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5-Acetylthiophene-2-Carboxylic Acid

    • Product Name 5-Acetylthiophene-2-Carboxylic Acid
    • Alias 5-Acetyl-2-thiophenecarboxylic acid
    • Einecs EINECS 415-650-8
    • 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

    734647

    Chemical Name 5-Acetylthiophene-2-Carboxylic Acid
    Cas Number 13679-86-2
    Molecular Formula C7H6O3S
    Molecular Weight 170.19 g/mol
    Appearance White to off-white powder
    Melting Point 174-177°C
    Solubility Soluble in DMSO, partially soluble in water
    Purity Typically ≥98%
    Smiles CC(=O)c1ccc(C(=O)O)s1
    Inchi InChI=1S/C7H6O3S/c1-4(8)5-2-3-6(7(9)10)11-5/h2-3H,1H3,(H,9,10)
    Storage Temperature Store at 2-8°C
    Synonyms 5-Acetyl-2-thiophenecarboxylic acid

    As an accredited 5-Acetylthiophene-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Acetylthiophene-2-Carboxylic Acid, 25g: Supplied in a sealed amber glass bottle with a tamper-evident cap and clear label.
    Shipping 5-Acetylthiophene-2-Carboxylic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. It is transported under ambient conditions, following all relevant chemical handling and safety regulations. Proper labeling and documentation accompany the shipment to ensure compliance with international and local hazardous material transport guidelines.
    Storage Store 5-Acetylthiophene-2-carboxylic acid in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Ensure appropriate labeling and use secondary containment to prevent spills. Follow established laboratory safety procedures and local regulations for handling and storage.
    Application of 5-Acetylthiophene-2-Carboxylic Acid

    Applications of 5-Acetylthiophene-2-Carboxylic Acid in Industrial Manufacturing

    As a direct manufacturer, we support global industries by supplying 5-Acetylthiophene-2-Carboxylic Acid for downstream production. Our expertise enables accurate integration of this heterocyclic intermediate into specialty chemicals, advanced pharmaceutical synthesis, electronic material development, and agrochemical innovations. Below are the primary industrial application sectors, each with specific regulatory, process, and final product details.

    1. Pharmaceutical API Intermediate Synthesis

    Leading pharmaceutical manufacturers select this compound as a key intermediate in the multi-step synthesis of thiophene-based active pharmaceutical ingredients, including drugs targeting central nervous system disorders, anti-inflammatory agents, and select antibiotics. The strictest quality attributes are required, and downstream processing often involves condensation, esterification, and heterocycle-functionalization reactions. Our production meets the purity and trace impurity thresholds required for large-scale cGMP manufacture of regulatory-submitted APIs.

    Industry compliance standards

    • USP, Ph.Eur., JP pharmacopeial requirement alignment (intermediate-grade, not final API)
    • ICH Q7/Q11 cGMP for intermediates
    • FDA 21 CFR Part 210/211 controls where used in US-bound API synthesis
    • EU Guidelines for Good Manufacturing Practice, Part II (intermediates)

    Typical usage ratio

    • 2–10 mol% relative to target API batch, depending on final structural requirements and scale
    • Loading adjusted based on downstream yield targets and route optimization
    • Excess use avoided to minimize byproduct formation and purification steps

    Downstream process integration

    • Charged post-reaction vessel charge-in of other heterocyclic intermediates
    • Integrated at stage 2–3 of 5+ step synthesis during ring construction or functionalization
    • Filtered and isolated intermediates proceed to subsequent amination, acylation, or cyclization

    Final product types

    • Thiophene-based neurological disorder drugs (e.g., anti-epileptic compounds)
    • Atypical anti-inflammatory agents
    • Sulfur-containing antibiotic scaffolds
    • Experimental oncology candidates

    2. Synthesis of Organic Electronic Materials

    Producers of advanced organic electronics employ this compound for the synthesis of conjugated thiophene derivatives, which are crucial monomers for organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and thin-film semiconductors. The material’s precise acetyl and carboxyl functionalities enable controlled polymerization and facilitate further derivatization, crucial for obtaining stable, high-mobility electronic materials with repeatable batch consistency.

