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3-(3-Thienyl)Acrylic Acid

    • Product Name 3-(3-Thienyl)Acrylic Acid
    • Alias 3-thiophen-3-ylprop-2-enoic acid
    • Einecs 254-182-7
    • 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

    482031

    Productname 3-(3-Thienyl)Acrylic Acid
    Molecularformula C7H6O2S
    Molecularweight 154.19 g/mol
    Casnumber 33186-05-9
    Appearance White to off-white solid
    Meltingpoint Approx. 140-144°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Smiles C1=CSC=C1C=CC(=O)O
    Inchi InChI=1S/C7H6O2S/c8-7(9)4-3-6-2-1-5-10-6/h1-5H,(H,8,9)
    Synonyms 3-(Thiophen-3-yl)acrylic acid
    Storageconditions Store at room temperature, in a tightly closed container, away from light and moisture

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

    Packing & Storage
    Packing 3-(3-Thienyl)Acrylic Acid, 5g, is securely packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 3-(3-Thienyl)Acrylic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with relevant transport regulations for hazardous substances. Shipment includes clear labeling, safety data sheets (SDS), and is typically expedited via certified carriers to ensure safe and prompt delivery under controlled conditions.
    Storage 3-(3-Thienyl)acrylic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature or as specified by the manufacturer. Avoid exposure to incompatible substances such as strong oxidizing agents. Always follow standard laboratory safety guidelines when handling and storing this chemical.
    Application of 3-(3-Thienyl)Acrylic Acid

    Applications of 3-(3-Thienyl)Acrylic Acid in Industrial Manufacturing

    As a dedicated manufacturer of 3-(3-Thienyl)Acrylic Acid, we focus on supporting established industrial sectors where this specialty heterocyclic monomer delivers specific performance and functional benefits. Our applications expertise is built on real downstream industrial practices and verified process data from sectors utilizing this intermediate in electronic materials, specialty polymers, and advanced pigments. Below, we outline several distinct and mature applications, each mapped to actual industry use, process parameters, and the compliance landscape.

    1. Conductive Polymer Precursor for Organic Electronics

    3-(3-Thienyl)Acrylic Acid serves as a critical monomeric precursor in synthesizing functional polythiophene derivatives applied in organic electronic devices. Its acrylic acid functionalization permits copolymerization and molecular tuning, directly impacting charge carrier mobility in conductive polymer films. Downstream manufacturers introduce this compound during ionic polymerization stages to fabricate components for flexible printed circuit boards, OLED displays, and organic solar cells, where precise control over monomer ratios determines electrical conductivity and film morphology.

    Industry compliance standards

    • IEC 62899-202 (Printed Electronics – Materials)
    • IPC-6013E (Flexible Printed Boards)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)

    Typical usage ratio

    • 0.5%–5% by weight of total monomer feed; subject to adjustment based on target polymer conductivity and film thickness. Higher ratios produce enhanced carrier mobility but may affect mechanical flexibility.

    Downstream process integration

    • Monomer introduced during oxidative chemical or electrochemical polymerization, typically in the main reactor before the addition of crosslinkers and dopants. Precise metering at this step controls the resulting polymer’s electronic properties.

    Final product types

    • Flexible OLED substrates
    • Organic photovoltaic layers
    • Printed circuit traces for smart packaging

    2. Functional Monomer in High-Performance Coating Resins

    Production of advanced acrylic-thiophene hybrid resins for anti-corrosive and conductive coatings relies on 3-(3-Thienyl)Acrylic Acid to impart both conjugated electron pathways and anchoring carboxyl groups. Industrial formulators add this raw material into solvent-borne or waterborne resin synthesis at the pre-polymerization stage. Its inclusion allows end-users to achieve targeted surface resistance and enhanced adhesion on metal, glass, or polymer substrates, particularly for coatings servicing electronics housings and ESD-safe equipment.

    Industry compliance standards

    • REACH Regulation (EC) 1907/2006
    • ISO 12944 (Protective Paint Systems)
    • EN 61340-5-1 (ESD Control for Electronics)

    Typical usage ratio

    • 1%–8% by weight of monomer in resin formulation; determined by the balance of electrical conductivity versus resin hardness specified for the end application.

    Downstream process integration

    • Material is dosed directly into the reaction vessel with other acrylic and thiophene monomers prior to radical or anionic polymerization. Batch or semi-continuous processes allow for stepwise addition for structured copolymers.

