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2-Acetyl-3-Methylbenzo[B]Thiophene

    • Product Name 2-Acetyl-3-Methylbenzo[B]Thiophene
    • Alias 2-Acetyl-3-methyl-1-benzothiophene
    • Einecs 629-426-2
    • 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

    114045

    Chemical Name 2-Acetyl-3-Methylbenzo[B]Thiophene
    Cas Number 72082-25-8
    Molecular Formula C11H10OS
    Molecular Weight 190.26 g/mol
    Appearance Yellow to brown solid
    Synonyms 2-Acetyl-3-methyl-1-benzothiophene
    Structure Type Aromatic heterocycle with acetyl and methyl substituents
    Inchi Key XECOEKJRODYKTI-UHFFFAOYSA-N

    As an accredited 2-Acetyl-3-Methylbenzo[B]Thiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g quantity of 2-Acetyl-3-Methylbenzo[B]Thiophene is supplied in a sealed amber glass vial with a tamper-evident cap.
    Shipping 2-Acetyl-3-Methylbenzo[B]Thiophene is shipped in sealed, certified chemical containers to prevent leaks and contamination. It is transported according to relevant hazardous materials regulations, with proper labeling and documentation. The shipment is protected from moisture, heat, and direct sunlight to preserve stability and ensure safe delivery to laboratories or industrial destinations.
    Storage Store 2-Acetyl-3-Methylbenzo[B]thiophene in a cool, dry, and well-ventilated area, tightly sealed in a compatible container. Keep away from direct sunlight, ignition sources, and incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to trained personnel. Use secondary containment to prevent leaks or spills, and follow local regulations for chemical storage and handling.
    Application of 2-Acetyl-3-Methylbenzo[B]Thiophene

    Applications of 2-Acetyl-3-Methylbenzo[B]Thiophene in Industrial Manufacturing

    2-Acetyl-3-Methylbenzo[B]Thiophene serves demanding roles as a key intermediate in advanced fine chemical synthesis. We enable industrial and specialty chemical manufacturers to integrate this compound into tightly controlled production lines, meeting strict specification and regulatory standards at scale.

    1. Pharmaceutical Intermediate for Thienopyridine Drug Synthesis

    Pharmaceutical companies select this thiophene derivative as a core starting material in the synthesis of thienopyridine class actives, such as certain antiplatelet agents. The acetyl-methyl-thiophene structure forms a building block in multi-step reactions leading to active pharmaceutical ingredients (APIs). Customers require high consistency during batch-to-batch procurement to maintain reaction reliability and achieve targeted API yields. Our strict lot release testing supports compliance and downstream reaction efficiency by minimizing side product formation.

    Industry compliance standards

    • cGMP guidelines (ICH Q7)
    • EU Guidelines for APIs (Directive 2011/62/EU)
    • USP and Ph. Eur. reference substance controls for intermediates
    • FDA 21 CFR Part 211 for process controls

    Typical usage ratio

    • Used at 1-8% molar ratio as the initial structure in synthesis pathways
    • Stoichiometry adjusted based on target API and scale; kinetic studies set optimum loading

    Downstream process integration

    • Charged as primary substrate in closed reactor systems
    • Combined with nitration, cyclization, or condensation agents
    • Purified by crystallization before further transformations
    • Residual levels strictly monitored in the produced API

    Final product types

    • Platelet aggregation inhibitor APIs (e.g., thienopyridines)
    • Cardiovascular bulk drugs
    • High-purity pharmaceutical intermediates for export
    • Reference standards for QC labs

    2. Intermediate for Agrochemical Active Synthesis

    Leading crop protection manufacturers use this compound as part of their process to build sulfur-heterocycle motifs common in modern herbicides and fungicides. Its defined position of acetyl and methyl groups enables regioselective reactions and clean final products. We supply tightly specified material to avoid catalyst poisoning in subsequent steps, supporting scalable active ingredient output aligned with agricultural sector demand cycles. Process control protocols maintain integrity and traceability for agrochemical use.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • REACH Regulation (EC) No 1907/2006 Annex VII
    • FAO/WHO JMPR residue standards for intermediates
    • Local EPA discharge and workplace exposure limits

    Typical usage ratio

    • Used at 0.5-5% molar percentage in target molecule construction
    • Adjusted depending on the specific herbicide or fungicide pathway

