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4-(2-Thienyl)But-3-En-2-One

    • Product Name 4-(2-Thienyl)But-3-En-2-One
    • Alias Thiophene vinyl ketone
    • Einecs 216-491-7
    • 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

    223604

    Chemical Name 4-(2-Thienyl)but-3-en-2-one
    Molecular Formula C8H8OS
    Molar Mass 152.22 g/mol
    Cas Number 13679-86-2
    Appearance Pale yellow liquid
    Boiling Point 78-80°C at 8 mmHg
    Density 1.136 g/cm³
    Smiles C=CC(=O)CC1=CC=CS1
    Inchi InChI=1S/C8H8OS/c1-2-8(9)5-7-3-4-6-10-7/h2-4,6H,1,5H2
    Pubchem Cid 3092428
    Solubility Slightly soluble in water
    Storage Conditions Store at 2-8°C in a cool, dry place
    Refractive Index 1.599

    As an accredited 4-(2-Thienyl)But-3-En-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 25 grams of 4-(2-Thienyl)but-3-en-2-one, sealed with a screw cap and labeled with safety information.
    Shipping 4-(2-Thienyl)but-3-en-2-one is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled by qualified personnel, following all relevant safety regulations. Shipments comply with local and international chemical transport guidelines, with clear hazard labeling and accompanying safety documentation to ensure safe delivery.
    Storage 4-(2-Thienyl)but-3-en-2-one should be stored in a tightly sealed container, away from direct sunlight and sources of ignition, in a cool, dry, and well-ventilated area. Keep it separated from strong oxidizers, acids, and bases. Ensure storage conditions minimize moisture exposure and temperature fluctuations. Clearly label the container and follow standard safety protocols for handling potentially hazardous organic compounds.
    Application of 4-(2-Thienyl)But-3-En-2-One

    Applications of 4-(2-Thienyl)But-3-En-2-One in Industrial Manufacturing

    As an original manufacturer, we supply 4-(2-Thienyl)But-3-En-2-One directly for established, material-driven industries requiring advanced heterocyclic building blocks. The following sectors utilize this compound in well-documented, process-critical roles, each with a focused application and regulatory context.

    1. Pharmaceutical Intermediates in Antithrombotic Synthesis

    Drug API manufacturers deploy this compound as a unique intermediate for the synthesis of selective antithrombotic agents featuring a thiophene moiety. Its electron-rich structure enables targeted coupling reactions in advanced heterocycle assembly. Formulators adjust use levels based on targeted yield and downstream purification strategies. Strict adherence to GMP protocols, validated process control, and compliance documentation govern batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (FDA cGMP regulations)
    • EU GMP Guidelines (EudraLex Vol. 4)
    • USP–NF and EP monograph conformity for intermediates and residuals

    Typical usage ratio

    • 0.8–1.2 mol equivalents relative to active pharmaceutical core substrate, based on stoichiometry in route design and impurity thresholds

    Downstream process integration

    • Introduced in the key coupling or condensation stage after initial scaffold construction, followed by controlled reflux and selective crystallization before purification

    Final product types

    • Antithrombotic API intermediates
    • Thienyl-substituted pharmaceutical actives
    • Certified GxP-compliant bulk APIs for contract manufacturing

    2. Organic Electronic Materials Manufacturing

    Producers of organic semiconductors and light-emitting materials integrate this compound as a critical monomer in the assembly of conjugated polymer backbones. The thiophene-vinyl motif promotes delocalization and charge carrier mobility, making it valuable in OLED, OFET, and OPV device fabrication. Precise ratios are determined by the target conjugation length and molecular weight distribution for layer uniformity and reproducibility across production runs.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU) for hazardous substance content
    • IEC 60747-1 (Semiconductor devices basic requirements)
    • JEDEC JESD625 for materials control
    • REACH (EC No. 1907/2006) registration for industrial use

    Typical usage ratio

    • 3–12% weight by mass within pre-polymerization feedstock, balanced according to bandgap engineering targets and downstream device specifications

    Downstream process integration

    • Dosed during the Suzuki-Miyaura or Stille cross-coupling polymerization step, prior to solution processing or film deposition under inert atmosphere

    Final product types

    • Poly(thiophene vinylene) semiconductors
    • Emissive layers for OLED panels and displays
    • P-type materials for flexible electronics and printed circuits

    3. Advanced Agrochemical Synthesis

    Specialty agrochemical formulators use this material as a synthon for constructing selective fungicidal actives featuring thienyl moieties. Its high reactivity in aldol-type and Michael addition steps allows efficient generation of next-generation crop protection agents. Formulation loading depends on targeted crop selectivity and local residue limits, with dedicated control on impurity carryover in downstream isolation.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • ISO 25198:2020 for chemical synthesis pesticides
    • China GB 2763-2021 (MRL regulation)
    • US EPA Pesticide Registration (40 CFR 152.46)

