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2-Thiophenecarboxylic Acid

    • Product Name 2-Thiophenecarboxylic Acid
    • Alias 2-Thiophenecarboxylic acid
    • Einecs 208-995-2
    • 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

    567034

    Name 2-Thiophenecarboxylic acid
    Cas Number 527-72-0
    Molecular Formula C5H4O2S
    Molar Mass 128.15 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 124-127 °C
    Density 1.431 g/cm³
    Solubility In Water Slightly soluble
    Iupac Name Thiophene-2-carboxylic acid
    Smiles C1=CSC(=C1)C(=O)O
    Inchi InChI=1S/C5H4O2S/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 2-Thiophenecarboxylic Acid, securely sealed with a screw cap and labeled for laboratory use.
    Shipping 2-Thiophenecarboxylic Acid is shipped in tightly sealed containers to prevent moisture and air exposure. It is classified as a chemical substance, requiring appropriate labeling and handling according to safety regulations. Shipping is conducted by certified carriers, often under controlled conditions, to ensure product integrity and compliance with all transportation guidelines.
    Storage 2-Thiophenecarboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Properly label the container and ensure good laboratory practices are followed to prevent contamination and accidental exposure.
    Application of 2-Thiophenecarboxylic Acid

    Applications of 2-Thiophenecarboxylic Acid in Industrial Manufacturing

    2-Thiophenecarboxylic acid plays a critical role in advanced synthesis across fine chemical, pharmaceutical, and specialty material industries. As a direct manufacturer, we supply this compound to diverse sectors where strict compliance, formulation precision, and integration into controlled processes are required for high-value end products.

    1. Active Pharmaceutical Ingredient (API) Intermediate Production

    2-Thiophenecarboxylic acid is a key intermediate for synthesizing a range of thienopyridine-based pharmaceuticals such as anti-platelet drugs. Pharmaceutical companies use it in amide coupling or heterocyclic modification steps, demanding high purity and traceability. Scale-up and batch synthesis require validated processes and full documentation from initial charge to final isolation and purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 US FDA Drug GMP
    • European Pharmacopoeia (Ph. Eur.) monographs for process intermediates
    • ISO 9001:2015 Quality Management System for pharmaceutical excipient and intermediate suppliers

    Typical usage ratio

    • Employed at 0.3 – 1.2 molar equivalents relative to the core reactant in thienopyridine frameworks, depending on target API yield and minimization of byproducts. Final ratio adjusted based on route-specific conversions and impurity thresholds.

    Downstream process integration

    • Charged during heterocycle construction or acylation step under solvent-controlled, nitrogen-blanketed conditions. Monitored via HPLC and isolated by crystallization before multi-step API synthesis.

    Final product types

    • Anti-platelet agents (e.g., ticlopidine, clopidogrel intermediates)
    • Novel thienopyridine derivatives
    • Research-grade screening compounds

    2. Agrochemical Synthesis (Fungicide and Herbicide Intermediates)

    Agrochemical manufacturers incorporate 2-thiophenecarboxylic acid in the synthesis of sulfonylurea and thiophene-based crop protection ingredients. The carboxylic moiety enables selective transformation for active molecule construction in multi-ton batch reactors with stringent residue and impurity requirements to meet global regulatory norms for environmental safety.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 17025 laboratory certification for quality control
    • Good Laboratory Practice (GLP) for agrochemical synthesis
    • REACH Regulation (EC) No 1907/2006 for chemicals in Europe

    Typical usage ratio

    • Utilized at 1:1 to 1:1.3 molar ratio relative to heteroaryl linkers, adjusted for conversion rate and minimization of waste. Scale determined by downstream product molecular weight and regulatory purity requirements.

    Downstream process integration

    • Fed into condensation or coupling reactions with chlorinated intermediates under basic or acid-catalyzed conditions, followed by purification and formulation into active pesticide concentrates.

    Final product types

    • Sulfonylurea herbicides (notably thiophene analogues)
    • Systemic fungicide intermediates (thienyl derivatives)
    • Plant growth regulator precursors

    3. Electronic and Functional Material Precursor

    The electronics and specialty material sectors employ 2-thiophenecarboxylic acid as a precursor for thiophene-based conjugated polymers, such as polythiophenes used in OLEDs, OFETs (organic field-effect transistors), and photovoltaic applications. Controlled polymerization and chemical modification protocols require electronic-grade purity and batch consistency to ensure targeted conductivity, film-forming, and light-absorption properties.

