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Methyl 3-Amino-4-Methylthiophene-2-Carboxylate

    • Product Name Methyl 3-Amino-4-Methylthiophene-2-Carboxylate
    • Alias MATC
    • Einecs 689-217-3
    • 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

    180406

    Product Name Methyl 3-Amino-4-Methylthiophene-2-Carboxylate
    Cas Number 55817-96-0
    Molecular Formula C7H9NO2S
    Molecular Weight 171.22 g/mol
    Appearance Light yellow to brown solid
    Purity Typically ≥98%
    Melting Point 72-74°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles CC1=CSC(=C1N)C(=O)OC

    As an accredited Methyl 3-Amino-4-Methylthiophene-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of Methyl 3-Amino-4-Methylthiophene-2-Carboxylate; tightly sealed with a screw cap and labeled.
    Shipping Methyl 3-Amino-4-Methylthiophene-2-Carboxylate is shipped in a tightly sealed container, kept away from light, moisture, and incompatible substances. The package is clearly labeled according to hazardous material guidelines. Transport conditions adhere to regulatory standards, ensuring safety during transit. Suitable cushioning and secondary containment are used to prevent leaks or breakage.
    Storage Store Methyl 3-Amino-4-Methylthiophene-2-Carboxylate in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances, such as strong oxidizers. Label the container clearly and keep it away from sources of ignition. Use appropriate PPE when handling and ensure compliance with all relevant safety and regulatory guidelines.
    Application of Methyl 3-Amino-4-Methylthiophene-2-Carboxylate

    Applications of Methyl 3-Amino-4-Methylthiophene-2-Carboxylate in Industrial Manufacturing

    As the direct manufacturer of high-purity Methyl 3-Amino-4-Methylthiophene-2-Carboxylate, we work closely with industry partners to support targeted applications in pharmaceuticals, agrochemicals, and advanced materials. Based on practical use cases and long-term supply records, the following sections detail four key downstream application scenarios, outlining sector-specific compliance requirements, standard dosage protocols, integration points in downstream processes, and the precise types of finished goods our partners produce using this intermediate.

    1. Pharmaceutical API Synthesis: Bacterial Infection Treatments

    Methyl 3-Amino-4-Methylthiophene-2-Carboxylate serves as a critical heterocyclic intermediate in the multi-step synthesis of cephalosporin and thienamycin antibiotic precursor molecules. Active pharmaceutical ingredient (API) manufacturers incorporate it in the heterocycle construction stage for next-generation β-lactam compounds designed to combat resistant Gram-negative pathogens. We supply this material in bulk lots consistently verified for residual solvents and trace metal content, supporting stringent GMP batch tracking and validated cleaning protocols in finished API production enterprises.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7) guidelines
    • USP <467> Residual Solvents limits for APIs/intermediates
    • European Pharmacopoeia (Ph. Eur.) monograph 5.2.1 compliance for impurities
    • FDA 21 CFR 211 Drug Product Processing and Packaging Control

    Typical usage ratio

    • 0.15–0.28 molar equivalents per API target batch, adjusted according to downstream chain extension reactions and target molecule yield requirements

    Downstream process integration

    • Reactant charge in heterocycle construction during Stage II of cephalosporin nucleus building via condensation or alkylation with protected aminothiophene moieties

    Final product types

    • Cephalosporin antibiotic active pharmaceutical ingredients (APIs)
    • Thienamycin series β-lactam APIs
    • Combination antimicrobial drug substances

    2. Agrochemical Intermediate: Synthesis of Fungicide Active Compounds

    Downstream agrochemical companies utilize our product as a key building block in the synthesis of thiophene-based fungicide actives. During multi-stage pesticide production, this heterocyclic ester is introduced at the condensation stage for constructing systemic fungicide frameworks effective against Fusarium and Botrytis pathogens. The supplied material supports robust impurity profiling, maintaining alignment with regional environmental and safety directives essential for pesticide registration dossiers.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications (FAO/WHO, latest edition)
    • ISO 9001:2015 Quality Management Systems for agrochemical manufacturing
    • REACH Annex II (Safety Data Sheet requirements for intermediate use in the EU)
    • China GB 2763 Maximum Residue Limits for Pesticides in Food in step-down assessment

    Typical usage ratio

    • 3-7% by weight per key intermediate batch, optimized based on final target molecular scaffold and stage yield balancing in process R&D or scale-up operations

    Downstream process integration

    • Condensation reactant at Stage I/II of fungicide core building, followed by amidation, halogenation, and protection group removal prior to formulation blending

    Final product types

    • Systemic fungicide actives for seed treatment and foliar spray
    • Technical concentrate intermediates for agricultural chemical formulators
    • Registered crop protection agents (co-formulated with adjuvants or wettable powders)

