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2-Acetylbenzo[B]Thiophene

    • Product Name 2-Acetylbenzo[B]Thiophene
    • Alias 2-Acetylbenzo[b]thiophene
    • Einecs 224-165-8
    • 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

    737366

    Cas Number 2468-84-8
    Molecular Formula C10H8OS
    Molecular Weight 176.24
    Iupac Name 1-(benzo[b]thiophen-2-yl)ethan-1-one
    Appearance Yellow solid
    Melting Point 99-103°C
    Density 1.23 g/cm3 (estimated)
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC(=O)C1=CC2=CC=CC=C2S1
    Inchi InChI=1S/C10H8OS/c1-7(11)8-6-9-4-2-3-5-10(9)12-8/h2-6H,1H3
    Synonyms 2-Acetylbenzo[b]thiophene, 2-Acetylbenzothiophene

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

    Packing & Storage
    Packing 2-Acetylbenzo[B]Thiophene is supplied in a 25g amber glass bottle with a secure screw cap, labeled with hazard information.
    Shipping **Shipping Description for 2-Acetylbenzo[B]Thiophene:** This chemical should be shipped in a tightly sealed container, away from direct sunlight and incompatible materials. During transit, maintain a cool, dry environment. Follow all local, national, and international regulations for transport; packaging should prevent leaks or spills. Hazard labeling and documentation are required. Handle with suitable personal protective equipment.
    Storage 2-Acetylbenzo[B]thiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. The container must be tightly sealed, clearly labeled, and made of a material compatible with organic compounds. Avoid exposure to direct sunlight and moisture. Follow all relevant safety guidelines and local regulations for chemical storage.
    Application of 2-Acetylbenzo[B]Thiophene

    Applications of 2-Acetylbenzo[B]Thiophene in Industrial Manufacturing

    2-Acetylbenzo[B]thiophene is an advanced specialty intermediate widely applied across fine chemical manufacturing. Our facility delivers industrial-scale capacity and stringent batch traceability, supporting diverse downstream sectors with reliable quality and regulatory documentation.

    1. Pharmaceutical Intermediate for Anti-inflammatory APIs

    2-Acetylbenzo[B]thiophene serves as a key building block in the synthesis of thiophene-linked anti-inflammatory actives, particularly in the early stage benzothiophene core construction. Its high purity ensures compatibility with late-stage high-purity crystallizations, and its predictable reactivity enables robust control of downstream functionalization during API route development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF standards applicable to intermediates
    • EDQM pharmaceutical quality guidelines
    • FDA 21 CFR Part 211 for cGMP API production

    Typical usage ratio

    • 0.8–1.1 mol equivalent relative to thiophene-indole acylation precursor; titrated by targeted API yield and minimization of byproducts

    Downstream process integration

    • Introduced at initial acylation and cyclization phase, preceding main scaffold assembly
    • Subject to analytical QC for residual metals and controlled substances before entering GMP suite
    • Batch documentation linked to DMF submissions for pharmaceutical partners
    • Used in both pilot and commercial-scale glass-lined reactor trains

    Final product types

    • Benzothiophene-based non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Pilot-scale clinical compound batches
    • Registered API lots for phase II/III trials
    • Commercial anti-inflammatory drug substances

    2. Intermediate for Agrochemical Synthesis (Fungicide Market)

    The material is a central intermediate in the synthesis of benzothiophene-derived fungicides, actively used in the preparation of heterocyclic compounds with targeted activity against high-resistance crop fungal pathogens. Its stable acetyl group facilitates selective substitution and minimizes undesired side reactions during alkylation or halogenation.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management System
    • REACH (EC) No 1907/2006 substance registration for export to EU
    • China National Agrochemical Standard HG/T 3950

    Typical usage ratio

    • 5–15% w/w based on total raw material mass in multi-step synthesis; adjusted by overall crop protection active ingredient target batch

    Downstream process integration

    • Charged in cyclization or acylation reactor during synthetic route construction
    • Monitored for residual water and impurities via in-line HPLC prior to downstream chlorination or methylation
    • Traceable supply for GMP-adjacent contract manufacturing
    • Final purification includes column chromatography and crystallization control

    Final product types

    • Benzothiophene-based broad-spectrum fungicides
    • Precursor molecules for triazole-type fungicidal actives
    • Formulated agricultural crop protection products
    • Registration trial samples for national pesticide approval

    3. OLED and Electroactive Material Intermediate

    Chemical process engineers utilize this compound for synthesizing thiophene-core monomers in organic light-emitting diode (OLED) materials. The acetyl functionality offers flexibility for subsequent conversion to aldehyde or carboxyl derivatives, important for modulating electronic properties required in blue- and green-emitting OLED layers, as well as for tuning solubility during ink formulation.

