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Methyl 3-Amino-2-Thiophenecarboxylate

    • Product Name Methyl 3-Amino-2-Thiophenecarboxylate
    • Alias MFCD06796996
    • Einecs 'EINECS 424-320-8'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    796559

    Chemical Name Methyl 3-Amino-2-Thiophenecarboxylate
    Cas Number 25299-68-9
    Molecular Formula C6H7NO2S
    Molecular Weight 157.19 g/mol
    Appearance Light yellow to brown crystalline powder
    Melting Point 70-74°C
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically >97%
    Smiles COC(=O)C1=CSC=C1N
    Inchi InChI=1S/C6H7NO2S/c1-9-6(8)4-2-3-10-5(4)7/h2-3H,7H2,1H3
    Storage Temperature Room temperature, keep tightly closed

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

    Packing & Storage
    Packing Methyl 3-Amino-2-Thiophenecarboxylate, 25 grams, supplied in a tightly sealed amber glass bottle with a tamper-evident cap.
    Shipping Methyl 3-Amino-2-Thiophenecarboxylate is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a laboratory chemical with no special hazardous transport restrictions. The package should include proper labeling and documentation, and be handled by trained personnel following standard chemical safety protocols during transit and storage.
    Storage Methyl 3-Amino-2-Thiophenecarboxylate should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Clearly label the container and avoid prolonged exposure to air to prevent degradation. Store according to all relevant chemical safety regulations.
    Application of Methyl 3-Amino-2-Thiophenecarboxylate

    Applications of Methyl 3-Amino-2-Thiophenecarboxylate in Industrial Manufacturing

    Methyl 3-Amino-2-Thiophenecarboxylate is a core intermediate in advanced chemical synthesis. As an original manufacturer, we support formulation, scale-up, and compliant integration across leading industrial sectors. Below we outline specific downstream applications, formulation standards, and manufacturing practices for this material.

    1. Pharmaceutical Intermediates – Synthesis of Antithyroid Agents

    Pharmaceutical manufacturers use our material as a building block in the synthesis of antithyroid drugs such as methimazole and analogous thioamide derivatives. The amino-thiophene structure directly supports heterocyclic ring construction, facilitating regioselective functional group substitution. Dedicated GMP production lines handle this intermediate to meet trace impurity and residual solvent specifications. Quality control steps include HPLC profiling and control of elemental impurities.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient intermediates
    • USP General Chapter <791> for pH and <232>/<233> for elemental impurities
    • EMA Guidelines for residual solvents (ICH Q3C)
    • Ph. Eur. 2.2.46 and 5.2.8 for chemical purity and heavy metals

    Typical usage ratio

    • Ranges from 0.8 to 1.3 molar equivalents per synthesis batch, adjusted by process yield and final assay requirements
    • Trace catalyst and auxiliary solvents controlled below 0.5% (mass/mass) in finished intermediate

    Downstream process integration

    • Enters during the initial heterocyclization step for drug precursor assembly
    • Follows dedicated overhead transfer into closed reactors to prevent cross-contamination
    • Feeds into batchwise or fed-batch reactor regimes for optimal conversion and quench
    • Subject to in-process sampling for NLT 98% conversion before proceeding to next synthesis stage

    Final product types

    • Methimazole (API)
    • Carbimazole derivatives
    • Other thioamide-containing pharmaceutical ingredients
    • Regioisomeric organic intermediates for medicinal chemistry programs

    2. Agrochemical Actives – Thiazole-Based Fungicide Synthesis

    Agrochemical formulators incorporate the amino-thiophene structure to construct thiazole rings, which serve as active cores of fungicides such as thiabendazole. Strict QC procedures track residual organic acids and maintain batch purity. Automated dosing stations handle pre-milling and solvent blending. The intermediate participates in ring-closure reactions under controlled atmospheres, monitored for reactant consumption and product crystallization endpoints.

    Industry compliance standards

    • FAO/WHO Specification for pesticides and their active ingredients
    • ISO 16140 for analytical control of pesticides – method performance
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • OECD Environment, Health and Safety Publications – chemical safety/transport conformity

    Typical usage ratio

    • Utilizes 1.0–1.5 molar equivalents relative to halogenated core substrates
    • Solvent use targeted at 2.0–4.0 L/kg, with recovery protocols

    Downstream process integration

    • Charged during nucleophilic substitution steps to form the thiazole nucleus
    • Feeds into jacketed reactors for temperature-controlled cyclization (80–120°C)
    • Integrates post-reaction filtration to remove insoluble by-products
    • Feeds directly to isolation and drying before conversion to pesticide technical grade

    Final product types

    • Thiabendazole technical (fungicide active ingredient)
    • Seed treatment fungicide premixes
    • Pesticide formulation intermediates for further downstream chemistry
    • Soil treatment agricultural chemicals based on thiazole moieties

    3. Dye and Pigment Synthesis – Thiophene-Based Colorants

    Advanced dye and pigment companies employ our intermediate for synthesizing sulfur-rich heterocyclic colorants—especially for disperse and metal complex dye families. It introduces a thiophene core necessary for specific absorption spectra, leading to high-performance pigments for textiles and plastics. Synthesis requires multi-step condensation and regioselective amination with subsequent purification.