    3. Advanced Dye Intermediate: Synthesis of Thiophene-Based Colorants

    Manufacturers of specialty dyes and pigments incorporate this thiophene derivative as a chromophore-building intermediate in the production of high-fastness yellow and orange dyes for synthetic fiber and polymer applications. The compound provides both the aromatic amine and sulfur-containing core required for exceptional light stability and washfastness properties demanded by textile, film, and coatings industries. We supply material via tightly controlled batch-to-batch consistency to ensure critical hue reproducibility in scale production.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • ISO 105-C06:2010 for color fastness in washing
    • ZDHC MRSL List V3.0 (Zero Discharge of Hazardous Chemicals)
    • EU REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance for dye intermediates

    Typical usage ratio

    • 0.5–2.0% by weight in the initial condensation stage during batch dye synthesis processes; final ratio varies by shade depth and polymer type targeted

    Downstream process integration

    • Condensation and diazotization in core chromophore extension stage, prior to coupling with aryl or alkyl substituents for color adjustment and solubility tuning

    Final product types

    • Reactive and acid dyes for PET and nylon fibers
    • Polymer-soluble pigments for plastic masterbatches
    • Solvent dye blends for industrial coatings and inkjet printing bases

    4. Specialty Material Precursor: OLED and Conductive Polymer Manufacturing

    Producers in the electronics industry value this thiophene ester as a functionalized building block for synthesizing advanced organic semiconductors, especially in OLED emitter and hole transport layer material programs. The amino- and methyl-substituted thiophene motif serves as a critical synthon for low-bandgap copolymer frameworks, promoting both charge mobility and processability in printed electronics. We supply ultra-pure lots with certificate of analysis confirming sub-ppm halogen and trace element profiles compliant with electronic chemicals standards.

    Industry compliance standards

    • IPC-4101E: Specification for Base Materials for Rigid and Multilayer Printed Boards
    • JEDEC J-STD-033: Handling, Packing, Shipping, and Use of Moisture/Reflow Sensitive Devices
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • IEC 62474: Material Declaration for Electrical and Electronic Products

    Typical usage ratio

    • 0.3–1.5 molar equivalents per copolymer synthesis; precise proportion tuned to chain length and targeted electronic bandgap in R&D labs or pilot lines

    Downstream process integration

    • Polycondensation or Suzuki-Miyaura cross-coupling with dibromo compounds in pre-polymerization stage for preparation of OLED charge transport or emissive layer material

    Final product types

    • Solution-processable organic semiconductors (p-type and ambipolar)
    • Hole transport layer materials for OLED displays and lighting panels
    • Active emissive components for printed/flexible electronics
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    Certification & Compliance
    More Introduction

    Methyl 3-Amino-4-Methylthiophene-2-Carboxylate: A Manufacturer’s Perspective

    Real Experience With a Specialty Building Block

    We have watched specialty thiophene chemistry gain momentum over the last decade, and Methyl 3-Amino-4-Methylthiophene-2-Carboxylate (MAMTC) stands out as a workhorse in many of our customer's most ambitious syntheses. From research labs to established process lines, this molecule has firmly secured its reputation as a valuable intermediate. Its use reaches far beyond the confines of rank-and-file fine chemicals. Whenever synthesis calls for rugged heterocycles that combine reliable reactivity with ease of functional group handling, MAMTC turns up on the bench.

    Our Approach to Consistent Manufacturing

    Producing MAMTC at scale brings more challenges than one might guess on paper. We have refined our process over years, drawing from both batch and semi-continuous setups, as customer demand fluctuates between multi-gram and multi-kilogram requirements. From the outset, our team faced persistent hurdles: managing sulfur sources, controlling methyl group placement, and introducing the amino group without byproduct drag. Overcoming color impurities after the key cyclization step required us to filter with precisely selected media and adopt multi-step distillation methods developed in our pilot plant.

    A final yield that satisfies both cost and purity rarely arrives without tradeoffs. If the thiophene ring picks up trace oxidation, batch-to-batch consistency collapses, and some research customers reported scattered analytical results before we overhauled our purification regime. Now, our in-house protocol delivers a product with minimum 98% HPLC purity. We use NMR and LCMS to confirm structural integrity, and our analysts keep water content low via Karl Fischer titration. Our customers depend on this transparent documentation. It supports their downstream success, especially where they incorporate MAMTC into regulated pharma projects or commercial agrochemical pipelines.

    The Role of Methyl and Amino Substituents

    Most generic thiophene esters falter when the situation demands both precision reactivity and manageable downstream modification. The methyl group at the 4-position locks in steric characteristics that block unwanted substituent shift during functionalization. The amino group on the 3-position introduces versatility. We’ve seen process chemists make the most of this: nucleophilic aromatic substitution, palladium-catalysed coupling, and various acylation approaches all start from a strong foundation here.