    Industry compliance standards

    • IEC 62321-7-1 for analytical detection of restricted substances
    • RoHS Directive 2011/65/EU compliance for finished display goods
    • ISO 9001 and ISO 14001 Environmental Management System
    • Company-specific raw material QC for electronics-grade organics

    Typical usage ratio

    • 2–6 mol% of total monomer feed in copolymer or oligomer synthesis; optimized on demand per device architecture

    Downstream process integration

    • Employed in Suzuki or Stille coupling steps for core conjugation
    • Purity controlled to <100 ppm metal ion content for electronic-grade material
    • Processed under inert atmosphere to avoid oxidative degradation
    • Final intermediates further purified for photoluminescent conversion

    Final product types

    • OLED emitter precursor molecules
    • Blue/green light-emitting active materials for display panels
    • Electroactive polymers for flexible displays
    • Prototype batches for device performance validation

    4. Flavor and Fragrance Synthetic Intermediate

    Flavors and fragrance producers incorporate this thiophene derivative in the creation of specialty sulfur aromatics and musk components. Its acetyl side chain supports clean conversion to ketone or alcohol derivatives, which serve as character impact molecules in high-value aroma formulations. The compound’s trace impurity profile falls within the levels required for further transformation in non-food fragrance bases.

    Industry compliance standards

    • IFRA (International Fragrance Association) standards for ingredient safety
    • FEMA GRAS listing for non-food use
    • ISO 9001:2015 for fragrance raw material quality
    • EU Cosmetics Regulation (EC) No 1223/2009 for restricted substances

    Typical usage ratio

    • 0.2–2.5% w/w in fragrance synthesis route; dosed as required by target olfactory profile and single-batch yields

    Downstream process integration

    • Fed to Grignard or Friedel–Crafts alkylation for musk and sulfur aroma creation
    • Monitored for volatile impurities and odor-neutrality before addition
    • Undergoes internal sensory evaluation for off-notes prior to release
    • Blended with carrier solvents for optimal reactivity in pilot facilities

    Final product types

    • Sulfur-based aroma compounds for fine fragrance blending
    • Musk analog intermediates
    • Synthetic aroma chemicals for perfumery
    • Specialty perfumery bases for personal care
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    Certification & Compliance
    More Introduction

    2-Acetylbenzo[B]Thiophene: A Factory Perspective on Its Value, Quality, and Practical Application

    Understanding the Character and Strengths of 2-Acetylbenzo[B]Thiophene—Straight from Our Production Line

    In the chemical world, every compound carves out its own place. After years of handling a wide array of products and seeing customer priorities up close, I can confidently say that 2-Acetylbenzo[B]Thiophene offers a depth of consistency and quality that always stands out. This compound, fashioned with precise engineering and rigorous checks across our facility, shows its strength not just in textbooks, but in the hands-on reality of research, manufacturing, and synthesis.

    Production Overview: From Raw Selection to Refined Crystal

    Making 2-Acetylbenzo[B]Thiophene is no trivial process. Our technicians have honed every step—from solvent selection and catalyst calibration to temperature staging and purification. We run every batch through repeated crystallization and advanced chromatography. Each batch receives scrutiny with high-performance liquid chromatography (HPLC), melting point measurements, and gas chromatography-mass spectrometry (GC-MS) checks. Visible clarity, color, and texture are repeatable from drum to drum. Years of listening to chemists has shaped our standards: nobody likes a compound that varies in grain size or slips outside the stated melting point.

    Consistent Model, Defined Specifications

    Our main offering comes with a purity level of 98% and above. Color holds a faint yellow hue, often described as straw-like by clients who measure every detail for sensitive reactions. The melting point routinely checks in at 72–74°C, with deviation rarely above half a degree. Packing is flexible by lot size, but for most projects, 1kg, 5kg, and 25kg drums remain the go-to scale. What do these figures actually mean for your lab bench or reactor? Stability translates directly to reproducible experimental outcomes and straightforward scaling for pilot or bulk runs.

