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2,5-Dimethyl-1-Phenylpyrrole

    • Product Name 2,5-Dimethyl-1-Phenylpyrrole
    • Alias 1-Phenyl-2,5-dimethylpyrrole
    • Einecs 246-951-6
    • 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
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    Specifications

    HS Code

    488496

    Chemical Name 2,5-Dimethyl-1-Phenylpyrrole
    Molecular Formula C12H13N
    Molar Mass 171.24 g/mol
    Cas Number 14679-10-4
    Appearance Pale yellow to brown solid
    Boiling Point 323.7 °C (predicted)
    Melting Point 58-60 °C
    Density 1.08 g/cm³ (estimated)
    Solubility In Water Insoluble
    Structure Type Aromatic heterocycle
    Smiles CC1=CC=C(N1C2=CC=CC=C2)C
    Refractive Index 1.597 (estimated)
    Storage Conditions Store in a cool, dry place
    Synonyms 1-Phenyl-2,5-dimethylpyrrole

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

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle with a secure screw cap, labeled with "2,5-Dimethyl-1-Phenylpyrrole," hazard symbols, and batch details.
    Shipping 2,5-Dimethyl-1-Phenylpyrrole is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with standard chemical safety regulations. The compound is transported as a non-hazardous material via ground or air freight, depending on destination requirements. Appropriate labeling and documentation ensure safe and regulatory-compliant handling throughout transit.
    Storage **2,5-Dimethyl-1-Phenylpyrrole** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store in a suitable, labeled chemical storage cabinet. Ensure proper labeling and use secondary containment to prevent spills or leaks. Follow standard laboratory chemical storage protocols.
    Application of 2,5-Dimethyl-1-Phenylpyrrole

    Applications of 2,5-Dimethyl-1-Phenylpyrrole in Industrial Manufacturing

    2,5-Dimethyl-1-Phenylpyrrole supports multiple high-value downstream chemical manufacturing sectors. Our production integrates with established customer process chains, addressing actual B2B market requirements in legal and industrial settings.

    1. Advanced Organic Pigment Synthesis

    Pigment producers utilize this compound as an intermediate in the synthesis of high-performance pyrrolic colorants. Its reactivity introduces essential methyl and phenyl functionalities in pigment structures, which enhances chromatic intensity and chemical resistance. Our technical teams supply this intermediate for controlled coupling reactions where color shade precision and compound purity remain critical criteria. The material enters premix reactors after aniline or other amine block-formers, allowing custom tuning of final pigment hues through precise stoichiometry adjustments.

    Industry compliance standards

    • REACH Registration (EU)
    • TSCA (USA Chemical Substance Inventory)
    • ISO 9001:2015 Quality Management
    • DIN EN 71-3 Safety Requirements (for colored toy coatings)

    Typical usage ratio

    • Routinely 0.15–0.25 molar equivalents in azo or pyrrole pigment core formation
    • Adjusted by pigment type and desired color yield

    Downstream process integration

    • Charged to condensation reactors post-amination stage
    • Mixed with diazonium salt or similar coupling partners
    • Undergoes controlled-temperature batch synthesis
    • Precipitated pigment filtered, washed, and milled for superior particle uniformity

    Final product types

    • C.I. Pigment Red 254
    • C.I. Pigment Violet 19
    • High-end automotive, coil, and powder coating pigments
    • Industrial grade printing ink dispersions

    2. Pharmaceutical Pyrrole Derivative Production

    Medicinal chemistry sectors use this material as a structural building block for small-molecule APIs in the anti-inflammatory and oncology segments. Its defined substitution pattern is essential for the targeted synthesis of heterocyclic drug candidates, supporting scalable GMP batch processing. The compound enters protected pyrrole formation routes, allowing precise modulation of pharmacologically relevant side chains. Downstream customers blend this intermediate during multi-step syntheses, emphasizing contamination control and reproducible yield.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance
    • Ph. Eur. and USP Monographs (where applicable for intermediates)
    • FDA Drug Master File (DMF) submission integrity
    • GMP traceability with batch recording

    Typical usage ratio

    • 0.9–1.1 equivalents per step, depending on the specific API synthetic route
    • Adjusted according to coupling and protection/deprotection efficiency

    Downstream process integration

    • Utilized post-cyclization in heterocycle segment assembly
    • Enters amidation or acylation step for final API preparation
    • Subject to in-process QC and impurity profiling
    • API extracted and purified for formulation or export

