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5-Nitrothiophene-2-Carboxylic Acid

    • Product Name 5-Nitrothiophene-2-Carboxylic Acid
    • Alias 5-Nitro-2-thiophenecarboxylic acid
    • Einecs 210-459-7
    • 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
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    Specifications

    HS Code

    885499

    Product Name 5-Nitrothiophene-2-Carboxylic Acid
    Cas Number 54810-75-8
    Molecular Formula C5H3NO4S
    Molecular Weight 173.15 g/mol
    Appearance Yellow to yellow-orange solid
    Melting Point 181-185°C
    Solubility Water Slightly soluble
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Smiles C1=CSC(=C1C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C5H3NO4S/c7-5(8)3-1-2-6-4(3)9(10)11/h1-2H,(H,7,8)
    Synonyms 5-Nitro-2-thiophenecarboxylic acid
    Ec Number N/A
    Hazard Statements Irritant

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

    Packing & Storage
    Packing The packaging contains 25 grams of 5-Nitrothiophene-2-Carboxylic Acid, sealed in an amber glass bottle with a secure screw cap.
    Shipping 5-Nitrothiophene-2-Carboxylic Acid is shipped in tightly sealed containers, protected from moisture and light. It should be handled according to standard chemical safety guidelines, including appropriate labeling and documentation. Transport must comply with local and international regulations for hazardous materials to ensure safe and secure delivery.
    Storage 5-Nitrothiophene-2-Carboxylic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat and ignition. Protect from moisture, direct sunlight, and incompatible substances such as strong oxidizers and bases. Use the chemical in a chemical fume hood and ensure proper labeling for safety and regulatory compliance.
    Application of 5-Nitrothiophene-2-Carboxylic Acid

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

    5-Nitrothiophene-2-carboxylic acid offers targeted functional reactivity for several specialty downstream sectors. As a direct manufacturer, we supply this intermediate to customers optimizing their proprietary processes for pharmaceutical API synthesis, specialty dye manufacturing, advanced agrochemical development, electronic material fabrication, and heterocycle-based research chemicals. The following content outlines exclusive segment applications with industry-focused specifications and process details.

    1. Pharmaceutical API Intermediates – Anti-Infective Synthesis

    Our material supports the synthesis of several nitrothiophene-based pharmaceutical intermediates, notably utilized during early-stage or key-step coupling in anti-infective drug production. R&D and manufacturing trends place heavy emphasis on high-purity heterocycle intermediates for structure-activity relationship exploration in nitro- and carboxy-functional agents. Our direct supply is integrated where validated impurity profiles and lot traceability are required for regulatory filings or process validation batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP <795> & <797> Compounding Standards
    • 21 CFR Part 210/211 US FDA cGMP for Drug Products
    • EDQM CEP-related impurity controls for EU Active Substances

    Typical usage ratio

    • 0.08–0.20 molar equivalence as a coupling component, with process engineers adjusting the ratio based on targeted yield and minimization of nitro by-products

    Downstream process integration

    • Introduced post-initial heteroaryl activation, typically in the nitroaromatic coupling or Suzuki-Miyaura cross-coupling stages for advanced intermediate assembly

    Final product types

    • Active pharmaceutical ingredients for broad-spectrum antimicrobials (e.g., nitroheterocyclic antibiotics)
    • Key advanced intermediates for clinical trial API batches

    2. Specialty Dye and Pigment Manufacturing

    This material serves as a building block in nitrothiophene condensation reactions, supporting the production of high-performance dyes and electronic pigments. Customers in this domain value the distinct electron-donating and accepting character, which enables precise control of chromophore extension and bathochromic shift in target molecules. Batch consistency and impurity profile directly impact reproducibility in downstream coloration and pigment dispersion.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Dyes and Pigments
    • REACH Regulation (EC) No. 1907/2006 for import and use in Europe
    • EN 71-3:2019 Migration of Certain Elements (Toy Paint & Pigment Safety)
    • OEKO-TEX® Standard 100 for textile application compatibility

    Typical usage ratio

    • 3–12% w/w relative to total charge in heteroaromatic dye synthesis, with precise addition tailored to desired shade intensity and solubility in organic substrates

    Downstream process integration

    • Introduced at the stage of heterocycle core construction or as the primary nitro component for azo coupling/malonate condensation during dye elaboration

    Final product types

    • Nitrothiophene-based solvent dyes (inks, coatings)
    • Functional colorants for optical materials and specialized textile dye ranges

    3. Agrochemical Intermediate for Fungicidal Formulations

    The addition of our product in agrochemical pathways targets the synthesis of thiophene carboxylic acid derivatives, crucial in formulating new-generation fungicides. Process chemists optimize reactivity and selectivity at this stage to minimize environmental residue and maximize mode-of-action diversity. Batch origin, impurity control, and full backward traceability are fundamental for customers aligning with regional pesticide registration requirements.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • ISO 9001:2015 – Agrochemical Quality Management
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market (EU)
    • GB 2763-2021 Maximum Residue Limits for Pesticides in Food (China)

