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2-Amino-Thiophene-3-Carboxylic Acid Amide

    • Product Name 2-Amino-Thiophene-3-Carboxylic Acid Amide
    • Alias 2-Aminothiophene-3-carboxamide
    • Einecs 628-100-0
    • 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

    746954

    Chemical Name 2-Amino-Thiophene-3-Carboxylic Acid Amide
    Molecular Formula C5H6N2OS
    Molecular Weight 142.18 g/mol
    Cas Number 6968-93-6
    Appearance Off-white to yellow solid
    Melting Point 206-210°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Smiles NC1=CC(=CS1)C(=O)N
    Inchi InChI=1S/C5H6N2OS/c6-4-2-1-9-3(4)5(7)8/h1-2H,6H2,(H2,7,8)

    As an accredited 2-Amino-Thiophene-3-Carboxylic Acid Amide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic screw-cap bottle labeled "2-Amino-Thiophene-3-Carboxylic Acid Amide, 25g, For Laboratory Use Only," tamper-evident seal.
    Shipping 2-Amino-Thiophene-3-Carboxylic Acid Amide is shipped in tightly sealed containers to prevent moisture and contamination. Typically packaged in amber glass bottles or HDPE containers, it is transported under ambient conditions unless specified otherwise. Ensure compliance with local regulatory requirements for chemical transportation and proper labeling for handling and safety.
    Storage **2-Amino-Thiophene-3-Carboxylic Acid Amide** 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. Keep away from heat and moisture. Store at room temperature, protected from light. Properly label the container and ensure compliance with local chemical storage regulations.
    Application of 2-Amino-Thiophene-3-Carboxylic Acid Amide

    Applications of 2-Amino-Thiophene-3-Carboxylic Acid Amide in Industrial Manufacturing

    As a direct manufacturer of 2-Amino-Thiophene-3-Carboxylic Acid Amide, we supply this advanced intermediate for several industrial application fields, where precise control of processes and compliance with stringent industry guidelines remains a key requirement.

    1. Pharmaceutical Active Ingredient Synthesis

    This raw material serves as a reliable heterocyclic intermediate for the preparation of specific active pharmaceutical ingredients, such as thiophene-based antihypertensive and antimicrobial agents. Industrial pharmaceutical plants employ it in the key amide functionalization step during multi-stage synthesis. Our products support demanding quality specifications for both generic drug and innovative molecule development where the presence of 2-aminothiophene motifs is critical for biological activity.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacture
    • U.S. Pharmacopeia (USP) Monograph suitability, where applicable
    • European Pharmacopoeia (Ph. Eur.) general chapter 5.10
    • FDA 21 CFR Part 211 for process control and traceability

    Typical usage ratio

    • 0.5–2.5 molar equivalents per batch, depending on API target and route optimization. Fine-tuning occurs based on yield optimization and impurity profiling protocols for each drug candidate.

    Downstream process integration

    • Introduced during the early condensation or amidation stages of API synthesis, often following halogenation or sulfonation of the thiophene core. Used in continuous stirred tank reactors or sealed autoclave systems to ensure controlled reaction kinetics and reproducibility.

    Final product types

    • Active pharmaceutical ingredients (APIs) for hypertension or anti-infective therapies
    • Intermediate bulk pharmaceutical chemicals
    • Small-molecule research compounds for clinical trial supply

    2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)

    The amide derivative is an essential synthetic building block for agrochemical formulations, serving particularly in the manufacture of selective herbicide and fungicide actives with thiophene moieties. Major crop protection corporations and CMO partners use the material in targeted amide coupling and cyclization chemistries, enabling new active ingredient discovery and patent extension projects while ensuring environmental and regulatory compatibility.

    Industry compliance standards

    • European Union REACH Regulation (EC) No 1907/2006
    • FAO/WHO Technical Guidelines for Pesticide Specification Development
    • ISO 9001:2015 for process and batch consistency
    • China GB 2763-2021 Maximum Residue Limit (where exporting formulations)

    Typical usage ratio

    • 1.1–1.6 molar equivalents relative to primary coupling agents, adjusted for technical purity and downstream target structure.

    Downstream process integration

    • Enters during the condensation or ring-closure stage after initial activation of aromatic substrates. Integrated in controlled jacketed glass-lined reactors and monitored via in-line HPLC to ensure conversion and minimize byproduct formation.

    Final product types

    • Active ingredients for post-emergence herbicides
    • Systemic fungicide intermediates
    • Technical concentrate (TC) pesticides for formulation blending

    3. Electronic Chemical Intermediates (OLED and Photovoltaics)

    In the electronics chemical manufacturing sector, our material is valued as a precursor for the synthesis of high-purity thiophene derivatives, which are indispensable in organic light-emitting diode (OLED) emitters, hole-transport layers, and novel organic photovoltaic cell components. The consistent supply of semiconductor-grade material with tight impurity thresholds is vital for downstream companies specializing in next-generation display technologies and organic electronics research.