    The Working Chemist’s Experience: What Sets This Product Apart

    Bench chemists rarely praise a compound just because the catalog says it’s available. Praise comes when a batch dissolves as expected—no clumping, no unwanted particles—and products flow through to downstream steps without unpredictable loss or contamination. Over many years, repeat customers return for 2-Acetylbenzo[B]Thiophene not due to abstract promises, but because their researchers and engineers find little to criticize in our batches. The batch-to-batch regularity matters not just for documentation; it speeds up product development and clears up data sets in medicinal chemistry, flavor synthesis, and agrochemical development.

    Main Usage Areas and the Demands of Synthesis

    2-Acetylbenzo[B]Thiophene tags into aromatic chemistry with real value. Its acetyl and thiophene rings offer a flexible gateway for building more intricate molecules, whether in pharmaceuticals, material science, or fine chemical research. We see it picked up for intermediate synthesis in anti-inflammatory drug projects, structural motif insertion in organic electronics, and as a scaffold for dye molecule research. Unlike blander aromatic ketones, its fused thiophene ring brings nuanced reactivity—leading to novel nucleophilic addition options or serving as a precursor in ring-expansion and functionalization schemes. The difference gets practical: a customer working on anti-tumor agents found that substituting this compound for a standard acetylbenzothiophene analog led to higher yields and cleaner NMR spectra. These aren’t rare stories—they follow a pattern we hear from teams in both pharma R&D and materials start-ups.

    Purity: Why It Matters in Downstream Chemistry

    Impurities complicate everything. Our quality control team has seen how slightly off-color or high-residue batches, even with nominally high purity, can ruin multi-step reactions or show up as ghost peaks in HPLC traces. Years ago, one key customer in a major pharmaceutical company flagged a trace-level sulfurous impurity that had gone undetected by basic GC. We upgraded to deeper GC-MS calibration protocols and shifted some cleaning stages. That investment in better detection helped many clients trust that their downstream yield changes reflected their experiment, not noise from bad input.

    Comparing 2-Acetylbenzo[B]Thiophene to Structural Relatives

    Not every aromatic ketone behaves the same. Sometimes customers wonder if they can swap in benzo[b]thiophene, simple acetylthiophene, or other benzothiophene derivatives. The electrophilicity, solubility, and sometimes even scent set 2-Acetylbenzo[B]Thiophene apart. In cross-coupling and Friedel–Crafts acylation work, this compound’s ketone position on the fused ring system changes reactivity pathways—often producing cleaner main products and fewer polyacylated byproducts. One academic group traced the efficiency in C–H activation to the precise electronic effects from the acetyl location.

    What Repeat Orders Say about Product Strengths

    Our operations team always pays attention when buyers return, year after year. Many customers began with a small 100-g evaluation lot and rapidly switched to multi-kilo quantities after running a handful of test batches. Strong performance in pilot studies convinced process chemists to lock in this compound during scale-up, avoiding the classic problems of revalidation. The takeaway: for working chemists, the math amounts to more than cents per gram—it’s about trust and avoiding costly project failures due to inconsistent input.

    Real Lab Feedback Drives Continuous Refinement

    We don’t just send off shipments and close files. Our technical support field engineers talk with users every week. Common feedback centers on three factors: ease of dissolving, odor stability, and clarity in NMR and HPLC results. There’s little tolerance for batches loaded up with extra stabilizers or buffer salts. Some research labs need the product packaged under inert gas to prevent air-induced yellowing. We learned to dry-pack and quality-test every container, minimizing headspace oxygen. That tweak alone reduced complaints among long-term storage buyers by half. In the world of chemical supply, little changes make big impacts.

    Addressing Application-Specific Needs: What Customers Actually Ask For

    Some buyers request batch splits for parallel project tracks, each with a tight analytical certificate. Our analysts share not just a COA PDF but the actual chromatograms on request. Pharmaceutical groups sometimes send back proposed testing schemes—our team welcomes this kind of communication, since passing these external checks makes everybody’s job more predictable. Compared to tradition-bound suppliers, we see success in collaborative problem solving rather than policing boundaries.

    Safe Handling Practices and Practical Advice from the Factory Floor

    As a crystalline solid, 2-Acetylbenzo[B]Thiophene avoids many of the volatility problems seen in lower-weight ketones. Still, our workers handle it in well-ventilated, dust-controlled environments. Long sleeves, gloves, and eye protection feature in every batch run. Even small batches create noticeable odor—while not sharp, the subtle sulfur note lingers. These handling details pass on to our instructions to end-users: store in sealed, moisture-free containers, away from direct light, and avoid extended exposure to air. Simple steps keep both product and lab teams safe.