    Typical usage ratio

    • 1.5–2.5 mol equivalents based on desired actives yield within a multi-step synthesis, adjusted for conversion efficiency in pilot and commercial scale

    Downstream process integration

    • Charged to the C–C bond formation stage, post-derivatization of the aromatic ring, then purified via extraction and preparative chromatography

    Final product types

    • Heterocycle-based fungicide actives
    • Liquid and wettable powder crop protection concentrates
    • Custom contract intermediates for agrochemical majors

    4. Specialty Fragrance Intermediate Production

    Fragrance ingredient manufacturers introduce this compound as a precursor to construct high-impact sulfur-containing notes typical in niche perfumery, especially for “leathery” and “earthy” accords. Because such note profiles require controlled sulfur integration and trace purity, formulators optimize charge relative to key aldehyde or ketone partners, with downstream process flow designed to minimize oxidative byproduct levels.

    Industry compliance standards

    • IFRA Standards for ingredient use and purity
    • REACH (EC No. 1907/2006) registration and CLP Regulation (EC) No 1272/2008
    • EU Cosmetics Regulation (EC No. 1223/2009, for end-use acceptability)
    • ISO 9235:2013 (Aromatic Natural Raw Materials—Vocabulary)

    Typical usage ratio

    • 0.3–1.0% by weight in precursor blend, finely tuned by GC–MS profile analysis and final effluent monitoring for olfactory consistency

    Downstream process integration

    • Dosed in the controlled synthesis of heterocycle-fragrance cores during the aldol condensation or cyclization phases, followed by fractionation and hydrocarbon stripping

    Final product types

    • Specialty sulfur-rich bases for fine fragrance formulation
    • Earthy–leathered aromachemicals for premium perfumery
    • Intermediate packages for aroma chemical houses and boutique perfumers
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    Certification & Compliance
    More Introduction

    4-(2-Thienyl)But-3-En-2-One: Real-World Insights from the Manufacturing Floor

    Understanding the Character of 4-(2-Thienyl)But-3-En-2-One

    In the business of fine chemicals, 4-(2-Thienyl)but-3-en-2-one stands out as much more than a line item on an inventory list. Walking past reactors and columns, watching every batch progress from raw feed to precise product, you start to appreciate how every molecule speaks to an end use. Our team, with years spent scaling synthesis and managing the real challenges of process chemistry, sees this compound—sometimes called a thienyl enone by regular customers—as a sharp tool in the toolkit of modern synthesis. Its structure, pieced together with a thienyl ring and an enone chain, gives it that edge, enabling reliable performance under demanding conditions.

    Making a material like this at commercial scale, not just in a well-equipped lab, tests the limits of what both people and equipment can do. Routine analysis and persistent tweaking—skill built up over actual drum production, not only bench experiments—creates a consistency that bench chemists and process engineers trust. Sulfur-containing aromatics such as thienyl compounds tend to raise eyebrows due to their sensitivity and volatility, but rigorous process controls keep each batch within tight specifications. Tolerance for impurities sits low here, since even minor off-spec can domino through downstream reactions.

    Performance and Reliability in Synthetic Routes

    Customers on the receiving end often mention how slight variations in heteroaromatic building blocks shift the entire tone of a reaction. We hear this echoed from medicinal chemists, contract manufacturers, and academic labs. The double bond conjugated to the thienyl group lets synthetic teams push their chemistry right where they want it—electrophilic additions, Diels-Alder cycloadditions, and more. In making this enone, getting the regiochemistry right is critical: extra effort in purification pays off quickly at any scale. From our repeated batches, it’s obvious that yields and side-product management hinge on both solvent choice and timing, especially for those who need to avoid sulfur-based byproducts downstream.

    We’ve seen research groups use 4-(2-thienyl)but-3-en-2-one as a precursor for assembling more elaborate heterocycles or small molecule probes. With each customer feedback or product adaptation, it becomes clear which qualities actually matter: reproducible purity above 98%, trace-level handling of thienyl isomers, and packaging that keeps out moisture. Delivering this over and over again for gram-to-kilo-scale orders defines the trust the industry places in a manufacturer instead of a trader.

