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4-Oxo-4-(2-Thienyl)Butyric Acid

    • Product Name 4-Oxo-4-(2-Thienyl)Butyric Acid
    • Alias 4-Thienylsuccinic acid
    • Einecs 609-040-5
    • 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

    954617

    Product Name 4-Oxo-4-(2-Thienyl)Butyric Acid
    Cas Number 39843-62-2
    Molecular Formula C8H8O3S
    Molecular Weight 184.21 g/mol
    Appearance White to off-white solid
    Melting Point 92-95°C
    Solubility Soluble in DMSO, slightly soluble in water
    Purity Typically >98%
    Smiles O=C(CC(=O)O)C1=CC=CS1
    Inchi InChI=1S/C8H8O3S/c9-7(5-8(10)11)6-2-1-3-12-6/h1-3,7H,5H2,(H,10,11)
    Storage Temperature 2-8°C

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

    Packing & Storage
    Packing The 10g of 4-Oxo-4-(2-Thienyl)butyric acid comes in a sealed amber glass bottle with a printed hazard label.
    Shipping 4-Oxo-4-(2-Thienyl)butyric acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically dispatched via ground or air freight, following all applicable chemical transport regulations, including labeling and documentation. Suitable protective packaging ensures safe transit, maintaining product integrity during handling and delivery.
    Storage Store **4-Oxo-4-(2-thienyl)butyric acid** in a tightly sealed container, protected from light and moisture. Keep it at room temperature or as recommended by the manufacturer, away from sources of ignition and strong oxidizing agents. Ensure the storage area is well-ventilated and equipped for handling chemical spills. Label all containers clearly, and follow standard laboratory safety procedures.
    Application of 4-Oxo-4-(2-Thienyl)Butyric Acid

    Applications of 4-Oxo-4-(2-Thienyl)Butyric Acid in Industrial Manufacturing

    4-Oxo-4-(2-Thienyl)butyric acid plays a functional role as an intermediate across targeted chemical manufacturing sectors where thienyl-based building blocks drive product innovation. As the producer, we supply this compound directly to integrators demanding consistent quality for downstream synthesis and production. The following application scenarios reflect high-confidence, established usage within the industrial landscape, each with specific requirements for compliance, ratio, process stage, and end product.

    1. Pharmaceutical Intermediates for API Synthesis

    Pharmaceutical manufacturers use 4-Oxo-4-(2-Thienyl)butyric acid as a key intermediate in the custom synthesis of heterocyclic APIs, including thienyl-substituted beta-keto derivatives relevant to central nervous system (CNS) and antiepileptic drugs. The material enters multi-step organic syntheses, typically serving as a precursor for coupling or cyclization steps, where tight purity and trace control support downstream GMP batch production. Formulators select the precise dosing based on route-of-synthesis and reaction stoichiometry, optimizing yields through in-process analytical monitoring.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs (as applicable intermediate)
    • US FDA 21 CFR Part 211 (finished pharmaceuticals)
    • WHO GMP guidelines for pharma intermediates

    Typical usage ratio

    • 0.9–1.2 molar equivalent as dictated by synthetic pathway; adjusted per reaction yield analysis

    Downstream process integration

    • Charged into reactor post initial condensation step; involved in heterocycle formation under controlled temperature and inert gas conditions

    Final product types

    • Thienyl-based pharmaceutical intermediates
    • Antiepileptic drug APIs (e.g., modified thiophene derivatives)
    • CNS drug candidates evaluated in clinical research
    • Regulatory starting materials for custom synthesis partners

    2. Agrochemical Actives Research & Formulation

    Agrochemical development groups incorporate the thienyl moiety from this acid into the synthesis of new classes of selective herbicides and fungicides, leveraging its aromatic thiophene function for bioactivity screening. R&D and process teams calibrate the dosage into combinatorial chemistry routes and scale-up trials, with specific attention to environmental safety and process residuals to comply with agrochemical regulatory filings. Usage remains tightly controlled according to pilot synthesis conversion rates and downstream functionalization efficiency.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • OECD Principles of Good Laboratory Practice
    • ISO 9001: Quality Management for Agrochemicals
    • REACH registration for substance handling in EU

