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Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate

    • Product Name Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate
    • Alias MATC
    • Einecs 6663-45-4
    • 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

    657957

    Chemical Name Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate
    Cas Number 6628-74-6
    Molecular Formula C4H6N4O2
    Molecular Weight 142.12
    Appearance White to off-white powder
    Melting Point 181-184°C
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles COC(=O)c1nnc(N)n1
    Inchi InChI=1S/C4H6N4O2/c1-10-4(9)3-6-2(5)7-8-3/h1H3,(H3,5,6,7,8)
    Pubchem Cid 446298
    Storage Temperature Store at room temperature

    As an accredited Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle containing 100 grams, sealed with a screw cap, labeled with chemical name, formula, CAS number, and hazard symbols.
    Shipping Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate is shipped in tightly sealed containers to prevent moisture ingress and contamination. It should be stored and transported at room temperature, away from incompatible substances. Shipping complies with relevant chemical regulations and includes proper labeling and documentation for safe handling and regulatory compliance.
    Storage Store Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Store at room temperature, unless otherwise specified, and ensure proper labeling. Avoid direct contact and handle using appropriate personal protective equipment.
    Application of Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate

    Applications of Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate in Industrial Manufacturing

    As the direct manufacturer of Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate, we supply this specialty chemical to established downstream producers across high-value sectors. Our in-plant experience has built detailed process insights, compliance management protocols, and knowledge of formulation-specific integration for this intermediate in actual production environments. Below, we outline core industrial applications with scenario-specific compliance requirements, composition parameters, integration stages, and the downstream product categories manufactured by our customers.

    1. Synthesis of Triazole-based Agrochemical Active Ingredients

    Downstream agrochemical manufacturers utilize this intermediate for building triazole ring systems essential to fungicidal and herbicidal APIs. In these facilities, the molecule enters multi-step organic syntheses, providing both nitrogen heterocycle and carboxyl-containing frameworks. Regulatory compliance for agrochemicals mandates scrutiny of process impurities, traceability of raw materials, and documented risk management throughout API synthesis and formulation packaging lines.

    Industry compliance standards

    • ISO 9001:2015 for quality management
    • REACH Annex II requirements for chemical safety in EU
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • China GB 2763 National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Applied at 2.5–12% mass ratio in triazole pesticide technical concentrate synthesis, with levels adjusted according to target compound molar conversion and efficiency; lower for single-step routes, higher in multistep processes with intermediate isolation

    Downstream process integration

    • Charged to reaction vessels after solvent charging for stepwise condensation with azoles
    • Reacted under anhydrous or acidic catalysis conditions; monitored by HPLC for endpoint determination
    • Introduced prior to key cyclization or N-functionalization step, forming API backbone

    Final product types

    • Triazole-based fungicide active ingredients (e.g., tebuconazole, propiconazole technical)
    • Triazole herbicide intermediates
    • Pre-formulated agrochemical end use solutions and suspension concentrates
    • Ready-to-pack technical grade APIs for further downstream formulation

    2. Pharmaceutical Intermediate for Heterocyclic Drug Synthesis

    Pharmaceuticals rely on reliable supply of synthetic intermediates for regulated API production, especially for heterocyclic scaffolds prevalent in anti-infectives and CNS actives. Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate allows streamlined construction of pharmaceutical triazole moieties via direct coupling, amidation, and ring-system modifications. All steps must ensure trace-level impurity control, validated analytical release, and GMP-aligned batch recording.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA GMP for finished pharmaceuticals)
    • European Pharmacopoeia standards for triazole APIs
    • Certificate of Suitability (CEP) per EDQM for API import into Europe

    Typical usage ratio

    • 5–20 mol% relative to main coupling reagent; levels customized for reaction yield, downstream purification load, and target impurity profile

    Downstream process integration

    • Introduced after solvent degassing and prior to coupling catalyst addition
    • Directly charged in heterocyclic core assembly or as a coupling partner in functionalized triazole synthesis
    • Processed through crystalline isolation or flash chromatography prior to API finishing steps

    Final product types

    • Active pharmaceutical ingredients for anti-fungal (azole-class), anti-viral, and CNS-modulating drugs
    • GMP-grade triazole intermediates for use in subsequent synthetic sequences
    • Clinical trial material for new chemical entity (NCE) registration batches

    3. Heterocyclic Additive for High-Performance Industrial Coatings

    Industrial coating formulators deploy this molecule as a performance-enhancing additive in specialty primers, anti-corrosive agents, and environmental barrier coatings. Its heterocyclic structure introduces functional groups promoting cross-linking, corrosion inhibition, and improved film durability, especially in metal protection systems. Regulatory compliance here includes both chemical formulation safety and functional end-use durability criteria.