    Putting It to Use in the Lab and Factory

    Every year brings a new demand profile. Sometimes it’s early-stage pharmaceutical work focused on sulfur-linked scaffolds. Other times, it’s the specialty materials segment, where the thienyl motif catches the eye of researchers in electronics or polymer chemistry. The versatility of the enone handle marks this product with a distinct advantage over plain thienyl acetones or typical alpha,beta-unsaturated ketones lacking heteroaromatic rings. Where some customers try to cut corners using generic enones, issues with reactivity and downstream selectivity crop up. By producing at scale with robust controls, we give teams confidence so that screen-to-scale-up work actually translates to real throughput.

    From inside the plant, managing the solid form and ensuring dry, uniform batches becomes an everyday focus. Too much moisture in shipping or storage throws off weighing accuracy and invites degradation. So, we pack using foil-lined drums and always recommend nitrogen backfilling for extended storage. Details like this—often skipped in quick-turn trading—matter most to those who know the pain of troubleshooting failed runs after weeks of planning.

    High Standards in Production: What Sets Us Apart

    As a company active at every technical touchpoint, we’ve learned that producing a specialty intermediate like 4-(2-thienyl)but-3-en-2-one demands more than basic adherence to a published synthesis. Any deviation, from the source of the thiophene feedstock to the purification path, ripples through to the end customer. Many manufacturers opt for shortcuts, such as using recycled solvents without proper cleanup or ignoring early-stage impurities—decisions that cost less in the short run but create lasting headaches for users.

    Our approach takes each step apart. We monitor not only the usual suspects—melting point, assay by HPLC, and identity via NMR—but also inspect for subtle markers like UV-Vis shifts that hint at trace co-elution or byproducts in the aromatic region. The plant operators, not just the quality control lab, keep real-time records. Every time we switch a reactor or update a solvent source, it’s logged and tracked. That diligence is not about meeting an abstract standard; it’s about knowing that better input equals safer and more successful chemistry downstream.

    Working with the Chemical: What Chemists Actually Experience

    Any time we check in with a long-time customer, the first stories involve bench results or process headaches—not spreadsheets. Those running discovery projects lean into thienyl enones for conjugate addition, Michael reactions, or as masked functionalities for later transformations. Some describe difficulties with moisture: thienyl enones tend to hydrolyze or polymerize if treated roughly, so we emphasize proper sealing and drying. We’ve learned that even minor delays in transit, unplanned warehouse exposures, or careless drum handling can change measured stability in subtle but impactful ways. These are insights only visible after producing and shipping real product, batch after batch, through the seasons.

    Compared to classical enones with phenyl rings, users point out that the sulfur in our compound alters reactivity enough to open doors (or close them), depending on the chemistry. For those targeting specific cross-coupling transformations, it’s the difference between a straightforward process or days lost picking through purification. Our repeat clients regularly send us data on new synthetic tricks, and we, in turn, tighten our controls. The feedback loop never really ends; our entire process shifts based on what customers uncover at the bench and pilot plant.

    The Real Costs and Stakes of Quality Control

    No seasoned manufacturer overlooks the costs. Proper waste handling, careful solvent management, and high-integrity logistics all eat into margins. Cheap shortcuts work for traders chasing a quick margin, but repeated failures burn trust—the one thing that brings researchers back for the next order. Over the last decade, our quality costs have ballooned, but so have the reliability metrics our partners demand. When a single out-of-spec load derails months of research, customers do not forget.

    We test random samples after packaging, not just at the end of synthesis. On a busy week, more drums are held for spot checks than for shipping, brushing aside complaints about lost turnaround speed. Internally, every operator learns to spot telltale hints of off-spec product: a whiff of sulfur, faint discoloration, or offbeat melting points. Teams are cross-trained to watch for problems before they grow. This makes a difference you can feel, even if it rarely shows up as a neat certification label.

    Comparison: Why Thienyl Enones Beat Out Standard Ketones

    We’ve run side-by-side syntheses so many times that the distinctions jump out. Standard enones—think cinnamoyl or acetylacetone derivatives—lack the electron-rich sulfur ring, which shifts both reactivity and selectivity. In alkylation, conjugate additions, or cycloadditions, this difference influences rates and outcomes, especially in complex settings where every percentage point matters. Feedback from our partners points to sharper, more reproducible results with thienyl variants, as long as they source from a manufacturer willing to control impurities below noise level.

    One clear strength lies in downstream customization. Chemists use our 4-(2-thienyl)but-3-en-2-one to build fused heterocycles, functionalize positions not available in simpler enones, and avoid workups complicated by persistent side-products. The sulfur atom, though a blessing in synthetic flexibility, brings challenges in smell and oxidation—so process design and packaging have to address those head-on. Our solution means keeping drums sealed, rotating stock frequently, and never letting unsold material linger past its optimal shelf life. Practically, this commitment stabilizes both our process and the customers’ experiments.