    Industry compliance standards

    • IEC 60747 standards for semiconductor materials
    • RoHS Directive 2011/65/EU for hazardous substance control in electronics
    • OEM customer-specific analytical method validation (UPLC, GC-MS)
    • ISO 14001:2015 for environmental management in specialty materials

    Typical usage ratio

    • Incorporated at 10–25 wt% monomer basis in copolymerization, depending on targeted film thickness and device architecture. The exact ratio is set by polymer optical and conductive tolerance levels in downstream electronic device engineering.

    Downstream process integration

    • Polymerized via oxidative coupling (e.g., FeCl3 catalysis) or Suzuki coupling to form conjugated backbones, then blended with electronic additives and processed via spin-coating or ink-jet deposition onto substrates.

    Final product types

    • Organic photovoltaic films
    • OLED (Organic Light Emitting Diode) thin film materials
    • Polymer-based transistors (OFETs and OTFTs)

    4. Dye and Pigment Intermediate

    Specialty dye houses and pigment manufacturers use 2-thiophenecarboxylic acid as an intermediate for sulfur- and thienyl-substituted chromophores. Its role in azo and quinone dye synthesis ensures intense color development and fastness properties for applications in textile and polymer coloration. The compound’s reactivity supports selective substitution to tune absorption maxima and chemical resistance in finished pigments.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile auxiliary chemicals
    • EN 71-3 for pigment migration in toys and consumer goods
    • ISO 9001:2015 for pigment and colorant manufacturing
    • Registration, Evaluation, Authorization and Restriction of Chemicals (REACH) for dye intermediates

    Typical usage ratio

    • Applied at 0.5–1.8 molar equivalents relative to aminobenzoic or phenol chromophores in dye-coupling steps. Modification of ratio based on bath composition, target shade, and solubility in final dispersion medium.

    Downstream process integration

    • Condensed with aromatic amines or substituted anilines under diazotization or Ullmann-type coupling conditions, followed by crystallization, washing, and formulation into dye powders or dispersions.

    Final product types

    • Azo dyes for textile fibers
    • Quinone-based pigments
    • Sulfur-containing high-performance colorants

    5. Flavors and Fragrance Ingredient Synthesis

    In the flavor and fragrance industry, 2-thiophenecarboxylic acid is utilized in the synthesis of sulfur-containing aroma compounds. Its thiophene structure enables molecular transformations for savory flavors and tobacco blends. Manufacturing requires traceable raw materials and adherence to food-grade purification and allergen control protocols, especially when intended for direct inclusion in end-user consumables.

    Industry compliance standards

    • FCC (Food Chemicals Codex) for food-grade intermediates
    • IFRA (International Fragrance Association) guidelines
    • Hazard Analysis Critical Control Point (HACCP)
    • ISO 22000:2018 Food Safety Management System

    Typical usage ratio

    • Applied at <0.05% w/w in the composition of finished flavors, but higher in synthetic aroma chemical synthesis steps, typically 0.1–2.0 molar equivalents, with ratio refined for strongest aroma profile and compliance with flavor safety limits.

    Downstream process integration

    • Condensed with aldehydes or alcohols in a controlled batch process, followed by distillation and fractionation to isolate the desired sulfur-compound intermediates. Product is then further purified based on customer GC profile requirements.

    Final product types

    • Sulfurous flavoring agents
    • Tobacco aroma precursors
    • Specialty synthetic fragrance bases
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    Certification & Compliance
    More Introduction

    2-Thiophenecarboxylic Acid: Experience from the Manufacturer’s Bench

    Understanding 2-Thiophenecarboxylic Acid in Today’s Chemical Landscape

    Several years back, the team at our manufacturing plant set out to improve the way 2-thiophenecarboxylic acid gets produced and supplied. This compound—known in labs by its CAS number, 527-72-0—has a small molecular footprint but an outsized role across a cluster of industries. Chemists recognize its five-membered heterocycle linked to a carboxylic acid group, a structure that consistently shows up in projects spanning from pharmaceuticals to specialty material synthesis. Over time, we’ve learned it’s not the ask of making the molecule that defines quality; it’s the discipline and knowledge at every step, from how the precursors are sourced to how the final crystal gets packaged.

