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Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate

    • Product Name Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate
    • Alias 5-Methyl-2-Pyrrolecarboxylic acid ethyl ester
    • Einecs 681-055-6
    • 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

    402299

    Chemicalname Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate
    Molecularformula C8H11NO2
    Molecularweight 153.18 g/mol
    Casnumber 13191-15-6
    Appearance Colorless to pale yellow liquid
    Boilingpoint 265-267°C
    Density 1.09 g/cm3
    Solubility Soluble in organic solvents such as ethanol and chloroform
    Refractiveindex 1.523
    Purity Typically >97%
    Flashpoint 116°C

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

    Packing & Storage
    Packing Brown glass bottle, 25 grams, with tamper-evident cap; labeled with chemical name, CAS number, hazard pictograms, and manufacturer details.
    Shipping Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate is carefully packaged in sealed, chemical-resistant containers to prevent leakage and ensure stability during transport. The shipment is labeled according to relevant safety and regulatory guidelines, and is handled by certified carriers specializing in chemical logistics to ensure safe delivery under ambient conditions, avoiding direct sunlight and excessive heat.
    Storage Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store at room temperature in a cool, dry, well-ventilated area, and keep away from incompatible substances such as strong oxidizing agents. Label containers clearly, and ensure storage in compliance with relevant safety and chemical handling guidelines.
    Application of Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate

    Applications of Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate in Industrial Manufacturing

    Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate supports advanced product development in several specialized industries. As a direct manufacturer, we supply this pyrrole derivative to global firms for uses requiring controlled purity, precise synthesis, and reliable traceability across regulated downstream markets.

    1. API Intermediate for Pyrrole-Based Pharmaceuticals

    Many pharmaceutical companies use Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate as a key intermediate during multi-step syntheses of pyrrole-containing active pharmaceutical ingredients (APIs). It enters the route for antihypertensives and CNS agents where methyl-pyrrole motifs are essential. We support customers requiring material for schemes under full regulatory documentation, with consistently tight impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) per 21 CFR Parts 210/211 (USA)
    • European Pharmacopoeia (Ph. Eur.) excipient and API guidance
    • REACH registration for non-EU importers/production sites

    Typical usage ratio

    • 0.9–1.3 molar equivalents relative to the downstream API yield, depending on route; batch size scaling from multi-kilogram to multi-ton. Ratio fine-tuned based on targeted coupling efficiency and desired impurity threshold.

    Downstream process integration

    • Added at early N-alkylation or Friedel-Crafts acylation reaction stage
    • Subjected to controlled hydrolysis or further ring-functionalization steps under nitrogen
    • Requires in-process HPLC monitoring for impurity and conversion tracking
    • Material transfer managed in dedicated clean rooms to avoid cross-contamination

    Final product types

    • Antihypertensive agent APIs (e.g. analogs in the Losartan family)
    • CNS drug intermediates using methylpyrrole cores
    • Oncology research compounds involving heterocyclic structures
    • Pharmaceutical reference standards for method validation

    2. Crop Protection Synthesis: Herbicides and Insecticides

    Agrochemical synthesis workflows incorporate this compound as a pyrrole building block when designing target-specific herbicides and innovative insecticidal agents, especially where selectivity for resistant weed species is critical. Our QC processes address stringent limits for metal impurities and residual solvents.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System for raw material traceability
    • Regulation (EC) No 1107/2009 for Plant Protection Products in the EU
    • EPA 40 CFR Part 180 for pesticide chemical residues (USA)

    Typical usage ratio

    • 0.8–1.1 molar equivalents in actives synthesis, with further dilution in formulation to 5–25% active ingredient in end-user product; minor excess managed for recycling or reprocessing during scale-up

    Downstream process integration

    • Employed in cyclization or amide coupling steps for final active compound assembly
    • Integrated in inert solvent media under controlled pH and temperature
    • QC sampling performed at crude and pure isolate stages to confirm consistent yield and low by-product formation
    • Prepared in dust-controlled areas for operator safety and product purity