    Typical usage ratio

    • 0.5–2.5% w/w relative to total reaction mass; optimized for specific structure-activity screening protocols

    Downstream process integration

    • Fed into pilot-scale reactors immediately after initial chlorination or carboxylation steps for target scaffold assembly

    Final product types

    • Experimental thienyl-substituted herbicide leads
    • Fungicidal actives for lab and greenhouse screening
    • Prototype agrochemical intermediates for structure-activity exploration
    • Commercial registration samples for regulatory submission

    3. Synthesis of Electronic Materials (Organic Semiconductors)

    Manufacturers in the organic electronics space use this thienyl-functionalized acid as a core building block for the preparation of small-molecule semiconductors and solution-processable oligomers. Its integration dictates doping efficiency, charge carrier mobility, and film-forming properties after further cross-coupling and esterification steps. Usage precision directly impacts device layer uniformity, prompting dosage decisions based on molar balance with complementary reagents in the initial material synthesis.

    Industry compliance standards

    • IPC-4101: Specification for Base Materials for Printed Boards
    • RoHS Directive (EU) for electronic chemical substances
    • ISO 14001: Environmental Management for Electronics Manufacturing
    • Quality system audits for semiconductor grade raw materials

    Typical usage ratio

    • Variable, 1.0–1.3 equivalents relative to organometallic coupling partner; batch-specific calibration to control final polymer properties

    Downstream process integration

    • Introduced in monomer synthesis tank pre-coupling; purification and processing performed under drybox conditions to prevent contamination

    Final product types

    • Thienyl-based organic semiconductors
    • Small molecule hole-transport materials for OLEDs
    • Thiophene-derivative intermediates for printable electronics
    • Precursor batches for R&D photoactive layers

    4. Fine Chemicals for Fragrance Building Blocks

    Specialty fragrance ingredient producers adopt this thienyl acid in the synthesis of sulfur-containing aroma compounds, where controlled addition contributes to earthy, tobacco, or roasted accord notes. The acid undergoes subsequent esterification or cyclization steps, and formulating chemists control the loading to optimize olfactory strength while maintaining IFRA limits on trace substances. Inclusion of the acid is based on GC-MS profiles targeting finished oil composition and regulatory conformance.

    Industry compliance standards

    • IFRA Code of Practice (for raw materials in fragrances)
    • EU Regulation (EC) No 1223/2009 on Cosmetics
    • GMP ISO 22716 for fragrance ingredient manufacture
    • US Food Chemicals Codex (for downstream flavor use)

    Typical usage ratio

    • 0.3–0.7% w/w of reaction feed; adjusted per target volatility and end-use olfactory profile

    Downstream process integration

    • Charged into reaction vessel during initial aromatic skeleton assembly, prior to esterification or selective hydrogenation

    Final product types

    • Sulfur-containing aroma intermediates
    • Specialty fragrance chemicals for fine perfumes
    • Notes contributors for flavor & fragrance blends
    • GC-standardized building blocks for aroma R&D houses

    5. Polymer Modifier Synthesis for Advanced Materials

    Advanced materials researchers and manufacturers use this thienyl keto acid to produce functionalized polymer modifiers, particularly targeting optical and sensor applications where the thienyl system enhances electronic communication and functional group reactivity. The compound’s dosage enters amidation, esterification, or Michael addition reactions, with parameter choices governed by targeted modulus, flexibility, or photoreactivity in the final formulation. Analytical labs check incorporation by spectroscopy to ensure functional performance.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Processing
    • ASTM D883: Standard Terminology Relating to Plastics
    • EU REACH substance registration guidelines for polymer processing
    • RoHS compliance audits for specialty plastics

    Typical usage ratio

    • 1.0–3.0% by weight, tuned for polymer compatibility and functional group demand

    Downstream process integration

    • Injected during intermediate modification stage—post-initiation, pre-polycondensation; in-situ monitored for grafting efficiency

    Final product types

    • Thienyl-functionalized polymer additives
    • Custom optical sensors with modified surface features
    • Performance polymers for electronics encapsulation
    • Photoreactive masterbatches for advanced processing
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    Certification & Compliance
    More Introduction

