Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Ethyl Tetrazole-5-Carboxylate

    • Product Name Ethyl Tetrazole-5-Carboxylate
    • Alias Ethyl 5-tetrazolecarboxylate
    • Einecs 415-730-8
    • 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
    VTB
    Specifications

    HS Code

    521518

    Chemical Name Ethyl Tetrazole-5-Carboxylate
    Cas Number 3524-67-0
    Molecular Formula C4H6N4O2
    Molecular Weight 142.12 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 130-134°C
    Solubility Soluble in polar organic solvents (e.g., methanol, ethanol)
    Density 1.54 g/cm³ (estimated)
    Purity Typically ≥98%
    Smiles CCOC(=O)c1nnn[nH]1
    Inchi InChI=1S/C4H6N4O2/c1-2-10-4(9)3-5-6-7-8-3/h1-2H2,(H,5,6,7,8)
    Synonyms 5-Carboxyethyl Tetrazole, Ethyl 1H-tetrazole-5-carboxylate

    As an accredited Ethyl Tetrazole-5-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl Tetrazole-5-Carboxylate is supplied in a 25g amber glass bottle with tamper-evident cap and detailed chemical labeling.
    Shipping Ethyl Tetrazole-5-Carboxylate is shipped in tightly sealed containers to protect it from moisture and contamination. It is typically packed in compliance with relevant hazardous material regulations, labeled appropriately, and transported at ambient temperature. Handling and shipping must follow local and international chemical safety guidelines to ensure safe delivery and storage.
    Storage Ethyl Tetrazole-5-Carboxylate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizing agents. Protect from moisture and direct sunlight. Recommended storage temperature is 2–8°C (refrigerator). Always handle with appropriate personal protective equipment to prevent skin and eye contact.
    Application of Ethyl Tetrazole-5-Carboxylate

    Applications of Ethyl Tetrazole-5-Carboxylate in Industrial Manufacturing

    Ethyl Tetrazole-5-Carboxylate serves as a critical intermediate in several specialized chemical production chains. As a manufacturer, we supply this material to established downstream sectors, supporting precise formulation and strict regulatory adherence in pharmaceuticals, agricultural actives, advanced materials, electronic chemicals, and custom synthesis operations. Below are key industrial application scenarios with in-depth manufacturing details.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    This material forms a core building block in pharmaceutical manufacturing, especially in tetrazole-containing API synthesis such as angiotensin II receptor blockers and certain oncology drugs. Regulatory and formulation precision is required, with strict in-process controls to ensure final product purity. Our direct material integration supports multi-step organic processes where tetrazole ring integrity critically determines pharmacological activity. Handling and environment meet stringent cGMP requirements for human therapeutic manufacture in regulated markets.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP–NF, EP, JP Pharmacopoeias (for final API)
    • EMA and US FDA API registration requirements
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Mol ratios: 1.0 eq vs. coupling partner (varies by specific API route)
    • Typically 3–7% w/w of total synthetic mass in step inclusion
    • Usage may adjust ±10% based on yield optimizations and impurity profile controls

    Downstream process integration

    • Introduced during heterocycle formation in the core API structure assembly
    • Coupling with alkyl, aryl, or acyl functionalized reagents
    • Solvent phase or solid-phase synthesis compatible (DMF, DMSO, or green solvents as per process design)
    • Subject to in-process purity confirmation via HPLC/GC analysis

    Final product types

    • Losartan Potassium API
    • Candesartan cilexetil API
    • Olmesartan medoxomil API
    • Custom clinical candidate APIs containing tetrazole substructures

    2. Agrochemical Intermediate Production

    Main downstream users in the agrochemical sector apply this raw material for constructing heterocyclic moieties in herbicides, insecticides, and select fungicides. It enables yield improvement agents designed for targeted biochemical mechanisms in modern crop protection. Its application requires careful batch verification and adaptation to increasingly strict food safety regulations, mandating trace contaminant controls and full-process documentation to assure end product compliance.