    Final product types

    • Selective herbicide actives for cereals and oilseeds
    • Systemic insecticidal formulations for cotton and horticulture
    • Nematicide actives for soil pathogen control
    • Original agrochemical lead compounds for regulatory study submission

    3. Fragrance and Flavor Ingredients Manufacturing

    Major aroma chemical producers utilize this pyrrole ester as a starting block in synthesizing aroma molecules and flavor enhancers, especially pyrazine and pyrrole derivatives found in roasted, nutty, or cocoa-like notes. Production lines require batch records and allergen declarations in accordance with global food and cosmetic regulations, alongside fully characterized residual solvent profiles.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Amendments
    • FEMA GRAS status for flavor ingredient safety assessment
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • Food Chemicals Codex (FCC) compliance on purity and contaminants

    Typical usage ratio

    • 0.05–0.5% in end flavor/aroma blends; intermediate synthesis yield optimization typically uses 1.0–1.2 equivalents of starting ester. Ratios are adjusted to minimize off-odor byproducts in specialty notes.

    Downstream process integration

    • Introduced at the heterocyclization or selective reduction stage, generating key odorant molecules
    • Processed in food-safe reactors; thorough cleaning validation ensures allergen cross-contact avoidance
    • Final distillation or crystallization monitored for flavor profile consistency
    • Formulation logs maintained for full traceability to product batches

    Final product types

    • Chocolate/cocoa aroma enhancers for confectionery
    • Roasted/nutty note creators for fine fragrance compositions
    • Complex savory or smoked flavors for culinary products
    • Flavored oils and beverage base concentrates

    4. Specialty Polymer Building Block

    Advanced polymer manufacturers integrate this compound into production lines for functional polymers and conductive materials, particularly in pyrrole-based oligomers and co-polymers used in sensors, antistatic coatings, and biomedical applications. We maintain consistent particle size, water content, and trace metals below 10 ppm to support sensitive downstream reactions.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • ISO 10993-5:2009 for cytotoxicity in biomedical polymers
    • ASTM D543 for chemical resistance testing of polymers
    • ISO 13485:2016 for medical device quality assurance (where relevant)

    Typical usage ratio

    • 5–15% by weight in functional polymerization reactions, adjusted based on chain length, conductivity target, and mechanical performance profile; excess further recovered in solvent extraction or recycling.

    Downstream process integration

    • Introduced during oxidative polymerization or co-polymerization stages with aniline or thiophene-based units
    • Dissolved or suspended for blend uniformity before catalyst addition
    • Inline monitoring controls viscosity parameters and conversion rates
    • Post-reaction washing and purification to remove low molecular weight fractions

    Final product types

    • Electroactive materials for sensor films
    • Antistatic and ESD protective coatings
    • Bio-compatible polymer scaffolds for tissue engineering
    • Specialty adhesives and functional binder components

    5. Fine Chemical Synthesis: Heterocyclic Research Intermediates

    Specialty chemical R&D and custom synthesis operations require this compound as a core heterocycle for developing novel research molecules, reference standards, and building blocks in combinatorial libraries. We guarantee full lot-specific traceability and can provide extended impurity profiling for regulated environments.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • GLP (Good Laboratory Practice) for research intermediates
    • REACH notification for lab-scale substance handling in the EU
    • Responsible Care® chemical stewardship principles

    Typical usage ratio

    • 0.8–1.5 equivalents per synthesis step, scaled to molecular diversity targets; small-mole batch work uses lower end, while scale-up/high-throughput screening may approach the upper end.