    4-Oxo-4-(2-Thienyl)Butyric Acid: A Look Inside Our Factory’s Experience

    Introduction to 4-Oxo-4-(2-Thienyl)Butyric Acid

    Producing fine chemicals takes more than following a recipe. Every process demands patience, investigation, and a practical understanding of both molecules and markets. Every day, our team builds on lessons learned from batches past, and 4-Oxo-4-(2-Thienyl)butyric acid is a product where that practical experience comes through at each step of the journey—from raw material handling right to product quality in the drum. In our shop, this compound goes by its concise name, and employees know the subtle signals that mean a batch is on track or something’s off.

    We don’t view this chemical as a generic offering. Its structure, marked by the unique blend of a four-carbon acyl chain and a thienyl ring, gives it qualities chemists seek out for solid reasons. In practice, bringing together the thiophene and the butyric acid fragments in reproducible yield never becomes routine. Our operators stand by their training, and each batch leaves with that knowledge woven through.

    Handling and Specifications: Experience Shapes the Outcome

    4-Oxo-4-(2-Thienyl)butyric acid tends to arrive in research labs or production floors as a slightly yellowish or tan crystalline powder, though shades sometimes shift depending on upstream thiophene quality. Batch consistency, more than impressively high yields, has proven the most telling benchmark for the long run. Lab and plant techs flag color or odor shifts before analytics ever confirm them because variances often trace back to small tweaks during oxidation—and predictable color means trace-level impurities have been held down.

    We set our purity standard by actual downstream tolerances. For gram-scale or multi-kilogram requests aiming at pharmaceutical intermediate applications, GC-MS and NMR sometimes batch out over 98%—more than meets normal demand. On occasion suppliers or clients ask whether “99.9%” matters, but on the ground, we see recoverable loss in workups and have witnessed no difference in their performance at these threshold marks. Our shipments usually pack between 98% and 99% assay, plus HPLC traces to document the outcome.

    Care in Processing: Each Step Builds on the Last

    Shaping this molecule involves lessons only a few years of real-world production can teach. Early trials using certain oxidants, for example, generated persistent sulfurous notes, which lingered in downstream synthetic steps. It’s tempting—in the rush of campaign deadlines—to over-pressurize reactors or skip extra-filtration in pursuit of time. Patience and double-checks, though, consistently pay off in odor-free, ease-of-weighing product. Process variables stretch beyond temperature or pH; drying time, glassware cleanout, and sequence order all matter.

    Our team understands that thiophene ring sources dictate both impurity profiles and subtle physical differences after final crystallization. A few changes in source or grade can shift flow properties or leave behind hard-to-remove traces. After enough batches, the hands in our plant know which incoming thiophene lots press out too much off-white byproduct in oxidation and which ones give clean cuts for acidification. With experience, we’ve developed a protocol rooted more in field observation than textbook readings.

    Usage: Applications Grounded in Practice

    In our years of receiving feedback from collaborators and end-users, the same theme repeats: 4-Oxo-4-(2-Thienyl)butyric acid acts as a trusted intermediate in discovery research and commercial production lines. Its structure gives a chemist space to build—both the keto group and thienyl ring open doors to useful transformations that would otherwise require much more complicated routes. Utility often swings between pharmaceutical research—where final molecules demand a backbone reminiscent of this motif—and specialty material synthesis, where sulfur and carbonyl groups help create more stable or more reactive materials.

    Our partners in custom synthesis tell us that, especially during lead optimization runs, a small family of butyric acid derivatives helps quickly tune both solubility and electronic properties of candidate drugs. They set aside this specific acid for targets where sulfur presence or a certain polarity window proves critical. In contrast, we hear from colleagues in materials labs that the acid group works wonders in surface modification schemes—anchoring to substrates with more reliability than shorter, more volatile analogs.

    Experience has taught us not to overpromise—4-Oxo-4-(2-Thienyl)butyric acid is no panacea. It outperforms only in scenarios where a thienyl-carboxylate motif becomes a bottleneck. It does not suit every chemistry, especially if cost or reactivity with common amines becomes a rate-limiting concern. Still, its track record speaks clearly—repeated small-to-medium orders from certain research centers suggest the acid’s unique place in molecular innovation.