    Downstream process integration

    • Fed into step-wise alkylation or halogenation reactions
    • Operates under controlled temperature and inert conditions
    • Downstream intermediates isolated prior to formulation
    • All process streams monitored for impurity carryover

    Final product types

    • Sulfur-containing herbicide technicals
    • Fungicidal active ingredient concentrates
    • Agrochemical bulk intermediates
    • Analytical reference standards for GLP residue testing

    3. Functional Dye and Pigment Precursor

    Manufacturers in the specialty dye sector integrate this thiophene derivative into multi-ring aromatic frameworks to achieve advanced color fastness and UV stability for textile coloration and optical materials. The acetyl group enhances solubility in organic synthesis stages, while the sulfur moiety supports specific electronic transitions in pigment molecules. We provide high-purity grades to eliminate trace metals and side contaminants, essential for chromophore performance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (limit values for intermediates)
    • ETAD guidelines for chemical safety
    • EN 71-3 for pigment applications in toys
    • ISO 9001 certified pigment process controls

    Typical usage ratio

    • Standard loading 2-10% weight percent in total pigment precursor batch
    • Adjusted for hue intensity and target shade depth

    Downstream process integration

    • Introduced during diazotization or acylation steps
    • Coupled with aromatic amines or phenols
    • Subjected to oxidation or metal complexation post-reaction
    • Residue monitored for synthetic byproducts

    Final product types

    • Functional dyes for polyamide and polyester textiles
    • High-performance printing ink pigments
    • Colorant intermediates for plastics compounding
    • Solar cell light-absorbing materials

    4. Fine Flavor and Fragrance Intermediates

    Aromatic chemistry specialists in the flavors and fragrances sector rely on 2-Acetyl-3-Methylbenzo[B]Thiophene as a key building block for producing sulfur-containing heterocyclic notes, especially in savory, meaty, roasted sweet, or nutty flavor accords. Our controlled purity supports reproducible olfactory profiles by reducing off-note formation, supporting both large-scale flavor houses and high-value fragrance molecule synthesis for consumer products under tight safety regulations.

    Industry compliance standards

    • IFRA Code of Practice for ingredient purity
    • FEMA GRAS listing for regulated intermediates
    • CFR 21 172.515 for synthetic flavoring substances
    • ISO 9001:2015 and HACCP for food chain safety

    Typical usage ratio

    • Dosed at 0.2-2.5% relative to final aromatic blend
    • Specific loadings designed per finished flavor impact

    Downstream process integration

    • Entered directly into high-pressure, high-temperature aroma synthesis reactors
    • Undergoes condensation or cyclization reactions
    • Purified by distillation or extraction systems
    • Checked for compliance with olfactory purity requirements

    Final product types

    • Nutritional flavor enhancers for snack and ready-meal sectors
    • Specialty fragrance ingredients for cosmetics and personal care
    • Food safe roasted-meat type flavor bases
    • Complex aroma compounds for fine parfumerie
    Free Quote

    Competitive 2-Acetyl-3-Methylbenzo[B]Thiophene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Acetyl-3-Methylbenzo[B]Thiophene: A Manufacturer’s Perspective

    Understanding the Chemistry and Character of 2-Acetyl-3-Methylbenzo[B]Thiophene

    Working in a plant that synthesizes 2-Acetyl-3-Methylbenzo[B]Thiophene offers a front-row seat to the practical side of fine chemical production. This is not just another chemical on a product list. The process of creating this compound demands both technical skill and an appreciation for what the molecule offers. With the formula C11H10OS, the structure features a benzothiophene core, subtly altered by acetyl and methyl substitutions. These small additions to the molecular scaffold fundamentally shift its chemical behavior compared to simpler benzothiophenes.

    Producing this compound calls for precision at every step. Upstream, the quality of starting thiophenes, choice of catalysts, and solvent purification make or break the downstream yield. Workers in our control room understand the importance of regular monitoring. We verify melting point, color, purity (often upwards of 98% when sent for use in pharma R&D), and not just by routine: any departure, even small, signals a need for close inspection somewhere along the line.

    Applications: Why End Users Keep Asking for This Molecule

    Demand for 2-Acetyl-3-Methylbenzo[B]Thiophene keeps rising for several good reasons. Laboratories use it as a building block in the synthesis of advanced materials and drug intermediates. The ketone group in position 2, paired with the methyl group on the fused aromatic ring, allows targeted reactivity that researchers value. This structure suits certain Friedel-Crafts reactions and can serve as a precursor for a range of substitutions or couplings.