    Industry compliance standards

    • OEKO-TEX® Standard 100 testing for harmful substances in textile dyes
    • REACH regulation (EC) No 1907/2006 compliance for dye and intermediate registration
    • RoHS Directive 2011/65/EU for pigment use in electrical/electronic equipment
    • ISO 105 series for color fastness in dye end-products

    Typical usage ratio

    • Applied at 0.7–1.2 molar equivalents relative to aryl coupling partners
    • Batch adjustments based on target chromophore intensity and coverage requirements

    Downstream process integration

    • Added to the initial condensation reaction for chromophore assembly
    • Supports staged addition in continuous flow reactors for large-batch pigment synthesis
    • Participates in post-reaction oxidation and milling to achieve desired particle size distribution
    • Feeds product filter presses or spray dryers prior to formulation

    Final product types

    • Sulfur-containing disperse dyes for polyester and synthetic fibers
    • Colorant intermediates for metal-complex dye manufacture
    • High-performance yellow and orange pigments with thiophene chromophores
    • Masterbatch colorants for plastics and fibers

    4. Specialty Chemicals – Development of OLED and Organic Electronics Materials

    High-purity grades serve research and mass production labs developing organic semiconductors, particularly for OLED and advanced display technologies. The material's electron-rich thiophene and amino functionalities enable precise tuning of energy band gaps for light-emitting and conductive polymers. Stringent moisture and trace metal control address performance reliability and device yield targets, integrating in both small molecule and polymer syntheses.

    Industry compliance standards

    • ISO 9001:2015 for quality management of electronic materials production
    • RoHS 2 (Directive 2011/65/EU) for electronic substance restrictions
    • IEC 62474 for material declaration in electronic supply chains
    • IPC/JEDEC J-STD-033 for handling, packaging, shipping, and use of moisture/reactive chemicals

    Typical usage ratio

    • Chemical feed adjustable from 0.5 to 1.0 molar equivalents relative to alkyl halide and STN co-monomers
    • Electronic-grade purity (>99.5%) maintained with water content below 200 ppm

    Downstream process integration

    • Enters direct arylation polymerization pathways for OLED emitter synthesis
    • Processed in glovebox and dry room environments to prevent contamination
    • Feeds continuous stirred-tank reactors for polymer backbone assembly
    • Final product undergoes solvent exchange and spin-coating trials for device testing

    Final product types

    • Organic light-emitting diode (OLED) emitting layers
    • Conductive and semiconductive polymer films
    • Solution-processable organic transistors
    • Functional materials for flexible display backplanes
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    Certification & Compliance
    More Introduction

    Methyl 3-Amino-2-Thiophenecarboxylate: A Practical Perspective from the Manufacturer

    Introduction: Putting Expertise into Practice

    Producing specialty thiophenes in-house has taught us to value both precision and consistency. Every batch of Methyl 3-Amino-2-Thiophenecarboxylate tells a story of methodical process control and hands-on problem solving. This fine crystalline product draws keen interest from pharmaceutical, agrochemical, and advanced material innovators. Large-scale reliability in manufacturing this compound grows out of deep experience, not just access to raw materials or theories about synthetic chemistry. Over years in this field, we’ve fine-tuned every parameter that shapes the quality of this product—because even small variances alter downstream processes for our industrial customers.

    Model, Specifications, and Batch Consistency

    We produce Methyl 3-Amino-2-Thiophenecarboxylate under controlled conditions with a keen eye on reproducibility. Each lot is benchmarked by clear chemical markers, with minimum purity levels matched by few producers. Stringent impurity testing defines every run, since users rely on tight specifications to keep synthetic routes efficient and predictable. In particular, minimizing residual solvents and adjusting crystallization to produce the right particle profile pays dividends across complex syntheses—fewer losses, less rework, and stable yields for the most demanding chemistries. From the color of the powder to the exact melting point, repeatability shows the difference between routine intermediates and precision-engineered chemicals.