    Industry compliance standards

    • IPC-5701 Cleanroom Material Guidelines
    • RoHS (Restriction of Hazardous Substances) Directive (2011/65/EU)
    • ISO 14001:2015 for environmental management
    • ITU-T L.1200 trace heavy metal content restrictions

    Typical usage ratio

    • 0.8–1.3 molar equivalents, closely controlled by custom synthesis protocols based on OLED or OPV molecular design specifications and desired bandgap tuning.

    Downstream process integration

    • Charged during the pivotal heterocycle-extension sequence for emitter or semiconductor backbone construction. Purified by preparative chromatography to electronic grade before use in vacuum deposition or spin-coating processes for device assembly.

    Final product types

    • OLED emitter and transport materials
    • OPV (organic photovoltaic) active layer precursors
    • Organic semiconductor intermediates for flexible electronics

    4. Specialty Chemical Synthesis for Dye Manufacturing

    Industrial dye manufacturers integrate this compound for synthesizing sulfur-containing heterocyclic dyes and pigments. Its unique amide-thiophene structure enables improved chromophore stability and light fastness in textile and specialty polymer coloration, especially for high-value technical textiles. Formulators require strict batch-to-batch consistency and must meet global standards on non-hazardous ingredient profiles, particularly for exports to regulated consumer markets.

    Industry compliance standards

    • ECHA SVHC (Substances of Very High Concern) candidate list assessment
    • OEKO-TEX Standard 100 for non-toxic dye components
    • ISO 9001:2015 for continual process improvement in dye production
    • ZDHC MRSL (Manufacturing Restricted Substances List) conformance

    Typical usage ratio

    • 0.3–0.7 molar equivalents, modulated by intended chromophore intensity and compatibility with substrate fiber types. Color strength testing dictates in-process adjustments.

    Downstream process integration

    • Added in primary coupling or diazotization steps for dye molecule construction. Incorporated in high-shear reactors and subjected to colorimetric QC protocols prior to downstream blending into dye formulations.

    Final product types

    • Reactive and disperse dyes for polyester and cellulose fibers
    • Specialty pigments for automotive and anti-counterfeit inks
    • Dye intermediates for liquid crystal display and technical coating applications
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    Certification & Compliance
    More Introduction

    2-Amino-Thiophene-3-Carboxylic Acid Amide: Experience from the Manufacturer’s Perspective

    Walking through the daily operations of our chemical plant, 2-Amino-Thiophene-3-Carboxylic Acid Amide comes up in more than one production meeting. Teams from research, production, and quality assurance understand it as a routine compound, but there’s much more to recognize beneath its formula. We see it not just as another intermediate, but as a building block that influences medicinal chemistry and advanced material science projects. This paragraph aims to put our experience with this compound into perspective, highlight its main uses, explain how we manufacture and handle it, and draw attention to differences compared to similar products in the same chemical family.

    How We Approach Manufacturing

    Consistency remains the backbone of our operation. A clean production environment, tight monitoring of reaction conditions, and thorough purification at every step play critical roles in reaching the right standard. For 2-Amino-Thiophene-3-Carboxylic Acid Amide, batch-to-batch reproducibility holds extra weight because this molecule often serves as a core in multi-stage syntheses for clients. Purity sits at the top of our checklist, as impurities even in tiny amounts can break a downstream reaction. Our technicians repeatedly check for water content, residual solvents, and trace metals—items that frequently get overlooked unless they turn into a problem in scale-up or further reaction steps.

    Raw thiophene-3-carboxylic acid comes in first, followed by amination under strict temperature control. Fine details in the process set apart a reliable product from a troublesome one. Acidic and basic impurities, for example, can leach into the product during neutralization. We use pH meters, not just by-the-books titration, and regularly verify them with standards. There’s a lot to say for modern chromatography, but sometimes just running a TLC in the middle of a batch gives an early warning that helps save the whole production. These daily habits form the foundation of confidence in the quality we deliver.

    Specifications: Beyond Numbers on a Sheet

    Some buyers judge chemicals by their COA numbers alone. Our experience says that paper values don’t capture the real usability of 2-Amino-Thiophene-3-Carboxylic Acid Amide in research or industrial settings. Purity above 99 percent becomes the norm here, but we have seen how batch color hints at subtle differences in handling, aging, or even unnoticed side reactions. Particle size distribution rarely emerges as a selection criterion, but if the compound tends to clump or has a high static charge, weighing errors and loss can run through a production line fast.