    Customers working on fragment-based drug discovery mention that MAMTC allows for rapid scaffold assembly without excessive protection/deprotection steps. Whether coupling with electrophilic moieties or modifying the ester end for solid-phase immobilization, they gain flexibility—something that other derivatives of methylthiophene, like the 2-amino-4-methyl variant, simply don’t match. In crop protection research, the amino group gets incorporated into bioactive ring systems, delivering both synthetic efficiency and new intellectual property space.

    From Inquiry to Delivery: Meeting Different Project Scales

    We handle inquiries from university spin-outs, scale-up teams, and multinationals. Each has specific needs, and we've learned that packaging and supply size often matter as much as technical support. Some universities need small glass bottles for rapid trial runs, while contract manufacturers ask for drum lots to feed pilot reactors. We maintain standing inventory ranging from 100 grams to 25 kilograms, storing in amber jugs or HDPE drums to shield from light and moisture.

    Shipping fragile, sulfur-rich intermediates brings another challenge. Our logistics team chooses packaging solutions that prevent leaks or odor issues—important not just for safety but also for maintaining lab harmony. If a package of methylthiophene arrives at an analytical center with a sulfurous smell, complaints follow, and we've built careful labeling and secondary containment into our regular protocol.

    Why High Quality Standards Set MAMTC Apart

    Every batch of Methyl 3-Amino-4-Methylthiophene-2-Carboxylate undergoes quality review by a cross-functional team. Analytical data from NMR, LCMS, and HPLC get checked against both our historical standards and new impurity benchmarks set through customer feedback. Our experience shows that some processes demonstrate real sensitivity to trace byproducts from early-stage cyclization or alkylation. Working closely with process partners, we've adapted quenching procedures and changed reagents to suppress these issues on scale-up.

    We notice clear performance differences between our MAMTC and off-brand alternatives, especially when delicate downstream reactions follow. Some outside material shows yellow tint or contains minor unidentified peaks by HPLC. Sourcing from us means skipping the debugging step—our customers can focus their attention on the transformative chemistry that adds value to their businesses, not on remediating problems from raw material origin.

    Understanding Customer Needs Through Dialogue

    Not every application calls for the purest available intermediate. Some downstream users value cost containment for high-throughput screens or non-regulated application development. Over time, we've set up feedback channels—direct lines where chemists and procurement managers can speak with our technical staff. This two-way communication helps us fine-tune specifications or adjust supply methods project by project. In several cases, we've provided custom-sized lots or adjusted crystal forms based on solvent compatibility in uniquely-engineered syntheses.

    We don't push for compliance or regulatory overkill where it isn’t needed. When a customer needs only basic analytical support and rapid turnaround for early discovery projects, we advise accordingly. If the application points toward later cGMP manufacture—such as for an API building block or agrochemical registration—we step up documentation and traceability to satisfy audits without inflating costs for bench-scale users.

    Technological Background: Our Process Development

    MAMTC production usually begins with appropriately methylated and aminated thiophene, proceeding through selective carboxylation. One of the trickier steps involves venting and neutralizing gas off-flow from the methylthiophene precursor to avoid exposure hazards. Early attempts at open-vessel operations brought humidity control issues and odor emissions. Our solution—after multiple lab-scale and plant-scale failures—involved applying closed-loop nitrogen purging to limit oxygen ingress and byproduct formation.

    With every major campaign, we document lessons and feed them back into continuous improvement. During a recent capacity expansion, we experimented with catalytic water removal and fine-tuned acid/base ratios. These incremental tweaks brought both higher yields and a brighter, more uniform product. Analysts observe that our best batches retain less than 0.1% residual solvents—a standard that simplifies downstream solvent-switching for customers.

    Safe Handling in the Manufacturing Setting

    Anyone who works in a chemical plant recognizes the pungency of methylthiophene derivatives. At scale, a few drops leave a lingering scent in even the best-ventilated synthesis bay. Routine handling requires full PPE—goggles, sleeves, and face shields. Despite myths circulating about its toxicity, our industrial hygiene records confirm that, with regular air monitoring and diligent glove protocol, workplace safety remains high. We provide our production staff with annual training, reinforced after every minor incident.

    We recognize that laboratory customers don’t work under the same controlled conditions. Technical support staff often provide handling guidance at no extra charge, especially for new users in universities or startups that may not have experience with sulfur heterocycles. Practical tips—like dispensing in ventilated hoods, using inert carrier gases, or storing material under nitrogen—help fight the nuisance associated with thiophene aroma, safeguarding both chemists and delicate downstream chemistry.

    The Role of MAMTC in Pharmaceutical and Agrochemical Synthesis

    Process development teams in pharma and agrochemicals consistently use MAMTC as a bridge between available raw materials and high-value, biologically active scaffolds. For lead optimization or library construction, the molecule fits into robust synthetic schemes. Its amino group offers ready access to amide, carbamate, or heteroaromatic derivatives via palladium- or copper-catalyzed couplings. The methyl group provides electron density and signals SAR (structure-activity relationship) value to medicinal chemists looking to exploit tunable positions for activity optimization.