    Our Model & Manufacturing Approach

    Inside the facility, every batch of 2-thiophenecarboxylic acid starts with material we have verified in-house. Reliability builds from the ground up, with skilled technicians conducting on-the-spot checks at each stage. Our model for the product is the plain, unmodified substance—no blends, no unnecessary additives, just clear, consistent 2-thiophenecarboxylic acid. This keeps it versatile, meaning labs can take advantage of its clean profile for their own sophisticated downstream reactions. For experienced chemists, the compound often appears as an off-white to tan crystalline solid with a mild, characteristic odor. Over time, we’ve found even minor impurities create trouble in reaction schemes, particularly for customers pushing for high-yield syntheses or stringent regulatory applications.

    Behind the scenes, our shift supervisors focus daily on tight controls. Every reactor gets calibrated for optimal temperature and agitation profiles. After reaction, crystallization often holds the key to sharp purity edges, so we handle this step under set humidity and temperature regimes, not just to please the eye but to favor clean spectroscopic signatures. Purity routinely exceeds 99% by HPLC, with analytical reports provided automatically—not as an afterthought but as a foundation of our transparency. These details matter: a compound’s trace background contaminants can throw off catalysts, short-circuit a step in an active pharmaceutical ingredient pathway, or even void an entire project timeline if not flagged early.

    Specifications: Beyond the Surface Numbers

    Specification sheets for 2-thiophenecarboxylic acid often end up as recitations of CAS, molecular formula C5H4O2S, and melting point. At the plant, every production round shows why these details only tell part of the story. Touch, smell, and even slight color variations mean something to an experienced operator. We set target melting points between 138-142°C and flag anything outside this band for retesting. Water content stays below 0.5%. Every kilogram bags the same way, but the difference slips in if a batch fields even half a percent more moisture or if the filtrate sits too long before drying. Our technicians have faced seasons where a drop in ambient humidity sent drying rates out of spec, and we had to refine procedural windows to lock in best results safely.

    Particle size impacts how readily the acid dissolves for downstream reactions. For labs scaling up, quick and full dissolution matters more than is often admitted up front. Customers planning to feed the acid straight into coupling or condensation sequences benefit directly from tight particle size distribution, and so we regularly check for clumping and take corrective action. Sophisticated coatings, compound libraries, and even agricultural applications—where the molecule serves as a precursor—require a substance that won’t introduce unwanted variables. Reliable specification makes for reliable downstream chemistry.

    Usage: What Sets 2-Thiophenecarboxylic Acid Apart

    On any day, orders from pharmaceutical makers, university labs, flavor and fragrance houses, and specialty polymer researchers bump up against each other on our production queue. Each sector asks for a slightly different performance window. In medicinal chemistry, 2-thiophenecarboxylic acid gets used as an intermediate for drugs and candidate molecules. In custom synthesis, it stands as a popular building block for aryl-thiophene frameworks, thanks to its ease of functionalization. APIs like tenoxicam or various antibacterial candidates trace their ancestors to this heterocycle.

    Polymer researchers call for 2-thiophenecarboxylic acid as a monomer and functional group anchor; the carboxylic acid enables the formation of linkers and end-capping moieties for specialty materials or electronic polymers. Flavor chemists sometimes ask for food-safe substance declarations—not because 2-thiophenecarboxylic acid goes directly into food, but because it often participates as a trace reactant for synthesis of sophisticated aroma compounds. The molecule’s thiophene core can survive harsh chemical environments, so customers can plan cross-couplings, Suzuki reactions, and other palladium-catalyzed procedures with attention to final product profiles. Each type of user shares stories of how even a sliver of extra contaminant rewrites biochemical reactivity or reliability; our job always circles back to hitting the tightest specification possible.

    The Difference From Other Similar Compounds

    Chemistry professionals sometimes compare 2-thiophenecarboxylic acid with its siblings—3-thiophenecarboxylic acid or thiophene-2-acetic acid. From a synthetic perspective, a subtle difference in point of attachment on the thiophene ring can flip selectivity in multi-step sequences. In some cases, the 2-position carboxylic acid, which we supply, locks in regioselectivity for subsequent coupling, while its 3-position counterpart may favor routes requiring alternate functionalization sites. Academic groups probing binding affinities often report clean 2-position carboxylation delivers more predictable biological effects thanks to the electronic influence across the aromatic system. Industrial users confirm this property translates to more robust intermediates and tighter process control.

    Structurally, adding length or bulk to the side chain—such as swapping the carboxylic acid for an acetic acid group—changes the solubility and influences how the substance behaves in phase transfer or crystallization processes. Pure 2-thiophenecarboxylic acid proves its worth in giving chemists a sharp, reproducible platform for diverse transformations, outclassing less pure or incorrectly substituted versions. Any deviation can complicate future synthesis or regulatory approval, especially where trace contaminants risk GMP compliance or downstream product safety.