    Industry compliance standards

    • ASTM D3276 Safety Standard for Handling & Mixing Paints and Coatings
    • RoHS and REACH regulations limiting hazardous components in end-use coatings
    • ISO 12944 for Corrosion Protection of Steel Structures
    • Chinese GB/T 25251 Code for Anticorrosive Coatings for Industrial Use

    Typical usage ratio

    • 0.3–1.5% w/w in total formulation, increased to 2% for heavy-duty marine or infrastructure coatings; adjusted by substrate compatibility and targeted salt spray resistance

    Downstream process integration

    • Dissolved into pre-polymerized resin mix prior to pigment and filler dispersion
    • Added at letdown stage with careful agitation to prevent precipitation
    • Monitored for full dissolution and compatibility with other anti-corrosive agents

    Final product types

    • Industrial metal primers with high salt spray test performance
    • Chemical-resistant topcoats for tank and structural steel
    • Protective automotive underbody coatings
    • Bridge and marine structure protective paint systems

    4. Building Block in Specialty Chemical Synthesis for Electronics Applications

    Within the electronics sector, specifically in advanced material synthesis, this compound functions as a key nitrogen donor and heterocyclic scaffold in manufacturing functional polymers, electronic adhesives, and circuit board protection chemistries. Electronic-grade production places emphasis on minimal trace metal contamination, batch-to-batch consistency, and recording of all toxicological data for cleanroom operations.

    Industry compliance standards

    • IEC 61249-2 for base materials for printed circuit boards
    • RoHS Directive 2011/65/EU for hazardous substances restriction
    • ISO 14644 for cleanroom process compliance
    • JPCA-ES-01 and IPC-4101 (for laminates and electronic insulating materials)

    Typical usage ratio

    • 0.1–0.8% in resin composite mass for specialty electronic adhesives, or up to 1.2% in high-end thermoset protective films

    Downstream process integration

    • Premixed into resin backbone or masterbatch prior to casting or extrusion
    • Added with reactive diluents in electronic encapsulation resins
    • Enter the lamination or patterning steps in circuit board manufacturing

    Final product types

    • Electronic-grade adhesives for PCB assembly
    • High-resistance encapsulants for semiconductor packages
    • Protective conformal coatings for microelectronic devices
    • High-durability polymer films used in flexible electronics

    5. Intermediate for Fine Chemical and Analytical Reagents Production

    Specialty chemical producers incorporate this raw material as an intermediate in synthesis of analytical reagents used for metal ion detection and as building blocks in research chemical catalogs. These production processes require purity assurance, documented batch records, and full traceability for analytical-grade supply chains.

    Industry compliance standards

    • ISO 17034 General Requirements for the Competence of Reference Material Producers
    • ISO/IEC 17025 for laboratory testing and calibration
    • GHS labeling compliance for safety documentation
    • Analytical purity standards defined by Sigma-Aldrich, Merck, and other catalog reagent benchmarks

    Typical usage ratio

    • Varies from 0.5–2 mol equivalents depending on synthesis target; adjusted for yield/purity tradeoff in multi-step reagent production

    Downstream process integration

    • Used in batch or semi-continuous reactors prior to final purification
    • Charged as an initial building block or as a coupling partner for structure extension
    • Subject to stringent in-process QC and post-synthesis validation

    Final product types

    • Chromatographic standards for laboratory use
    • Analytical indicators and metal complexing reagents
    • Reference compounds in research and diagnostic kits
    • Specialty triazole derivatives for further R&D in universities and industrial labs
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    Certification & Compliance
    More Introduction

    Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate: Global Quality, Local Know-How

    Direct from the Source: Our Manufacturing Perspective

    Every day on the production floor, we see how strong attention to detail transforms raw starting materials into reliable fine chemicals. For decades, chemists and process engineers on our team have dedicated themselves to refining the synthesis of heterocyclic building blocks. Among our specialty lines, Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate stands out not just for its chemical structure, but also for the tight process control and experience that go into every kilogram we produce. Handling the full route from raw material assessment to finishing, we stand behind the consistency we offer, batch after batch.

    Chemical Identity and Seasoned Production

    Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate, often called MATC by researchers who work with it, is not a name you see on general-use chemical lists. Its value comes from a unique three-nitrogen ring core, an amino group at position five, and a methyl ester at position three. In our facility, engineers monitor both time and temperature carefully at critical points in the process, ensuring purity and reproducibility. We avoid unsound shortcuts as they almost always lead to downstream issues. Over the years, we have fine-tuned our recrystallization and drying steps to minimize contaminants and moisture content. Our technicians draw on both data logs and years of working with triazole derivatives, understanding how subtle tweaks impact both solubility and reactivity for the next step in the customer’s application.

