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Ethyl Pyrrole-2-Carboxylate

    • Product Name Ethyl Pyrrole-2-Carboxylate
    • Alias Ethyl 1H-pyrrole-2-carboxylate
    • Einecs 220-962-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    571621

    Cas Number 1071-97-2
    Molecular Formula C7H9NO2
    Molecular Weight 139.15 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 108-110°C at 19 mmHg
    Density 1.101 g/cm³ at 25°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Refractive Index 1.519-1.521
    Flash Point 94°C
    Purity Typically ≥ 98%
    Synonyms Ethyl 1H-pyrrole-2-carboxylate
    Smiles CCOC(=O)C1=CC=CN1
    Storage Temperature Store at 2-8°C, protect from light
    Uses Intermediate in organic synthesis

    As an accredited Ethyl Pyrrole-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl Pyrrole-2-Carboxylate is supplied in a 100g amber glass bottle with a secure screw cap, labelled with hazard information.
    Shipping **Shipping Description for Ethyl Pyrrole-2-Carboxylate:** Ethyl Pyrrole-2-Carboxylate is shipped in tightly sealed containers, protected from light and moisture. It should be handled in accordance with local, national, and international transport regulations, typically shipped as a chemical substance in compliance with applicable UN and DOT guidelines. Keep away from strong oxidizers during transit.
    Storage Ethyl Pyrrole-2-Carboxylate should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to heat, moisture, and direct sunlight. Handle under an inert atmosphere, such as nitrogen or argon, if highly sensitive. Ensure proper labeling and follow local regulations for hazardous chemicals.
    Application of Ethyl Pyrrole-2-Carboxylate

    Applications of Ethyl Pyrrole-2-Carboxylate in Industrial Manufacturing

    Ethyl Pyrrole-2-Carboxylate serves as a specialized intermediate across several chemical sectors. Its defined reactivity and pyrrole moiety position it in advanced synthesis lines for pharmaceuticals, agrochemicals, specialty aroma compounds, and material science applications. Below are the principal downstream scenarios our manufacturing customers employ this intermediate within large-scale operations.

    1. Pharmaceutical Intermediates for Antifungal and Anti-inflammatory APIs

    Our customers in active pharmaceutical ingredient (API) synthesis utilize Ethyl Pyrrole-2-Carboxylate as a crucial building block in multi-step reactions for antifungal and anti-inflammatory drug substances. Its unique ester functionality reacts under controlled conditions to yield specific heterocyclic compounds integral to the pharmaceutical compound backbone. Integration mostly occurs in condensed-phase condensation or amidation reactions, followed by strict purification steps. End users demand narrow quality metrics for the absence of non-pyrrolic byproducts to ensure the safety and efficacy of the resulting medicines.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary)
    • EU GMP (EudraLex Volume 4 Part II)
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • Used at 0.05–0.15 molar equivalents depending on synthetic route and yield requirements
    • Adjustments based on batch sizes from pilot to commercial scale

    Downstream process integration

    • Introduced at the intermediate condensation or esterification step
    • Purification and QC sampling align with GMP in-process controls

    Final product types

    • Itraconazole intermediates
    • Non-steroidal anti-inflammatory drug (NSAID) heterocycles
    • Advanced pyrrole-based pharmaceutical actives

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    Industrial agrochemical manufacturers regularly introduce Ethyl Pyrrole-2-Carboxylate within their fine chemical divisions to obtain substituted pyrrole rings used as core scaffolds in herbicide and fungicide molecule synthesis. Controlled reaction conditions—particularly during acylation, hydrogenation, or ring modification—are imposed to maintain functional group integrity. End products undergo dedicated downstream isolation to meet stringent residue and environmental profiles.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticides)
    • REACH (EC Regulation 1907/2006) Chemical Safety Assessment
    • ISO 9001:2015 for quality management in agrochemical manufacturing

    Typical usage ratio

    • Usually applied at 2–7% by weight of the active ingredient synthesis batch
    • Adjusted in stepwise reactions depending on conversion and downstream derivatization

    Downstream process integration

    • Enters early-stage nucleophilic substitution or cyclization phases
    • Subject to in-process monitoring for structural verification

    Final product types

    • Pyrrole-based triazole herbicides
    • New-generation fungicidal scaffolds
    • Custom fine chemical intermediates for crop protection

    3. Aroma Compound Manufacture (Flavor & Fragrance)

    Flavor and fragrance compound formulators value Ethyl Pyrrole-2-Carboxylate as a precursor to complex aroma molecules which impart signature roasted, nutty, or savory notes in high-value food and perfumery formulations. Industrial processes involve controlled hydrolysis or further esterification, closely monitored to prevent off-taste generation. These sensitive applications require certification under food-grade standards and continuous analysis for volatile organic compound impurities.