    In pharmaceutical development, the benzothiophene backbone delivers properties relevant for candidate screening. Our technical team has learned through client feedback that research teams prefer it due to the balance it strikes between reactivity and manageable toxicity. Compared with unsubstituted benzothiophenes, the acetyl group enhances functionalization options, giving medicinal chemists greater flexibility to design targeted molecules for their pipelines.

    Product Specifications: What Sets This Material Apart During Real-World Synthesis

    The product we deliver comes as a pale yellow crystalline solid, usually shipped in sealed glass containers to keep out moisture and airborne contaminants. Years of running the same production line offered clear lessons: crystal clarity can dip if solvents are not fully removed, or if storage conditions drift too far from recommended parameters.

    Each batch lands in our QC department, where we run not just HPLC but also NMR and elemental analysis. Experience has shown that small discrepancies in signal strength can point to impurities that, although minor, impact the reliability of downstream chemistry. We do not ship unless all benchmarks are passed. Customers looking to scale up reactions for pilot plant or larger batch work regularly report that the format and purity we provide saves them rework and unplanned troubleshooting.

    Compared to other benzothiophene derivatives, 2-Acetyl-3-Methylbenzo[B]Thiophene offers a distinct compositional advantage. For example, 2-acetylbenzo[b]thiophene (without the methyl) or 3-methylbenzo[b]thiophene (without the acetyl) both lack the fine-tuned reactivity offered by the combination here. This pairing of functional groups has made the product preferred in screening for heterocyclic libraries and targeted catalyst development.

    Our Role as Manufacturer: From Lab Bench to Kilo Scale and Beyond

    Every improvement or adjustment we make comes straight from the realities of the production floor. Take temperature control—too hot, and you get unwanted byproducts; too cool, and the reaction stalls. We work with sensors and feedback loops, but human oversight plays a big part. Operators gauge bubbling, color change, and even sample odor as informal markers during the run. Having a team with decades of combined experience means those cues guide intervention sooner than any remote dashboard can.

    Moving from gram-scale to kilo-scale brings its challenges. Crystal growth in larger batches, heat removal during exothermic additions, and the logistics of safe solvent handling all demand attention. We have had to adapt our glassware and, later, steel reactors, to guarantee safety and batch consistency. Currently, most of our output heads to clients focused on medicinal chemistry and specialty intermediates, who value both the technical documentation we provide and our willingness to discuss process yield improvements.

    Safety, Handling, and Environmental Impact

    The bench chemist often opens a container and notes the aromatic odor—not too strong, but distinctive enough to be noticed. We designed our packaging for easy, safe transfer, whether the material’s destined for a hood in a university research lab or an automated synthesis robot in a pharmaceutical company. Inside the factory, our staff routinely works with gloves and goggles to avoid direct contact, cleaning any accidental spills immediately with appropriate absorbents. Years in this business taught us that minor lapses in protocol can result in real issues, both for worker health and for the quality of material shipped.

    From an environmental angle, waste minimization matters. Rather than dumping spent mother liquors or used filter aids, we direct streams for solvent recycling and have invested in scrubber upgrades to handle any sulfur-containing vapors. Stringent process records and batch tracings keep regulatory compliance straightforward and build trust during customer audits. Responsible manufacturing has always required more than meeting a spec—it means building relationships based on transparency and consistent delivery.

    Comparisons: What Makes Ours Stand Out Against Other Benzothiophenes

    People sometimes ask why they should pay a premium for 2-Acetyl-3-Methylbenzo[B]Thiophene when other thiophenic intermediates seem similar on paper. Our years working with diverse researchers and formulators taught us that no two substituted benzothiophenes behave in the same way, especially once introduced to real synthetic routes.

    The acetyl and methyl pairing gives this molecule a versatile edge. Compared to relatives with only a methyl or only an acetyl group, this compound’s dual functionalization provides both electron-withdrawing and electron-donating effects within the aromatic framework. That translates directly to more control during stepwise functionalization or library synthesis—a lighter touch for protecting-group strategies, fewer side reactions, and better reproducibility. Our plant has fielded many requests to customize physical form or particle size for specific reactions, and we have proven that this product’s flow properties suit common transfer and dispensing setups.