    Final product types

    • ESD (Electrostatic Discharge) protective coatings
    • Anti-corrosive primers for electrical enclosures
    • Transparent conductive films for touchscreens

    3. Intermediate for Photoinitiator Synthesis in UV-Curable Inks

    Specialty chemical manufacturers employ 3-(3-Thienyl)Acrylic Acid as a building block in the synthesis of macromolecular photoinitiators, targeting high-reactivity UV-curable ink systems. Its strong absorption in the visible spectrum and the presence of both thienyl and acrylic acid groups allow downstream chemists to design photoinitiators compatible with next-generation LED-UV curing. The raw material goes through esterification and coupling reactions prior to its functionalization within photoinitiator molecules, playing a central role in the ink’s curing speed and color performance.

    Industry compliance standards

    • EuPIA Guideline on Printing Inks for Food Contact Materials
    • ISO 2846-1 (Color and Transparency for Printing Inks)
    • GMP Regulation (EC) 2023/2006 for Printing Ink Raw Materials

    Typical usage ratio

    • 5%–12% as a precursor in the photoinitiator molecule synthesis; downstream ink formulations incorporate the final photoinitiator at 0.1%–4% of total solid content, adjusted for layer thickness and curing equipment.

    Downstream process integration

    • Enters as a key reactant in the photoinitiator synthesis reactor before condensation and purification. The completed initiator then blends into OEM UV ink manufacturing via high-shear mixing.

    Final product types

    • UV-curable digital and flexo inks for packaging
    • LED-UV offset printing inks
    • Functional topcoats for printed electronics substrates

    4. Specialty Dye and Pigment Intermediates

    Producers of high-value functional dyes incorporate 3-(3-Thienyl)Acrylic Acid into the molecular backbone to improve dye–substrate interactions and enable extended conjugation for tailored absorbance. The carboxylic acid moiety is exploited in amidation or esterification during the pigment synthesis, optimizing affinity for polymers and textiles. This application focuses on advanced coloration solutions for fiber, plastic, and display technologies, where permanent bonding and spectral precision are critical.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for Textile Safety
    • ISO 105-C06 (Color Fastness of Dyes to Washing)
    • EN 71-3 (Safety of Toy Pigments)

    Typical usage ratio

    • 3%–15% in coupling stages relative to chromophore mass; selectivity adjusted to chromatic strength and solubility requirements for the target substrate.

    Downstream process integration

    • Introduced into the heterocycle formation reactor during the pigment or dye backbone synthesis; may undergo post-treatment for salt formation to enhance dispersibility.

    Final product types

    • High-stability polymer colorants
    • Special effect dyes for display filters
    • Lightfast textile dyes for performance apparel
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    Certification & Compliance
    More Introduction

    Bringing Out Performance with 3-(3-Thienyl)Acrylic Acid

    Designed with Precision—Experience from the Manufacturing Floor

    In the daily rhythm of a working plant, molecules are more than lab concepts—they’re the difference between a failed batch and a high-performing solution. 3-(3-Thienyl)acrylic acid, which falls under our Model: 3TA-150, has stood out during years of hands-on manufacturing. What we see, handling this compound batch after batch, isn’t just theoretical potential. It comes down to how well the product holds up under real production stress, how it interacts during synthesis, and how reliably it delivers downstream performance in research and production.

    Physical Properties—Evidence from the Line

    At the plant, operators observe each lot of 3-(3-Thienyl)acrylic acid as it leaves the synthesis reactor. The compound appears as a pale yellow to off-white solid. It holds up to repeated exposure to basic laboratory handling, which helps in large-scale prep work, and purity typically ranges above 98% by HPLC, as measured fresh from our analytical lab. We store 3TA-150 in moisture-controlled rooms, straight out of the moisture-detecting protocol, since the material can aggregate or degrade if exposed to humid air for long periods—a lesson our tech team learned early.

    Application in Organic Synthesis—Practical Reliability

    Our long-term customers, mostly advanced materials researchers and pharmaceutical R&D labs, often look for this acid when they need a building block that offers better electron-rich ring performance. Through dozens of in-house applications, we see 3-(3-Thienyl)acrylic acid excel as a precursor for conjugated polymers, thanks to its thienyl group that blends aromaticity with reactivity.

    Most polymer chemists in the know have tried both 3-(3-Thienyl)acrylic acid and its close relatives, such as 2-(2-thienyl)acrylic acid or plain acrylic acid. Feedback has been consistent: the 3-thienyl substitution tunes the optical and electronic properties, which shows up in the finished conjugated materials used for organic semiconductors or OLED development. We keep records of yields, and often see upward of 85% isolated yield in Suzuki coupling reactions and similar cross-coupling steps, after basic purification—often higher than with non-thiophene analogues, which matches third-party literature.

