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HS Code |
738825 |
| Cas Number | 1468-83-3 |
| Molecular Formula | C6H6OS |
| Molecular Weight | 126.18 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 193-195°C |
| Melting Point | -12°C |
| Density | 1.13 g/cm³ at 25°C |
| Refractive Index | 1.549 |
| Flash Point | 73°C |
| Purity | Typically ≥98% |
| Chemical Name | 3-Acetylthiophene |
| Synonyms | Thiophene-3-yl methyl ketone |
| Solubility | Soluble in organic solvents; slightly soluble in water |
As an accredited 3-Acetylthiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Acetylthiophene is packaged in a 100 mL amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | 3-Acetylthiophene is shipped in tightly sealed containers, away from heat, sparks, and open flames due to its flammable nature. It should be stored in a well-ventilated, cool, and dry area, and properly labeled according to hazard regulations. Handling requires appropriate personal protective equipment to avoid exposure. |
| Storage | 3-Acetylthiophene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. The storage area should be equipped to prevent moisture ingress and exposure to direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental leaks or spills. |
Applications of 3-Acetylthiophene in Industrial Manufacturing3-Acetylthiophene is a key intermediate synthesized in-house at an industrial scale for integration into specialist downstream markets. We supply this thiophene derivative to manufacturers operating under precise formulation constraints, regulatory oversight, and advanced process controls. Below, we outline established application scenarios where 3-acetylthiophene plays a direct and traceable role in the composition of end-use goods. 1. Pharmaceutical Intermediates for Thienopyridine API SynthesisMany manufacturers rely on this thiophene compound as a starting material in the multi-step synthesis of thienopyridines, a class of orally active platelet aggregation inhibitors. It enters early-stage coupling reactions, enabling selective functionalization crucial to the active pharmaceutical ingredient (API) structure. The final compounds serve as globally regulated prescription medicines. Material flow, usage ratio, and purification procedures must conform to international pharmacopoeial and GMP standards. Industry compliance standards
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2. Building Block for Agrochemical Active Ingredient SynthesisLeading agrochemical companies incorporate this material as a heterocyclic scaffold in the chemical synthesis of selective herbicides and fungicides. Its structural motif enables precise molecular modifications critical for activity spectrum, patent differentiation, and regulatory registration. Integration occurs at tightly controlled stages to ensure consistent performance in crop protection formulas. Industry compliance standards
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3. Fragrance Ingredient Precursor in Fine Chemical ManufacturingSpecialty fragrance manufacturers use this thiophene ketone to synthesize sulfur-containing aroma molecules. It enables the production of nuances characteristic of roasted, nutty, and smoky notes found in flavor and fragrance compositions for premium consumer goods. Purity, residual solvent control, and odor profile undergo consistent testing to comply with industry safety restrictions and sensory quality benchmarks. Industry compliance standards
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4. Intermediate for Advanced Dye and Pigment SynthesisDye manufacturing plants utilize this raw material as a key intermediate for constructing thiophene-containing π-conjugated systems used in high-value specialty dyes and functional pigments. The unique aromaticity and electron-donating characteristics support color stability and lightfastness essential for demanding technical textile, inkjet, and pigment dispersions. Industry compliance standards
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5. Precursor for Electronic Material Synthesis in Organic ElectronicsProducers of organic electronic materials rely on this molecule for constructing advanced thiophene-based monomers and oligomers, which serve as the backbone for high-mobility semiconductors. Process engineers tightly control purity and isomer ratios to ensure device-grade electrical performance and reproducibility in optoelectronic applications. Industry compliance standards
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Producing 3-Acetylthiophene at an industrial scale involves more than simply managing a reaction vessel and a few pieces of glassware. Our experience crafting this ketone demonstrates its valued place in the world of chemical synthesis. The molecule, with the formula C6H6OS and CAS number 1468-83-3, deserves a closer look for anyone invested in pharmaceutical research, intermediates development, or fine chemical manufacturing.
Our team has spent years addressing the challenges of thiophene derivative production, always prioritizing reaction reliability and reproducibility. 3-Acetylthiophene isn’t a lab curiosity; it lives at the crossroads of academic synthesis and high-volume manufacturing. We run this product through multi-step batch operations, employing precise control over acylation procedures, while balancing reaction kinetics with environmental health and safety requirements. Through all this, the priorities remain consistent: minimize impurity formation, optimize yields, and ship a product that performs predictably in downstream chemistry.