    What We Ship: Appearance, Purity, and Handling Know-how

    Customers rely on us to deliver a material that meets their needs, whether they are scaling up agrochemical actives, creating specialty coatings, or developing new pharmaceutical syntheses. Batches leave our site as a white to off-white crystalline powder. Whether a research lab asks for a single kilogram, or an industrial partner needs tonnage, our controls stay the same. High-performance liquid chromatography and proton NMR supplement older classic assays to confirm purity—an essential, not a luxury, with compounds that sit at the heart of expensive multi-step syntheses. With melting point and loss-on-drying standards held tight, we do not face surprises in the warehouse or at our customers’ benches. This approach also limits wasted time on reworking or correcting intermediate stages down the supply chain.

    Solid Reasons for Popularity in Synthesis

    Why do chemists come back for our Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate, given all the alternatives? Much comes down to the sharp reactivity profile of the molecule. The arrangement of nitrogen atoms, flanked by the methyl ester and amino substituent, makes this compound a versatile intermediate. In pharmaceutical development, it’s leveraged for building more complex, bioactive triazoles, which often show strong antifungal or anticancer properties. Agrochemical firms use our material where targeted pest control or herbicidal selectivity matter. Researchers use it as a scaffold for further functionalization, taking advantage of the free amino position or unreacted nitrogens in the triazole ring. What sets this compound apart is the predictable outcome in cyclization, amidation, and other heterocycle transformations. Many literature examples underline its role as a gateway to even higher value triazole derivatives.

    How MATC Differs from Other Triazole Derivatives

    Our customers often compare Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate against other triazole building blocks. For process chemists, substitution matters. The ester function at position three means the compound takes part in ester-amide transformations effectively, unlike carboxylic acid analogues which often present solubility or stability problems. Meanwhile, the amino group creates a handle for N-acylation or diazotization. Series like 3-amino-1,2,4-triazoles cannot offer the same dual functionality for step-economy in routes where convergent synthesis is a must. Compared to methyl esterification at other ring positions, MATC’s profile balances shelf stability with reactivity, supporting both storage and in-line reactivity. Whether for pilot-scale optimization or small-batch novel development, this unique balance saves costs on purification and avoids multi-step protecting group strategies.

    Consistency, Traceability, and Safety Backed by Evidence

    On the factory side, we have learned the hard way that poor traceability causes headaches on both sides—yours and ours. Every lot we dispatch comes with detailed batch records, not out of bureaucracy, but because in regulated industries, knowing your material’s story makes the difference between smooth production and costly delays. We do not rely solely on the front line for quality. Our laboratory checks feed back into process improvements. For example, by tracking melting point drift over several hundred batches per year, we have pinpointed raw material source issues before they cause downtime.

    Another aspect gets attention at the packing hall: Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate can generate dust if handled roughly. Our operators cap moisture ingress from the start, pack the product with antistatic liners, and ship using tamper-evident seals. This detail seems small, but for downstream formulations—especially in sterile or low-excipient environments—avoiding cross-contamination pays off. Advice for handling and storage draws on both in-house MSDS testing and shared real-world experience with our biggest customers.

    Supporting Research and Regulatory Progress

    Those working on regulated applications pay close attention to both material source and integrity. Over the years, our support staff have answered hundreds of requests for additional documentation: impurity profiling, solvent-residue screening, or renewable energy data related to synthesis. Because we run our own laboratories, getting custom analytical support is just another part of how we help clients cross formulation or registration hurdles. From a regulatory standpoint, whenever new directives like REACH or updates from environmental agencies threaten to disrupt older supply chains, our data archive—built over continuous compliance cycles—helps customers maintain audit readiness. We pay close attention to requests for detailed impurity lists, especially for projects moving from early-stage R&D into GMP or FSSC-certified lines.

    Evolution of Sourcing and the Importance of Direct Manufacturing

    The last decade brought a steady stream of questions about the real origin of chemicals. End users now push for clarity: no more accepting products that have crossed five hands with unclear provenance. With Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate, every batch in our facility receives a unique identifier. We trace it from initial raw stocks right through to finished drum or container. This focus on direct manufacturing reduces risk of counterfeiting or quality drift. Each lot that leaves our site responds to customer feedback, regulatory changes, or new technical challenges, not marketplace trends set by traders with no ties to the chemistry itself. For long-term end-users in pharma and agrichemicals, this direct relationship means issues can be resolved with someone who controls the process.