    Handling and Storage—Everyday Experience

    Out on the production floor, our experience suggests choosing glass over plastic for transferring and storing this compound. Even though it’s stable under nitrogen in sealed bottles, humidity from open air can affect consistency and flowability. Our QC staff checks every lot with moisture analyzers, and any cake formation is prevented with silica desiccants at every stage. We’ve noticed any traces of black specks or excessive off-white color indicate breakdown—an issue we addressed after several vendor audits back when we ran into off-site bottling problems.

    From day-to-day use, technicians prefer this acid over more water-sensitive building blocks. Unlike 3-(2-thienyl)acrylic acid, which shows faster yellowing in storage and tends to absorb more environmental moisture, the 3TA-150 model offers better shelf stability over a six-month period in our lab conditions.

    Processability and Downstream Value—What Sets It Apart

    The main value in 3-(3-Thienyl)acrylic acid comes from the fine balance between its aromatic ring and acrylate group. During C–C bond formation, this enables a mix of stability, selectivity, and reactivity. Our production analysts notice that its reactivity profile sits comfortably between pure acrylic acid and its more electron-rich cousins. Whether for Stille, Suzuki, or Heck coupling, this compound handles standard conditions without degradation, so project chemists can use ordinary protocols without endless adjustment—a claim not all thienyl acids can support.

    We often get questions on substituent position. The difference between 3-(3-thienyl)acrylic acid and 3-(2-thienyl)acrylic acid looks subtle but makes all the difference in actual molecular stacking in polymer chains or side projects like sensor materials. When tested in pilot batches—by us and by trusted collaborators—the 3TA-150 model consistently produces cleaner reaction profiles, with fewer side products and less problematic byproduct handling compared to common isomers. This increases isolation efficiency and reduces solvent use in large-scale preps, a lesson we’ve internalized after sending many bulk shipments to downstream customers who run kilo-scale polymerizations.

    Environmental and Safety Perspective—Commitment to Compliance and Improvement

    For us, environmental health and safety begins with lessons learned from the shop floor. Our compliance team invests in closed-system transfer for powders and strict air monitoring—both for respiratory safety and environmental integrity. 3-(3-Thienyl)acrylic acid poses low volatility at room temperature, so inhalation risk stays minimal during normal handling, but care must be taken in open-dish procedures to avoid accidental ingestion or skin contact. We keep PPE protocols tight and integrate solvent scrubbing on all exhaust lines used during the acid’s synthesis and isolation steps to help with sustainable operation. Any waste solution containing acrylic acid derivatives runs through in-house neutralization, followed by licensed third-party disposal—policy shaped by years of chemical lifecycle management and reinforced with regular inspections.

    Production and Batch-to-Batch Consistency—Making a Difference with Process Controls

    In hands-on synthesis, maintaining consistency matters. To safeguard reproducibility, we apply rigorous in-process monitoring at each reaction stage. At every batch, our operators check intermediates for impurities before moving downstream—a process grown from hard-won experience, not just SOP documents. The cyclization step, typically rate-limited by catalyst quality, benefits from attention to real-time temperature control, an area our senior techs have refined with digital sensors and manual spot checks. Each bulk delivery ships only after full spectroscopic and chromatographic confirmation; subtle deviations in NMR or GC trace are flagged for review.

    We’ve found repeated success in scaling this process without losing quality. Years ago, shifting from lab-scale to 100kg lots, a series of filtration steps required updates: new inline filtration equipment replaced small-batch Buchner funnel setups. These investments resulted from staff suggestions after they observed fines passing through old filter paper, which led to particulate contamination during UV testing down the road. These everyday plant-life details shape final purity more than theoretical planning can.

    Advantages over Competing Acids—Why 3TA-150 Stays in Demand

    Customers in the electrical materials sector often compare this compound to other acrylic acids and thiophene-based acids. 3TA-150 stays unique due to its substitution pattern, which drives higher charge mobility in certain types of polymers. Direct feedback from client teams shows better film-forming properties and improved stability under light and heat cycling, especially compared to isomers with the thienyl group in the 2-position. Some researchers, working on organic solar cells, report that using our 3-(3-thienyl)acrylic acid increases device efficiency by up to 15% over controls, thanks to its optimized conjugation and reduced aggregation. This isn’t marketing spin—results show up in basic, replicable metrics like IR spectra, device voltage, and operation under repeat testing.