    Industry compliance standards

    • FAO and WHO Specifications for Plant Protection Products
    • ISO 9001 Quality Management Systems
    • REACH Regulation (EC 1907/2006) for intermediates
    • National food residue MRL standards (e.g., EPA, EFSA)

    Typical usage ratio

    • 1.1–1.5 eq. against reactive partner in crop protection active synthesis
    • Typically 4–12% w/w in finished technical-grade agrochemical intermediates
    • Adjusted for conversion efficiency and downstream impurity risk reduction

    Downstream process integration

    • Integrated during key coupling or cyclization stages in heterocycle formation
    • Used as a direct precursor to triazolopyrimidine or similar actives
    • Combined with halogenating or oxidizing agents as per molecule blueprint
    • QC samples drawn at transformative steps for NMR and LC-MS control

    Final product types

    • Sulfonylurea herbicide intermediates
    • Tetrazole-derived crop protection actives
    • Custom insecticidal research compounds
    • Pre-cursors for environmental fate studies in regulatory approval

    3. Advanced Material Synthesis for Energetic Compounds

    Manufacturers in the high-performance explosives and propellants sector incorporate this tetrazole derivative during formulation of next-generation energetic materials. It acts as a source of high-nitrogen content moieties for improved stability and energetic output, meeting international regulations for handling and environmental impact. The use of this raw material occurs under controlled, license-specific conditions with detail to energetic safety and quality traceability.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods (Orange Book)
    • US ATF Explosives Regulatory Requirements
    • EN 13631 Standards – Explosives for Civil Uses
    • ISO 17025 Accredited Laboratory Testing

    Typical usage ratio

    • 2–6% w/w as energetic-building fragment in main charge or primer formulation
    • Exact dosage adapted for target velocity of detonation and thermal properties
    • Process optimization based on sensitivity and environmental assessment

    Downstream process integration

    • Reacted via condensation or substitution reactions with energetic binders or plasticizers
    • Functionalized prior to melt-pour, cast-cure, or compressed powder formation
    • Monitored for nitrogen release and compatibility in OT & RT thermal cycling tests
    • Requires temperature-controlled additions to minimize hazard risk

    Final product types

    • High-performance detonators and initiators
    • Gas-generator propellant grains
    • Laboratory reference explosives for sensitivity studies
    • Novel insensitive munitions (IM) candidates

    4. Electronic and Functional Material Precursor

    This compound is essential in the synthesis of specialty polymers and functional materials for the electronics sector. It supports precision formation of tetrazole-based ligands used in conductive polymer backbones and high-performance coatings for circuit boards. End users demand trace metal control, ultra-high purity, and real-time analytical traceability across the entire batch.

    Industry compliance standards

    • RoHS and REACH regulations for electronic chemicals
    • IEC 62474 Material Declaration Standard
    • IPC-4101 Laminate and Prepreg Specification
    • ISO 14001 Environmental Management

    Typical usage ratio

    • 0.5–3 mol% in functional monomer mix for specialty polymers
    • 0.2–6% w/w in final resin solutions for printed circuit board coatings
    • Adapted to achieve specific dielectric constant and conductivity characteristics

    Downstream process integration

    • Dissolved and reacted during monomer solution preparation for polymerization
    • Introduced pre- or post-functionalization for ligand crosslinking or surface treatments
    • Blended in controlled atmosphere to minimize oxidation and impurity intrusion
    • Monitored for residual solvents by headspace GC

    Final product types

    • Conductive polymer films for flexible displays
    • High-durability PCB protective coatings
    • Functionalized resins for microelectronic encapsulation
    • Specialty adhesives for electronic assembly

    5. Custom Chemical Synthesis and Contract Manufacturing

    Our direct industrial clients use this material for custom intermediate generation in contract and toll chemical synthesis. These projects often demand precise adaptation of reaction parameters and detailed batch certification, supporting early-stage pharmaceutical, agrochemical, and material science programs. Each campaign meets end-user IP protection, secure logistics, and strict chain-of-custody documentation as defined by international contracts.

    Industry compliance standards

    • ISO 9001 and ISO 14001 Management Systems
    • Confidentiality and data integrity under CMO/CDMO Good Practice Protocols
    • Client-specified regulatory audits (e.g., US FDA, ECHA, MOH)
    • GMP or ISO 13485 for medical and diagnostic intermediates

    Typical usage ratio

    • Usage specified by client-provided synthetic route, typically 0.5–10% w/w depending on complexity
    • Adjustment based on target compound yield, batch size, and risk assessment
    • Excess may allow for pilot plant scale-up and analytical validation

    Downstream process integration

    • Material charged at the initial step for core heterocycle assembly or as a functionalization agent in multi-step pathways
    • Documentation includes batch genealogy and in-line analytical snapshots for every critical control point
    • Integration in pressure reactors or continuous flow equipment as per project scope
    • End-to-end quality review with release against customer specifications