    Typical usage ratio

    • 5–15% molar input relative to total heterocycle batch, with precise adjustment guided by active ingredient yield optimization and regulatory residue constraints

    Downstream process integration

    • Entry at thiophene core coupling or functionalization, followed by stepwise halogenation, amination, or esterification as specified by the patented fungicide synthesis procedure

    Final product types

    • Active fungicidal ingredients (e.g., thiophene carboxylate pesticides)
    • Finished granule and suspension concentrate formulations for seed and foliar treatments

    4. Precursor for Electronic Materials (Organic Semiconductors)

    In advanced electronics manufacturing, this compound supports the preparation of thiophene-based monomers incorporated into organic thin-film transistor (OTFT) and photovoltaic material technologies. Research and pilot-scale customers pursue high lot-to-lot consistency, minimized metal/halide residues, and quantifiable nitro and carboxylate functional group integration to enable controlled charge transport in finished films.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substances
    • ISO 14001:2015 for environmental management in electronics chemicals
    • IEEE 1680.1 Standard for the Environmental and Social Responsibility Assessment of Electronic Products
    • IPC-5704 Cleanliness Requirements for Unpopulated Printed Boards

    Typical usage ratio

    • Typically 0.5–4% w/w in the monomer feedstock for controlled oligomerization or polymer backbone tailoring, with ratios set by electronic performance targets (e.g., carrier mobility)

    Downstream process integration

    • Material charged directly during monomer synthesis or post-polymerization modification for subsequent solution casting or vacuum deposition onto device substrates

    Final product types

    • Organic semiconducting films for OTFT circuits
    • Active layers in organic photovoltaic cells or OLED components

    5. Research & Fine Chemical Synthesis – Heterocyclic Compound Libraries

    Specialty fine chemical manufacturers and research-based organizations use our product as a functionalized thiophene scaffold, incorporating it into custom batch production for chemical library expansion or lead finding. Application requirements focus on customization of functional group patterns, isotopic labeling options, and minimal trace contaminants to support downstream structure-activity and reactivity studies, especially where multistep elaborations rely on reliable core batch identity.

    Industry compliance standards

    • ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
    • GLP Principles as per OECD Guidelines for chemical synthesis
    • REACH (EC) No 1907/2006 for new chemical development within Europe
    • Local authority notification for Schedule II research chemicals (if applicable)

    Typical usage ratio

    • 0.1–2.0 equiv. in research-scale preparations, with dosage fine-tuned by synthetic route requirements and target scaffold complexity

    Downstream process integration

    • Incorporated as a primary heterocycle donor or acceptor unit in initial building block formation or as a substrate for subsequent cross-coupling transformations, halogenations, amide formations, and esterifications

    Final product types

    • Custom heteroaromatic compound libraries
    • Reference standards, probe molecules, or synthetic intermediates for medicinal chemistry and analytical method development
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    Competitive 5-Nitrothiophene-2-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Nitrothiophene-2-Carboxylic Acid: Experience from the Production Floor

    Making 5-Nitrothiophene-2-Carboxylic Acid: Years in the Trenches

    In our production plant, 5-Nitrothiophene-2-Carboxylic Acid has seen steady demand year after year. Its unique aromatic thiophene core, paired with a nitro and carboxylic acid functional group, gives this compound wide appeal in both medicinal chemistry and material science circles. Our manufacturing team has put countless hours into refining the nitro-thiophene pathway and post-synthesis purification. Each batch tells the story of experience, process improvements, and tough lessons learned from scale-up.

    The bright yellow crystals coming off our drying trays look simple, but behind that color stands a multi-step process with strict attention to detail. Moisture control, safe handling of reagents, and close monitoring of nitration steps form the backbone of our approach. We have built this process through repeated runs, not just textbook procedures.

    Specifications from the Manufacturer’s Hands

    Our typical model for 5-Nitrothiophene-2-Carboxylic Acid follows CAS number 54814-64-1, with molecular formula C5H3NO4S. We isolate material at a purity that regularly tests above 99% by HPLC, and every container matches that spec before it leaves our doors. The melting point clocks in around 192-195°C, an indicator for us that the purification stage hit the mark. Water and inorganic residue content are kept low because we bolster every stage of filtration and drying with real-world QC checks.

    Previous years taught us the value of tight specification. A few tenths of a percent impurity in the nitro group skews downstream reactivity for API synthesis. Residual acid traces limit coupling efficiency. Final products heading for electronic applications cannot tolerate deviation in melting range or color. We have learned to scrutinize every metric because a missed detail means downtime, not just in our plant but in customers’ reactors as well.