    Downstream process integration

    • Employed in directed functionalization or cross-coupling reactions for scaffold diversification
    • Purified by flash chromatography or preparative HPLC for trace impurity removal
    • Documentation of chain of custody for regulatory and patent filing audits
    • SOP-controlled handling in research analytical labs

    Final product types

    • Custom heterocyclic intermediates for biotech research
    • Reference standards for analytical method development
    • Fine chemical libraries for SAR (structure–activity relationship) studies
    • Precursors for dye and pigment molecule synthesis
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    Certification & Compliance
    More Introduction

    Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate: A Manufacturer’s Perspective

    Decades of Practical Know-how in Chemical Synthesis

    Here at the plant, every batch of Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate comes off the line under the eye of experienced staff who have long become familiar with its telltale scent and character. Decades on the floor have shown us that this compound, sometimes referenced by model EMPC-2317 in our own tracking, offers both reliability and appeal across multiple fields in chemical manufacturing. The work isn’t only about producing consistent product, but also about understanding the specific demands that chemists and process engineers bring to their syntheses.

    Specifics That Set the Product Apart

    We prepare Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate with a keen attention to purity and structural confirmation. Standard output runs at 98% minimum purity, GC-verified, and always matches the NMR fingerprint we log for quality assurance. This isn’t a by-product or a “side stream” rescue as sometimes found in the market; these are controlled, purpose-driven batches. One quality that regular customers mention is the ease with which our material dissolves in typical organic solvents—ethyl acetate, dichloromethane, and acetonitrile, to name a few. This allows for straightforward scaling in both R&D bench projects and commercial reactors, a quality rooted in the tight control over moisture and residual solvent levels during the drying stage.

    Understanding Practical Use in Synthesis

    From pharmaceuticals to specialty fine chemicals and agrochemicals, the compound’s value resides in its robust pyrrole skeleton and its carboxylate ester group. Medicinal chemistry customers often aim to use the pyrrole as a precursor in small-molecule construction, especially when seeking compounds that benefit from the methyl group at position five. That methyl offers steric and electronic effects not present in unsubstituted pyrrole esters, which regulars in the lab appreciate when they’re after specific pharmacophore tuning or metabolic stability.

    Agrochemical users lean on its reactivity; the ester group proves quite handy for derivatization. A well-maintained batch of our EMPC-2317 goes straight into processes that require selective alkylation, acylation, or even straightforward hydrolysis when shifting toward the acid derivative. Over the years, we’ve even seen some creative use in dye manufacture, where the slightly electron-rich methyl group imparts subtle changes to absorption spectra once the product gets incorporated into complex rings.

    Reliability from Plant to Project Bench

    Our production workflow doesn’t leave much to luck. Staff keep tabs on temperature, pH, and solvent ratios from charge-in to separation, then log key steps to ensure repeatability. Each drum gets its own batch sheet, and customers occasionally tour the drying and packing rooms to see firsthand the level of detail in documentation and monitoring. This transparency reassures researchers and formulators who can’t afford surprises at scale. Years ago, as our volume began to expand, we took steps to automate several monitoring systems, which led to tighter control ranges for yield and purity—not only allowing us to fill bulk orders but also guaranteeing that the product characteristics stay unchanged year after year.

    Why Not Just Settle for Another Pyrrole Derivative?

    It’s tempting to see ethyl pyrrole-2-carboxylates as all the same, but our repeat interactions with process chemists have taught otherwise. The methyl group at the five position shifts both boiling range and selectivity in common reactions. Take acylation: the presence of the methyl group alters the orientation of incoming substituents, sometimes reducing unwanted by-products in later steps. Formulators in pharma consistently report lower impurity profiles downstream. This attention to molecular detail defines why people keep ordering this specific structure rather than generic pyrrole esters with broader or less predictable effects.

    Down-to-Earth Quality Control: No Mystique, Just Practice

    We don’t view analytical chemistry as paperwork, but as the practical toolkit that lets us confidently stand behind each drum, bottle, or kilogram. Our QC lab keeps reference spectra and chromatograms from every run. This means material refilled six months later matches what left the plant previously—no unwelcome surprises in boiling point spread or IR bands. Staff tell the same story: every shift, routine calibrations and cross-checks reinforce the discipline that high-value sectors expect.

    More than once, we’ve spotted subtle changes in purity when scheduled maintenance slipped on a minor valve or filter housing. Experience says that even minor crude transfer issues or drying anomalies can nudge levels out of spec. By investing in redundancies and hands-on troubleshooting, we limit scrap and rework batches—translating to more confidence for everyone downstream.