    Final product types

    • Custom heterocyclic intermediates for clinical or field trial supply
    • Elaborated tetrazole structures for lead optimization in drug/agro discovery
    • Spec-defined specialty materials for advanced diagnostics
    • Intermediate feedstock for further fine chemical processing
    Free Quote

    Competitive Ethyl Tetrazole-5-Carboxylate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing Ethyl Tetrazole-5-Carboxylate: A Chemist's Take from the Factory Floor

    Behind the Reactor Doors: Daily Experience with Ethyl Tetrazole-5-Carboxylate

    Inside our plant, Ethyl Tetrazole-5-Carboxylate stands as a specialty that drew its value from the demands of precision chemistry. Each batch leaves the reactors after a journey of stringent controls, but our commitment to consistency starts long before raw materials hit the mixing tanks. Chemists watch every thermal cycle and pressure change, knowing this compound—sometimes written as 5-Ethoxycarbonyl-1H-tetrazole—isn’t just another chemical in the toolbox. Processing comes down to the details: water content, color, residual solvent, and spectra integrity. Without these, the downstream jobs—mainly in pharmaceutical intermediate synthesis—hit trouble. Nobody working with exotic azoles simply hopes quality falls into place. Instead, we hit targets because we trace every deviation, regularly refusing to release a lot that falls even slightly outside the mark.

    Over the past several years, our crew watched Ethyl Tetrazole-5-Carboxylate rise in demand as research arms chase next-generation medicines and high-value intermediates. Researchers need tight controls on every impurity, demanding that our separation and drying teams pay attention to every step. You hear older operators say the raw odor of a batch still tells stories—hints about cooling rates or unreacted starting material from far upstream. Those cues wind up in practical changes, and most improvements come from hands-on experience, not outside consultants or generic flowcharts. The tetrazoic core is touchy; if you get careless with moisture or pH, you risk rearrangements or ring-opening, which ruins yield and set purity. Consistency across years has built us a reputation for reliability that newcomers in the market struggle to match.

    Specifications: The ‘Why’ Behind the Numbers

    Specifications aren’t just pieces of paper in a folder. Consistently achieving a purity of 98% or greater took years of trial and error. Most buyers don’t appreciate the headaches from off-color product or minor contamination until a process grinds to a halt or patent deadlines loom. We focus on UV and HPLC purity because trace side-products sabotage high-throughput screens in pharmaceutical research. Even one percent impurity can trigger regulatory headaches or require extra purification down the line.

    Our typical batches of Ethyl Tetrazole-5-Carboxylate fall between off-white and very pale yellow crystals, sometimes a powder, depending on the final process steps. Moisture matters just as much as purity, since this molecule’s tendency to absorb water interferes during storage and in the first steps of coupling reactions. Standard residual moisture levels stay below 0.5%, measured by Karl Fischer titration. Each lot comes with its own chromatograms. NMR and mass spectrometry support all releases, since spectra drift signals deeper problems than a single number can show.

    Every time our team checks melting points, the story comes down to the same issue: functional groups on tetrazole rings don't always behave under heat. You don’t want premature decomposition, and lab accidents from unknown impurities cost more than any shortcut savings. Product leaves our plant only after a cascade of human checks, not just instrument printouts. Without hands-on review, years of know-how go to waste.

    Real-World Applications: Reputation Forged Through Results

    On the customer side, researchers in drug discovery and industrial process design look for performance, stability, and reliable lead times. This tetrazole derivative gets plenty of attention for its role in building angiotensin receptor blockers and several small-molecule candidates. Inside the plant, the attention lands on making sure each shipment lives up to the promise. Someone might use Ethyl Tetrazole-5-Carboxylate to link up with a carboxylic acid, spin up a protected amide, or move further into a heterocyclic core. Lab scientists want the same set of properties batch to batch. If the melting point drifts or the spectrum shows a ghost peak, trust erodes quickly, and we spend more time on phone calls and problem-solving than making product.

    We don’t just ship powder and hope for the best. Every repeat order from a major R&D house carries the unspoken warning: any slip in quality, and someone else gets the contract next year. This feedback loop made us focus even harder on stability tests, photostability, and the impact of packaging on long-haul shipments. Over the summers, metal drums heat up fast, but tanks inside our plant run under controlled nitrogen, with regular monitoring to pick up any slow hydrolysis or thermal stress. That’s no theoretical risk—one shipping document error offloaded a container three weeks late, and the sample on arrival had degraded, teaching us to follow temperature from factory to dock. Our partners in API development have noticed the improvement over time.