    Worker Hazards and Responsible Handling

    From the beginning, sulfur-rich intermediates call for careful handling—both in the lab and on the shop floor. We train operators to handle minor leaks or spills wearing full PPE, not just gloves and eyewear. Odor can sneak into non-processing areas if a valve isn’t seated right. Limiting such lapses takes regular drills and real accountability, not just paperwork. Every incident review feeds back into how the process is set up. Nobody wants a story about a ruined batch or workplace exposure circulating through the team.

    Our environmental plans go beyond checklists. Containing thienyl residues avoids cross-contamination with other product streams. Liquid waste gets neutralized and separated, never just bulked and dumped, even if disposal costs climb. Air handling systems see frequent filter swaps to catch volatilized organics before they head out through vents. The goal isn’t just regulatory compliance but being able to walk through the plant without a sharp tang of sulfur in the air. Site visits from clients show off not only our chemical storage but our people’s attitude toward safety and environmental care—elements that matter to operators and partners alike.

    Unique Challenges of Scale-Up

    Bringing a synthesis up from gram to kilo or multi-ton scale reveals hidden issues every time. Mixing, temperature control, and separation routines that work in a beaker often turn temperamental in a reactor. We’ve encountered batch variability stemming from ambient temperature swings, reagent age, even the type of silica gel used in downstream purification. Instead of burying problems, we log every process hiccup and pursue process improvements. Batch history—the real numbers—not generalizations, steers both routine work and emergency troubleshooting.

    Scaling up 4-(2-thienyl)but-3-en-2-one, the thienyl portion sometimes adds unexpected complexity. Shifting solvent mixtures, evaporation rates, and thienyl ring stability under heat demand constant vigilance. Running dozens of real batches—each with tightly monitored process data—has shaped our standard procedures. This experience doesn’t come from reading a catalog or transactional order history but from years of lived production. Each successful delivery is the result of many rounds of learning, adjustment, and more than a little perseverance from everyone on the line.

    Long-Term Value for Researchers and Industry

    What makes our version of 4-(2-thienyl)but-3-en-2-one valuable isn’t just a clean label or meeting a minimum purity standard. The tangible difference is the peace of mind users get knowing their supply won’t surprise them with an off smell, hidden impurity, or stubborn degradation. This security lets researchers move beyond troubleshooting the raw material and instead focus on the chemistry that counts.

    Experience has shown that customers quickly notice when a supplier’s quality slips. Production runs grind to a halt. Data points scream inconsistency. As a manufacturer, making the process as transparent and stable as possible earns more loyalty than any marketing slogan. Decades in this business demonstrate that reliability always wins over the long horizon.

    Looking Forward: Meeting the Demands of a Tighter Market

    Many changes in the chemical sector—tighter regulations, rising raw material costs, and a push for greener chemistry—keep us on our toes. The baseline expectation for products like 4-(2-thienyl)but-3-en-2-one keeps rising. Customers want lower contamination, more traceability, and deeper technical feedback. These requests don’t just land in an inbox; they spark new approaches in our pilot plant, push our analytics department to hunt for sub-ppm contaminants, and challenge shipping teams to get materials to the right place, undamaged, every time.

    So, each batch rolling out of the line tells a story—not just about the starting materials or the chemistry, but about the knowledge and persistence behind it. The difference between a commodity intermediate and a trusted material lies inside these details. The extra mile we walk on compliance and performance offers more than a promise; it stands as a guarantee forged by repeated success, visible to everyone who’s spent a day troubleshooting a reaction or waiting for a reliable shipment.

    Building Long-Term Trust with End Users

    Shortcuts erode trust. Today’s research teams don’t just order product, they stake their reputations on it. By sticking to meticulous process records, refusing to accept corners cut, and prioritizing full transparency, we’ve kept relationships throughout industry and academia that last beyond the usual transaction cycles. Our regular customers have deep insight into both our process and our philosophy—we keep them in the loop about every improvement or material change, no matter how small.

    This direct connection with users is essential. Troubleshooting, rare product requests, or joint investigations into process failures are part of the daily reality on the production floor. Even under pressure, batch quality stays high because everyone, from operator to chemist to final client, has a stake in the outcome. The extra effort pays off; most problems get solved before they reach a key experiment or production run.

    Concluding Thoughts: Why Continuous Improvement Drives Success

    At the end of the day, producing and delivering 4-(2-thienyl)but-3-en-2-one at scale takes more than clean glassware and well-maintained reactors. It takes commitment to detail, experience honed over countless batches, and ongoing feedback from the real users who push chemistry forward. As the bar continues to rise in specialty chemical manufacturing, only manufacturers willing to walk the hard road of quality, transparency, and sustained improvement will continue to earn the trust of the chemists and companies building the future.