    The Role of Batch Records and Documentation

    Over the years, compliance demands from global clients have only grown. Laboratories in Europe, the US, and Japan all expect full documentation, including lot traceability and detailed residual solvent analysis. As a manufacturer, we log all raw materials back to original sources, run cross-record checks at every stage, and keep digital and paper logs on hand for any audit or recall. In bulk chemical manufacturing, these records don’t just satisfy auditors—they prevent downtime and give researchers confidence in experiment validity.

    Supporting the Move to Greener Chemistry

    A trend has surfaced in every segment of specialty chemistry: routes that use less chlorinated solvent, produce less hazardous waste, and avoid highly toxic ligands. We’ve tuned some synthesis steps in 2-Acetylbenzo[B]Thiophene production toward greener alternatives, and we’re candid with buyers about process changes. Clients working on environmental remediation or green pharma projects take an interest in how their inputs are sourced. Our shift to less waste-intensive acid scavengers and solvent recycling processes cut the plant’s waste stream by over 10% in recent years. Collaborative customers have helped identify further “greener” substitutions without compromising product quality.

    What to Watch Out for with Blends, Knockoffs, or Low-Grade Imports

    We know some buyers shop around for “cheaper” sources. The industry is filled with blends, off-grade lots, and relabeled material. Reports from university labs describe false melts, impurities not listed on COAs, and unexplained darkening during reactions. We secure supply chains tightly to prevent cross-batch contamination, and random third-party lab checks confirm our purity claims. For research at the cutting edge, unknowns in material composition spell delay, data inconsistency, and the risk of throwing out weeks of work.

    Adaptability and Scale—Meeting Both Small Labs and Industry Needs

    Over the decades, our production lines have evolved from single-liter glassware to multi-hundred-liter reactors. For a rare intermediate like 2-Acetylbenzo[B]Thiophene, flexibility is vital. Each kilo run passes the same scrutiny as the smallest research lot. Our technicians adjust running parameters for seasonal fluctuations, batch size, and even custom requests for solvent residuals or lot-specific grind size. Many competitors focus solely on cost, ignoring feedback from the field. Our model emphasizes real-world use: we measure our success by how easy our product fits into downstream operations without adjustment or complaint.

    What Comes Next: Insights from Customer Projects

    The real test of a chemical’s value comes from how it functions beyond the supplier’s gates. Medicinal chemists have shared data that our product often proves key to unlocking new synthetic approaches for sulfur-containing heterocycles. Polymer groups find our tightly controlled lots crucial for reproducible upscaling of semiconducting films and sensors. Agrochemical discovery teams, working on new fungicide scaffolds, have selected our compound not for lowest cost, but because they can run 50 or 100 parallel reactions without worrying about odd color changes or microimpurities. Direct technical feedback gets folded into each year’s production cycle.

    Connecting Directly with Researchers, Not Just Purchasing Agents

    Our team regularly answers questions from principal investigators, grad students, and industrial chemists, not just procurement staff. We know chemists ask about detailed impurity profiles, lot-specific spectra, and proposed alternatives for side reactions. In the push for innovation and transparency, we share as much technical detail as possible, including NMR scans or freshly run spectral data upon request. By fostering open communication, we’ve sidestepped old frustrations where buyers felt left in the dark about what actually arrived on their doorstep.

    Continuous Learning Means Better Outcomes for All

    Each round of production or troubleshooting brings new lessons. Sometimes a shift in raw material source requires a weeks-long period of co-validation. Now and then, a user flags a minor issue—a slight bump in water content or a faint off-note in a bioassay—which prompts a refresh of both in-process controls and final checks. These real-world signals keep the product sharp and reliable, pushing our technicians to adapt procedures and reinforce best manufacturing practices. Over time, the back-and-forth with demanding end-users translates into a stronger, more stable product line that earns its place in advanced labs and production floors worldwide.

    Our Commitment to Researchers and the Future

    Producing 2-Acetylbenzo[B]Thiophene inside a working chemical plant isn’t about simply ticking off checkboxes on a product data sheet. It’s the ongoing commitment to quality, reliability, and open dialogue that lets research teams move faster with fewer hiccups and reduced uncertainty. Real experience tells us that in specialty chemistry, a good compound does more than meet a numbered specification—it fits smoothly into ambitious projects and helps bring new science into reality. Our entire team—engineers, analysts, floor chemists, and support staff—stays focused on that promise with every lot produced. As the field evolves, we keep listening and improving, turning customer feedback into practical changes on the line and better results for every project that uses our product.