    From Synthesis to Purification: Lining Up Chemistry with Needs

    Ethyl Tetrazole-5-Carboxylate’s synthesis takes experience under pressure. Diazotization hazards and nitrogen outgassing are real. We keep emergency shutoffs and local ventilation running around the clock. Chlorinating agents and acidic precursors can throw a whole batch off if feed rates aren’t tightly managed. Early on, during pilot-scale development, we lost almost twenty percent of trial runs to misjudged additions or over-aggressive crystallization. Nobody working the reactors wants to see sludge or tar in a vessel, because cleanup puts production behind for days.

    Purification can be even trickier. Sometimes people think a few column runs guarantee clean product. Misjudging solvent ratios leads to streaky fractions, and if water sneaks into the mix, the end result gets sticky and discolored. Once, a change in supplier for a minor component shifted the trace metal profile, and it took weeks to identify the cause behind later-stage HPLC ghosting. This commitment to chasing down all root causes has become second nature among our staff, and we always involve the team from the lab who built the original process.

    Comparison: Ethyl Tetrazole-5-Carboxylate and Its Siblings

    Other tetrazole derivatives sometimes offer easier handling or less moisture uptake. Methyl or sodium tetrazole carboxylates appear similar on paper, but in hands-on work, the ethyl form outperforms in coupling reactions with sensitive amino acids and protected groups. Maybe less obvious, but crystal form and solubility profiles in major organic solvents push more customers toward the ethyl derivative. Our own process research supports that observation; we saw higher yields in solvent-based reactions and longer shelf life compared to closely related analogues.

    Some buyers ask about cost comparison with methyl or sodium salts, believing cheaper precursors offset risks. Our experience proves cost savings vanish with every failed batch or stuck filter. The ethyl ester provides a balanced reactivity, letting chemists switch between hydrolysis or direct coupling as their process demands without major rework. Sodium salts often face clumping and harbor trace sodium that can poison metal catalysts. The ethyl form’s only real competitor comes from bespoke custom-made derivatives, which lack the data and track record that years of commercial-scale manufacturing bring.

    Our storage containers rarely develop pressure build-up, compared to other tetrazole-based reagents. That’s important for customers running longer campaigns, as it means less worrying about container ruptures or unplanned downtime. In practice, feedback always flows back to us about which variant runs cleanest, and Ethyl Tetrazole-5-Carboxylate commands repeat demand because it supports higher throughput in both pharma discovery and commercial pilot plants.

    Tighter Process, Fewer Surprises: Minimizing Batch-to-Batch Variation

    Dealing with heterocyclic carboxylates means unexpected things crop up—batch variation, tank fouling, even unusual odors point toward minor side reactions. Back when our facility ran older reactor suites, every week delivered some strange off-note. We started rigorous root-cause checks—tracking batch logs, monitoring subtle color shifts, and developing more reliable in-line sensors. This investment changed the way the plant runs. Today, not much goes unnoticed. Operators spot a misplaced seal or temperature drift before a whole week’s worth of production gets tossed out.

    Direct ties to the pilot team make a difference. Recipes aren’t treated as static; adjustments happen, whether in how quickly to ramp a jacket or bring in a feed. If wastewater benches report foaming or new odors, process tweaks follow. In the long run, these habits translate to measurable success—not just in quality numbers, but in customer loyalty.

    Customer Success Stories: Research Innovation Driven by Consistent Supply

    One story comes to mind from a customer scaling up an advanced intermediate for a cardiovascular candidate. Initial gram-scale work proved simple, but moving to pilot-plant quantities exposed vulnerability to micro-impurities, especially in coupling stages. Early batches stalled, and the culprit traced back to trace-level salts missed by less-sensitive detection. After working together to set new baseline specs and implement more granular purification, we both won: our customer kept timelines, and our team turned the learning into better production practice.

    Another example found a generics developer fighting process drift during the crucial amidation step. Using an alternate raw material led to consistency issues and longer cycle times, with staff working overtime to troubleshoot. Once they switched back to our ethyl-based material—produced using tighter in-process controls—batch success rates climbed, and rework costs plummeted. These aren’t isolated cases; over years, similar feedback led us to fine-tune both our process and the way we communicate openly when things go wrong.

    Sustainability in Manufacturing: Live Concerns, Not Marketing Spin

    Most green-chemistry advancements get over-hyped. In our factory, efforts focus on real outcomes. Operators invested in solvent recycling and waste heat capture only after seeing annual energy bills and stricter government rules. For Ethyl Tetrazole-5-Carboxylate, this meant upgrading our distillation train to minimize solvent loss and tighten waste streams. Teams review every ton of material in and out, since hazardous streams can’t just be flushed into municipal systems.