    Key Differences: What Sets It Apart From Related Compounds

    Comparison matters in chemical manufacturing. On paper, 4-Oxo-4-(2-Thienyl)butyric acid would seem to differ little from other keto acids or standard butyric acid. In reality, the thienyl ring introduces both technical challenges and advantages. Standard butyric acids lack the aromatic sulfur, which brings electron-rich and hydrophobic attributes to the table. That changes how the molecule behaves in both solution and reaction setups.

    Our own technical group has run several head-to-head tests against simple acetoacetic acid, 4-oxo acids with phenyl rings, and even thienyl-acetic acid. In straightforward alkylation or amide formation, the thienyl analog sometimes reacts with more predictability when handled at carefully controlled pH. Some team members, with a decade or more in kilo lab scaling, argue that our acid’s unique molecular weight (186.22) and solid-state properties give more reliable melting and solubility behavior compared to near cousins, especially when handling temperature-sensitive steps.

    Differences show up clearly when considering aroma and thermal stability. Pure butyric acids often carry a persistent, unpleasant odor. By contrast, the thienyl derivative, when prepared with high-purity thiophene, rarely emits strong or problematic scents at room temperature or upon gentle heating. Over long-term storage, changes in color or composition occur less often in properly sealed containers. These aren’t mere footnotes—chemists working late shifts appreciate a product that doesn’t foul air or require endless hood cycling, and operators speak plainly about trouble-free handling and transfer.

    We’ve heard from outside analysts who once raised concerns about potential ring opening or side reactions affecting downstream use. By monitoring batch history, we’ve gathered enough data to show stable, reproducible batches over many months. This stability reflects both compound identity and the labor invested in careful crystallization rather than any unique shelf-life trick.

    Working with the Product: Handling, Storage, and Practical Tips

    The reality of daily chemical manufacturing forces plant operators and chemists alike to balance convenience and safety. 4-Oxo-4-(2-Thienyl)butyric acid demands attention to simple, effective practice—airtight packaging, dry storage, and clear labeling. Our staff avoid moisture exposure as even brief contact increases clumping and lengthens redissolving or weighing time at the receiving bench. Years ago, a missed warehouse protocol check led to minor surface caking in summer humidity, driving home the lesson quickly.

    The acid dissolves well in common laboratory solvents—ethyl acetate, acetone, and, to a modest degree, ethanol or methanol. In our process, efficient use of solvent means batch recovery rarely falls below targeted thresholds, and tank cleaning involves fewer headaches at the end of a production run. The remaining solids filter off without persistent stickiness, making product recovery straightforward. These small process efficiencies add up over time, reducing downtime and personnel exposure.

    Forklift drivers and plant techs handle the packed drums daily, and feedback from these hands shapes our packaging choices. Double-bagged liners, clear batch numbers, and accurate net weights save time and hassle for our partners. To minimize spills, we moved away from rigid liners years ago, favoring more flexible, puncture-resistant bags sealed inside sturdy drums. Labels may sound like a small issue, but clear, solvent-resistant printing prevents mix-ups—not just internally, but also for customers dividing re-packed lots.

    Real-World Batch Challenges and Solutions

    Chemical manufacturing never unfolds without the unexpected. Past challenges with 4-Oxo-4-(2-Thienyl)butyric acid have included inconsistent color, batch-to-batch moisture variances, and the rare presence of oxidation byproducts. Based on our experience, most complications can be traced to raw material variation or process deviations. Quality in, quality out—one subpar stock of thiophene nine years back resulted in a series of tedious filtrations and batch quarantines before root cause analysis identified the impurity source.

    Team meetings after such challenges focus on actionable steps, not blame. Installation of final stage in-line water scrubbers, installation of more precise metering pumps, and investment in real-time pH monitoring brought both better yields and more uniform acid color. Some lessons came hard—one winter, condensation inside our warehouse led to increased post-crystalization caking. Now, we condition all storage spaces and track environmental variables not just for compliance, but because the product quality depends on it.