    Solving Real-world End-use Challenges

    Pharmaceutical clients often look for reactivity and shelf-life, while others worry about cost or ease of blending. We provide this pyrrole ester with attention to stability—careful exclusion of water and air during storage keeps hydrolysis to a minimum. Shelf studies run in-house show the product maintains specification under normal storage conditions for a year or more, and we’re always open to working with clients to solve special packaging or transport needs.

    As solvents and raw materials shift in the international market, chemists sometimes seek guidance about suitable substitutes in the synthetic routes utilizing our pyrrole derivative. We maintain a technical support line, staffed by team members who know the synthesis steps inside and out, to propose minor tweaks or recommend buffer changes along the route to suit new green chemistry standards or regulatory guidelines. The plant’s real-world bench experience often shortens the time to scale-up—and reduces costly missteps.

    Safety, Regulations, and Realistic Handling Guidance

    Staff at the plant handle every batch according to stringent workplace protocols. Gloves, goggles, and strict inventory tracking remain common sense, not just lines in a procedure manual. Even though EMPC-2317 doesn’t fall under particularly hazardous substance restrictions, we label and store it with the same care as more reactive intermediates. Frequent reviews with safety officers and environmental coordinators target not just waste reduction but also minimizing accidental exposure, spills, or cross-contamination.

    Years in the industry taught us that customers don’t appreciate surprises, whether it’s a drum that sat in a hot warehouse or an unexpected aromatic impurity. We always urge receiving chemists to check the COA and don’t shy from fielding calls about batch anomalies or unexpected test results. Tracebacks occur within hours, drawing on both lot tracking and retained sample testing. It’s part of the commitment to openness that keeps long-standing customers working with us season after season.

    Learning from Customer Feedback

    Most of the real lessons in chemical manufacturing come from customers. The best improvements have come because a process team insisted on ever-tighter water content, or a formulation chemist found a chromatographic tailing peak rare enough to slip under most radars. We have developed both feedback loops and regular discussion calls, often uncovering details that academic papers or regulatory checklists don’t surface.

    Several years ago, a customer in North America highlighted a slightly higher color index in one of our midsize lots. A focused investigation tracked the issue to a slight temperature drift in the final distillation cut. Fixing that not only improved appearance but, as follow-up showed, cut down on trace side-product formation too. These kinds of practical adjustments stick, shaping future batches in ways that documentation alone can’t capture.

    Production Process in Plain Terms

    We synthesize Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate by established routes, reacting carefully controlled methylated pyrrole intermediates under anhydrous conditions. Staff cycle through checklists on batch charges, monitoring the exothermic reactions and carefully timing the esterification and subsequent purification. It’s not automation alone; decades of hands-on oversight ensure each stage progresses as expected. Every operator in the room is qualified and authorized to call a halt if the process strays from the norm, no matter how tight the schedule.

    Some customers ask about green chemistry credentials. We’ve incorporated solvent recovery and modernized our waste streams to cut emissions and overall chemical use, while keeping costs down. Sometimes, raw material shortages push us toward minor process adjustments, but every change runs a full round of validation to confirm that end-user results won’t change. Only production lots that meet specification and customer-supplied method tests move out the warehouse gate.

    Importance of Supply Chain Integrity

    Years of uncertainty in the global chemical trade have taught the manufacturing team a few hard lessons: source transparency and supply-chain backup matter just as much as technical skill. We source key starting materials from audited, reliable suppliers who deliver consistent quality, avoiding the fluctuations or unplanned shutdowns that can ripple through to finished product batches. Regular review of supplier certificates and updated SDS documents keep our approval database current, so we’re not scrambling to adapt if outside conditions shift.

    Since certain international clients now require sharply defined traceability or third-party audit access, our full batch records and retained samples offer more than just legal compliance—they mean peace of mind for every regulatory or QA visitor who steps onto our site.