    Production Bottlenecks and How We Overcome Them

    Peak demand for MATC tends to hit unpredictably, especially as new crop protection products or drug candidates pass key milestones. We keep a pipeline of intermediate stock and calibrated reactor capacity to avoid long lead times. Past experience showed that waiting for partner suppliers of hydrazine or related triazole precursors increased our risk. Now, dedicated storage of these sensitive reagents, combined with more robust procurement contracts, steadies our in-house workflow. By rebuilding our filtration and drying equipment, we eliminated bottlenecks tied to seasonal humidity swings, a common problem among other suppliers who buy finished material offshore. This responsiveness has helped our clients seize commercial opportunities with less time pressure.

    Environmental Impact and Sustainable Choices

    Environmental responsibility is not a slogan for us; it’s a process woven into every equipment upgrade and technical evaluation. During MATC synthesis, solvent choice can mean the difference between effective isolation and burdensome waste streams. Our team continually trials alternative mother liquors and phase-separation methods to drive down emissions and water use. Several years ago, we replaced a routinely used chlorinated solvent with a lower-toxicity option, reducing overall hazardous waste output per ton by over 35%. In our effluent plant, process engineers run regular checks for triazole breakdown products, ensuring our discharge does not impact local ecosystems. Persistent scrutiny and regular third-party audits let customers with sustainability mandates trust the real impact of their supply.

    Operational Experience Shaping Product Quality

    Much of what makes a consistent MATC product comes down to people, not just process diagrams. Operators working the reactors catch early signs of color change or failed crystallization before QA ever takes a sample. Over the years, we’ve learned that investing in technician training pays dividends in product quality and equipment uptime. A strong safety culture also keeps both people and product protected. For instance, advice from shift supervisors led to tray dryer design changes that almost eliminated particle size outliers, reducing downstream sieving needs at customer plants. This synergy between technical skill and practical know-how can’t be replaced by automation alone.

    Market Challenges and Meeting Customer Needs

    Raw material prices swing and regulations shift. Some argue it’s tough to guarantee a stable cost structure for specialty chemicals like Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate. Still, advanced demand planning and regular customer dialogue allow us to offer reliable quotes and on-time deliveries. The real margin for error comes from unplanned demand spikes, so we built buffer stocks and redundant QA testing into our workflow. Customers who struggled to get pharmaceutical-grade intermediates in the past have noted higher batch-to-batch consistency and faster onboarding to their projects, compared to resellers or brokers unable to validate their product’s origin.

    For international clients, gaining regulatory approval means full transparency. We provide supporting documents, shipment samples, and regulatory data packages—not just generic paperwork, but timely responses that incorporate the latest changes in local or international statutes. Our attention to these requirements keeps projects moving forward even in complex compliance environments.

    Practical Uses Driving Continued Demand

    The unique structure of this molecule opens up practical applications beyond high-profile pharmaceuticals. In specialty agrochemical development, MATC fits new modes of action that target resistant weed strains. Its efficacy as a precursor in custom intermediates also supports crop protection pipelines facing rapidly mutating pests. In advanced polymer science, companies have used it to introduce controlled nitrogen content and polar functionalities into their backbones, improving thermal or chemical resistance.

    Downstream researchers see the benefits during late-stage derivatization. Skilled synthetic chemists exploit the methyl ester’s reactivity, which tolerates a variety of catalytic or base-driven conditions. In one example, a university research group developed a novel anti-cancer agent using MATC as the key starting material. Process safety and high yield in amidation steps owes much to the compound’s clean leaving group and selective amino functionality.

    Learning from Feedback and Continuous Improvement

    True to our manufacturing roots, we rely on direct dialogue with customers for both incremental and breakthrough process improvements. Chemists on the client side often propose tighter impurity limits, and we respond by reworking separation steps or retraining analytical staff. Feedback after on-site technical visits or product-use trials feeds directly into batch record reviews, so every request pushes us closer to the ideal product profile. No third-party distributor has a closer connection to these ongoing refinements, and this cycle of critique and improvement has raised the bar for specialty triazoles coming out of our facility.

    Conclusion: Building Confidence, Not Just Molecules

    Supplying Methyl 5-Amino-1H-1,2,4-Triazole-3-Carboxylate comes with responsibility—all the way from sourcing, through synthesis, to delivery into demanding hands. Our team treats every order as a reflection of decades-long investment in both chemistry and customer trust. Knowing both the technical and practical challenges that can emerge at any stage, we serve not just as suppliers but as partners dedicated to making each client’s workflow smoother, more reliable, and ready for the next breakthrough. The promises we make are anchored in direct experience and constant refinement—not just theory, and never just words.