    Production and Quality: Hard Lessons Learned on the Floor

    After years of manufacturing, the trial and error never entirely disappears. Process scaling stays the source of headaches—small batch purity often loses clarity on larger reactors, where mixing and temperature gradients appear in ways that only running a real vessel can teach. Technicians quickly learn why too-fast acid addition sours overall yield, and why a change in solvent grade ripples through to impact the next customer’s analytical run. Old losses and customer complaints forced us to tighten raw material vetting and to conduct unannounced in-process checks—HPLC and NMR confirmation aren’t a marketing badge, but the minimum threshold for guaranteeing consistent chemical integrity and a clear inventory.

    We’ve rebuilt our filtration and drying infrastructure twice in the last decade, based on customer requests and regulatory nudges. Small design tweaks—upgrading to inert-gas drying rather than heated air, introducing closed-loop solvent recycling—each improved purity and environmental safety, even at the cost of longer turnaround. Over time, every tweak became standard. Now, our output meets more than just industry baseline—repeat clients explain this is the difference between spending energy troubleshooting and staying on schedule with their own R&D or bulk manufacturing commitments.

    Supporting Documentation & Analytical Assurance

    Our facility regards documentation as another layer of product reliability. Every shipment packs thorough analytical profiles, full spectra, and batch-specific data. Return customers reach out most over questions of process stability and trace impurity data—they recognize that the acid’s performance in real conditions often depends on details invisible to the naked eye. Requests for impurity mapping, elemental analysis, or process residuals are met without reluctance; transparency has always proven a better investment than salesmanship. Consistent high purity and well-documented impurity profiles allow chemists to map side reactions before they happen, saving time and grant money for innovation rather than remediation.

    Recent audits found that our choice of analytical tools—HPLC for main purity, gas chromatography for volatile organics, and ICP for trace metals—matches what customers expect, but the difference shows in the numbers for batch-to-batch reproducibility. Raw data availability and archived reference samples mean new clients can verify our claims, and regulatory submissions have never bounced back for lack of detail or authenticity. Over the years, dealing openly with unexpected test results and product recalls built trust, cementing long-term relationships with those who cannot afford surprises in their chemical supply.

    Shipping, Storage, and the Practical Side of Customer Needs

    Handling 2-thiophenecarboxylic acid isn’t about ticking off procedural boxes. Moisture and light degrade it if left unprotected too long, so every drum and bag goes out in dark, tight-sealed liners with clear labeling. Repeated requests for smaller packages led us to scale down as well as up, so now both kilogram lots for pilot batches and multi-ton shipments for larger production lines pass the same rigorous checks. Over time, clients reported less caking and fewer off-odors with these packaging adjustments, which means less downtime and fewer wasted lots in their own facilities.

    Our shipping team stays sharp on both ground and air compliance, updating transport protocols with changing regulations and always flagging shipment routes with known customs bottlenecks. This approach gets orders to both local and international clients faster and with fewer incidents. Storage advice gets grounded in what we see affect product integrity on a real-world timeline—cool, dry, and sealed conditions limit degradation and keep the acid ready for immediate use. Training warehouse partners to inspect seals and monitor humidity has radically dropped the incidence of customer complaints tied to product aging.

    Global Compliance: Navigating Evolving Regulatory Demands

    A major trend impacting supply chains is the growing stringency around chemical usage and documentation. Regulators expect more than technical compliance—they want auditable trails and risk-conscious life cycle tracking. Our site now integrates batch tracking software to map every container through every stage, leaving a digital fingerprint ready for post-market inspection or recall. This oversight isn’t about bureaucracy, but about protecting downstream clients—pharma, especially, carries no patience for contamination or undocumented history.

    Chemical regulation, especially in North America and Europe, means compliance officers spend more time requesting traceability, sustainability declarations, and environmental stewardship. Our records go back years, and a dedicated compliance team keeps up with SARA, REACH, TSCA, and similar evolving lists. We’ve managed chemical registration, hazard labeling, and export declarations in-house and respond quickly to market requests for regulatory documentation. Our production logs, solvent inventories, and material origin certifications hold up to inspection and have given customers extra assurance in their own audits.