    Comparisons to Other Pyrrole Ester Products

    Not all pyrrole esters act or perform alike. Our experience says that non-methylated analogues can bring about subtle shifts in synthetic reactivity; labs in both pharmaceutical and agrochemical development confirm that methylation at the five position offers steric protection and altered electron density. This translates directly to differences in side-reactions, yield, and ultimate purity in the hands of skilled chemists.

    We’ve produced other pyrrole esters in parallel, and the learning curve in handling, storage, and even raw material variability has highlighted that not every compound stores equally well or handles residual solvent with the same resilience. Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate, kept tightly sealed and protected from direct sunlight, passes stability checks at a higher rate than some less sterically protected analogues that tend to degrade or discolor on shelf. Practical work shows that scale-up yields stay consistently higher, with less batch-to-batch drift, when sticking with this modified structure.

    Response to Market Pressures

    International price pressures and raw material swings regularly test the manufacturing team’s planning and adaptability. We don’t cut corners to maintain costs, since this would directly undercut the trust built over years of steady supply to technical customers. Instead, we’ve invested in process efficiency—heat recovery systems, better filtration, continuous small-scale distillations—to keep costs reasonable while retaining the technical characteristics that separate our product from cut-rate mass-market alternatives.

    Clients often approach with curiosity about alternative suppliers they’ve found online, usually offering significant price discounts. Experience has shown that these “equivalents” often miss the mark on purity, and rarely hold up under the scrutiny of detailed physical and analytical property checks. By providing a reliable, traceable, and technically responsive product, we avoid the false economy of accepting sub-par quality at a lesser price.

    Building Trust Through Consistency

    Over the years, we’ve seen customers navigate shifting research goals, evolving quality requirements, and market expansion. Through these cycles, the team here has pledged to keep service and technical support grounded in real-time communication, so if a batch issue arises or a new derivatization need crops up, skilled staff can step in rapidly. This culture of accountability comes from the floor level as much as from management; deliver what’s promised, or revisit the approach until it matches.

    Adaptation in a Changing Regulatory and Technical Landscape

    As global standards keep evolving—tightening limits on allowable impurities or restricting certain solvents—our manufacturing group works ahead of the curve by engaging with regulators, QA consultants, and technical consumers. We often perform comparative studies for key clients, feeding back raw data rather than marketing claims, so they can make their own informed choices based on actual use scenarios. That’s how gradual improvements and more rigorous compliance find their way directly into ongoing product lines.

    Local and international compliance isn’t only about keeping documents in a drawer. The team participates in training—updating staff on labeling, documentation, and storage nuances as these get revised. This hands-on commitment means clients get up-to-date product, supported by clear paperwork that matches actual findings in the drums and bottles that leave the warehouse floor.

    Direct Communication and Supporting Ongoing Development

    Small and midsize customers, not just conglomerates, find benefit in direct access to technical manufacturing staff. Whether troubleshooting a tricky synthetic step, handling a scale-up, or simply looking for insight into a slight drift in physical properties, the doors remain open. Our practical advice comes from hands-on experience with both the chemistry and the logistics of shipping, storing, and using this specific compound.

    Not every product variation has made it to commercial scale, but continued feedback and proof-of-concept syntheses—often carried out in the on-site pilot plant—help qualify minor tweaks and potential new derivatives. Sometimes, a simple shift in process parameters encourages a new application or offers a technical edge, and those advantages feed directly back to customers working at the front line of product innovation.

    Why Ethyl 5-Methyl-1H-Pyrrole-2-Carboxylate Continues to Stand Out

    In a sector crowded by resellers, middlemen, and shifting regulatory requirements, the manufacturing team’s experience keeps the focus on what matters: purity, traceability, practical reactivity, and open communication. This compound, built molecule by molecule under the careful eye of practiced staff, continues to fill a clear and present need for specialty chemical and pharmaceutical manufacturers. Instead of generic, mass-produced stock, clients gain the confidence of product born from attentive practice and honest feedback. Years of production and accumulated field reports confirm that there are few shortcuts to consistency, and that quality, communication, and accountability remain irreplaceable.