Thorough solvent control and temperature management are more than checkboxes—they’re essential to getting the right GC/HPLC profile batch after batch. Our process knowledge lets us navigate complications such as byproduct formation or overreaction, which may not always be obvious to those who limit themselves to bench research. The ultimate goal is to enable our customers to focus on their goals, not wrestle with variations in quality from one drum to another.
Over years of dialogue with formulation teams, analytical specialists, and scale-up engineers, we have honed our finished 3-Acetylthiophene to deliver the purity and lot-to-lot consistency that serious projects require. Key factors—appearance, purity by GC, water content, and residual solvents—deserve scrutiny, because their impact on catalytic reactions and synthetic reliability isn’t theoretical. Medicinal chemists and production managers don’t want variance causing delays in medicinal lead optimization campaigns or pilot plant runs.
Our 3-Acetylthiophene ships as a clear, pale yellow liquid, with purity levels reaching 99% or higher (GC area %). Strict visual and chemical control has emerged from feedback: some projects cannot tolerate any unusual tints or excess water. Residual solvents, especially acetic acid or DMF, must never cross accepted thresholds. Moisture, even when present in trace amounts, can disrupt fryes, Grignard reactions, or sulfonation—experience has taught us to watch for it. Quantitative analysis by Karl Fischer titration lets us guarantee water below 0.2%, so reactivity stays reliable, batch after batch.
It’s satisfying to follow our product’s journey from the plant into labs where creativity happens. Our 3-Acetylthiophene often becomes part of synthesis routes for new pharmaceuticals, agrochemicals, or electronic chemicals. Large-scale projects prize this compound as a building block for heterocyclic scaffolds, especially those destined for advanced research in anti-inflammatory and anti-infective drugs. Structural clarity—no isomeric contamination, no excess water—enables precise downstream transformations like Suzuki couplings or electrophilic aromatic substitutions.
Academic researchers depend on predictability and purity, especially when their syntheses pivot on gram-scale reactions or short timelines for publication. Commercial producers need reliability at scale; deviations in color, odor, or trace impurities can spell costly process rework or end-product degradation. We have concentrated on feedback from both communities to focus our operational investments: refining the rectification step, purifying intermediates, and verifying every outgoing batch by a full set of analytical methods, including NMR, GC-MS, and HPLC.
Customers sometimes ask about the difference between 3-Acetylthiophene and its close relatives, particularly 2-Acetylthiophene. Both species look similar in a bottle, but any practicing bench chemist will tell you that their chemistry diverges sharply. Directing effects—where the acetyl group sits on the aromatic ring—change everything from reactivity to final product outcome.
3-Acetylthiophene features an acetyl group at the third position. This location offers unique opportunities for selective halogenation, alkylation, or Suzuki-Miyaura cross-coupling which cannot be reliably duplicated with either the simple thiophene or the 2-acetyl isomer. This difference becomes crucial in route scouting for new drugs or materials, where the orientation of substituents determines biological activity or final device performance. Real-world experience with reaction selectivity reminds us that chemical intuition only goes so far—test reactions confirm that 2-acetyl and 3-acetyl variants produce different outcomes under identical conditions.
Scaling up 3-Acetylthiophene production goes beyond multiplying lab reaction quantities. During early efforts, we encountered bottlenecks in maintaining product purity at higher volumes. The formation of minor sulfur-containing side products required new purification schemes and tighter monitoring of reagent quality. As process chemists, we learned firsthand that slight changes in solvent grade, temperature ramp rates, or reaction time can push impurity profiles beyond customer tolerance. Our continuous monitoring and adjustment, guided by real process data, enables us to keep quality within specified boundaries.
Solvent recovery and waste management form key aspects of responsible manufacturing. Dealing with odorous thiophene residues and acetylation waste pushed our team toward new containment, off-gassing, and scrubbing systems, minimizing plant impact and preserving local air quality. By optimizing the acylation and purification stages, we have reduced both raw material consumption and waste output.