    Industry compliance standards

    • FCC (Food Chemicals Codex) specifications
    • ISO 22000:2018 (Food Safety Management Systems)
    • 24 CFR 582 (Food additives: flavoring agents and adjuvants)
    • IFRA Standards (International Fragrance Association)

    Typical usage ratio

    • Flavor compositions: up to 0.5% of final formulation, depending on intensity targets
    • Fragrance intermediates: typically 0.1–0.3% in concentrated bases

    Downstream process integration

    • Undergoes initial hydrolysis or reduction step prior to aroma development
    • Inline GC-MS monitoring for batch consistency

    Final product types

    • Maillard reaction flavors
    • Nutty fragrance accord bases
    • Roasted flavor enhancers for food processing

    4. Advanced Materials and Organic Electronic Precursors

    Producers in specialty materials and organic electronics integrate Ethyl Pyrrole-2-Carboxylate to functionalize π-conjugated polymers, supplying monomer units for organic field-effect transistors (OFETs) and conductive coatings. The compound’s structure allows downstream selective substitution, providing tunable electronic properties and oxidative stability. Reactors maintain strict atmosphere and temperature control throughout the coupling and polymerization steps, with high-purity batch QC standards tracked from monomer preparation to device-grade material production.

    Industry compliance standards

    • ISO 9001:2015 for material traceability and quality management
    • RoHS Directive (EU Restriction of Hazardous Substances in electronics)
    • IEC 62660 (Battery and device component standards)
    • ASTM D6288 for purity in organic electronic materials

    Typical usage ratio

    • Monomer feed: 5–20 mol% in polymerization mixtures
    • Optimized through pre-formulation R&D for intended conductivity or device application

    Downstream process integration

    • Fed into Grignard coupling, Stille, or Suzuki-Miyaura polymerizations
    • Followed by purification for device fabrication

    Final product types

    • Pyrrole-modified polymers for OFETs
    • Conductive organic coatings
    • Functionalized electronic ink precursors
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    Certification & Compliance
    More Introduction

    Ethyl Pyrrole-2-Carboxylate: Bringing Precision to Fine Chemical Synthesis

    Decades of Insight into Pyrrole-Derived Chemistry

    Ethyl Pyrrole-2-Carboxylate offers a rare precision and consistency in a field where minor deviations can make or break downstream syntheses. Over years of direct chemical production experience, certain molecules have gained importance for their transformative effect on pharmaceutical, agrochemical, aroma, and material science projects. This ester, with its white to pale brown crystalline or oily appearance and subtle chocolate-like odor, proves vital each time a synthesis demands both integrity and reactivity. Drawing from countless in-process controls, I can say consistency in pyrrole chemistry only answers to intense process monitoring, fine-tuned purification, and a practiced understanding of real-world impacts on batch yield.

    Our Standard: Model, Purity, and Batch Integrity

    Across our manufacturing lines, Ethyl Pyrrole-2-Carboxylate emerges from carefully selected pyrrole and controlled esterification routes. Typical batches exhibit purities exceeding 98%, a benchmark maintained not just for compliance but also for reliability in end-use. By employing solvent systems that cut down side reactions and refining distillation protocols, we address the nagging risk of residual starting materials or unknown byproducts. Appearance metrics – color, clarity, odor – receive continuous attention, since even minor contamination can cause downstream issues for pharmaceutical intermediates. With years spent scrutinizing each variable in commercial batches, my team remains focused on repeatable production at the scale our customer base expects from a manufacturer, not a distributor or broker.

    Why Chemists Keep Asking for Pyrrole Esters

    Requests for Ethyl Pyrrole-2-Carboxylate come not out of tradition, but out of necessity. Medicinal chemists see it as a solid building block for a wide stretch of nitrogen heterocycle drugs: anticonvulsants, antivirals, even high-potential kinase inhibitors. Its ester group introduces just the right protection and synthetic flexibility to push complex molecules through multi-step syntheses. Agrochemical teams favor it for years of confirmed performance in selective fungicides and insecticides targeting leaf blight and rust. In fragrance manufacture, its warm, cocoa-like aroma and easy handling expand flavor profiles for bakery, candy, and specialty liquor clients. Enzyme and material scientists tell me that ethyl esters outcompete methyl esters by offering better solubility in common organic solvents and a better fit with downstream functionalization steps.