    Industry compliance standards

    • RoHS Directive 2011/65/EU compliance (for electronics manufacturing)
    • JEDEC JESD625 for electrostatic discharge (ESD) precaution
    • ISO 9001:2015 for production quality systems
    • REACH Annex XVII restrictions for electronic downstream users

    Typical usage ratio

    • 5–20 wt% in co-monomer feed depending on target polymer chain length and application
    • Ratio tailored for controlled copolymerization with other aromatic or heterocycle monomers
    • Reactive group content adjusted to achieve target film thickness and charge carrier mobility

    Downstream process integration

    • Introduced in solution or melt-phase monomer blend for chemical polymerization
    • Feeds directly into in-situ cross-coupling or oxidative polymerization stage
    • Modifies electronic structure based on insertion point and functional group conversion

    Final product types

    • Conducting polymer films for OPV devices
    • OFET semiconducting layers
    • Photovoltaic module thin films
    • Organic light-emitting diode (OLED) precursor materials

    3. Advanced Agrochemical Synthesis

    Specialty agrochemical formulators utilize this compound as a building block for the development of selective fungicides and pesticides, where sulfur- and acetyl-containing heterocycles deliver unique mode-of-action properties. Used in strictly controlled environments, the material undergoes reactions such as acylation and heterocycle extension to yield active compounds optimized for bioavailability and crop specificity, ensuring compliance with agricultural chemical residue limits.

    Industry compliance standards

    • FAO/WHO technical guidelines for pesticide manufacturing
    • EU Regulation (EC) No 1107/2009 for active substance approval
    • US EPA requirements for new chemical registration (FIFRA)
    • ISO 17025 for analytical test method validation in agrochemical production

    Typical usage ratio

    • 1–8 mol% relative to agrochemical target based on synthetic design
    • Stoichiometry depends on desired functional load and reactivity with crop-protective moieties
    • Ratio adjusted to optimize efficacy and minimize process byproducts

    Downstream process integration

    • Reacted in early or mid-stage synthesis with other aromatic intermediates
    • Forms acetylated or sulfur-modified intermediates ahead of final formulation
    • Chemical batch processed under inert, moisture-free conditions to control impurity profiles

    Final product types

    • Systemic fungicide actives
    • Herbicidal intermediates for cereal protection
    • Insect repellent scaffolds
    • Seed treatment active ingredient precursors

    4. Specialty Dye and Pigment Additive Manufacture

    Producers of technical dyes and pigments incorporate this molecule during the synthesis of sulfur-containing conjugated chromophores, especially in the production of industrial colorants for plastics, inks, and coating systems. The material’s dual reactive groups enable finely tuned color modulation and yield enhanced photostability, a critical feature for applications requiring fade-resistance and high color fastness under severe environmental conditions.

    Industry compliance standards

    • REACH (EC Regulation 1907/2006) for chemical dyes
    • ISO 9001:2015 quality management for pigment manufacturing
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) recommendations
    • US FDA 21 CFR Part 74 for color additives (where applicable)

    Typical usage ratio

    • 2–6 mol% as modifying intermediate, based on absorption spectrum specification
    • Adjusted according to required chromophore length and hue consistency
    • Lower end for process color inks; upper end for technical coatings

    Downstream process integration

    • Introduced mid-process during condensation or coupling stages
    • Forms sulfur-containing chromogenic intermediates with other aromatic structures
    • Integrated under controlled pH to prevent secondary color formation

    Final product types

    • Disperse dyes for PET fiber
    • Technical pigments for high-performance coatings
    • Colorant bases for inkjet and offset printing
    • Plastisol pigment concentrates
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    Certification & Compliance
    More Introduction

    5-Acetylthiophene-2-Carboxylic Acid: Practical Insights from Direct Manufacturing

    Real-World Performance and Commitment in Synthetic Chemistry

    Walking the production floor, we rely on experience to shape our approach to specialty organic compounds such as 5-acetylthiophene-2-carboxylic acid. Demand for this product doesn’t only come from research benches or formulation labs. Chemists and process engineers trust us because year after year, we deliver material that holds up under industrial scrutiny, from pilot scale to full production. Those of us engaged in daily plant operations know that repeatable quality means more to a customer than a tech sheet ever could. Quality for us stems from managing raw material purity, controlling water content in the final product, and verifying every lot by tested analytical profiles.

    Production Model and Specification Strategy

    Our main model of 5-acetylthiophene-2-carboxylic acid follows a robust process built for stability and scale. Each batch features high purity, usually not less than 98% by HPLC, and minimal water content thanks to controlled crystallization and precise drying parameters. Color typically ranges from off-white to pale yellow, which signals a clean synthesis with minimal byproducts. These signals are benchmarks for quality in our facility, with chromatographic traces checked against historical standards for every lot.