    Many of our competitors source from upstream traders, meaning the original plant conditions are unclear and batch reproducibility suffers. By contrast, we manufacture from the ground up. Our records trace everything from incoming raw materials to shipment documentation. That difference, while invisible to the purchaser looking at a kilogram drum, shows up during reaction optimization, where purity and low trace impurity levels allow R&D teams to explore with greater confidence.

    Working With Researchers: Responding to Real-World Synthetic Needs

    We do not just ship and forget. Researchers often need minor tweaks—sometimes a drier product, sometimes smaller batch splits, and occasionally a melt-point adjustment for an esoteric application. Our technical staff runs each request through a feasibility meeting, balancing safety, throughput, and regulatory requirements. This direct feedback loop has led us to adjust our crystallization and drying methods over time, with real improvements seen in purity and product yield.

    Working closely with process chemists, we have tracked the way 2-Acetyl-3-Methylbenzo[B]Thiophene holds up under hydrogenation, lithiation, or oxidative conditions. Most early-stage synthesis groups report good tolerance in mixed solvent systems, compared to more touchy, highly conjugated analogs. This resilience, combined with scalability, makes our product the lead pick in gram-to-kilo synthetic transformations.

    Real Impact on Downstream Innovation

    Looking back on years in the plant, one thing stands out: compounds like 2-Acetyl-3-Methylbenzo[B]Thiophene fuel far more than incremental change. Medicinal chemists building new scaffolds cite it as enabling quick iterations. Catalysis groups use it to tune selectivity in reactions where structure-activity relationships remain poorly understood. Some materials scientists leverage the compound’s stability for new optoelectronic prototypes. Across these disciplines, success often hinges on sourcing material with consistent, high-end purity and minimal batch-to-batch drift in color, melting range, or impurity profile.

    We keep refining the manufacturing process with regular input from these innovators. Their results in the field offer the clearest guide to what matters in real-world use, far more than any published data sheet. Outliers—unusual side products, reactivity loss in pilot runs, or odd solubility patches—all feed back into our process reviews. As much as chemists value technical specifications, ongoing dialogue between manufacturer and user builds the reliability that underpins new discoveries.

    Commitment to Reliability and Responsible Manufacture

    Running a chemical plant asks for discipline and foresight. Our team knows shortcuts risk much more than occasional rework—they undercut trust built over years. Every packed drum that heads out the door reflects the standards we set for ourselves, shaped by real consequences: customer complaints, wasted time, and lost opportunity. By investing in modern QC and training our operators to recognize subtle cues, we catch small deviations before they snowball into bigger problems.

    We also take pride in process transparency. Visitors on technical audits see nothing hidden: calibration logs, solvent origins, reprocessing records, and environmental controls are all open for inspection. That openness reassures clients running tightly regulated projects, especially in pharmaceuticals, that they can trace each input and processing step. For many, this means less time spent qualifying a new supplier—a win for project schedules and bottom lines.

    Future Directions: Adapting to Evolving Demands

    Research never stands still. From our standpoint, new requests for custom purities, form factors, or packaging configurations point to ongoing innovation among our clients. We are currently evaluating pilot efforts to further cut solvent volumes, improve recycling, and simplify product isolation. Instead of adding complexity, our aim is to make downstream use even smoother: easier weighing, improved dissolution, and more adaptive batch splits.

    We notice projects in green chemistry and sustainable synthetic methods increasingly ask detailed questions about the origin and fate of the chemicals upstream. As manufacturers, we respond with improved lot traceability and readily available COA and SDS documentation. The baseline for ‘acceptable’ process transparency is changing, and we intend to stay ahead through investment in both people and process.

    Recap: Why 2-Acetyl-3-Methylbenzo[B]Thiophene Keeps Its Place in Modern Chemistry

    From our vantage point inside the plant, the long runs, regular QC checks, and constant dialogue with end users bring a detailed understanding of what matters. 2-Acetyl-3-Methylbenzo[B]Thiophene delivers reliable results across industries because each batch reflects both hard-earned process expertise and a commitment to client-driven improvement. Compared with simpler or more heavily substituted benzothiophenes, the product we batch and ship gives research groups an optimal mix of functional group availability and chemical resilience.

    Trust in a chemical product grows through each successful reaction, each reproducible yield, and every transparent answer to a client’s technical or regulatory query. Our approach relies on real-world learning: adapting methods as actual feedback dictates, keeping eyes open for subtle process improvement, and not cutting corners no matter the commercial pressure. The result: innovators return for more, knowing they will get not just a product, but a reliable partner in discovery.