers engaged in specialty pigment and dye synthesis utilize this raw material for constructing colorants with tailored electronic interactions, capitalizing on the electron-rich thiophene core to modify absorption peaks or solvent compatibility. The compound becomes crucial when producing charge-transport dyes for solar cells, functional coatings, or photoresponsive polymers; strict color fastness and toxicity controls apply throughout the production cycle to meet downstream electronics and polymer sector regulations.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—Annex XVII for pigments and dyes
    • EN 71-3 (Migration of certain elements for dye use in consumer products)
    • ISO 105-X12 (Textile color fastness standards)
    • RoHS and Proposition 65 for pigments in electrical goods

    Typical usage ratio

    • 5–25% by molar fraction in dye precursor mixture, set based on final color strength and extinction coefficient requirements in downstream applications

    Downstream process integration

    • Condensation or coupling in diazo, Schiff base, or metal complex dye syntheses
    • Post-coupling purification via recrystallization or membrane filtration
    • Integration into masterbatch, ink, or polymer matrix prior to industrial application

    Final product types

    • Organic dyes for plastic electronics
    • Functional pigments in photovoltaic polymers
    • Photochromic coatings
    • Solar cell dye-sensitized layers

    5. Advanced Polymer and Crosslinked Resin Additive Synthesis

    Resin and polymer formulators engaged in high-performance composites harness the thiophene-benzaldehyde motif to form unique crosslinked networks, imparting thermal and chemical stability enhancements. The material plays a role as a co-monomer or pendant group precursor, introduced ahead of curing reactions or crosslinking stages. Industry standards dictate precision in monomer ratio to achieve specified mechanical performance benchmarks for aerospace, automotive, or microelectronics substrate applications.

    Industry compliance standards

    • ASTM D638 (Tensile properties of plastics)
    • ISO 11357-2 (Differential scanning calorimetry—Thermal analysis for polymers)
    • IEC 61249-2 (Base materials for printed wiring)
    • UL 94 (Flammability ratings for polymer components)

    Typical usage ratio

    • Generally 0.5–10% by weight within the monomer mix, tunable depending on end-use glass transition point and desired crosslink density

    Downstream process integration

    • Pre-mixed with main polymer backbone or added to reaction vessel during melt phase
    • Covalently incorporated during in situ polycondensation or free radical curing
    • Post-curing mechanical and chemical testing for batch release

    Final product types

    • Crosslinked resin laminates for PCBs
    • Thermoset composites for automotive components
    • Encapsulation materials for electronic devices
    • Heat-resistant engineering plastics
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    Certification & Compliance
    More Introduction

    Bringing Precision and Consistency to Chemistry: 3-Thiophen-2-Yl-Benzaldehyde

    Introducing the Realities of 3-Thiophen-2-Yl-Benzaldehyde Production

    Every batch of 3-Thiophen-2-Yl-Benzaldehyde we manufacture carries the results of careful process control and decades of experience working with heterocyclic compounds. The product walks a fine line between aromatic and heteroaromatic functionalities—a benzenoid aldehyde bearing a thiophenyl group at the three position. That structure has opened doors in diverse sectors, from specialized research in new organic materials, to synthetic intermediates in pharmaceutical development, to fine chemical research. Over the years, conversations with our partners have shown that reliability means more than just hitting specification—it means predictability in performance, and ease in working up downstream chemistries, batch after batch.

    In our manufacturing facility, the choice to produce this compound did not come as a response to short-term demand. Instead, it grew from a continued, direct collaboration with bench chemists in R&D environments. They spoke about the challenges around off-spec material, the impact of trace impurities like unreacted starting materials, and the sensitivity of various syntheses to trace sulfur byproducts. In scaling up 3-Thiophen-2-Yl-Benzaldehyde production, we took those conversations seriously. We designed our process to minimize side-products, control isomer formation, and stabilize against oxidation—a point that often escapes notice until product degrades on the shelf or during storage.

    Understanding Performance: More Than a Simple Molecule

    Downstream users quickly recognize the importance of purity, especially in projects where further transformations demand reliable reagents. 3-Thiophen-2-Yl-Benzaldehyde may look straightforward on paper, but it requires careful control at every processing stage. The model we produce generally maintains a purity above 98%, measured by both HPLC and NMR analysis, with verified residual solvent levels far below the commonly accepted cutoffs for sensitive organic syntheses. Early in our scale-up years, some customers pointed out occasional color instability. After years of iterative improvements, we now consistently observe a pale yellow crystalline appearance—an indicator of minimized decomposition and oxidative side products.