    Grain size affects handling in the workshop. Inconsistent texture complicates both storage and weighing, so we modify milling times for each production run to ensure free-flowing powder, not caked lumps. Our packaging keeps moisture and ambient contaminants at bay—important for this compound, since uncontrolled absorption in storage could knock a process batch off spec.

    Applications: Fine Chemicals and Specialty Synthesis

    Requests most often come from pharmaceutical intermediates, agrochemical research, and material science labs. Colleagues in pharma focus on its role in synthesizing potent building blocks for heterocyclic motif development. Some groups exploit the carboxylic acid site for direct amidation, others use the acetyl moiety for downstream condensation steps. We sit with formulation teams to discuss not just the basic chemistry, but the process side—how clean reaction profiles have saved hours in downstream isolation by cutting out contaminant byproducts.

    Agrochemical partners use it for novel herbicide scaffolds. Precise pH control matters in these syntheses, and we respond by pushing each batch through additional titration checks so product actually matches the reactivity profile their route demands. In the dye and pigment sector, some technically challenging couplings depend on the acetylothiophene core for color modulation. We test for those markers directly onsite with UV spectroscopy, to spot subtle batch-to-batch differences before drums go out the door.

    How It Stacks Up Against Related Compounds

    Colleagues sometimes ask why this product holds a niche over simple thiophene derivatives. It comes down to functional versatility. The para-placement of acetyl and carboxylic acid groups across the thiophene ring doesn’t just lend synthetic flexibility—a direct result of our tuned process. Because both groups offer unique sites for reaction, chemists gain more control in building molecular complexity at later stages. Simple 2-acetylthiophene or 2-carboxythiophene limit possibilities; chemoselectivity becomes an extra puzzle in those cases, and yields often drop, headaches we hear about from frustrated researchers.

    We regularly compare purity and physical characteristics against similar intermediates from external benchmarks. Direct customer feedback matters here. Teams report that our material dissolves efficiently in common organic solvents, without trailing haze or persistent residues. Handling properties like pourability and dustiness have been adjusted through plant trials, responding directly to customer input. This responsiveness often leads researchers to specify our material when robustness in project scale-up is a must.

    Lessons from the Bench and the Plant

    As manufacturers, we face ongoing challenges with oxidation during storage. Exposure to air triggers subtle color shifts and sometimes conversion to trace impurities, especially when storage tanks run low and air ingress rises. Our answer has been to decant under inert nitrogen and use moisture-scavenging liners for every drum. We built our protocols by learning the hard way—scrapping entire batches after just a few days of mishandling, then re-working protection methods until the shelf life extended beyond six months at ambient temperature. This experience isn’t theoretical for us; lost batch costs hit hard, and only real data convinced us to change course.

    Trace metals in raw materials cause headaches in various applications. Sourcing high-purity starting thiophenes from vetted producers and testing for iron and copper at receipt helped us reduce final metal levels to the ppm range. The benefits show up most plainly in pharma and pigment work, where even trace contamination can sabotage expensive syntheses.

    Supporting Sustainable and Safe Operations

    Handling aromatics—especially sulfur-containing ones like this—puts safety and environmental impact at the forefront. We maintain vapor recovery systems at reactor heads and treat spent mother liquor with advanced oxidants before disposal. Our team monitors sulfurous effluent metrics to ensure emissions stay far below local regulatory limits. Maintaining these controls protects not just the immediate team but the communities beyond plant boundaries.

    Reducing waste pays off directly in cost and compliance. We recapture solvents through fractional distillation, use closed-loop cooling circuits, and prioritize batch production to minimize scale-up losses. Deviations from process specs rarely slip uncorrected, thanks to plant-floor empowerment—operators flag issues before QC has to reject a drum. These practices matter when moving hundreds of kilos per month.

    Supply chain unpredictability isn’t new. We deal with customs snarls or raw material shortfalls by maintaining buffer stocks and actively qualifying alternate vendors. Buying teams keep an eye on global thiophene production, which can swing in price based on unrelated polymer market fluctuations. Constant review of supplier quality data lets us pivot quickly, and frequent communication with procurement ensures steady production.

    Direct Value of Experience-Driven Manufacturing

    Users often understate the difference between direct manufacturing control and indirect sourcing through dealers or brokers. With us, every step—from sulfur source distillation through final packaging—happens under one roof. If troubleshooting is needed, technical questions draw on the chemists and engineers who ran the batch, not an intermediary with secondary knowledge. Responsive feedback loops between production and R&D give us the flexibility to tweak process parameters for novel requests, rather than being stuck with rigid external specs.