    Meeting the Needs of Chemistry and Industry

    5-Nitrothiophene-2-Carboxylic Acid steps into several roles once it leaves our facility. For medicinal chemists, our material becomes a prized building block for anti-infectives and anti-inflammatory research. The resonance stabilization from the thiophene ring, combined with electron withdrawal from the nitro group, makes it an excellent substrate for a range of coupling reactions, amide formations, and reductions.

    Our walk-in customers from research labs often seek it for Suzuki and Heck reactions. Electronic materials teams value its purity in the development of OLED intermediates. Polymer synthesis groups appreciate the reliability of its melting range and moisture control, eliminating one variable in new material scale-up. Organic synthesis teams rely on the sharp signal it gives in NMR and mass spectrometry, knowing their product characterization will not be clouded with noise from trace by-products.

    What Sets Our Grade Apart

    Across the industry, a dozen suppliers might offer nitrothiophene acids. Our process controls trace iron and copper even after using metal catalysts earlier in the chain, verified through repeated ICP-OES checks. The polyacrylate used in some routes to stabilize the nitro group after initial introduction can persist at low ppm; our plant found that extra wash cycles, while costly in water and time, prevent API development headaches for our most demanding customers.

    Years spent troubleshooting purification led us to avoid common blend tricks—no bulking with sodium salt forms or excess crystallization solvents, just solid, predictable product. Feedback from partners told us early on that even slight odor carryover from acid-washed glassware means the difference between a promising candidate and a failed QC batch at the formulation site.

    While lab-made material sometimes comes at higher nominal purity, true industrial batches need low metal, low water, no common residual solvents (like DMF, DCM, or methanol), and minimal flow-through of nitrate byproducts. Our techs track batches through full life cycles—every issue in a customer’s bench test or pilot scale synthesis gets traced back to a lot, and we adapt. This iterative feedback loop sharpens the controls, batch by batch.

    The Technical Story: Not Just a Number

    A molecule is not just a registry number to us as the people who make it. Early in our journey, scale-up from flask to reactor brought headaches that no catalog supplier cares about. Exothermic control in the nitration stage determined if a day’s work became a safe batch or an avoidable loss. Getting the reaction mixture dry enough after quenching set the residue profile for months. Teams developed in-line monitoring at crystallization, shifting from open trays to enclosed chromatography, spurred on by customer requests for even stricter impurity profiles for medicinal projects.

    Some commercial facilities resort to quick recrystallization under less stringent conditions for volume. Experience taught us this shortens the shelf life, brings clumping, and adds questions when the product lands on an HPLC bench. We keep things slow and controlled, checking every stage end-to-end, especially during hot and humid seasons when minor impurities can ride through unnoticed until a sharp-eyed analyst catches them.

    From Research Help to Full Production: What Users Tell Us

    Process chemists in pharma tell us consistency ranks above speed; skipping a QC step or recycling filtrate to speed up delivery leaves more to be fixed later. Peptide chemists dislike surprise peaks in their mass spectra, so our lot certificates cover more than usual impurity windows—any outlier triggers a review before shipping. Advanced material developers ask about stability, thermal degradation, and color changes with light exposure. We swapped packaging for UV-proof liners and reported findings back, closing the loop between production and real-world lab benches.

    Our facility does not see 5-Nitrothiophene-2-Carboxylic Acid as just another commodity. Each user, from molecule makers to electronics fabricators, works at the edge of their field. If we fail on the basics—purity, moisture, trace residue—entire product runs stall or fail, turning weeks of research into setbacks. That feedback drives reinvestment in both our process and the training behind it.

    Handling: Plant Lessons from Day One

    Every operator learns quickly that nitro compounds in general require respect. Proper airflow, containment, and monitoring during nitration operations keep accidents off our record. Carboxylic acid handling brings its own set of challenges. Static management, dust control, and continuous pH checks keep our workflows smooth. Our QC lab trains every technician to test with both standard and in-house reference material, catching errors that slipped by before we adopted these routines.

    Packaging and shipment do not end at drum sealing. Our process includes desiccant inclusion as a rule, with real-world humidity checks at the dock. We document the open time for each batch, the age of reagents, and the maintenance history on transfer lines—nothing is left to chance, from the reactor through shipping. These standard practices grew from hard-won lessons, not theory.

    Applications That Drive Improvement

    Pharmaceutical companies have used our 5-Nitrothiophene-2-Carboxylic Acid in early-stage research for both anti-microbial programs and anti-inflammatory targets. Researchers explained to us how sensitivity to metal content can cause problems with subsequent catalytic hydrogenations or reductions. After learning about failed scouting experiments, we adopted extra filtration and ICP testing, even at concentrations thoughtful suppliers might skip. Real complaints led to real upgrades.