    We’ve supported several pharmaceutical launches using material produced at our plant. Each case underscored how critical clean-up steps become as the project moves beyond initial research-grade demands. IP protection for new drug candidates often rests on rare and well-defined intermediates, and MAMTC's unusual substitution pattern makes it a strong candidate for unique molecular claims. For agrochemicals, regulations may call for data going back to primary batch samples—another reason our documentation and retention practices stay so rigorous.

    MAMTC in Electronic Materials and Advanced Polymers

    Not all of our customers come from life sciences. Some carboxylated thiophenes get used in electronic applications, especially in the search for high-performance, conductive, or light-emitting polymers. We’ve supplied research groups interested in organic semiconductors and OLEDs, where subtle differences in ring substitution cause major changes in conductivity or optical absorption. In several cases, custom formulations or solvent-switching were needed at the point of use, and our technical teams provided the real-world insights that sped these time-sensitive projects to completion.

    The versatility of MAMTC often reveals itself in applications that demand both purity and custom formulation. In polymer science, downstream users appreciate that our product arrives ready to fit into complex formulation sequences, reducing time wasted on repeated crystallization or drying steps. The ability to identify and suppress trace color-forming impurities adds value, especially for optical device customers where even faint yellow color in a sample jeopardizes device quality.

    Reliability and Transparency in a Crowded Market

    Customer trust builds one batch at a time. Over years of manufacturing and supply, we witnessed lesser-known competitors enter the market. Some offer sharply lower prices but cut corners on analytical depth, batch tracking, or after-sales support. Purchasing teams with tight budgets may be tempted, but our long-term customers report that hidden costs arise—lost productivity, wasted time on purification, or even full batch rejections when their processes depend on reliable material.

    In an environment where regulatory scrutiny and IP stakes keep rising, transparency makes the difference. Our records stretch back batch by batch, not just for traceability but to provide full confidence in material employed at every stage. During audits and technology transfers, we open our books, sharing historical data, process changes, and analytical method development, giving customers the confidence to move their projects forward unimpeded.

    Sustainability and Responsible Manufacturing

    Reduced waste and energy footprint matter to our team, not as a marketing tick-box, but as a concrete plant-floor reality. Sulfur-based chemistry carries legacy challenges—both in odor management and in effluent processing. Early in our history, we invested in closed-cycle recovery systems for organic solvents, and every year we push downstream partners to adopt greener alternatives. By carefully managing feed streams and actively collecting side streams, we have reduced annual waste output per ton produced.

    Digital manufacturing controls and automated off-gas treatment ensure that every campaign can withstand third-party environmental audits. We take pride in the fact that regulatory visits often end with recognition of the small but essential steps we’ve baked into daily production—not visible on an invoice but highly apparent to operators and downstream users.

    Key Differences Compared With Other Chemical Options

    Other methylthiophene intermediates can’t always match MAMTC in terms of both versatility and reliability. For example, the 2-methyl or unsubstituted versions don't provide the regioselective advantages needed for late-stage functionalization in pharmaceutical projects. The presence of both a methyl and amino group defines its utility: the amino group unlocks further amide, urea, and heterocycle chemistry; the methyl group's exact placement affords activation and stability unmatched by more generic thiophenes.

    Attempts to substitute closely related chemicals often meet with unwanted side reactions. The position of the amino group especially determines the success of key cross-coupling steps or stability under oxidizing conditions. We collaborate with chemists who discovered, through trial and error, that alternative scaffolds failed to deliver required yields or led to time-consuming byproduct purifications. MAMTC provides the right mix of stability and synthetic tractability, saving project teams both time and budget.

    Looking Ahead: Innovation, Partnerships, and Customer Focus

    The stories from our plant aren’t just about cold glassware, distillation columns, or pilot reactors. They're about the hundreds of chemists—including our own—who look for reliable starting points for some of the most innovative molecules made today. From discovery research at academic labs to process chemistry in global multinationals, MAMTC bridges the gap from early imagination to real-world production.

    Our team remains committed to responsive, informed partnership—hoping to pass along not just raw material but real expertise gained over years of manufacturing and supply. Future plans involve deeper integration of green chemistry, even tighter batch monitoring, and more flexible packaging options based on evolving customer needs.

    Industry is moving fast, and molecules like Methyl 3-Amino-4-Methylthiophene-2-Carboxylate open doors for those willing to take on challenging chemistry with confidence. We thrive on supporting those willing to tackle the next generation of molecules, armed with reliable intermediates, technical insight, and a manufacturing partner who understands that the smallest details make the largest difference.