    Research labs in organic electronics and pharmaceutical discovery often favor this molecule for its ability to introduce both aldehydic and thiophenic functionality in a single step, without extended protection/deprotection strategies. Reliability comes into play when making advanced materials such as polythiophenes, or when using it as a core building block for bioactive molecule discovery. No two users run the same transformation protocols, but consistent feedback tells us they notice when quality slips—so we set our standards by real user experience, not just regulatory minimums.

    Working with 3-Thiophen-2-Yl-Benzaldehyde: Our Practical Experience

    Scaled manufacturing unearths challenges that lab-scale trials fail to anticipate. Early runs at a pilot scale produced larger than expected levels of oligomeric by-products, especially under atmospheric conditions. Controlling moisture content and oxygen ingress became critical lessons; we moved to inert gas blanketing throughout purification and packaging. Even slight oxidative exposure can result in unwanted polymerized residues—hardly visible by eye, but profoundly destabilizing for those who rely on clean aldehyde chemistry in subsequent steps.

    Glassware, metal compatibility, and choice of solvents during synthesis also shaped our workflow. Thiophene rings, although more robust than some other heterocycles, still exhibit a tendency to undergo ring-opening or substitution under aggressive conditions. Stainless steel reactors with properly passivated surfaces gave us more consistent results than hastily tinned or older glass-lined equipment. These are details that rarely appear in specifications but matter deeply to those who make or use complex organic intermediates.

    Comparisons and Practical Differences from Other Aldehyde Intermediates

    Chemists comparing 3-Thiophen-2-Yl-Benzaldehyde to benzaldehyde or its common substituted analogs often notice marked differences. The fusion of the thiophenyl group changes both the physical profile and the reactivity landscape. For instance, relative to benzaldehyde alone, the presence of the sulfur-containing thiophene ring subtly shifts electron density across the molecule, influencing how it reacts under standard condensation, oxidation, or reduction protocols.

    The aldehyde group’s location at the benzene ring, positioned ortho to the thiophen-3-yl substituent, distinguishes our product from para- or meta-substituted isomers that sometimes crop up in batch processing from less disciplined sources. Off-site discussions with customer R&D teams highlighted how even minor deviations in the isomer ratio (such as a para impurity over 1%) can affect downstream pharmaceutical trial outcomes or cause reproducibility issues in high-performance material synthesis. Our efforts thus persistently target a single, well-defined isomer, even at scale.

    Physically, this produces a difference in melting point, solubility in both polar and nonpolar solvents, and even shelf stability. Some products developed by other manufacturers tend to present with a broader melting range or slight tinge in color, indicators of higher impurity or molecular complexity. We believe end users quickly notice these signals and appreciate being able to trace their starting material to a specific manufacturing approach rather than a bulk, catch-all product lot.

    Taking Responsibility for Product Lifecycle

    The chemical industry continues facing questions about stewardship: how products are sourced, made, and handled after delivery. Thiophene-derived compounds demand attention, especially given the historical tendency for uncontrolled sulfur emissions in less developed sectors. Our plant draws on closed-system reactor designs and on-site solvent reclamation; these choices do not only control operational risk—they reflect our responsibility toward our site neighbors and the global community. Several years ago, we redirected waste streams containing sulfur byproducts through a recovery line, ultimately reducing both emissions and the cost to treat effluent.

    We work with transport firms who understand special requirements for sensitive organics. Every package arrives with its chain-of-custody documentation, and drums are protected from both temperature swings and light exposure. These are practices evolving from years of troubleshooting—practices that keep both end users and supply chain partners confident. Small changes matter: from the silica-gel desiccant chosen for drum liners, to the freeze-seal closure minimizing air ingress until the first use.

    Transparency in Manufacturing and Testing

    Over the last decade, customers have pushed for greater visibility not just on certificates of analysis, but on process control and trace analysis methods behind the numbers. It’s common for partners to request chromatograms, spectroscopic datasets, or trace metals results before purchase. We maintain a library of batch data, including detailed NMR and IR spectra, which connect each lot shipped to its specific synthetic run.

    Some have questioned if multiple sourcing affects quality. Experience says otherwise—fragmented supply chains and disjointed outsourcing create too many points for variability to creep in. By producing in-house, we can make process adjustments in real time, troubleshoot unplanned deviations, and maintain chain-of-custody through dozens of handling stages. More than once, this has allowed us to pull and rework material before shipment following a late-stage analytical anomaly. This is direct, hands-on control—not just oversight on paper.