    Material science groups seeking new organic semiconductors provided insight into subtle color stability problems. Even tiny process changes to remove trace protic residues helped improve shelf life, as those groups pushed for material that did not yellow over months in ambient light. This information did not circulate in generic supplier brochures but came only through back-and-forth with scientists using the product at scale.

    The Difference in the Details

    Similar thiophene acids differ in nitro group position, substitution pattern, or ring activation. Our core product, 5-nitro on the 2-carboxylic acid holds both electron-withdrawing power and site selectivity for pharmaceutical intermediates and optoelectronics alike. Some groups find ortho or para-nitro forms problematic due to steric hindrance or mismatched reactivity; our years of running 5-nitro syntheses show this position balances reactivity and stability.

    Other suppliers sometimes blend or switch lots without traceability. For us, each vessel’s contents get walked through storage, not warehoused en-masse, so chemists track the batch lineage without headaches. Mixed-lot supply often triggers batch failures downstream—a reality we encountered years ago, leading us to set strict one-lot-one-container rules within our own plant and distribution.

    Challenges and Next Steps from Manufacturing View

    Outgassing and dust from nitro groups present constant challenges. Plants facing warm, humid conditions must remain alert for clumping or unwanted hydrolysis. We update our drying protocols each season, adjusting for atmospheric pressure and moisture. The product’s sensitivity to both high heat and basic solutions during storage requires constant evaluation.

    Some clients ask for customized sizing, from fine powder for solution-phase processes to larger crystals for direct solid handling in automated weighing systems. Not every production run lends itself to granulometry control, but we experiment where possible, and users see the value in batch-to-batch repeatability.

    Our teams turn research feedback into measurable changes on the floor. Whether it’s tweaking solvent recovery for a greener process or investing in new carbon filtration, every change starts with a conversation between our front-line technicians, production engineers, and the scientists using our acid somewhere on the other side of the world.

    Pricing and Value: Manufacturer’s Perspective

    Most customers seeking 5-Nitrothiophene-2-Carboxylic Acid appreciate a straightforward cost structure. Terms for bulk differ from small volumes only where real added value exists, like segregated packaging, customized documentation, or shipping conditions. Market swings in precursor chemicals and energy cost influence our quotes but not our commitment to maintaining steady supply.

    The trick in this sector is not being the cheapest, but preventing downtime in the labs and production floors who depend on our batch reliability. That’s where years of process refinement, equipment investment, and staff know-how build reputation. Reactive price cuts cut corners elsewhere—trained operators, solid waste handling, or enforced QC consistency start to slip under those pressures.

    Environmental Responsibility on the Production Line

    Nitration chemistry draws scrutiny for possible environmental impact. Our experience led to continual upgrades in fume handling, closed-reactor processing, and spent acid neutralization. Scrubber operation, implemented early and improved ever since, ensures compliance and a safer work environment. As regulations evolve, each improvement brings long-term security for us and confidence for our partners.

    We reduced VOC emissions compared to legacy methods, switching solvents and optimizing temperatures. These choices matter when handling releases from thousands of liters of batch operation each year. Most users never see those investments, but in the end, they affect everything from compliance documents to corporate sustainability reporting.

    Listening and Playing the Long Game

    Transparency with users sharpens our focus on continuous improvement. Years of partnership with research centers taught us that rapid answers to technical questions, clear documentation, and a readiness to trace even minor deviations produce real value. Every complaint gets evaluated, not just by sales but by process chemists and plant managers, because those lessons shape the next production campaign.

    This work never stands still. Synthetic targets get more complex, analytical tools uncover ever-finer impurities, and new user groups find demand in fields not considered a decade ago. Our approach stays rooted in daily realities: safe operations, up-to-date process knowledge, and honest feedback within our plant and from those who transform our molecules down the line.

    The Road Forward: Why the Manufacturer’s Perspective Matters

    Each kilogram of 5-Nitrothiophene-2-Carboxylic Acid leaves our plant as part of an ongoing conversation—a story of plant workers, process refinements, research partners, and quiet technological advance. The details behind every successful batch stack up over years: nimble team response, technical adjustments mid-campaign, and listening to the many scientists and engineers who stretch the boundaries of what thiophene chemistry can do.

    For us, thriving on the frontier of specialty organic chemistry demands a blend of discipline, humility, and close attention to the feedback from every corner of our user base. That is how 5-Nitrothiophene-2-Carboxylic Acid, a compound that could seem like just another product code, becomes a linchpin in research and development worldwide. We learn from every scrap of feedback, every process hiccup, and every satisfied repeat order. To us, that’s what it means to manufacture at a level you can trust—not just now, but as the field grows in invention and expectation each year.