    Ongoing Development and Adaptation

    Demand for 2-thiophenecarboxylic acid keeps shifting. Every new request tells us where innovation is moving next. Recently, customers in green chemistry started asking about renewable routes and lower-waste byproduct handling. In response, our R&D group has piloted new catalytic methods and explored solvent recycling loops to cut down environmental loads. These changes reduce byproduct salt formation and limit hazardous effluent. Even small shifts in process—switching out certain mineral acids for organocatalytic alternatives—bring measurable improvements to environmental compliance and worker safety without diminishing yield or purity.

    Pharma clients now challenge us to meet not just chemical but toxicological profiles, demanding impurity maps reaching down to parts per million and narrower batch variation to satisfy both regulatory and in vivo performance standards. The push for sustainable supply has reached into our bulk purchasing, so we audit suppliers for traceability back to their own sources, rewarding those who invest in documented, ethical raw material production. Over two decades, these adaptations have grown from optional to essential; missing even a single update now risks regulatory shutdown or supply disruptions across the market.

    Advice to Users and Collaboration with End Users

    Feedback drives improvement. The most vital lessons came from customers frustrated by unexpected results—low yields, failed isolations, or regulatory fines due to off-spec material. By inviting real-world feedback and failures back into our development pipeline, we sharpened our focus on what each sector actually needs. Regular workshops and site visits help keep our teams and partners on the same page, closing the gap between laboratory synthesis and industrial scale-up challenges.

    Some of our most reliable customers maintain long-term contracts to guarantee a stable pipeline of the acid, allowing them to plan novel reactions months or years in advance. We’ve seen the benefits of these partnerships in smoother operations, earlier notification of supply chain issues, and direct lines for supporting troubleshooting. Open channels with end-users bring head-starts on regulatory changes, so adjustments ripple upstream quickly, keeping everyone in step.

    Troubleshooting and Common Issues in Application

    Problems rarely happen in isolation. Often, customers using 2-thiophenecarboxylic acid as an intermediate report reaction anomalies—unexpected byproducts, color changes, or purification headaches. Over years, a pattern emerges; lots that stray from tight melting point or show extra water can change entire downstream syntheses. Sourcing the acid directly from manufacturers who understand batch consistency means these hitches are minimized or straightforward to fix.

    Our technical support learns the language of synthetic troubleshooting: what looks like a spectral anomaly on paper often matches up with a subtle shift in crystalline habit or incomplete removal of mother liquor on scale-up. We don’t shy from advising clients to rerun Karl Fischer, change solvents, or modify their workup when they describe an unfamiliar outcome. In several cases, joint investigations revealed impurities traceable to processing aids or side reactions, which we then eliminated from our process. Showing customers data and being ready to adapt leads to improvements across both sides of the supply chain.

    Industry Trends: Where We See 2-Thiophenecarboxylic Acid Going Next

    Market-driven synthesis evolves quickly. Increased interest in heterocyclic chemistry, green synthesis, and pharmaceutical innovation places new demands on staple intermediates like 2-thiophenecarboxylic acid. Custom synthesis groups push for greater batch granularity—not just annual bulk orders, but small, highly controlled lots ready for customized modification. This trend led us to build smaller, more agile reactors able to quickly flip between product runs and offer more flexible lead times.

    Electronic materials research now taps into thiophene derivatives for next-generation organic conductors and polymers. Academics exploring molecular electronics request advanced impurity mapping and ask about doping protocols, seeking to push the limits of conductivity and functional integration in devices. We support these efforts with targeted impurity controls; analytical teams characterize trace elements and organic residues to help customers fully realize their own project goals.

    As competition for high-purity sources intensifies, reliability stands as a defining asset. Markets penalize surprises, so we continuously revisit purification strategies, investing in operator training and next-generation analytical validation. The move toward greener, safer manufacturing inches forward each year, so production teams now track not just output, but energy and resource footprints. Collaborating closely with customers lets us anticipate needed changes before regulation demands them, which keeps volatility and downtime well away from the end user’s workflow.

    Conclusion: Why 2-Thiophenecarboxylic Acid Remains a Cornerstone

    The foundation for delivering a quality specialty chemical traces back to experience, vigilance, and a clear-eyed understanding of end-use requirements. Making and supplying 2-thiophenecarboxylic acid never really gets easy—each batch, each shipment, each customer feedback loop introduces new challenges and fresh solutions. What stays unchanged is the necessity for tight process control, honest reporting, and open collaboration. This creates the basis for real performance gains, smooth regulatory audits, and true innovation throughout the modern chemical supply chain.