    There is little replacement for long-term retention on the shop floor. Operators who’ve monitored reactors for years recognize subtle changes in viscosity or color before the analytical report lands. That kind of insight drove upgrades, such as shifting to low-ox steel in reactors after staff reported off-flavors hinting at corrosion. These lessons show up as increased reliability in the final product, especially for complex intermediates.

    Key Differences from Other Available Products

    Some sources offer coarser or less refined versions of acetylated thiophenes, usually at discounted rates. We noticed through returned customer samples that poorer drying or cuts taken too close to the solvent tailings can increase residual solvent content, which affects reactivity and downstream analysis. Washing protocols in some operations skip secondary extractions, trapping byproducts within the solid. By refining our process, including double-filtration and slow evaporation, our material passes stricter NMR, HPLC, and GC-MS checks.

    Cheaper competitors sometimes ship product with weak batch records or insufficient characterization. We maintain full documentation from bulk input to packaged output, storing spectroscopic, chromatographic, and purity data. Visitors and auditors can walk the shop floor and inspect traceability logs at every step. This transparency gives project leads confidence that every drum matches their original request, which translates to fewer rejected shipments or costly reworks.

    Responding to Industry Feedback and Meeting New Challenges

    The story of this product tracks ongoing shifts in the chemical landscape. Regulatory and sustainability demands rise, and our team adapts by auditing solvents annually, exploring greener alternatives, and collaborating with customers on safer end applications. If a pharma group targets new specs for genotoxic impurities, we run prototype batches, share pilot results, and optimize accordingly. Curiosity about process yield improvements isn’t just academic here; it shows up in hard-won percentage points backed by shop-floor changes.

    Research partners also want confidence against cross-contamination with other thiophene derivatives. To that end, dedicated reactor trains on specific product lines, enhanced with rigorous clean-out, ensure minimal carryover. Analytical samples run before and after each campaign spot any trace material from earlier runs. Such protocols came after customer-rooted investigations flagged cross-reaction concerns we hadn’t initially anticipated.

    Building Reliability Across the Supply Chain

    Downstream users sometimes underestimate cumulative impact from minor variances in input material. A batch with slight color change, or marginally drier than spec, can change solubility or filtration efficiency later. This knowledge reaches us directly from technical calls and complaint investigations—small findings that, left unaddressed, risk halting pilot campaigns across the supply chain. Our production adjusts batch-to-batch to preempt these recurring headaches, not as a luxury but as daily necessity.

    More than one major client shifted from third-party suppliers to us after experiencing reduced process yields. Feedback often highlighted cleaner mass spectra, higher conversions, and less process downtime thanks to reduced impurity drag from our product. Project teams in pharma, dyes, or materials synthesis prefer reliable sources for market scaling, as minor errors at kilo scale multiply at the ton level.

    Training, Retention, and Process Improvements

    Staff turnover can unravel progress in consistent manufacturing. We invest heavily in training and in cross-skilling, so more hands understand the nuances at each step—whether that’s tuning the distillation column profile or maintaining the right drying vacuum. Feedback loops, including early-morning meetings with the plant and QC teams, keep learnings in circulation and foster a sense of ownership. Staff expertise isn’t plug-and-play; it accumulates through repeated exposure, enhanced by process debriefs after unusual batches.

    Lessons from batch deviations guide ongoing upgrades and retrospectives. An incident last year revealed how a previously overlooked trace impurity stemmed from pH drift during esterification. Immediate review led us to recalibrate sensors, install more frequent checks, and share the original data with technical clients, closing the loop transparently.

    The Path Forward for Advanced Synthesis Inputs

    Demand continues to grow not just for quantity but for tailored quality, as chemists and engineers alike push for more sustainable, efficient, and adaptable inputs. As a direct producer, our team stands ready to adjust methods in light of regulatory change, emerging process requirements, or shifts in downstream technology. We work side by side with clients to explain results, advise on storage, and react to the changing needs of the field—because chemical manufacturing at this level isn’t about commoditized product, but about robust partnership between practitioner and end user.

    So as you explore options for your next advanced synthesis, our practical experience and plant-backed insights help drive your process forward, reducing trial-and-error, and ensuring quality with every unit supplied. The knowledge of lived shop-floor experience, combined with continual feedback from the field, keeps us focused on improvements that matter.