    No technology removes operator vigilance from the process. We keep training fresh; even experienced staff rotate through every process stage. If something looks, smells, or dries differently, it’s reported up the chain and traced back through logs immediately. Customers do not always see this, but the care runs deep—from scheduled downtime maintenance to routine pilot scale side-by-side trials testing new process equipment.

    Compliance, Safety and Environmental Responsibility

    No chemical process operates in isolation from laws, rules, and shared responsibility. We stay on top of evolving regulatory frameworks regarding thiophenes and related compounds. Reports detailing environmental impact, waste streams, and workplace safety run parallel to production logs. Over the past decade, stricter disposal rules influenced our choice in solvents and prompted investment in closed-loop filtration and recovery systems.

    Acids containing heterocycles present another layer of oversight. Every drum leaving our plant carries accurate safety and handling instructions written from experience, not generic labels. Direct conversations with warehouse stewards and end-users highlight where hazards arise, such as inappropriate mixing or disposal practices. Proactive communication prevents issues later down the line, and regular audits ensure staff awareness stays current.

    On environment, we have seen measurable reductions in both solvent waste and overall emissions by optimizing reaction concentrations, scaling up single campaigns, and reusing cleaned equipment wherever feasible. These shifts don’t come from external pressure but from a clear-eyed analysis of our own footprint, and the recognition that what leaves our plant shapes both reputation and local safety. Our operators track the reduction in hazardous drum disposals year to year with pride. Learning from both mishaps and successes drives the same responsible care approach through every tier of our production chain.

    Feedback Loop: Learning from Our Customers and Partners

    From research chemists in biotech startups to purchasing departments at major specialty chemical houses, all feedback about our 4-Oxo-4-(2-Thienyl)butyric acid gets logged, reviewed, and used for process adjustment. Years ago, one order returned for minor off-color prompted our QC team to refine final crystallization. Customer comments about particle size and solubility now inform our drying process. Sometimes the most useful improvements have come from details only regular users notice—like reduced bottle necks or easier scooping from packaging, which in turn improves on-site usage and lowers lab waste.

    We recognize that no two labs use our products in quite the same way. Providing detailed batch records and traceability for each shipment reassures partners repeating syntheses or scaling up from milligrams to kilos. For those scaling up for the first time, we always share stories from our shop floor—what storage works best, pitfalls in solvent choice, ways to avoid small-scale error magnification when transitioning to plant-scale runs.

    Continuous Improvement: The Manufacturer’s Promise

    Having handled, produced, and shipped many metric tons of 4-Oxo-4-(2-Thienyl)butyric acid over the years, we never see our role as finished at delivery. The market keeps evolving, regulatory documentation updates yearly, and new users surface novel needs. We take pride in calibrating our approach in real time—not by reacting to fads, but by sticking with what safeguarding the chemistry means to us. Batch notes, direct phone calls, and day-to-day troubleshooting knit together practical knowledge and science—not just for reliability today, but so that one mistake or success story improves the next batch tomorrow.

    Through every batch and every shipment, we remember who will open the next drum we ship. Quality matters most in its most practical form: product that’s easy to use, acts as advertised, and stands up under scrutiny. In our world, the numbers on an assay don’t just fill out paperwork; they mean trust—for our reputation and for the lab coat lining up glassware on the other end. That trust rests on everything from clear labeling to straightforward documentation, and it gets rebuilt one batch at a time.

    Beyond the Specification Sheet: A Human Approach

    At the end of the day, real chemistry involves people—those who make, test, package, ship, and ultimately run reactions using our 4-Oxo-4-(2-Thienyl)butyric acid. Each role plays its part, shaping how this chemical heads out into the world and what story it tells. Some team members have handled it for years, noting subtle cues in appearance or feel by hand; new arrivals bring sharp eyes and thoughtful questions. All of these perspectives keep standards sharp—and help us see beyond the process flowcharts.

    Every drum reflects more than yield figures or purity points. It brings together the daily problem-solving and cumulative memories of the people shaping the process. Listening to questions from customers and feedback on new research applications helps us keep the work aligned with real-world science and shifts in demand. As both science and industry continue to change, that blend of hands-on attention and technical precision will keep steering our manufacturing approach.