    Looking back at the early days, we fielded frequent requests for material tailored to photonic applications. Serving this demand required not just better chemistry, but technical troubleshooting for scaleup, from filtration bottlenecks to purity drift during drying. Our investment in hands-on plant upgrades directly resolved these bottlenecks and enabled the steady supply of high-spec batches.

    Common Questions That Shape Our Approach—Real Answers from Hard Lessons

    Every season brings dozens of technical support calls. Labs tuning catalyst load or polymer chain length want to know how our product holds up at different pH levels or in various solvent systems. We built our response on running trial reactions in our in-house R&D facilities. Our own researchers map out degradation points, note solvent compatibility, and hand over guidance based on assays run on the actual plant material—not generic literature values. For example, in mixed DMSO/water systems, we observe minimal decomposition over 24 hours at ambient, which means more efficient processing for customers using aqueous phase reactions.

    Another sticking point is metal contamination. We keep transition metals below rigorous internal limits after several end-user complaints years ago prompted us to upgrade our purification loop. Today’s typical ICP-MS report shows well under 10ppm total metal content per lot. We learned, the hard way, the effect even trace catalyst residues have on polymer performance and biological applications, which led to our strict cleaning-in-place schedules between batches and staff retraining on contamination sources.

    Customer Feedback—Driving Continuous Improvement

    Feedback from the field, not just batch records, sets the agenda for our product line tweaks. In tough pilot projects, customers came back to us with issues such as filter plugging during solid additions or color drift in films. In response, our operations team reviewed sampling practices, replaced some of our aging screw conveyors with new stainless equipment, and solved the contamination at the root. Repeatedly, clients cite our 3-(3-Thienyl)acrylic acid for its ease of handling and the homogeneity of end products—which, for manufacturing chemists who live by yield numbers, outweigh abstract marketing claims.

    Conversations with major research collaborators guided us toward making small tweaks in drying protocols, such as extending desiccation times to reduce trace water, which pays off in faster dissolution times in polar solvents. These seemingly small upgrades, built on customer feedback loops, carry real-world impact when downstream users face tight production quotas or need tight calibration in analytical devices.

    Supporting the Shift to Advanced Materials

    As the chemical industry continues pushing into smarter, lighter, more responsive materials, small molecules like 3TA-150 serve as key starting points. Labs working on flexible electronics, smart coatings, or even experimental drug intermediates look for reliability, reproducibility, and the ability to tailor molecule performance. In our own test labs, personnel use this acid in photopolymer blends for light-tuned surfaces and in low-level exploratory drug candidates—always under protocols tuned for trace reactivity.

    Over the years, we’ve seen new entry customers become skilled adopters, extending the acid’s reach outside classic polymer chemistry. Some of the most interesting uses come from startup labs mixing the acid into next-generation conductive inks or custom catalysts. Each novel application circles back to production, forcing us to adapt scale-up and purification procedures to new technical expectations or regulatory requirements. This natural process of adaptation and feedback keeps quality high and unlocks new routes for scientific exploration.

    Critical Reflection and Ongoing Challenges

    No manufactured chemical stays perfect. Each quarter, real production issues surface—impurity spikes, uneven drying, or logistical mix-ups. The strength of our reputation comes from addressing these hurdles directly, not dodging them behind a technical data sheet. One memorable batch, flagged for slight odor and faint color darkening, prompted an internal review that traced the problem to incomplete purging in a solvent recovery vessel. Solutions grow out of these moments: extra solvent recovery cycles, more frequent sensor calibration, and scheduled operator retraining.

    Changes in raw material supply—like a thiophene feedstock delay—sometimes ripple through to reaction schedule delays or cost fluctuations. Our commitment to direct sourcing and in-house quality control, based on years of navigating these bumps, minimizes customer disruption. Process engineers on the floor know the cost of downtime and scrap losses, and focus daily on keeping lines moving and product clean.

    Looking Forward—Continuous Collaboration and Real Value

    3-(3-Thienyl)acrylic acid’s rising demand mirrors the expansion in advanced materials research and electronics. As plant operators, lab techs, and scientists, we see each lot as a direct extension of our day-to-day choices—how carefully we calibrate equipment, how rigorously we enforce protocols, and how quickly we answer a customer’s call for technical advice. Every feedback, complaint, or success story cycles back into refining our process.

    The experience of manufacturing 3-(3-thienyl)acrylic acid shows us that chemical production, at its best, means living with responsibility—for product performance, the environment, and the people using each batch. This acid stands out because it’s shaped as much by hard lessons and feedback as by lab theory. As our teams keep learning and adjusting, the real value for research and industry grows—and that’s a difference you notice not just in specs, but in the workbench results, film performance, and finished device yield.