    Meeting Global User Needs

    Our primary user base includes advanced material researchers, pharmaceutical intermediate developers, and agrochemical innovators. Requests span the routine—gram-to-kilogram quantities for method validation—through to multi-ton runs underpinning commercial API campaigns. Some users need standard powders, others demand larger crystals or granular forms tailored for automated batch feeders. We developed processes for each form, tracking how physical properties influence flow, handling, and reactivity.

    Across all end uses, stability remains paramount. Exposure studies over multiple cycles emphasize the role of packaging and atmospheric conditions in shelf life. In settings where bench storage may linger for weeks or months, visible degradation correlates with real-world problems—off odors, uneven reactivity, and even downstream contaminant buildup in finished products. Years spent assessing sample retention under simulated warehouse conditions have nudged us toward packaging improvements, desiccant selections, and even packing density choices that extend usability for our customers, helping to reduce waste and keep project budgets predictable.

    Intellectual Property and the Rise of Copycat Products

    As global demand grows, copycat producers attempt to undercut established manufacturers through shortcuts in synthesis, often relying on lower-cost feedstocks, relaxed environmental controls, or incomplete purification. End users frequently underestimate the downstream costs posed by such off-spec or poorly characterized intermediates. Some learn the hard way as failed reactions, unreliable analytical results, or regulatory pushback challenge their projects. Maintaining transparency about our synthetic route, purification approach, and analytical traceability helps partners spot differences that matter—whether that be impurity fingerprinting or consistency in isomer ratios.

    There’s a reason we maintain relationships with research teams long after the initial order. Through iterative feedback—discussing issues observed under conditions no certificate could predict—we’ve adjusted not just our process, but the conversation around expectations and shared standards. This extends beyond compliance to building in real-world, practical reliability. Most users rarely see the full lifecycle behind each drum or bottle; our aim is to illuminate everything from upstream raw material testing, to real-time process monitoring, finishing protocols, and post-sale support.

    Learning from Field Failures and Turning Problems Into Progress

    Early batches a decade ago carried lessons we refused to ignore. Some customers reported stubborn filtration problems when working up their reactions; others flagged batch variation correlating with solvent grade or trace metal content. We responded by instituting batch-level trace analysis on both in-process and finished product, and by adjusting our reactor cleaning protocols to meet the need for sub-ppm cleanliness. Filter media choices, adjustments to crystallization conditions, and even timing the post-synthesis cleanup became areas for continuous improvement driven by user outcomes.

    Years in, the reality is that product development doesn’t end with the launch. From the first small-scale sample to today’s consistent tons-per-year output, we’ve taken each reported issue as a chance to improve—not only the product itself but the user experience for diverse end-users. Being able to track the entire process from start to finish, and share results openly, underlines our commitment to the trust placed in us by those who rely on our material as a foundation for their work.

    Shaping the Future: Sustainability and Adaptability in Chemical Manufacturing

    Today’s marketplace expects more than technical capability; expectations include reduced waste, closed-loop management, and process transparency. We audit each material choice, review solvent recovery rates, and participate in peer benchmarking initiatives to ensure continual progress. Few products better exemplify this mindset than 3-Thiophen-2-Yl-Benzaldehyde, where the intersection of complexity, performance, and responsibility all come into play.

    Adapting to user preferences also shapes the future of our production. From adjusting batch sizes for pilot projects, to scaling packaging for logistics, responsiveness forms the backbone of durable business relationships. In recent years, user feedback led us to develop tailored training for correct handling and optimized storage. The result? Fewer complaints, less waste, and improved feedback cycles benefiting everyone along the supply chain.

    The Real-World Value of Direct Manufacturer Partnerships

    Through countless conversations with researchers and process chemists, we have learned that the human factor drives innovation and reliability as much as technical data. Direct manufacturer partnerships, whether across the laboratory bench or the production floor, consistently produce better outcomes for everyone involved. We remain committed to hands-on engagement and never relying solely on faceless intermediaries or data sheets detached from reality.

    Growing global confidence in 3-Thiophen-2-Yl-Benzaldehyde depends not only on our technical performance but also on open communication, readiness to troubleshoot, and a commitment to learning from each use case. This outlook deepens our understanding of what success really looks like: end results achieved in your lab, not just on our spec sheet. Chemical manufacturing is more than a transfer of goods; it’s a collaboration built around practical challenges, persistent solutions, and the power of clear, honest dialogue.