    Why In-House Production Beats Outside Sourcing

    As a manufacturer, I build process knowledge that resellers often overlook. Roots in raw material handling control both cost and fate of the entire lot. Small changes in pyrrole source or acid catalyst suppliers shift the impurity profile in ways invisible to quick in/out testers. Downstream, the absence of carrier solvents eliminates the future headaches of forced solvent evaporation or contamination during critical synthetic steps. Only hands-on scaling – like maintaining sub-atmospheric pressures in purification or swapping out glassware material for high-sensitivity batches – keeps real consistency batch after batch. Third-party brokers might offer a document stating specification, but daily production has taught me that purity is dynamic, not static. So, customers return for the lived experience rather than the shelf promise.

    Tuning Reaction Conditions: Practical Advantages in Synthesis

    Ethyl Pyrrole-2-Carboxylate supports bold choices in synthetic design. Many medicinal projects demand mild hydrolysis or transesterification; the ethyl group cleanly departs under basic or acidic conditions, yet remains stable under moderate pHs, allowing for greater flexibility in multistep routes. Compare this with methyl analogs, which in my experience display higher volatility and occasionally unwanted byproducts under scaled-up hydrolysis. Our compound’s slightly higher boiling point lets process engineers hold tighter temperature controls, especially during rotary evaporation or vacuum transfer. This reduces the odds of accidental tube blockage or yield drops from premature evaporation – lessons learned not from data sheets but from cleaning up equipment after years of trial.

    Batch Testing and Traceability for Regulatory Confidence

    Direct manufacturing brings an obligation to each customer: the assurance that every bottle and drum comes traced back to a lot number with full analytical data. Each batch undergoes GC-MS, HPLC, and Karl Fischer titration to flag anomalies before single grams ever reach client labs. Decades of compliance cycles, audits, and technical root cause analyses have taught me that true regulatory confidence does not come from a specification certificate alone. It’s built in shared method validation, reproducible impurity fingerprinting, and the willingness to adjust process variables rather than just hiding behind COAs.

    Customer Applications Across the Spectrum

    Pharmaceutical researchers tell us they count on repeatable, high-purity pyrrole esters for developing new prodrugs, linking groups, and CNS-active scaffolds. Agrochemical innovators use our product in the synthesis of active pyrrole carboxylate core fungicides where impurity level can tip the balance from active to failed field test. In the food industry, top flavors and fragrance houses keep coming back because our ester delivers nuanced chocolate and nutty notes – something not easily replicated by analogues or less consistent bulk sources. Material science groups build conducting polymers and OLED layers with its help, finding its intermediate polarity lends flexibility to solvent choice and doping agent integration.

    Direct Comparisons: Ethyl vs. Methyl and Other Esters

    Years examining the performance of various pyrrole esters have documented a few points of divergence. Methyl Pyrrole-2-Carboxylate, often more volatile, brings greater risk of workplace exposure and can create a harsher hydrolytic environment, sometimes damaging sensitive functional groups. The ethyl ester, by contrast, handles better in open-batch workspaces, stays stable at slightly higher temperatures, and offers a slower, more predictable cleavage – critical for controlled-release drug candidates and responsive agrochemicals. Bulkier esters, like isopropyl or t-butyl, face solubility and steric hurdles and usually cost more, both in starting material and downstream protections. Ethyl consistently rides the sweet spot: fast enough reaction kinetics, coupled with easy isolation, and price efficiency over substitutions.

    No Substitute for In-Process Knowhow

    Pure chemical syntheses rarely follow a single textbook formula. Unexpected byproducts, small impurity carryovers, and batch-to-batch nuances often pop up during scale-up. Hundreds of runs have shown me that the right adjustments – whether to pH drift during esterification, temperature plateaus in purification, or even subtle shifts in pyrrole color before addition – distinguish high-grade product from mediocre. Simplistic sourcing misreads the value of seasoned process observation and adaptation. At our plant, it’s not uncommon for a chemist to halt a reactor mid-run, draw a slick of the intermediate, and tweak the addition rate hours ahead of what QC would flag. These unquantifiable, field-forged reflexes deliver quality beyond what labels and paperwork ever could.