    Solubility in DMF, DMSO, or other organic solvents gets tested, since our customers rely on solution-phase procedures. Solvent residues and water content are checked by Karl Fischer titration and NMR. We don’t point to these numbers to impress. In practice, one batch with slightly higher moisture can ruin an acylation step downstream. Since many of our clients run parallel medicinal chemistry routes, reliable reactivity under mild conditions matters more than just numbers on a certificate.

    Application Focus: Not Just a Research Reagent

    2-Amino-Thiophene-3-Carboxylic Acid Amide often shows up as an intermediate in the synthesis of heterocyclic scaffolds. In our history, more than a few customers are working with libraries of thiophene-based leads. Small differences in the amide can bring out new patterns of biological activity. It crops up in discovery programs for kinase inhibitors, antibacterial screens, or small molecule dyes.

    Some end-users ask for kilogram-scale lots, others only need a few grams. Requests for custom packaging—foil sacks, sealed glass, or inert gas—often come from those running moisture-sensitive syntheses. For a plant used to shipping drum-quantities of bulk chemicals, repackaging by hand sounds minor but earns client loyalty, especially in early-stage or high-value research. Our sales managers have heard more than once that careful, custom packaging avoided last-minute project delays.

    Often, the advantages of this compound show up in the way it stands up to harsher reaction conditions. Other analogues tend to decompose during strong oxidations or reductions, while 2-Amino-Thiophene-3-Carboxylic Acid Amide remains stable. Its NH2 and CONH2 groups provide anchor points for both nucleophilic and electrophilic transformations, allowing synthetic chemists to branch out into diverse substitution and modification schemes. This versatility makes a difference for teams who may be developing rapidly changing target molecules.

    Relevant Difference from Similar Products

    Comparison between 2-Amino-Thiophene-3-Carboxylic Acid Amide and its halogenated or alkylated cousins sparks constant discussion in the lab. For those who have handled 2-amino thiophene itself, the amide group dramatically reduces volatility. No more breathing in the sharp sulfur smell or dealing with product loss during rotary evaporation. In procedures where extreme temperatures or acid/base swings can degrade substituted thiophenes, the amide shows resilience. When other derivatives bind to glassware or foul chromatography columns, our experience says that the straightforward amide cleans off easily and handles smoothly.

    We often receive questions about 2-amino-thiophene-3-carboxylic acid and its amide. The carboxylic acid form dissolves poorly in many organic systems, complicating large-scale workups. On the other hand, the amide derivative dissolves better and crystallizes in a form that's easier to weigh, transfer, and store. Ironically, perceived ‘activity’ seems to run higher for the acid, but several medicinal chemistry teams tell us the amide is their first choice for SAR studies because it makes for fewer purification headaches.

    No product works in isolation. Researchers blend this amide into a variety of multi-step sequences, often switching from halides, esters, or acids depending on desired transformations. As a manufacturer, we understand why someone might request a custom modification, but our core amide stays in demand because it opens doors to amidines, ureas, thioamides, and even fused ring structures. Any project needing a reactive yet stable five-membered sulfur heterocycle has room for the amide. Based on past collaborations, we have witnessed how critical it becomes for scale-up; sometimes, changing to another intermediate introduces new issues—solubility, batch workup, purification—that our amide neatly sidesteps.

    Quality Assurance Rooted in Real-World Feedback

    Every lot goes through full HPLC and NMR traceability, with records to match. Customers supply their own feedback, sometimes days after a delivery, sometimes months later, in reports describing yields, color changes, or unexplained byproducts. We listen closely, as these notes tell us where to direct our next process improvement. For example, one customer alerted us to a side-product that inhibited a Suzuki coupling. We dug deeper upstream in drying conditions, modified our purification, and eliminated the interfering impurity. Later shipments received praise for more consistent results.

    Some competitors downplay minor differences in impurity profiles. Our standpoint relies on data: persistent, low-level impurities can show up as big issues when customers scale reactions or push for higher SAR throughput. Our teams use this real-world feedback in weekly meetings to adjust cleaning protocols, solvent switches, or process temperatures. Reproducibility across seasons forms another critical metric. We chart seasonal humidity and track how it affects final water content, implementing warehouse controls rather than only shifting paperwork.

    Responsivity to Customer Needs

    Every manufacturing facility wishes for a predictable order pattern, but reality tracks research funding cycles and project decisions. Rush orders for ‘freshest possible’ batches, detailed analytical documentation, or just-in-time packaging come in any time of year. We keep reserve lots of key intermediates to speed up these situations, learned by harsh experience that lead times can make or break a project. Often, a customer will ask for expanded impurity profiling or stability data, far beyond regulatory minimums. We take these requests as indications that researchers trust us with challenges their own work sets, especially when a synthetic route pushes up against the stability limits of sensitive partners.