    Final product types

    • Non-steroidal anti-inflammatory pharmaceutical intermediates
    • Experimental pyrrole kinase inhibitors
    • Precursor for anti-cancer heterocyclic scaffolds
    • Veterinary drug fine chemicals

    3. Specialty Conductive Polymer Additive Formulation

    Material scientists employ this pyrrole derivative in the custom synthesis of polypyrrole-based conductive polymers, improving electrical conductivity and stability profiles. In this application, the compound features as a monomer or copolymer feedstock for creating tailored electronic or sensor films. Its methyl and phenyl groups impart desired morphology and processability to the resulting polymer matrix, supporting downstream coating and device manufacturing.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic materials
    • IEC 62321 screening for restricted substances
    • ISO 14001:2015 Environmental Management
    • ISO 10993-5 for device cytotoxicity (if applicable to sensor devices)

    Typical usage ratio

    • 3–7% weight percent in monomer blend for conductive film formation
    • Tunable by film thickness and target resistance

    Downstream process integration

    • Pre-blended with oxidants and dopants in aqueous or solvent suspension
    • Polymerization initiated by electrochemical or chemical oxidization
    • Resulting polymer deposited or cast into films and coatings
    • Post-processed for device integration (curing, lamination, patterning)

    Final product types

    • Conductive polymer coatings for flexible electronics
    • Electrochromic display layer components
    • Printed circuit board (PCB) antistatic layers
    • Chemical sensor active films

    4. Agrochemical Intermediates for Crop Protection Agents

    Formulators in the agrochemical sector use this compound for the production of pyrrole-derived herbicide and fungicide intermediates. Its structural properties support the design of actives with UV stability and soil persistence tailored for modern crop systems. This intermediate is introduced at the pre-final condensation stage, after assembly of primary heterocyclic frameworks, to enable downstream formulation of actives into commercial formulations such as wettable powders and EC concentrates.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for active ingredient synthesis
    • FAO/WHO pesticide specification guidelines
    • ISO 17025 certified analytical validation
    • Regulatory authority registrations (EPA, EU PPP, China Ministry of Agriculture)

    Typical usage ratio

    • 0.2–0.5 parts by weight in final active intermediate synthesis
    • Adjusted for target molecule and environmental field persistence

    Downstream process integration

    • Charged into reactor in the penultimate synthesis step
    • Catalyzed coupling under controlled pH and temperature
    • Intermediate purified and crystallized before formulation
    • Final actives formulated with carriers and adjuvants for market-ready product

    Final product types

    • Pyrrole-based herbicidal actives
    • Fungicidal technical intermediates
    • Synthetic pesticides for field crops
    • Microencapsulated crop protection agents
    Free Quote

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    Certification & Compliance
    More Introduction

    2,5-Dimethyl-1-Phenylpyrrole: An Experienced Manufacturer’s Perspective

    What We’ve Learned Producing 2,5-Dimethyl-1-Phenylpyrrole

    After years of working with pyrrole derivatives, we recognize that not every synthetic route or batch yields the same stability and purity, especially with a compound like 2,5-Dimethyl-1-Phenylpyrrole. Each production run brings its own set of variables, whether it’s the handling of starting materials or the dialing-in of process temperatures. Our daily hands-on experience shapes how we control these factors for a reliable outcome. The differences show up not just in numbers on a certificate of analysis—yield quality in practice matters every bit as much as a tidy spec sheet.

    Core Insights: Characterizing This Compound

    2,5-Dimethyl-1-Phenylpyrrole stands out for its unique substitution pattern on the pyrrole ring. By introducing methyl groups at the 2 and 5 positions and a phenyl group at the 1 position, we see an altered electron distribution compared to unsubstituted pyrrole or even 1-phenylpyrrole without geminal methylation. These core shifts in structure affect how the molecule engages in further transformations, whether it’s coupling chemistry, cyclization, or even medicinal research.

    Our approach avoids shortcuts that can introduce unpredictable side products. We rely on gas chromatography and NMR at each production stage, confirming that ring substitution goes precisely as intended. By consistently monitoring these control points, we see directly just how much even a small impurity shifts downstream application performance. Researchers tell us that material purity makes a real difference to their reaction reproducibility.

    Specifications That Actually Matter in the Lab

    No matter how many times a catalog lists a purity figure, the real proof arrives on the bench—whether the reagent gives clean signals, whether reaction yields fall into place, whether further derivatization works without a hitch. Through direct collaboration with our customers, we’ve seen that assays above 98% (by GC and HPLC) form a solid foundation, but the last trace matters in medicinal and technical R&D. We track residual solvents and minor isomers, because experience tells us that process chemists and formulators want a reagent that won’t deliver surprises.