    We switched to a closed-loop water-cooling system last year, which paid off in lower costs and less risk of process contamination. Clean-in-place systems now run after every major batch—yes, it takes longer to prep for the next job, but it keeps contaminants out of subsequent runs. The team feels the daily pain of skipping steps; faster turnaround looks tempting, but the risk of cross-contaminated lots isn’t worth it.

    Keeping nitrogen use efficient, maintaining physical barriers between production lines, and investing in analytical tools all require cash and patience. Any shortcut gets exposed either by regulatory auditors or by angry downstream partners. So we do the work up front and train newcomers until old hands see them as trustworthy. Every short-term fix tends to boomerang, and repeat issues almost always land heavier on cost and team morale.

    Regulatory Pressures and Analytical Accountability

    Nobody operating on the manufacturing floor ignores the reach of global regulation. To ship Ethyl Tetrazole-5-Carboxylate to mainstream syntheses, pharma teams demand audit trails, chain-of-custody documents, and proof of certificate traceability. We don’t play games with data integrity; backup servers and locked archives hold every baseline reading, and management audits each shift’s paperwork. Our team keeps hard copies and digital records aligned, knowing that internal reviewers check for any mismatch.

    Trained analysts run QC checks rather than farm out validation work. That means routine batch-specific data, from FT-IR and NMR to multistep chromatographic profiles. We keep every standard updated, and senior chemists review methods whenever customers report unexpected results. Years back, a flagged batch taught us to build redundancy into the QC lab, since letting process drift slide even twice can land you on government watchlists or in patent trouble. This dedication to documentation lets downstream manufacturers avoid hold-ups months or years later.

    Challenges With Market Expectations: Lessons Learned

    Big-name customers ask for time-definite shipments, transparent documentation, and assurance they won’t face regulatory ‘black swans’ from trace impurities or storage irregularities. Teams remember the sting of rapid scale-up requirements, when new builds struggled with raw material bottlenecks or faster-than-expected drawdown rates. Calendar stress translates into live production risk; late deliveries or shorted orders cascade through whole project timelines.

    To avoid these problems, we built thicker inventory buffers and worked out tiered supply contracts for long-term accounts. Our empirical forecasting benefits from direct client feedback, not wild guesses about seasonal surges. No third-party logistics platform replaces historical records showing which months run hottest for urgent API requests.

    Overestimating how easy it is to make ultra-pure specialty chemicals remains one of the industry’s main pitfalls. Short-term marginal players may price low without the overhead of documentation, traceability, or retraining. They disappear fast after one or two problem batches. Real manufacturers don’t get to vanish after a slip-up; we live with every error, fix it, and let every subsequent customer benefit from the fix.

    Future Growth: Experience Teaches, Not Trend Reports

    In the world of tetrazole chemistry, innovation rarely arrives from business-school reports. Instead, day-to-day work with real-time feedback drives improvements. We hear often from researchers chasing more elaborate transformations or trying to speed up synthetic steps with fewer side-products. Proposals for new derivatives or downstream intermediates come up all the time, and our staff welcomes technical discussions on synthesis optimization and analytical support.

    Every alteration in reaction conditions gets debated closely: should we shift to continuous-flow? Is a solvent switch justified by measurable yield or safety gain? These aren’t hypothetical issues for us—they determine how well we can supply future demand, cut waste, and hold the trust of companies betting their next big patent on a reliable supply of Ethyl Tetrazole-5-Carboxylate. Versatility is less a marketing slogan and more an earned result of gradual, sometimes painful, progress in process parameters and analytical methods.

    Every Batch, An Ongoing Puzzle

    People on the outside see bags or drums and imagine uniformity. Each container reflects dozens of choices made across weeks: whether to run at a slightly lower temperature, dose reagents in a tighter window, or extend drying time an hour more. No single solution guarantees perfection, and that’s why new hires spend months pairing up with experienced hands before running a reactor or packing product. Mistakes get logged and solutions traded across generations.

    Ethyl Tetrazole-5-Carboxylate stands as a story of trial, error, and the pursuit of reliable synthesis under real-world conditions. Our hands-on focus shows in the pride we take, the relentless tweaking of parameters, and the mutual respect that grows between plant workers and the distant researchers relying on a steady supply of a single specialty chemical. Every lot tells a story, and every improvement starts with a problem someone cared enough to solve.