    Environmental and safety factors weigh heavily in our protocols. With the comfort of handling the compound’s thermal and photochemical stability data, we train new operators using action-based drills, not just PowerPoint modules. A record-free handling history doesn’t mean we rest easy—near-misses get discussed not as rare events, but as opportunities to instill better habits before they become newsworthy. We maintain secondary containment systems and ventilation suited for sulfur-containing organics, since most plant incidents in our experience stem from scraps of leftover compounds, not the main process line itself.

    Environmental Considerations and Waste Management

    The thiophene core in this molecule means special care in managing sulfur residues. We channel spent solvents and byproducts to a closed loop recovery unit, separating useful materials and minimizing landfill output. Water washes from purification stages get neutralized and checked for trace contamination. Regulatory compliance forms a starting point, not an end goal. We involve off-site analytical firms for random batch checks, not because audits demand it, but because surprises have popped up in long-term residue analyses before. These practices reflect the concerns not just of plant managers, but of our neighbors and future employees.

    Process Improvement: Lessons Learned from Production

    We faced a few setbacks in early runs. A batch that crystallized too fine prompted filter clogs and delays. Another time, reagent freshness changed the reaction profile, leading to a slight odor and product discoloration. We followed these outcomes back to technical root causes, changing suppliers only after vetting several test runs, and switching equipment where material build-up threatened long-term throughput. Investment in a more precise temperature control module paid for itself inside a year, since the resulting uniformity saved hours on difficult work-ups.

    Pilot runs gave us a few unwelcome headaches: a dissolved glass thermometer in a batch, for instance, or a half-day delay when a process line backed up with viscous suspension. Real issues don’t arise out of the blue. We take failures apart with the same focus we bring to successful runs, mapping out what went right and wrong at every decision point. The most surprising lesson was that small shifts in solvent grade led to unexpectedly large differences in product morphology—affecting not only shelf life and packaging, but the ease of transfer for hundreds of employees down the line.

    Challenges That Remain and Strategies Moving Forward

    Not every synthesis order fits our usual pattern. Unpredictable raw material shortages sometimes throw a wrench into scheduling, especially as global events disrupt supply chains. Working with thiophene-based scaffolds means we can’t substitute just any supplier without risk. We’ve made it a point to maintain both long-term contracts and a small pool of local secondary suppliers to cover emergencies. Staffing turnover created its own knowledge gaps until we started a peer-mentoring approach among technicians. These lessons translate directly to less downtime and fewer out-of-spec batches.

    Long-term storage stability remains another area requiring vigilance. We run periodic tests on reserve inventory, checking for changes in melting point or NMR shifts that might not show up in routine analysis. Glass container compatibility tests, cold storage upgrades, and additional moisture barriers all came from practical experiences—sometimes from an unexpected shelf-life complaint, other times from our proactive stability program. Investing in staff training, refreshers, and open forums for reporting near-misses gives us early warning for new challenges.

    The Real Value of 2-Amino-Thiophene-3-Carboxylic Acid Amide

    After years of manufacturing and shipping this compound, we have seen its real value: reliability in diverse synthetic contexts, and ease of use compared to analogues with complicating functional groups. Its stability, both in storage and during most reaction conditions, lets chemists focus attention on more challenging reaction points. Projects targeting new pharmaceuticals, materials, or even electronics depend on intermediates like this being available on schedule and to specification.

    Customers frequently share project milestones with us—successful screens, new hit compounds, or finally achieving a publication—where small but critical details in the supply and consistency of 2-Amino-Thiophene-3-Carboxylic Acid Amide made an outsized difference. The back-and-forth among our team, quality labs, and the scientists working at the cutting edge of research keeps the process grounded in the realities of modern R&D. We view these collaborations not as a side effect, but as a central reason to keep investing in manufacturing practices that deliver both quality and adaptability.

    Supporting Innovation Across Applications

    Medicinal chemistry, advanced polymer design, agricultural screening—each uses our amide differently. The requests for custom analytical protocols, rare solvents, or odd lot sizes tell us that this compound lives at many intersections of science and technology. Our role isn’t just to produce kilograms, but to enable teams pushing frontiers in disease research, material discovery, or electronic molecule engineering. Each fresh project brings unique requirements and challenges that stretch our own capacities and make us a better manufacturing partner.

    Conclusion: Drawing from Practical Experience

    The story of 2-Amino-Thiophene-3-Carboxylic Acid Amide at our facility isn’t just in COAs or process flow diagrams. Experience comes from every step—raw materials, operator intuition, client feedback, and a steady focus on scale, quality, and safety. We find evidence of its value not only in lab successes, but in its resilience against production setbacks and mishaps. Each production run tells its own story, and the most enduring lesson is that deep attention to detail really does pay off in the long run. Our aim remains the same: deliver a product that works, so others can do the science that matters.