    Our batches generally offer specific rotation and melting point data, helping with incoming QC and identification. Molecular weight and empirical formula don’t tell the full story unless backed by batch-by-batch transparency. We produce in mid-sized lots, large enough for consistent supply, small enough to let us maintain full oversight over each stage of the vessel. When researchers return for more material that matches the first order, batch consistency proves its value.

    How Application Leads Our Mindset

    2,5-Dimethyl-1-Phenylpyrrole has seen action in diverse settings, from pharmaceutical building blocks to specialty material monomers. Chemists working on heterocyclic scaffolds appreciate this molecule’s reactivity, especially when exploring new ligands or fused ring systems. The dual methyl groups can influence aromaticity and stability, allowing for more predictable outcomes in cross-coupling or annulation strategies.

    Material researchers, especially those exploring organic electronics, value phenylpyrrole backbones for their charge-transport characteristics. In these fields, a trace impurity sometimes casts a long shadow over device efficiency. We have worked alongside academic and industrial partners at these frontiers, so we refine our crystallization and washing processes to remove fine particles and non-volatile residues that could impact both reproducibility and downstream performance.

    Handling Nuances: What We’ve Learned in Practice

    Stability is a recurring theme. Pyrrole derivatives don’t always enjoy long shelf lives; oxidization can darken or degrade the material over time, especially in badly sealed packaging. After years of working with this family, we’ve shifted to nitrogen-purging and triple-sealing methodologies, noticing a substantial difference in storage stability. Over the years, customer feedback looped back to us: storage in amber or opaque containers preserves color and limits decomposition.

    We also know that 2,5-Dimethyl-1-Phenylpyrrole handles better when dry, and exposure to high humidity invites clumping. Our operators keep track during packing and avoid overfilling bags, which has cut down on caking incidents by a noticeable margin. Those hands-on tweaks come from daily practice, not from books or specifications. Safety requires mindfulness; the compound delivers a mild odor, so we protect staff with proper ventilation even though safety limits remain manageable for a lab-scale aromatic heterocycle.

    Differences That Impact the End User

    Placing 2,5-Dimethyl-1-Phenylpyrrole beside similar compounds on the shelf draws certain contrasts. The presence of two methyl groups on the ring affects not only reactivity but solubility and volatility. Chemically, this substitution blocks some classic pyrrole reactivity at those positions, which reduces certain side reactions in extended syntheses. In practice, this can lead to higher selectivity in coupling operations or functionalizations downstream.

    Compared to 1-Phenylpyrrole without the methyl groups, we see a difference in melting point, storage requirements, and the likelihood of color changes during storage. Users pursuing electrophilic substitutions find that the confining effect from the methyls curbs overreaction and lets them achieve sharper selectivity in some syntheses of fused rings or aromatic networks. It also shows improved crystallization in many solvent systems—something formulators mention as a practical advantage.

    Against the parent pyrrole, both chemical behavior and physical properties shift; the molecule’s bulkier, more lipophilic profile translates to better compatibility with some organic phases, and now and then, this offers better solubility in certain solvent systems for process-scale applications. Formulators in paints and coatings, or resin manufacturers, can leverage this when tuning performance attributes in their product lines.

    What Traceability and Authenticity Mean in Daily Production

    Trying to distinguish a manufacturer’s batch from repackaged bulk quickly reveals whether care went into the original synthesis or only into relabeling drums. We track every can and every lot number back to raw material invoices, making it possible for downstream customers to trace process conditions as well as analytical signatures. We keep drum samples for batch reference stretching back years, offering peace of mind for return orders and regulatory audits.

    This detailed traceability builds trust—not because a regulator told us to, but because it has solved problems before they found their way to a customer’s laboratory. Contamination scares or out-of-specification events don’t appear in day-to-day practice if the origins of every precursor go on record in full. We’ve learned that open documentation and clear records save headaches not just for us, but for everyone downstream.

    Continuous Improvement Driven by Real Feedback

    Small-scale users and large-volume buyers alike bring valuable feedback. Academic groups care about batch-to-batch consistency; they want results that stand up to repeat experiments or publications. Industrial researchers worry about scale-up: different kettle sizes or agitation speeds can lead to subtle changes in impurity profiles. From this feedback, we fine-tune our reaction times, temperature ramps, and post-synthesis purification, testing changes in our pilot line before rolling them out widely.