    Inside the Synthesis: Why Methodology Matters

    Every step of our manufacturing reflects the chemical behavior of the thiophene core. Starting from well-characterized precursors, selective aminolysis and optimized esterification underpin the process. In the lab, technicians check every intermediate for unreacted starting material. Scaling up, our teams monitor agitation, pH, and temperature control, which become vital as reaction volumes grow. Equipment reliability and process discipline matter more than ever at industrial scale, and unplanned deviations have a direct cost—lowered purity, more scrap, and unpredictable crystallization rates. Our ability to keep parameters in line hour after hour, day after day, guarantees not only what goes into the drum but what stays out of it.

    Understanding the Applications: Why Real-World Use Drives Our Decisions

    Few chemicals illustrate the gap between theory and everyday results as clearly as Methyl 3-Amino-2-Thiophenecarboxylate. Its value traces to the nucleophilic amino group, tightly linked to the electron-rich thiophene ring. Chemists rely on this framework to build up more elaborate heterocycles—often in advanced pharmaceutical targets, agrochemical actives, and specialty dye systems. Downstream users do not just want any methyl ester; they need it to withstand robust coupling reactions, process without unexpected byproducts, and dissolve or recover under industrial filtration regimes. Failures in upstream quality multiply costs for those handling scale-up or GMP campaigns. Direct conversations with leading R&D groups have shaped our internal controls as much as any published paper: small clues flagged by reaction engineers, unique loss points identified in real-world reactors, or subtle incompatibilities with catalyst choices shared by our partners.

    Differences from Other Heterocyclic Products

    Many who source thiophenes ask how Methyl 3-Amino-2-Thiophenecarboxylate stands apart from comparable esters and substituted thiophenes. Side-chain electronics do more than shift analytical readings—they radically alter reactivity. The position of the amino moiety on the 3-position combined with the methyl ester at the 2-carboxylate region sets this molecule apart from straightforward thioesters or 2-aminothiophenes. In practice, this translates into higher coupling efficiency for certain amide-forming reactions and a lower tendency to cyclize under hydrogenation. Direct experience working with both close analogues and off-the-shelf alternatives confirms the greater selectivity and reduced formation of side products seen with our material. Instead of merely benchmarking against literature standards, we routinely process runs alongside predecessor and competitor compounds to see where hydrolytic stability or side-chain migration leads to better finished yield or fewer purification steps.

    Cleanliness, Downstream Reactions, and Practical Yields

    Customers’ process engineers often share feedback with us that each modification to the thiophene skeleton changes filtration and isolation behavior far more than textbook projections suggest. The methyl group on the ester offers practical benefits for handling: it balances lipophilicity and crystallization speed, making downstream work-ups smoother. Subtle shifts in pH tolerance due to electronic effects also prevent decomposition during robust reaction sequences. Many users aiming to move toward greener technologies have noted that our product’s consistent melting and solubility profiles enable solvent minimization in large-scale crystallizations, offering both cost and environmental benefits.

    Typical Usage: Meeting Demands in Pharma, Agrochemicals, and Research

    Large pharmaceutical companies have integrated our Methyl 3-Amino-2-Thiophenecarboxylate in synthesis of kinase inhibitors, complex antimicrobials, and antiviral scaffolds. Structural biologists value the ready availability of this intermediate as it aids in producing probe molecules designed to map protein–ligand interactions. Our largest agroscience partners build on this compound to introduce sulfur-rich heterocycles into plant protection formulations, exploiting its selectivity in cross-coupling and amide-bond formation. Academic research groups have cited our batches in dozens of peer-reviewed publications on thiophene reactivity and novel catalyst discovery. Each of these fields sets its own critical requirements: assay yield, byproduct suppression, robustness against trace metal interference, and scalable recovery.

    Addressing Challenges: Real-World Stories from Our Plant

    Supplying this ester at capacity often means solving fresh puzzles. In one particularly hot summer campaign, variable cooling water temperatures forced us to rethink crystallizer operation. When exotherms pushed a batch ahead of schedule, in-process impurities threatened to breach our internal specification ceiling. Through quick adjustment, the team controlled seed addition, adjusted solvent ratios, and restored granule habit. Focusing on controlling the endpoint rather than sticking to a rigid time target made the difference between out-of-spec waste and material our customers could trust. Years of hands-on troubleshooting have fueled a continuous feedback loop: process data, customer application results, and ongoing analytical investment.

    Quality Assurance: Rigor That Stems from Experience

    Quality for us is not just a paper promise. Our technicians sample each batch mid-process and pre-pack, running side-by-side HPLC and NMR confirmations. They look for outlier peaks, baseline shifts, or subtle contamination from prior campaigns. We invest in validated reference materials prepared using orthogonal synthetic routes. Material out of line with internal data gets reprocessed, not relabeled. This commitment to truth in data comes from living with the downstream consequences: every failed lot means hours of rework, increased solvent waste, and unpredictable costs, both for us and for the end user. What matters is not just clearing regulatory bars, but delivering material that sets up our customer’s chemistry for low-risk success.