    Real-World Storage and Handling

    Clients use our Ethyl Pyrrole-2-Carboxylate with confidence because experience has shown it remains robust under ordinary storage and bench-top handling. Years spent tracing stability in warehouses and under variable temperatures prove this product resists slow hydrolysis and discoloration if kept sealed, cool, and shielded from light. Water activity must be kept low; otherwise, minor hydrolysis leads to free pyrrole and acid, skewing reactions and reducing shelf-life. Rather than offering abstract guidelines, I recommend airtight containers, clear labeling, and regular inventory turnover based on actual storage data. Overexposure to open air in production rooms sometimes leaves the characteristic chocolate scent hanging long after the drum leaves, so short transfer lines and efficient ventilation make all the difference.

    Optimizing Scale-Up: Lessons from the Line

    Scale brings its own set of challenges. Early runs at bench scale rarely predict heat load, mixing efficiency, or side-product buildup on jacketed reactors. I recall several initial production batches where modest exothermic release, ignored at flask scale, threatened to overshoot safety limits at kilo scale. Only after adapting stirring speeds, refining cooling profiles, and retraining staff on real-time trend spotting did stable, repeatable, high-quality output follow. Since then, scale-up protocols have centered on integrating live process data, not relying on static one-time reports. We have invested in plant historian databases that allow retrospective tracking – each adjustment, spike, or pause in production mapped over years.

    Supporting Sustainable Chemistry

    Sustainability remains an ongoing commitment in pyrrole chemistry. Our process optimization has allowed us to switch from high-waste legacy acid catalysis to near-quantitative greener catalytic systems that cut solvent and water use, cut single-pass waste, and rollback overall VOC emissions. By recovering excess alcohol for chemical feedstock rather than flaring or dumping, we see real reductions both in waste bill and public reporting. Purification adopts closed-loop solvent recycling wherever possible, ensuring client projects meet rising regulator and stakeholder expectations for green chemistry. This isn’t just for show; it keeps product price, quality, and lead time stable in uncertain supply markets.

    Troubleshooting: What Experience Taught Us

    Unexpected issues in chemical manufacture test every improvement plan. Once, a midwinter shipment lost potency from unnoticed condensation inside a reefer container. Only after backtracking distribution, measuring residual moisture, and overhauling cold chain protocols did the solution come clear. Another time, a competitor’s batch failed in a client’s critical synthesis when their broker cut corners on purification and supplied a solvent-heavy material in disguise. The fallout – halted project, lost time, regulatory headwinds – illustrates why seasoned control over every production stage guards against hidden risk. Over the years, these lessons drive each improvement in our protocols, empower faster client troubleshooting, and define trust between our teams and theirs.

    Collaboration Built on Transparency, Not Hype

    Ethyl Pyrrole-2-Carboxylate draws the attention of innovative teams because our production method, batch-level transparency, and willingness to share real process data set our supply apart from bulk market offers and generic resellers. Every inquiry gets a technically grounded answer, not sales filler. Analytical results, process outlines, and feedback from prior runs help clients integrate our product into increasingly complex syntheses. Our chemical team takes pride in handling even specialized requests – such as low-particulate filtration for polymer applications or freshly distilled lots for ultra-sensitive pharmaceutical work – without delay or pushback. This level of partnership stems from direct communication, rapid problem-solving, and the flex to adapt ongoing process improvements to new industry requirements.

    Looking Ahead: Investing in Next-Generation Pyrrole Chemistry

    The future of pyrrole derivatives lies in deeper integration with biocatalysis routes, greener technologies, and data-driven batch monitoring. We devote R&D to exploring enzyme-mediated transformations that could lower energy use, widen functional group compatibility, and boost selectivity beyond what classic acid-base chemistries allow. On the analytics front, advanced LC-MS fingerprinting and ongoing impurity profiling open pathways to even tighter specifications and earlier detection of batch drift. By combining hands-on plant experience with next-generation process technology, manufacturers gain the edge needed to support drug discovery, agricultural innovation, and advanced material design as requirements and regulations evolve.

    Conclusion: Experience Makes the Difference

    In the hands of chemists with years of manufacturing grit, Ethyl Pyrrole-2-Carboxylate does more than fill a supply chain gap; it builds a bridge between repeatable synthesis and new molecular frontiers. Confident application, rooted in day-to-day lessons, ensures that clients—from drug discovery pioneers to aroma designers—receive not just high-purity material but also reliable support, transparent guidance, and faster troubleshooting. For those building tomorrow’s molecular architectures, only first-hand manufacturer experience brings confidence that each batch will perform, every time.