Our 3-Acetylthiophene has appeared in routes for cardiovascular, CNS, and antiinfective drug candidates. Many of these analogs rely on the unique reactivity of thiophene rings to anchor moieties critical for binding to enzyme pockets or receptor sites. We often get feedback from project managers and medicinal chemists, who describe how reliable supply at consistent purity liberates project teams to pursue clinical lead development without regulatory or analytical surprises.
In specialty materials, 3-Acetylthiophene has uses in organic semiconductors and precursor polymers for OLEDs, where even minor trace metal contaminants or residual chloride can sabotage device efficiency or lifetime. Our batch testing screens for common contaminants introduced through plant piping, valves, or glassware, ensuring pure material reaches electronics clients. For flavor and fragrance applications, where off-odors or trace organosulfur residues must stay below sensory limits, we monitor product by both instrumental and sensory panels.
The plant environment in which we produce 3-Acetylthiophene sees robust safety protocols, shaped by years of handling thiophene systems. Our crew faces daily hazards associated with acylating agents and sulfur chemicals, which can produce unpleasant odors or react strongly if procedures lapse. Regular worker retraining, incident reviews, and emergency drills keep the risk profile at manageable levels, protecting both product and people.
Personal protective gear, local exhaust ventilation, and closed-loop solvent handling have all advanced in the past decade. We have logged thousands of work-hours in small-batch and large-plant runs, with a safety record that reflects vigilance more than luck. Any lessons learned from near misses or process deviations get fed into regular operational reviews and adjustment of our process documentation.
Trust in a raw material in industry often grows through repeated, successful runs. Our records show that upstream process engineers, medicinal chemists, and formulation managers return to our 3-Acetylthiophene because it stands up across multiple projects. Customer case studies highlight lot traceability and batch record availability, which facilitate both troubleshooting and regulatory filings.
We regularly exchange technical data packages with customers, sharing latest batch analyses and addressing queries about particular impurity profiles, solubility behavior, or reaction outcomes. The conversation runs two ways: real-time field feedback from synthetic users or QA professionals turns into process improvements. For example, after obtaining user input about marker compounds interfering with a downstream hydrogenation, we tweaked purification conditions, which brought measurable improvement to both yield and analytical clarity.
Minimizing our manufacturing footprint without sacrificing quality stands as an ongoing challenge. Through solvent recycling improvements and waste reduction projects, we’ve cut emissions and lowered utilities demand. Water/solvent usage for washing and extraction receives continuous review. Data from our in-plant operations team reveals steady progress: less solvent evaporation, reduced sulfur odors, and lower hazardous waste pickup frequency. Every significant change undergoes validation to ensure customer-facing metrics—like purity, appearance, and stability—remain stable.
We track energy usage, emissions, and occupational metrics at every batch campaign. This information drives decisions about plant upgrades, preventive maintenance, and raw material supplier selection. Sourcing greener, higher-quality precursors pays off both in lower environmental impact and fewer downstream process disruptions. Some plant modifications—such as in-line metal filtration or advanced condenser recovery systems—have enabled us to edge closer to both environmental benchmarks and cost targets.
Chemical procurement teams managing GMP- or ISO-compliant production lines demand full transparency. Every batch of 3-Acetylthiophene we ship includes origin, batch record, and analytical certifications. Digital archiving aids in traceability, letting project teams backtrack every raw material, assay data point, and process step even several years after purchase. Our manufacturing records have been reviewed by regulatory and QA teams at facilities all over the world. Familiarity with regulatory documents, MSDS management, and chemical inventory protocols improves logistics for pharmaceutical and specialty customers alike.
Client collaboration drives next-gen process development. Increasing demand for cleaner, more efficient 3-Acetylthiophene—especially with stricter downstream specifications and new sustainability mandates—pushes research and production to integrate greener chemistry and novel synthesis methods. Our process development group operates a pilot facility for continuous advances in yield, resource use, and process intensification. Each process or plant improvement aims to enhance the reliability and performance of our product.
We take seriously the role our product plays in multi-step synthesis, device fabrication, and final formulation. Whether contributing to the next active pharmaceutical ingredient or OLED material, every outgoing shipment embodies lessons learned through years of experience, dialogue with customers, and constant attention to evolving standards in the global chemical industry.