    Supporting Sustainable Chemistry Efforts

    Building a future in chemical manufacturing depends on more than economies of scale or incremental recipe tweaks. Sustainability in producing Methyl 3-Amino-2-Thiophenecarboxylate reflects years of focused investment in waste reduction, solvent recovery, and optimized reaction conditions. We draw lessons from every round of solvent exchange, learning which methods maximize product recovery per unit of energy, or cut waste in neutralizations by fractions of a percentage. The team reviews batch records not just for outliers, but for trends that signal new opportunities—unexpected improvements to atom economy, new supplier partnerships that lower the embedded carbon footprint, or in-line purification equipment that protects both workers and the ecosystem. We track performance by kilograms of final product, but also by reduction in reprocessing and number of off-spec events. This makes environmental goals more than something you ‘align’ with; it makes them a core part of driving yield and quality at every stage.

    Supply Chain Assurance Built from Direct Relationships

    Relationships with precursor suppliers and logistics partners remain as critical as any internal protocol. Sourcing pure starting material at competitive cost often calls for months of trust-based negotiation and technical cooperation. Our team visits suppliers at their plants, confirms stability of supply through sample batch processing, and keeps backup quantity in place for every major input. During pandemic and transport disruptions, this buffer saved months of potential downtime and let us fulfill customer commitments that others could not. Avoiding outages and ensuring on-schedule delivery, especially for pilot production or time-sensitive R&D, require ongoing vigilance in a world where every link in the supply chain carries risk. Customers value not just documentation, but honest feedback on lead time risk and transparency that grows from direct experience, not advertising gloss. Every full container that makes port without delay or spoilage comes from this blend of planning, relationship, and technical detail.

    Listening to Customers, Adjusting Processes

    No two production campaigns run the same way, and no two customers use the material in identical processes. A major pharmaceutical client recently needed tighter moisture control to streamline a continuous flow synthesis. Their lab flagged even minor hydrate formation as a source of both filter clogging and lower ultimate yield. We revised our drying sequence, upgraded inert transfer, and tracked the impact on particle morphology and packing density. Regular feedback—from bench chemist to plant manager—shapes our lot release standards as much as internal analytics. This gives users flexibility to keep process costs low or avoid requalification runs. It fosters a rhythm of improvement that comes not from generic checklists but from hands-on partnership and open discussion.

    Why This Compound Remains a Go-To Intermediate

    Beyond reliable performance, Methyl 3-Amino-2-Thiophenecarboxylate draws repeat business due to its versatility in robust, high-value synthetic routes. Many medicinal chemists appreciate how the amino and ester groups unlock selective functionalization, favoring it over bulk thiophene esters that lack programmable reactivity. The molecule’s resistance to harsh basic or reductive conditions delivers more predictable step yields and less need for downstream purification. Customers scaling up library production for clinical studies cite reduced need for rescreening and lower isolation costs as reasons to rely on our supply. These case studies help us refine purification standards, drying protocols, and packaging choices year by year to support evolving needs both in discovery chemistry and commercial manufacturing.

    Moving Forward: Innovation, Investment, and Responsibility

    Sustaining high-quality production year after year takes ongoing investment in both equipment and people. Training new chemists, piloting alternative routes, and testing advanced in-line monitoring systems all reflect commitment to better results, not just bigger output. We encourage plant staff to keep active links with university labs, learning from academic breakthroughs in green chemistry and catalytic efficiency that hold promise for future upgrades. Discussions with our largest customers also steer internal R&D, helping us anticipate regulatory shifts and new applications so there is less risk of product obsolescence. As the science evolves, so does our plant—incremental improvements, targeted retrofits, and never losing sight of both the environmental and human stakes in the work.

    Trust Earned Through Years of Direct Manufacture

    Delivering on promises means more than meeting spec. Every drum of Methyl 3-Amino-2-Thiophenecarboxylate that leaves our site reflects years of learning, adaptation, and daily discipline. Shared metrics, customer test logs, and supplier audits shape what ends up on the formulation line or in the pilot reactor. Teams here take pride in not just supplying a commodity, but in offering a consistent, trusted intermediate that speeds up development and brings predictability to chemical processes around the world. That sense of shared responsibility—from the operator at the reactor to the client’s lab bench only comes from direct, ongoing production experience. We know what goes into the product, and we know the value of outcomes that exceed expectations.