    As process chemistry changes, environmental controls and regulatory expectations evolve. We work with greener solvents where the chemistry supports it, keeping both efficiency and worker safety in mind. Over time, many of our most robust improvements came not from top-down management, but from our floor operators spotting ways to simplify clean-in-place routines or shorten cooling times, cutting down both waste and turnaround time.

    Supply Chain in Practice: Why Source Directly from the Manufacturer

    Direct buyers avoid supply uncertainty. As the original producer, we control the drum from the vessel to the truck dock, adapting lead times during raw material shortages or ramping up output if a sudden surge in demand arrives. Weather, customs delays, or force majeure may not always stay predictable, but having visibility into actual inventory and on-site lab capability means we can communicate realistic timelines.

    Buyers know what they’re getting. We have control over every kilogram and know exactly which lot gives which analytical profile. If researchers spot an issue—unexpected byproducts, unusual color, or changes in crystallization—we look at the original synthesis protocol and data records directly, without guessing which third party packaged or blended the batch. This responsiveness supports time-sensitive R&D and helps avoid both wasted man-hours and scrap costs.

    Current Industry Demands and Market Direction

    The demand for pyrrole derivatives shifts year by year as application research matures. Lately, more of our requests come from research into drug-like molecules, bioactive heterocycles, and conductive polymer backbones. With designers of next-generation OLEDs or organic field-effect transistors exploring new chemistries, the purity and batch origin of specialty monomers like 2,5-Dimethyl-1-Phenylpyrrole matter more. The high specificity of these industries puts pressure on all suppliers to reduce minor contaminants, keep solvent residue undetectable, and deliver crystal material that meets both bench and pilot plant standards.

    Regulators also examine specialty organic intermediates more closely. That means tighter scrutiny of both process history and compliance paperwork. Our compliance department works continuously with up-to-date material safety data, and our technical team answers regulatory questions fielded by customers working across borders. Not every batch triggers the same set of questions, but we’ve learned which records are most critical for export, and which documentation helps our buyers pass their own audits without delay.

    Challenges and Real-World Solutions

    Every synthesis has a lesson to teach, whether it’s from a product spill, an analytical error, or a packaging mishap. Through hands-on work, we’ve learned to run regular root cause reviews after any out-of-spec event. After several lessons learned, we set up a second check for every drum weight and label at the packing line, not relying on line workers’ memory under time pressure. After scattered complaints about changes in product moisture and flow, we changed our storage and packing workflow, keeping material in a humidity-controlled space from synthesis through shipment. These concrete adjustments reduced error rates and minimized end-user problems, supporting demand for ever-consistent material.

    We maintain a built-in feedback loop—lab, production, and logistics teams review both routine shipments and any nonconformance. It’s not just about problem response; it’s about preemptive shifts that stave off future complications. Robust communication between teams leads to shorter investigation times and greater accountability up and down the supply chain.

    Unpacking the Real Value: Expertise, Not Just Molecules

    Chemical manufacturing at this specialty level comes down to trust and experience. We don’t see ourselves as just vendors; our goal is to solve problems, streamline syntheses, and open the door to new applications for our clients. Real expertise doesn’t come from repeating spec sheets—it’s built on thousands of hours spent tracking, tuning, and refining each step of production. Customers return not just for the molecule but for the reliability and the real-world backing that stand behind every batch.

    It is through accumulated experience—born of both successes and missteps—that we continue improving our offering of 2,5-Dimethyl-1-Phenylpyrrole. Whether your work takes the form of exploring uncharted chemical space or achieving the same benchmark results every week, having a manufacturer who understands the practical realities of this compound can make a tangible difference.

    Closing Thoughts on the State of Specialty Pyrroles

    We take pride in our continuous relationship with the chemical development community. Over the years, through evolving techniques and closer partnerships, we have seen dramatic improvements in quality, reproducibility, and support surrounding our 2,5-Dimethyl-1-Phenylpyrrole. Familiarity with the compound’s quirks—whether in reaction vessel design, in stability over time, or in the day-to-day needs of researchers and formulators—lets us adapt to changing market needs without compromising on the fundamentals that distinguish a genuine manufacturer from a passing trader.

    We recognize that every customer wants to minimize uncertainty and maximize successful outcomes. Our ongoing efforts in analytical transparency, storage practices, and direct communication keep us prepared to serve new projects as well as established production runs. Experience tells us that the difference between good and great chemical supply isn’t only the number on a certificate—it’s everything that goes into getting that number, and everything that follows when questions or challenges arise. For anyone considering the next research step or scale-up, the route always runs smoother with a manufacturer who knows the material inside and out.